---
OA_place: repository
OA_type: green
_id: '18748'
abstract:
- lang: eng
  text: "We present models for dusty high–redshift Lyα emitting galaxies by combining
    the Press–Schechter formalism with a treatment of inhomogeneous dust distribution
    inside galaxies. These models reproduce the surface density of emitters inferred
    from recent observations, and also agree with previous non–detections. Although
    a detailed determination of the individual model parameters is precluded by uncertainties,
    we find that (i) the dust content of primordial galaxies builds up in no more
    than ∼ 5 × 10^8 yr, (ii) the galactic HII regions are nhomogeneous with a cloud
    covering factor of order unity, and (iii) the overall star formation efficiency
    is at least ∼ 5%. Future observations should be able to detect Lyα galaxies upto
    redshifts of z ∼ 8. If\r\nthe universe is reionized at zr ∼< 8, the corresponding
    decline in the number of Lyα\r\nemitters at z ∼> zr could prove to be a useful
    probe of the reionization epoch.\r\n"
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Zoltán
  full_name: Haiman, Zoltán
  id: 7c006e8c-cc0d-11ee-8322-cb904ef76f36
  last_name: Haiman
  orcid: 0000-0003-3633-5403
- first_name: M.
  full_name: Spaans, M.
  last_name: Spaans
citation:
  ama: Haiman Z, Spaans M. Models for high-redshift Lyα emitters. <i>AIP Conference
    Proceedings</i>. 1999;470(1):63-67. doi:<a href="https://doi.org/10.1063/1.58635">10.1063/1.58635</a>
  apa: 'Haiman, Z., &#38; Spaans, M. (1999). Models for high-redshift Lyα emitters.
    <i>AIP Conference Proceedings</i>. College Park, MD, United States: AIP Publishing.
    <a href="https://doi.org/10.1063/1.58635">https://doi.org/10.1063/1.58635</a>'
  chicago: Haiman, Zoltán, and M. Spaans. “Models for High-Redshift Lyα Emitters.”
    <i>AIP Conference Proceedings</i>. AIP Publishing, 1999. <a href="https://doi.org/10.1063/1.58635">https://doi.org/10.1063/1.58635</a>.
  ieee: Z. Haiman and M. Spaans, “Models for high-redshift Lyα emitters,” <i>AIP Conference
    Proceedings</i>, vol. 470, no. 1. AIP Publishing, pp. 63–67, 1999.
  ista: Haiman Z, Spaans M. 1999. Models for high-redshift Lyα emitters. AIP Conference
    Proceedings. 470(1), 63–67.
  mla: Haiman, Zoltán, and M. Spaans. “Models for High-Redshift Lyα Emitters.” <i>AIP
    Conference Proceedings</i>, vol. 470, no. 1, AIP Publishing, 1999, pp. 63–67,
    doi:<a href="https://doi.org/10.1063/1.58635">10.1063/1.58635</a>.
  short: Z. Haiman, M. Spaans, AIP Conference Proceedings 470 (1999) 63–67.
conference:
  end_date: 1998-10-14
  location: College Park, MD, United States
  start_date: 1998-10-12
date_created: 2025-01-03T12:37:12Z
date_published: 1999-04-27T00:00:00Z
date_updated: 2025-01-07T14:26:07Z
day: '27'
doi: 10.1063/1.58635
extern: '1'
external_id:
  arxiv:
  - astro-ph/9811396
intvolume: '       470'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/astro-ph/9811396
month: '04'
oa: 1
oa_version: Preprint
page: 63-67
publication: AIP Conference Proceedings
publication_status: published
publisher: AIP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Models for high-redshift Lyα emitters
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 470
year: '1999'
...
---
OA_place: repository
OA_type: green
_id: '18750'
abstract:
- lang: eng
  text: Empirical studies of the first generation of stars and quasars in the Universe
    will likely become feasible over the next decade. The Next Generation Space Telescope
    will provide direct imaging and photometry of sub-galactic objects at (math formular)
    while microwave anisotropy experiments, such as MAP or Planck, will set constraints
    on the ionization history of the intergalactic medium due to these sources. We
    describe the expected signals that will be detectable with these future instruments.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Zoltán
  full_name: Haiman, Zoltán
  id: 7c006e8c-cc0d-11ee-8322-cb904ef76f36
  last_name: Haiman
  orcid: 0000-0003-3633-5403
- first_name: A.
  full_name: Loeb, A.
  last_name: Loeb
citation:
  ama: Haiman Z, Loeb A. Empirical constraints on the first stars and quasars. <i>AIP
    Conference Proceedings</i>. 1999;470(1):34-47. doi:<a href="https://doi.org/10.1063/1.58620">10.1063/1.58620</a>
  apa: Haiman, Z., &#38; Loeb, A. (1999). Empirical constraints on the first stars
    and quasars. <i>AIP Conference Proceedings</i>. AIP Publishing. <a href="https://doi.org/10.1063/1.58620">https://doi.org/10.1063/1.58620</a>
  chicago: Haiman, Zoltán, and A. Loeb. “Empirical Constraints on the First Stars
    and Quasars.” <i>AIP Conference Proceedings</i>. AIP Publishing, 1999. <a href="https://doi.org/10.1063/1.58620">https://doi.org/10.1063/1.58620</a>.
  ieee: Z. Haiman and A. Loeb, “Empirical constraints on the first stars and quasars,”
    <i>AIP Conference Proceedings</i>, vol. 470, no. 1. AIP Publishing, pp. 34–47,
    1999.
  ista: Haiman Z, Loeb A. 1999. Empirical constraints on the first stars and quasars.
    AIP Conference Proceedings. 470(1), 34–47.
  mla: Haiman, Zoltán, and A. Loeb. “Empirical Constraints on the First Stars and
    Quasars.” <i>AIP Conference Proceedings</i>, vol. 470, no. 1, AIP Publishing,
    1999, pp. 34–47, doi:<a href="https://doi.org/10.1063/1.58620">10.1063/1.58620</a>.
  short: Z. Haiman, A. Loeb, AIP Conference Proceedings 470 (1999) 34–47.
date_created: 2025-01-03T12:38:26Z
date_published: 1999-04-27T00:00:00Z
date_updated: 2025-01-07T14:30:28Z
day: '27'
doi: 10.1063/1.58620
extern: '1'
external_id:
  arxiv:
  - astro-ph/9811395
intvolume: '       470'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/astro-ph/9811395
month: '04'
oa: 1
oa_version: Preprint
page: 34-47
publication: AIP Conference Proceedings
publication_status: published
publisher: AIP Publishing
quality_controlled: '1'
scopus_import: '1'
status: public
title: Empirical constraints on the first stars and quasars
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 470
year: '1999'
...
---
_id: '2592'
abstract:
- lang: eng
  text: Metabotropic glutamate receptors (mGluRs) consist of eight different subtypes
    and exert their effects or second messengers and ion channels via G- proteins.
    The function of individual mGluR subtypes in the CNS, however, largely remains
    to be clarified. We examined the fear response of freezing after electric shock
    in wild-type and mGluR7(-/-) knockout littermates. Wild- type mice displayed freezing
    immediately after and 1 d after footshock. In comparison, mGluR7(-/-) knockout
    mice showed significantly reduced levels in both immediate postshock and delayed
    freezing responses. However, the knockout mice exhibited no abnormalities in pain
    sensitivity and locomotor activity. To further examine amygdala-dependent behavior,
    we performed conditioned taste aversion (CTA) experiments. In wild-type mice,
    the administration of saccharin followed by intraperitoneal injection of the malaise-inducing
    agent LiCl resulted in an association between saccharin and LiCl. This association
    caused strong CTA toward saccharin n contrast, mGluR7(-/-) knockout mice failed
    to associate between the taste and the negative reinforcer in CTA experiments.
    Again, the knockout mice showed no abnormalities in taste preference and in the
    sensitivity to LiCl toxicity. These results indicate that mGluR7 deficiency causes
    an impairment of two distinct amygdala-dependent behavioral paradigms. Immunohistochemical
    and immunoelectron-microscopic analyses showed that mGluR7 is highly expressed
    in amygdala and preferentially localized at the presynaptic axon terminals of
    glutamatergic neurons. Together, these findings strongly suggest that mGluR7 is
    involved in neural processes subserving amygdala-dependent averse responses.
acknowledgement: This work was supported in part by research grants from the Ministry
  of Education, Science and Culture of Japan, the Ministry of Health and Welfare of
  Japan, the Sankyo Foundation, the Yamanouchi Foundation, and the Biomolecular Engineering
  Research Institute. We thank Takashi Yamamoto for advice on CTA experiments, Fumitaka
  Ushikubi for advice on the nociception test, Markus Schroeder for back-crossing
  of mutant mice, Ayae Kinoshita for the kind gift of antibodies, Akira Uesugi for
  photography, and Kumlesh K. Dev for careful reading of this manuscript.
article_processing_charge: No
article_type: original
author:
- first_name: Miwako
  full_name: Masugi, Miwako
  last_name: Masugi
- first_name: Mineto
  full_name: Yokoi, Mineto
  last_name: Yokoi
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Keiko
  full_name: Muguruma, Keiko
  last_name: Muguruma
- first_name: Yasuyoshi
  full_name: Watanabe, Yasuyoshi
  last_name: Watanabe
- first_name: Gilles
  full_name: Sansig, Gilles
  last_name: Sansig
- first_name: Herman
  full_name: Van Der Putten, Herman
  last_name: Van Der Putten
- first_name: Shigetada
  full_name: Nakanishi, Shigetada
  last_name: Nakanishi
citation:
  ama: Masugi M, Yokoi M, Shigemoto R, et al. Metabotropic glutamate receptor subtype
    7 ablation causes deficit in fear response and conditioned taste aversion. <i>Journal
    of Neuroscience</i>. 1999;19(3):955-963. doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-03-00955.1999">10.1523/JNEUROSCI.19-03-00955.1999</a>
  apa: Masugi, M., Yokoi, M., Shigemoto, R., Muguruma, K., Watanabe, Y., Sansig, G.,
    … Nakanishi, S. (1999). Metabotropic glutamate receptor subtype 7 ablation causes
    deficit in fear response and conditioned taste aversion. <i>Journal of Neuroscience</i>.
    Society for Neuroscience. <a href="https://doi.org/10.1523/JNEUROSCI.19-03-00955.1999">https://doi.org/10.1523/JNEUROSCI.19-03-00955.1999</a>
  chicago: Masugi, Miwako, Mineto Yokoi, Ryuichi Shigemoto, Keiko Muguruma, Yasuyoshi
    Watanabe, Gilles Sansig, Herman Van Der Putten, and Shigetada Nakanishi. “Metabotropic
    Glutamate Receptor Subtype 7 Ablation Causes Deficit in Fear Response and Conditioned
    Taste Aversion.” <i>Journal of Neuroscience</i>. Society for Neuroscience, 1999.
    <a href="https://doi.org/10.1523/JNEUROSCI.19-03-00955.1999">https://doi.org/10.1523/JNEUROSCI.19-03-00955.1999</a>.
  ieee: M. Masugi <i>et al.</i>, “Metabotropic glutamate receptor subtype 7 ablation
    causes deficit in fear response and conditioned taste aversion,” <i>Journal of
    Neuroscience</i>, vol. 19, no. 3. Society for Neuroscience, pp. 955–963, 1999.
  ista: Masugi M, Yokoi M, Shigemoto R, Muguruma K, Watanabe Y, Sansig G, Van Der
    Putten H, Nakanishi S. 1999. Metabotropic glutamate receptor subtype 7 ablation
    causes deficit in fear response and conditioned taste aversion. Journal of Neuroscience.
    19(3), 955–963.
  mla: Masugi, Miwako, et al. “Metabotropic Glutamate Receptor Subtype 7 Ablation
    Causes Deficit in Fear Response and Conditioned Taste Aversion.” <i>Journal of
    Neuroscience</i>, vol. 19, no. 3, Society for Neuroscience, 1999, pp. 955–63,
    doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-03-00955.1999">10.1523/JNEUROSCI.19-03-00955.1999</a>.
  short: M. Masugi, M. Yokoi, R. Shigemoto, K. Muguruma, Y. Watanabe, G. Sansig, H.
    Van Der Putten, S. Nakanishi, Journal of Neuroscience 19 (1999) 955–963.
date_created: 2018-12-11T11:58:33Z
date_published: 1999-02-01T00:00:00Z
date_updated: 2023-03-27T10:00:42Z
day: '01'
doi: 10.1523/JNEUROSCI.19-03-00955.1999
extern: '1'
external_id:
  pmid:
  - '9920659'
intvolume: '        19'
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782134/
month: '02'
oa: 1
oa_version: Published Version
page: 955 - 963
pmid: 1
publication: Journal of Neuroscience
publication_identifier:
  issn:
  - 0270-6474
publication_status: published
publisher: Society for Neuroscience
publist_id: '4306'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Metabotropic glutamate receptor subtype 7 ablation causes deficit in fear response
  and conditioned taste aversion
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 19
year: '1999'
...
---
_id: '2593'
abstract:
- lang: eng
  text: In cat and monkey, lamina I cells can be classified into three basic morphological
    types (fusiform, pyramidal, and multipolar), and recent intracellular labeling
    evidence in the cat indicates that fusiform and multipolar lamina I cells are
    two different types of nociceptive cells, whereas pyramidal cells are innocuous
    thermoreceptive-specific. Because earlier observations indicated that only nociceptive
    dorsal horn neurons respond to substance P (SP), we examined which morphological
    types of lamina I neurons express receptors for SP (NK-1r). We categorized NK-1r-
    immunoreactive (IR) lamina I neurons in serial horizontal sections from the cervical
    and lumbar enlargements of four monkeys. Consistent results were obtained by two
    independent teams of observers. Nearly all NK-1r-IR cells were fusiform (42%)
    or multipolar (43%), but only 6% were pyramidal (with 9% unclassified). We obtained
    similar findings in three monkeys in which we used double-labeling immunocytochemistry
    to identify NK-1r-IR and spinothalamic lamina I neurons retrogradely labeled with
    cholera toxin subunit b from the thalamus; most NK-1r-IR lamina I spinothalamic
    neurons were fusiform (48%) or multipolar (33%), and only 10% were pyramidal.
    In contrast, most (~75%) pyramidal and some (~25%) fusiform and multipolar lamina
    I spinothalamic neurons did not display NK-1r immunoreactivity. These data indicate
    that most fusiform and multipolar lamina I neurons in the monkey can express NK-1r,
    consistent with the idea that both types are nociceptive, whereas only a small
    proportion of lamina I pyramidal cells express this receptor, consistent with
    the previous finding that they are nonnociceptive. However, these findings also
    indicate that not all nociceptive lamina I neurons express receptors for SP.
acknowledgement: This study was supported by National Institute of Health Grants NS
  34022 to Y.D.K. and NS 25616 to A.D.C., by Canadian Medical Research Council (MRC)
  Grants MT 12942 to Y.D.K. and MT 12170 to A.R.S., and by the Barrow Neurological
  Foundation. Y.D.K. is a Scholar of the Canadian MRC. We thank A. Constantin and
  A. Forster for expert technical assistance and Dr. M. Wikstrom for generously supplying
  monoclonal antibodies against CTb.
article_processing_charge: No
article_type: original
author:
- first_name: Xiao
  full_name: Yu, Xiao
  last_name: Yu
- first_name: En
  full_name: Zhang, En
  last_name: Zhang
- first_name: Arthur
  full_name: Craig, Arthur
  last_name: Craig
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Alfredo
  full_name: Ribeiro Da Silva, Alfredo
  last_name: Ribeiro Da Silva
- first_name: Yves
  full_name: De Koninck, Yves
  last_name: De Koninck
citation:
  ama: Yu X, Zhang E, Craig A, Shigemoto R, Ribeiro Da Silva A, De Koninck Y. NK-1
    receptor immunoreactivity in distinct morphological types of lamina I neurons
    of the primate spinal cord. <i>Journal of Neuroscience</i>. 1999;19(9):3545-3555.
    doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-09-03545.1999">10.1523/JNEUROSCI.19-09-03545.1999</a>
  apa: Yu, X., Zhang, E., Craig, A., Shigemoto, R., Ribeiro Da Silva, A., &#38; De
    Koninck, Y. (1999). NK-1 receptor immunoreactivity in distinct morphological types
    of lamina I neurons of the primate spinal cord. <i>Journal of Neuroscience</i>.
    Society for Neuroscience. <a href="https://doi.org/10.1523/JNEUROSCI.19-09-03545.1999">https://doi.org/10.1523/JNEUROSCI.19-09-03545.1999</a>
  chicago: Yu, Xiao, En Zhang, Arthur Craig, Ryuichi Shigemoto, Alfredo Ribeiro Da
    Silva, and Yves De Koninck. “NK-1 Receptor Immunoreactivity in Distinct Morphological
    Types of Lamina I Neurons of the Primate Spinal Cord.” <i>Journal of Neuroscience</i>.
    Society for Neuroscience, 1999. <a href="https://doi.org/10.1523/JNEUROSCI.19-09-03545.1999">https://doi.org/10.1523/JNEUROSCI.19-09-03545.1999</a>.
  ieee: X. Yu, E. Zhang, A. Craig, R. Shigemoto, A. Ribeiro Da Silva, and Y. De Koninck,
    “NK-1 receptor immunoreactivity in distinct morphological types of lamina I neurons
    of the primate spinal cord,” <i>Journal of Neuroscience</i>, vol. 19, no. 9. Society
    for Neuroscience, pp. 3545–3555, 1999.
  ista: Yu X, Zhang E, Craig A, Shigemoto R, Ribeiro Da Silva A, De Koninck Y. 1999.
    NK-1 receptor immunoreactivity in distinct morphological types of lamina I neurons
    of the primate spinal cord. Journal of Neuroscience. 19(9), 3545–3555.
  mla: Yu, Xiao, et al. “NK-1 Receptor Immunoreactivity in Distinct Morphological
    Types of Lamina I Neurons of the Primate Spinal Cord.” <i>Journal of Neuroscience</i>,
    vol. 19, no. 9, Society for Neuroscience, 1999, pp. 3545–55, doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-09-03545.1999">10.1523/JNEUROSCI.19-09-03545.1999</a>.
  short: X. Yu, E. Zhang, A. Craig, R. Shigemoto, A. Ribeiro Da Silva, Y. De Koninck,
    Journal of Neuroscience 19 (1999) 3545–3555.
date_created: 2018-12-11T11:58:34Z
date_published: 1999-05-01T00:00:00Z
date_updated: 2023-03-27T09:54:40Z
day: '01'
doi: 10.1523/JNEUROSCI.19-09-03545.1999
extern: '1'
external_id:
  pmid:
  - '10212314'
intvolume: '        19'
issue: '9'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782224/
month: '05'
oa: 1
oa_version: None
page: 3545 - 3555
pmid: 1
publication: Journal of Neuroscience
publication_identifier:
  issn:
  - 0270-6474
publication_status: published
publisher: Society for Neuroscience
publist_id: '4305'
quality_controlled: '1'
scopus_import: '1'
status: public
title: NK-1 receptor immunoreactivity in distinct morphological types of lamina I
  neurons of the primate spinal cord
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 19
year: '1999'
...
---
_id: '3444'
abstract:
- lang: eng
  text: This study examined intermittent, high-frequency (100-200 Hz) oscillatory
    patterns in the CA1 region of the hippocampus in the absence of theta activity,
    i.e., during and in between sharp wave (SPW) bursts. Pyramidal and interneuronal
    activity was phase-locked not only to large amplitude (&gt;7 SD from baseline)
    oscillatory events, which are present mainly during SPWs, but to smaller amplitude
    (&lt;4 SD) patterns, as well. Large-amplitude events were in the 140-200 Hz, &quot;ripple&quot;
    frequency range. Lower-amplitude events, however, contained slower, 100-130 Hz
    (&quot;slow&quot;) oscillatory patterns. Fast ripple waves reversed just below
    the CA1 pyramidal layer, whereas slow oscillatory potentials reversed in the stratum
    radiatum and/or in the stratum oriens. Parallel CA1-CA3 recordings revealed correlated
    CA3 field and unit activity to the slow CA1 waves but not to fast ripple waves.
    These findings suggest that fast ripples emerge in the CA1 region, whereas slow
    (100-130 Hz) oscillatory patterns are generated in the CA3 region and transferred
    to the CA1 field.
article_processing_charge: No
article_type: original
author:
- first_name: Jozsef L
  full_name: Csicsvari, Jozsef L
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
- first_name: Hajima
  full_name: Hirase, Hajima
  last_name: Hirase
- first_name: András
  full_name: Czurkó, András
  last_name: Czurkó
- first_name: Akira
  full_name: Mamiya, Akira
  last_name: Mamiya
- first_name: György
  full_name: Buzsáki, György
  last_name: Buzsáki
citation:
  ama: Csicsvari JL, Hirase H, Czurkó A, Mamiya A, Buzsáki G. Fast  network  oscillations 
    in the  hippocampal  CA1 region of the behaving rat. <i>Journal of Neuroscience</i>.
    1999;19(16). doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-16-j0001.1999">10.1523/JNEUROSCI.19-16-j0001.1999</a>
  apa: Csicsvari, J. L., Hirase, H., Czurkó, A., Mamiya, A., &#38; Buzsáki, G. (1999).
    Fast  network  oscillations  in the  hippocampal  CA1 region of the behaving rat.
    <i>Journal of Neuroscience</i>. Society for Neuroscience. <a href="https://doi.org/10.1523/JNEUROSCI.19-16-j0001.1999">https://doi.org/10.1523/JNEUROSCI.19-16-j0001.1999</a>
  chicago: Csicsvari, Jozsef L, Hajima Hirase, András Czurkó, Akira Mamiya, and György
    Buzsáki. “Fast  Network  Oscillations  in the  Hippocampal  CA1 Region of the
    Behaving Rat.” <i>Journal of Neuroscience</i>. Society for Neuroscience, 1999.
    <a href="https://doi.org/10.1523/JNEUROSCI.19-16-j0001.1999">https://doi.org/10.1523/JNEUROSCI.19-16-j0001.1999</a>.
  ieee: J. L. Csicsvari, H. Hirase, A. Czurkó, A. Mamiya, and G. Buzsáki, “Fast  network 
    oscillations  in the  hippocampal  CA1 region of the behaving rat,” <i>Journal
    of Neuroscience</i>, vol. 19, no. 16. Society for Neuroscience, 1999.
  ista: Csicsvari JL, Hirase H, Czurkó A, Mamiya A, Buzsáki G. 1999. Fast  network 
    oscillations  in the  hippocampal  CA1 region of the behaving rat. Journal of
    Neuroscience. 19(16).
  mla: Csicsvari, Jozsef L., et al. “Fast  Network  Oscillations  in the  Hippocampal 
    CA1 Region of the Behaving Rat.” <i>Journal of Neuroscience</i>, vol. 19, no.
    16, Society for Neuroscience, 1999, doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-16-j0001.1999">10.1523/JNEUROSCI.19-16-j0001.1999</a>.
  short: J.L. Csicsvari, H. Hirase, A. Czurkó, A. Mamiya, G. Buzsáki, Journal of Neuroscience
    19 (1999).
date_created: 2018-12-11T12:03:22Z
date_published: 1999-08-15T00:00:00Z
date_updated: 2022-09-07T13:41:18Z
day: '15'
doi: 10.1523/JNEUROSCI.19-16-j0001.1999
extern: '1'
external_id:
  pmid:
  - '10436076'
intvolume: '        19'
issue: '16'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782850/
month: '08'
oa: 1
oa_version: Published Version
pmid: 1
publication: Journal of Neuroscience
publication_identifier:
  issn:
  - 0270-6474
publication_status: published
publisher: Society for Neuroscience
publist_id: '2943'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Fast  network  oscillations  in the  hippocampal  CA1 region of the behaving
  rat
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 19
year: '1999'
...
---
_id: '3445'
abstract:
- lang: eng
  text: The medial septal region and the hippocampus are connected reciprocally via
    GABAergic neurons, but the physiological role of this loop is still not well understood.
    In an attempt to reveal the physiological effects of the hippocamposeptal GABAergic
    projection, we cross-correlated hippocampal sharp wave (SPW) ripples or theta
    activity and extracellular units recorded in the medial septum and diagonal band
    of Broca (MSDB) in freely moving rats. The majority of single MSDB cells (60%)
    were significantly suppressed during SPWs. Most cells inhibited during SPW (80%)
    fired rhythmically and phase-locked to the negative peak of the CA1 pyramidal
    layer theta waves. Because both SPW and the negative peak of local theta waves
    correspond to the maximum discharge probability of CA1 pyramidal cells and interneuron
    classes, the findings indicate that the activity of medial septal neurons can
    be negatively (during SPW) or positively (during theta waves) correlated with
    the activity of hippocampal interneurons. We hypothesize that the functional coupling
    between medial septal neurons and hippocampal interneurons varies in a state-dependent
    manner.
acknowledgement: This work was supported by National Institutes of Health Grants NS34994
  and MH54671. We thank Z. Borhegyi, H. Hirase, C. King, and Z. Nadásdy for help and
  support and T. F. Freund for his comments on this manuscript.
article_processing_charge: No
article_type: original
author:
- first_name: George
  full_name: Dragoi, George
  last_name: Dragoi
- first_name: Daniel
  full_name: Carpi, Daniel
  last_name: Carpi
- first_name: Michael
  full_name: Recce, Michael
  last_name: Recce
- first_name: Jozsef L
  full_name: Csicsvari, Jozsef L
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
- first_name: György
  full_name: Buzsáki, György
  last_name: Buzsáki
citation:
  ama: Dragoi G, Carpi D, Recce M, Csicsvari JL, Buzsáki G. Interactions between hippocampus
    and medial septum during sharp waves and theta oscillation in the behaving rat.
    <i>Journal of Neuroscience</i>. 1999;19(14):6191-6199. doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-14-06191.1999">10.1523/JNEUROSCI.19-14-06191.1999</a>
  apa: Dragoi, G., Carpi, D., Recce, M., Csicsvari, J. L., &#38; Buzsáki, G. (1999).
    Interactions between hippocampus and medial septum during sharp waves and theta
    oscillation in the behaving rat. <i>Journal of Neuroscience</i>. Society for Neuroscience.
    <a href="https://doi.org/10.1523/JNEUROSCI.19-14-06191.1999">https://doi.org/10.1523/JNEUROSCI.19-14-06191.1999</a>
  chicago: Dragoi, George, Daniel Carpi, Michael Recce, Jozsef L Csicsvari, and György
    Buzsáki. “Interactions between Hippocampus and Medial Septum during Sharp Waves
    and Theta Oscillation in the Behaving Rat.” <i>Journal of Neuroscience</i>. Society
    for Neuroscience, 1999. <a href="https://doi.org/10.1523/JNEUROSCI.19-14-06191.1999">https://doi.org/10.1523/JNEUROSCI.19-14-06191.1999</a>.
  ieee: G. Dragoi, D. Carpi, M. Recce, J. L. Csicsvari, and G. Buzsáki, “Interactions
    between hippocampus and medial septum during sharp waves and theta oscillation
    in the behaving rat,” <i>Journal of Neuroscience</i>, vol. 19, no. 14. Society
    for Neuroscience, pp. 6191–6199, 1999.
  ista: Dragoi G, Carpi D, Recce M, Csicsvari JL, Buzsáki G. 1999. Interactions between
    hippocampus and medial septum during sharp waves and theta oscillation in the
    behaving rat. Journal of Neuroscience. 19(14), 6191–6199.
  mla: Dragoi, George, et al. “Interactions between Hippocampus and Medial Septum
    during Sharp Waves and Theta Oscillation in the Behaving Rat.” <i>Journal of Neuroscience</i>,
    vol. 19, no. 14, Society for Neuroscience, 1999, pp. 6191–99, doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-14-06191.1999">10.1523/JNEUROSCI.19-14-06191.1999</a>.
  short: G. Dragoi, D. Carpi, M. Recce, J.L. Csicsvari, G. Buzsáki, Journal of Neuroscience
    19 (1999) 6191–6199.
date_created: 2018-12-11T12:03:22Z
date_published: 1999-07-15T00:00:00Z
date_updated: 2022-09-07T13:37:41Z
day: '15'
doi: 10.1523/JNEUROSCI.19-14-06191.1999
extern: '1'
external_id:
  pmid:
  - '10407055'
intvolume: '        19'
issue: '14'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783073/
month: '07'
oa: 1
oa_version: Published Version
page: 6191 - 6199
pmid: 1
publication: Journal of Neuroscience
publication_identifier:
  issn:
  - 0270-6474
publication_status: published
publisher: Society for Neuroscience
publist_id: '2942'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Interactions between hippocampus and medial septum during sharp waves and theta
  oscillation in the behaving rat
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 19
year: '1999'
...
---
_id: '3518'
abstract:
- lang: eng
  text: Information in neuronal networks may be represented by the spatiotemporal
    patterns of spikes. Here we examined the temporal coordination of pyramidal cell
    spikes in the rat hippocampus during slow-wave sleep. In addition, rats were trained
    to run in a defined position in space (running wheel) to activate a selected group
    of pyramidal cells. A template-matching method and a joint probability map method
    were used for sequence search. Repeating spike sequences in excess of chance occurrence
    were examined by comparing the number of repeating sequences in the original spike
    trains and in surrogate trains after Monte Carlo shuffling of the spikes. Four
    different shuffling procedures were used to control for the population dynamics
    of hippocampal neurons. Repeating spike sequences in the recorded cell assemblies
    were present in both the awake and sleeping animal in excess of what might be
    predicted by random variations. Spike sequences observed during wheel running
    were “replayed” at a faster timescale during single sharp-wave bursts of slow-wave
    sleep. We hypothesize that the endogenously expressed spike sequences during sleep
    reflect reactivation of the circuitry modified by previous experience. Reactivation
    of acquired sequences may serve to consolidate information.
acknowledgement: This work was supported by National Institutes of Health Grants NS34994
  and MH54671 and by the Human Science Frontier Program. We thank Moshe Abeles, Michale
  Fee, Stuart Geman, Stephen Hanson, Darrell Henze, Günther Palm, Michael Recce, and
  Matthew Wilson for their suggestions with data analysis and comments on this manuscript.
article_processing_charge: No
article_type: original
author:
- first_name: Zoltán
  full_name: Nádasdy, Zoltán
  last_name: Nádasdy
- first_name: Hajima
  full_name: Hirase, Hajima
  last_name: Hirase
- first_name: András
  full_name: Czurkó, András
  last_name: Czurkó
- first_name: Jozsef L
  full_name: Csicsvari, Jozsef L
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
- first_name: György
  full_name: Buzsáki, György
  last_name: Buzsáki
citation:
  ama: Nádasdy Z, Hirase H, Czurkó A, Csicsvari JL, Buzsáki G. Replay and time compression
    of recurring spike sequences in the hippocampus. <i>Journal of Neuroscience</i>.
    1999;19(21):9497-9507. doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-21-09497.1999">10.1523/JNEUROSCI.19-21-09497.1999</a>
  apa: Nádasdy, Z., Hirase, H., Czurkó, A., Csicsvari, J. L., &#38; Buzsáki, G. (1999).
    Replay and time compression of recurring spike sequences in the hippocampus. <i>Journal
    of Neuroscience</i>. Society for Neuroscience. <a href="https://doi.org/10.1523/JNEUROSCI.19-21-09497.1999">https://doi.org/10.1523/JNEUROSCI.19-21-09497.1999</a>
  chicago: Nádasdy, Zoltán, Hajima Hirase, András Czurkó, Jozsef L Csicsvari, and
    György Buzsáki. “Replay and Time Compression of Recurring Spike Sequences in the
    Hippocampus.” <i>Journal of Neuroscience</i>. Society for Neuroscience, 1999.
    <a href="https://doi.org/10.1523/JNEUROSCI.19-21-09497.1999">https://doi.org/10.1523/JNEUROSCI.19-21-09497.1999</a>.
  ieee: Z. Nádasdy, H. Hirase, A. Czurkó, J. L. Csicsvari, and G. Buzsáki, “Replay
    and time compression of recurring spike sequences in the hippocampus,” <i>Journal
    of Neuroscience</i>, vol. 19, no. 21. Society for Neuroscience, pp. 9497–9507,
    1999.
  ista: Nádasdy Z, Hirase H, Czurkó A, Csicsvari JL, Buzsáki G. 1999. Replay and time
    compression of recurring spike sequences in the hippocampus. Journal of Neuroscience.
    19(21), 9497–9507.
  mla: Nádasdy, Zoltán, et al. “Replay and Time Compression of Recurring Spike Sequences
    in the Hippocampus.” <i>Journal of Neuroscience</i>, vol. 19, no. 21, Society
    for Neuroscience, 1999, pp. 9497–507, doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-21-09497.1999">10.1523/JNEUROSCI.19-21-09497.1999</a>.
  short: Z. Nádasdy, H. Hirase, A. Czurkó, J.L. Csicsvari, G. Buzsáki, Journal of
    Neuroscience 19 (1999) 9497–9507.
date_created: 2018-12-11T12:03:45Z
date_published: 1999-11-01T00:00:00Z
date_updated: 2022-09-07T12:48:08Z
day: '01'
doi: 10.1523/JNEUROSCI.19-21-09497.1999
extern: '1'
external_id:
  pmid:
  - '10531452'
intvolume: '        19'
issue: '21'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782894/
month: '11'
oa: 1
oa_version: Published Version
page: 9497 - 9507
pmid: 1
publication: Journal of Neuroscience
publication_identifier:
  issn:
  - 0270-6474
publication_status: published
publisher: Society for Neuroscience
publist_id: '2866'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Replay and time compression of recurring spike sequences in the hippocampus
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 19
year: '1999'
...
---
_id: '3524'
abstract:
- lang: eng
  text: We examined whether excitation and inhibition are balanced in hippocampal
    cortical networks. Extracellular field and single-unit activity were recorded
    by multiple tetrodes and multisite silicon probes to reveal the timing of the
    activity of hippocampal CAI pyramidal cells and classes of interneurons during
    theta waves and sharp wave burst (SPW)-associated field ripples. The somatic and
    dendritic inhibition of pyramidal cells was deduced from the activity of interneurons
    in the pyramidal layer [int(p)] and in the alveus and st. oriens [int(a/o)], respectively.
    int(p) and int(a/o) discharged an average of 60 and 20 degrees before the population
    discharge of pyramidal cells during the theta cycle, respectively. SPW ripples
    were associated with a 2.5-fold net increase of excitation. The discharge frequency
    of int(a/o) increased, decreased (”anti-SPW” cells), or did not change (”SPW-independent”
    cells) during SPW suggesting that not all interneurons are innervated by pyramidal
    cells. Int(p) either fired together with (unimodal cells) or both before and after
    (bimodal cells) the pyramidal cell burst. During fast-ripple oscillation, the
    activity of interneurons in both the int(p) and int(a/o) groups lagged the maximum
    discharge probability of pyramidal neurons by 1-2 msec. Network state changes,
    as reflected by field activity, covaried with changes in the spike train dynamics
    of single cells and their interactions. Summed activity of parallel-recorded interneurons,
    but not of pyramidal cells, reliably predicted theta cycles, whereas the reverse
    was true for the ripple cycles of SPWs. We suggest that network-driven excitability
    changes provide temporal windows of opportunity for single pyramidal cells to
    suppress, enable, or facilitate selective synaptic inputs.
acknowledgement: This work was supported by National Institutes of Health Grants NS34994,
  MH54671, and 1P41RR09754 and by the Human Frontier Science Program. We thank Darrell
  A. Henze and M. Recce for their comments on this manuscript and Jamie Hetke and
  Ken Wise for supplying us with silicon probes.
article_processing_charge: No
article_type: original
author:
- first_name: Jozsef L
  full_name: Csicsvari, Jozsef L
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
- first_name: Hajima
  full_name: Hirase, Hajima
  last_name: Hirase
- first_name: András
  full_name: Czurkó, András
  last_name: Czurkó
- first_name: Akira
  full_name: Mamiya, Akira
  last_name: Mamiya
- first_name: György
  full_name: Buzsáki, György
  last_name: Buzsáki
citation:
  ama: Csicsvari JL, Hirase H, Czurkó A, Mamiya A, Buzsáki G. Oscillatory coupling
    of hippocampal pyramidal cells and interneurons in the behaving rat. <i>Journal
    of Neuroscience</i>. 1999;19(1):274-287. doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-01-00274.1999">10.1523/JNEUROSCI.19-01-00274.1999</a>
  apa: Csicsvari, J. L., Hirase, H., Czurkó, A., Mamiya, A., &#38; Buzsáki, G. (1999).
    Oscillatory coupling of hippocampal pyramidal cells and interneurons in the behaving
    rat. <i>Journal of Neuroscience</i>. Society for Neuroscience. <a href="https://doi.org/10.1523/JNEUROSCI.19-01-00274.1999">https://doi.org/10.1523/JNEUROSCI.19-01-00274.1999</a>
  chicago: Csicsvari, Jozsef L, Hajima Hirase, András Czurkó, Akira Mamiya, and György
    Buzsáki. “Oscillatory Coupling of Hippocampal Pyramidal Cells and Interneurons
    in the Behaving Rat.” <i>Journal of Neuroscience</i>. Society for Neuroscience,
    1999. <a href="https://doi.org/10.1523/JNEUROSCI.19-01-00274.1999">https://doi.org/10.1523/JNEUROSCI.19-01-00274.1999</a>.
  ieee: J. L. Csicsvari, H. Hirase, A. Czurkó, A. Mamiya, and G. Buzsáki, “Oscillatory
    coupling of hippocampal pyramidal cells and interneurons in the behaving rat,”
    <i>Journal of Neuroscience</i>, vol. 19, no. 1. Society for Neuroscience, pp.
    274–287, 1999.
  ista: Csicsvari JL, Hirase H, Czurkó A, Mamiya A, Buzsáki G. 1999. Oscillatory coupling
    of hippocampal pyramidal cells and interneurons in the behaving rat. Journal of
    Neuroscience. 19(1), 274–287.
  mla: Csicsvari, Jozsef L., et al. “Oscillatory Coupling of Hippocampal Pyramidal
    Cells and Interneurons in the Behaving Rat.” <i>Journal of Neuroscience</i>, vol.
    19, no. 1, Society for Neuroscience, 1999, pp. 274–87, doi:<a href="https://doi.org/10.1523/JNEUROSCI.19-01-00274.1999">10.1523/JNEUROSCI.19-01-00274.1999</a>.
  short: J.L. Csicsvari, H. Hirase, A. Czurkó, A. Mamiya, G. Buzsáki, Journal of Neuroscience
    19 (1999) 274–287.
date_created: 2018-12-11T12:03:47Z
date_published: 1999-01-01T00:00:00Z
date_updated: 2022-09-07T10:00:45Z
day: '01'
doi: 10.1523/JNEUROSCI.19-01-00274.1999
extern: '1'
external_id:
  pmid:
  - '9870957'
intvolume: '        19'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782375/
month: '01'
oa: 1
oa_version: Published Version
page: 274 - 287
pmid: 1
publication: Journal of Neuroscience
publication_identifier:
  issn:
  - 0270-6474
publication_status: published
publisher: Society for Neuroscience
publist_id: '2860'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Oscillatory coupling of hippocampal pyramidal cells and interneurons in the
  behaving rat
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 19
year: '1999'
...
---
_id: '3582'
abstract:
- lang: eng
  text: We study edge contractions in simplicial complexes and local conditions under
    which they preserve the topological type. The conditions are based on a generalized
    notion of boundary, which lends itself to defining a nested hierarchy of triangulable
    spaces measuring the distance to being a manifold.
acknowledgement: The second author thanks Wolfgang Haken and Min Yan for interesting
  discussions and Günter Ziegler for suggesting the knot construction in the triangulation
  of the 3-sphere mentioned in Section 7.
article_processing_charge: No
article_type: original
author:
- first_name: Tamal
  full_name: Dey, Tamal
  last_name: Dey
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
- first_name: Sumanta
  full_name: Guha, Sumanta
  last_name: Guha
- first_name: Dmitry
  full_name: Nekhayev, Dmitry
  last_name: Nekhayev
citation:
  ama: Dey T, Edelsbrunner H, Guha S, Nekhayev D. Topology preserving edge contraction.
    <i>Publications de l’Institut Mathématique</i>. 1999;66:23-45.
  apa: Dey, T., Edelsbrunner, H., Guha, S., &#38; Nekhayev, D. (1999). Topology preserving
    edge contraction. <i>Publications de l’Institut Mathématique</i>. Mathematical
    Institute, Serbian Academy of Sciences and Arts.
  chicago: Dey, Tamal, Herbert Edelsbrunner, Sumanta Guha, and Dmitry Nekhayev. “Topology
    Preserving Edge Contraction.” <i>Publications de l’Institut Mathématique</i>.
    Mathematical Institute, Serbian Academy of Sciences and Arts, 1999.
  ieee: T. Dey, H. Edelsbrunner, S. Guha, and D. Nekhayev, “Topology preserving edge
    contraction,” <i>Publications de l’Institut Mathématique</i>, vol. 66. Mathematical
    Institute, Serbian Academy of Sciences and Arts, pp. 23–45, 1999.
  ista: Dey T, Edelsbrunner H, Guha S, Nekhayev D. 1999. Topology preserving edge
    contraction. Publications de l’Institut Mathématique. 66, 23–45.
  mla: Dey, Tamal, et al. “Topology Preserving Edge Contraction.” <i>Publications
    de l’Institut Mathématique</i>, vol. 66, Mathematical Institute, Serbian Academy
    of Sciences and Arts, 1999, pp. 23–45.
  short: T. Dey, H. Edelsbrunner, S. Guha, D. Nekhayev, Publications de l’Institut
    Mathématique 66 (1999) 23–45.
date_created: 2018-12-11T12:04:05Z
date_published: 1999-01-01T00:00:00Z
date_updated: 2023-03-22T13:20:32Z
day: '01'
extern: '1'
intvolume: '        66'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.emis.de/journals/PIMB/080/3.html
month: '01'
oa: 1
oa_version: None
page: 23 - 45
publication: Publications de l'Institut Mathématique
publication_identifier:
  issn:
  - 0350-1302
publication_status: published
publisher: Mathematical Institute, Serbian Academy of Sciences and Arts
publist_id: '2803'
quality_controlled: '1'
status: public
title: Topology preserving edge contraction
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 66
year: '1999'
...
---
_id: '1449'
abstract:
- lang: eng
  text: In this paper we consider a canonical compactification of M, the moduli space
    of stable Higgs bundles with fixed determinant of odd degree over a Riemann surface
    Σ, producing a projective variety M̄ = M ∪ Z. We give a detailed study of the
    spaces M̄, Z and M. In doing so we reprove some assertions of Laumon and Thaddeus
    on the nilpotent cone.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Tamas
  full_name: Hausel, Tamas
  id: 4A0666D8-F248-11E8-B48F-1D18A9856A87
  last_name: Hausel
citation:
  ama: Hausel T. Compactification of moduli of Higgs bundles. <i>Journal fur die Reine
    und Angewandte Mathematik</i>. 1998;1998(503):169-192. doi:<a href="https://doi.org/10.1515/crll.1998.096">10.1515/crll.1998.096</a>
  apa: Hausel, T. (1998). Compactification of moduli of Higgs bundles. <i>Journal
    Fur Die Reine Und Angewandte Mathematik</i>. Walter de Gruyter. <a href="https://doi.org/10.1515/crll.1998.096">https://doi.org/10.1515/crll.1998.096</a>
  chicago: Hausel, Tamás. “Compactification of Moduli of Higgs Bundles.” <i>Journal
    Fur Die Reine Und Angewandte Mathematik</i>. Walter de Gruyter, 1998. <a href="https://doi.org/10.1515/crll.1998.096">https://doi.org/10.1515/crll.1998.096</a>.
  ieee: T. Hausel, “Compactification of moduli of Higgs bundles,” <i>Journal fur die
    Reine und Angewandte Mathematik</i>, vol. 1998, no. 503. Walter de Gruyter, pp.
    169–192, 1998.
  ista: Hausel T. 1998. Compactification of moduli of Higgs bundles. Journal fur die
    Reine und Angewandte Mathematik. 1998(503), 169–192.
  mla: Hausel, Tamás. “Compactification of Moduli of Higgs Bundles.” <i>Journal Fur
    Die Reine Und Angewandte Mathematik</i>, vol. 1998, no. 503, Walter de Gruyter,
    1998, pp. 169–92, doi:<a href="https://doi.org/10.1515/crll.1998.096">10.1515/crll.1998.096</a>.
  short: T. Hausel, Journal Fur Die Reine Und Angewandte Mathematik 1998 (1998) 169–192.
date_created: 2018-12-11T11:52:05Z
date_published: 1998-10-01T00:00:00Z
date_updated: 2022-09-01T13:51:07Z
day: '01'
doi: 10.1515/crll.1998.096
extern: '1'
external_id:
  arxiv:
  - math/9804083
intvolume: '      1998'
issue: '503'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/math/9804083
month: '10'
oa: 1
oa_version: Preprint
page: 169 - 192
publication: Journal fur die Reine und Angewandte Mathematik
publication_identifier:
  issn:
  - 1435-5345
publication_status: published
publisher: Walter de Gruyter
publist_id: '5746'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Compactification of moduli of Higgs bundles
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 1998
year: '1998'
...
---
_id: '1450'
abstract:
- lang: eng
  text: In this paper we consider the topological side of a problem which is the analogue
    of Sen's S-duality testing conjecture for Hitchin's moduli space M of rank 2 stable
    Higgs bundles of fixed determinant of odd degree over a Riemann surface ∑. We
    prove that all intersection numbers in the compactly supported cohomology of M
    vanish, i.e. &quot;there are no topological L2 harmonic forms on M&quot;. This
    result generalizes the well known vanishing of the Euler characteristic of the
    moduli space of rank 2 stable bundles N of fixed determinant of odd degree over
    ∑. Our proof shows that the vanishing of all intersection numbers of H* cpt(M)
    is given by relations analogous to the Mumford relations in the cohomology ring
    of N.
acknowledgement: "First of all I would like to thank my supervisor Nigel Hitchin for
  suggesting Problem 1, and for his help and \r\n encouragement. I am grateful to
  Michael Thaddeus for his inspiring paper [Thai], enlightening communications and
  his constant interest in my work. I am also indebted to Manfred Lehn for the idea
  of the proof of Theorem 6.2. I have found\r\nconversations with Michael Atiyah,
  Frances Kirwan and Graeme Segal very stimulating. I thank the Mathematical Institute
  and St. Catherine's College, Oxford for their hospitality during the preparation
  of this work. Finally I thank Trinity College, Cambridge for financial support."
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Tamas
  full_name: Hausel, Tamas
  id: 4A0666D8-F248-11E8-B48F-1D18A9856A87
  last_name: Hausel
citation:
  ama: Hausel T. Vanishing of intersection numbers on the moduli space of Higgs bundles.
    <i>Advances in Theoretical and Mathematical Physics</i>. 1998;2(5):1011-1040.
    doi:<a href="https://doi.org/10.4310/ATMP.1998.v2.n5.a3">10.4310/ATMP.1998.v2.n5.a3</a>
  apa: Hausel, T. (1998). Vanishing of intersection numbers on the moduli space of
    Higgs bundles. <i>Advances in Theoretical and Mathematical Physics</i>. International
    Press. <a href="https://doi.org/10.4310/ATMP.1998.v2.n5.a3">https://doi.org/10.4310/ATMP.1998.v2.n5.a3</a>
  chicago: Hausel, Tamás. “Vanishing of Intersection Numbers on the Moduli Space of
    Higgs Bundles.” <i>Advances in Theoretical and Mathematical Physics</i>. International
    Press, 1998. <a href="https://doi.org/10.4310/ATMP.1998.v2.n5.a3">https://doi.org/10.4310/ATMP.1998.v2.n5.a3</a>.
  ieee: T. Hausel, “Vanishing of intersection numbers on the moduli space of Higgs
    bundles,” <i>Advances in Theoretical and Mathematical Physics</i>, vol. 2, no.
    5. International Press, pp. 1011–1040, 1998.
  ista: Hausel T. 1998. Vanishing of intersection numbers on the moduli space of Higgs
    bundles. Advances in Theoretical and Mathematical Physics. 2(5), 1011–1040.
  mla: Hausel, Tamás. “Vanishing of Intersection Numbers on the Moduli Space of Higgs
    Bundles.” <i>Advances in Theoretical and Mathematical Physics</i>, vol. 2, no.
    5, International Press, 1998, pp. 1011–40, doi:<a href="https://doi.org/10.4310/ATMP.1998.v2.n5.a3">10.4310/ATMP.1998.v2.n5.a3</a>.
  short: T. Hausel, Advances in Theoretical and Mathematical Physics 2 (1998) 1011–1040.
date_created: 2018-12-11T11:52:06Z
date_published: 1998-09-01T00:00:00Z
date_updated: 2022-09-01T14:09:49Z
day: '01'
doi: 10.4310/ATMP.1998.v2.n5.a3
extern: '1'
external_id:
  arxiv:
  - math/9805071
intvolume: '         2'
issue: '5'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://arxiv.org/abs/math/9805071
month: '09'
oa: 1
oa_version: Preprint
page: 1011 - 1040
publication: Advances in Theoretical and Mathematical Physics
publication_identifier:
  issn:
  - 1095-0761
publication_status: published
publisher: International Press
publist_id: '5747'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Vanishing of intersection numbers on the moduli space of Higgs bundles
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 2
year: '1998'
...
---
OA_place: repository
OA_type: green
_id: '17839'
abstract:
- lang: eng
  text: 'We study the observational signatures of a potential population of low-luminosity
    quasars at high redshifts in a ΛCDM cosmology. We derive the evolution of the
    quasar luminosity function at fainter luminosities and higher redshifts than currently
    detected based on three assumptions: (1) the formation of dark matter halos follows
    the Press-Schechter theory, (2) the ratio of central black hole mass to halo mass
    is the same for all halos, and (3) the light curve of quasars, in Eddington units,
    is universal. We show that a universal light curve provides an excellent fit to
    the observed quasar luminosity function at redshifts 2.6 < z < 4.5. By extrapolating
    the evolution of this luminosity function to higher redshifts (4.5 < z < 20),
    we find that the associated early population of low-luminosity quasars reionizes
    the universe at a redshift z ~ 12. The reprocessing of the UV light of these quasars
    by dust from early Type II supernovae distorts the microwave background spectrum
    by a Compton y-parameter y ~ 10-5, comparable to the lower limit set by COBE.
    The Next Generation Space Telescope could detect tens of quasars per arcmin-2
    from redshifts z > 10 with its proposed 1 nJy sensitivity at 1-3.5 μm. Absorption
    spectra of several such quasars would reveal the reionization history of the universe.'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Zoltán
  full_name: Haiman, Zoltán
  id: 7c006e8c-cc0d-11ee-8322-cb904ef76f36
  last_name: Haiman
  orcid: 0000-0003-3633-5403
- first_name: Abraham
  full_name: Loeb, Abraham
  last_name: Loeb
citation:
  ama: Haiman Z, Loeb A. Observational signatures of the first quasars. <i>The Astrophysical
    Journal</i>. 1998;503(2):505-517. doi:<a href="https://doi.org/10.1086/306017">10.1086/306017</a>
  apa: Haiman, Z., &#38; Loeb, A. (1998). Observational signatures of the first quasars.
    <i>The Astrophysical Journal</i>. American Astronomical Society. <a href="https://doi.org/10.1086/306017">https://doi.org/10.1086/306017</a>
  chicago: Haiman, Zoltán, and Abraham Loeb. “Observational Signatures of the First
    Quasars.” <i>The Astrophysical Journal</i>. American Astronomical Society, 1998.
    <a href="https://doi.org/10.1086/306017">https://doi.org/10.1086/306017</a>.
  ieee: Z. Haiman and A. Loeb, “Observational signatures of the first quasars,” <i>The
    Astrophysical Journal</i>, vol. 503, no. 2. American Astronomical Society, pp.
    505–517, 1998.
  ista: Haiman Z, Loeb A. 1998. Observational signatures of the first quasars. The
    Astrophysical Journal. 503(2), 505–517.
  mla: Haiman, Zoltán, and Abraham Loeb. “Observational Signatures of the First Quasars.”
    <i>The Astrophysical Journal</i>, vol. 503, no. 2, American Astronomical Society,
    1998, pp. 505–17, doi:<a href="https://doi.org/10.1086/306017">10.1086/306017</a>.
  short: Z. Haiman, A. Loeb, The Astrophysical Journal 503 (1998) 505–517.
date_created: 2024-09-06T12:16:27Z
date_published: 1998-08-20T00:00:00Z
date_updated: 2024-11-13T07:43:28Z
day: '20'
doi: 10.1086/306017
extern: '1'
external_id:
  arxiv:
  - astro-ph/9710208
intvolume: '       503'
issue: '2'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.48550/arXiv.astro-ph/9710208
month: '08'
oa: 1
oa_version: Preprint
page: 505-517
publication: The Astrophysical Journal
publication_identifier:
  eissn:
  - 1538-4357
  issn:
  - 0004-637X
publication_status: published
publisher: American Astronomical Society
quality_controlled: '1'
scopus_import: '1'
status: public
title: Observational signatures of the first quasars
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 503
year: '1998'
...
---
_id: '1955'
abstract:
- lang: eng
  text: 'The plastid genomes of several plants contain homologues, termed ndh genes,
    of genes encoding subunits of the NADH:ubiquinone oxidoreductase or complex I
    of mitochondria and eubacteria. The functional significance of the Ndh proteins
    in higher plants is uncertain. We show here that tobacco chloroplasts contain
    a protein complex of 550 kDa consisting of at least three of the ndh gene products:
    NdhI, NdhJ and NdhK. We have constructed mutant tobacco plants with disrupted
    ndhC, ndhK and ndhJ plastid genes, indicating that the Ndh complex is dispensible
    for plant growth under optimal growth conditions. Chlorophyll fluorescence analysis
    shows that in vivo the Ndh complex catalyses the post-illumination reduction of
    the plastoquinone pool and in the light optimizes the induction of photosynthesis
    under conditions of water stress. We conclude that the Ndh complex catalyses the
    reduction of the plastoquinone pool using stromal reductant and so acts as a respiratory
    complex. Overall, our data are compatible with the participation of the Ndh complex
    in cyclic electron flow around the photosystem I complex in the light and possibly
    in a chloroplast respiratory chain in the dark.'
acknowledgement: We thank Professor Süss (Institute of Plant Genetics and Crop Plant
  Research, Gatersleben, Germany) for the gift of the anti-FNR antiserum, Professor
  Masahiro Sugiura (Nagoya University, Japan) for the gift of plasmid pTB19 and Professor
  Peter Horton (University of Sheffield) for the loan of his ED-800T unit. P.B. is
  a recipient of a BBSRC studentship and the work was supported by grants from the
  BBSRC, The Royal Society (to P.J.N.) and The National Science Foundation (to P.M.).
article_processing_charge: No
article_type: original
author:
- first_name: Paul
  full_name: Burrows, Paul
  last_name: Burrows
- first_name: Leonid A
  full_name: Sazanov, Leonid A
  id: 338D39FE-F248-11E8-B48F-1D18A9856A87
  last_name: Sazanov
  orcid: 0000-0002-0977-7989
- first_name: Zóra
  full_name: Sváb, Zóra
  last_name: Sváb
- first_name: Pàl
  full_name: Maliga, Pàl
  last_name: Maliga
- first_name: Peter
  full_name: Nixon, Peter
  last_name: Nixon
citation:
  ama: Burrows P, Sazanov LA, Sváb Z, Maliga P, Nixon P. Identification of a functional
    respiratory complex in chloroplasts through analysis of tobacco mutants containing
    disrupted plastid ndh genes. <i>EMBO Journal</i>. 1998;17(4):868-876. doi:<a href="https://doi.org/10.1093/emboj/17.4.868">10.1093/emboj/17.4.868</a>
  apa: Burrows, P., Sazanov, L. A., Sváb, Z., Maliga, P., &#38; Nixon, P. (1998).
    Identification of a functional respiratory complex in chloroplasts through analysis
    of tobacco mutants containing disrupted plastid ndh genes. <i>EMBO Journal</i>.
    Wiley-Blackwell. <a href="https://doi.org/10.1093/emboj/17.4.868">https://doi.org/10.1093/emboj/17.4.868</a>
  chicago: Burrows, Paul, Leonid A Sazanov, Zóra Sváb, Pàl Maliga, and Peter Nixon.
    “Identification of a Functional Respiratory Complex in Chloroplasts through Analysis
    of Tobacco Mutants Containing Disrupted Plastid Ndh Genes.” <i>EMBO Journal</i>.
    Wiley-Blackwell, 1998. <a href="https://doi.org/10.1093/emboj/17.4.868">https://doi.org/10.1093/emboj/17.4.868</a>.
  ieee: P. Burrows, L. A. Sazanov, Z. Sváb, P. Maliga, and P. Nixon, “Identification
    of a functional respiratory complex in chloroplasts through analysis of tobacco
    mutants containing disrupted plastid ndh genes,” <i>EMBO Journal</i>, vol. 17,
    no. 4. Wiley-Blackwell, pp. 868–876, 1998.
  ista: Burrows P, Sazanov LA, Sváb Z, Maliga P, Nixon P. 1998. Identification of
    a functional respiratory complex in chloroplasts through analysis of tobacco mutants
    containing disrupted plastid ndh genes. EMBO Journal. 17(4), 868–876.
  mla: Burrows, Paul, et al. “Identification of a Functional Respiratory Complex in
    Chloroplasts through Analysis of Tobacco Mutants Containing Disrupted Plastid
    Ndh Genes.” <i>EMBO Journal</i>, vol. 17, no. 4, Wiley-Blackwell, 1998, pp. 868–76,
    doi:<a href="https://doi.org/10.1093/emboj/17.4.868">10.1093/emboj/17.4.868</a>.
  short: P. Burrows, L.A. Sazanov, Z. Sváb, P. Maliga, P. Nixon, EMBO Journal 17 (1998)
    868–876.
date_created: 2018-12-11T11:54:54Z
date_published: 1998-02-04T00:00:00Z
date_updated: 2022-09-01T13:17:49Z
day: '04'
doi: 10.1093/emboj/17.4.868
extern: '1'
external_id:
  pmid:
  - '9463365'
intvolume: '        17'
issue: '4'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1170436/
month: '02'
oa: 1
oa_version: None
page: 868 - 876
pmid: 1
publication: EMBO Journal
publication_identifier:
  issn:
  - 0261-4189
publication_status: published
publisher: Wiley-Blackwell
publist_id: '5129'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Identification of a functional respiratory complex in chloroplasts through
  analysis of tobacco mutants containing disrupted plastid ndh genes
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 17
year: '1998'
...
---
_id: '1956'
abstract:
- lang: eng
  text: "\r\nThe plastid genomes of several plants contain ndh genes-homologues of
    genes encoding subunits of the proton-pumping NADH:ubiquinone oxidoreductase,
    or complex I, involved in respiration in mitochondria and eubacteria. From sequence
    similarities with these genes, the ndh gene products have been suggested to form
    a large protein complex (Ndh complex); however, the structure and function of
    this complex remains to be established. Herein we report the isolation of the
    Ndh complex from the chloroplasts of the higher plant Pisum sativum. The purification
    procedure involved selective solubilization of the thylakoid membrane with dodecyl
    maltoside, followed by two anion-exchange chromatography steps and one size-exclusion
    chromatography step. The isolated Ndh complex has an apparent total molecular
    mass of approximately 550 kDa and according to SDS/PAGE consists of at least 16
    subunits including NdhA, NdhI, NdhJ, NdhK, and NdhH, which were identified by
    N-terminal sequencing and immunoblotting. The Ndh complex showed an NADH- and
    deamino-NADH-specific dehydrogenase activity, characteristic of complex I, when
    either ferricyanide or the quinones menadione and duroquinone were used as electron
    acceptors. This study describes the isolation of the chloroplast analogue of the
    respiratory complex I and provides direct evidence for the function of the plastid
    Ndh complex as an NADH:plastoquinone oxidoreductase. Our results are compatible
    with a dual role for the Ndh complex in the chloro-respiratory and cyclic photophosphorylation
    pathways."
acknowledgement: We gratefully acknowledge Dr. A.Carne (Institute of Cancer Research,
  London, U.K.) for help with N-terminal sequencing. We thank Prof. C. J. Leaver (University
  of Oxford, U.K.), Prof. K.-H. Süss (Institute of Plant Genetics and Crop Plant Research,
  Gatersleben, Germany), and Prof. L. J. Rogers (University of Aberystwyth, U.K.)
  for gifts of antiserum against maize mitochondrial cytochrome oxidase subunit 1
  and cytochrome bc1 complex, spinach FNR, and spinach ferredoxin, respectively. This
  work was supported by grants from The Royal Society and the Biotechnology and Biological
  Sciences Research Council.
article_processing_charge: No
article_type: original
author:
- first_name: Leonid A
  full_name: Sazanov, Leonid A
  id: 338D39FE-F248-11E8-B48F-1D18A9856A87
  last_name: Sazanov
  orcid: 0000-0002-0977-7989
- first_name: Paul
  full_name: Burrows, Paul
  last_name: Burrows
- first_name: Peter
  full_name: Nixon, Peter
  last_name: Nixon
citation:
  ama: 'Sazanov LA, Burrows P, Nixon P. The plastid ndh genes code for an NADH-specific
    dehydrogenase: Isolation of a complex I analogue from pea thylakoid membranes.
    <i>PNAS</i>. 1998;95(3):1319-1324. doi:<a href="https://doi.org/10.1073/pnas.95.3.1319">10.1073/pnas.95.3.1319</a>'
  apa: 'Sazanov, L. A., Burrows, P., &#38; Nixon, P. (1998). The plastid ndh genes
    code for an NADH-specific dehydrogenase: Isolation of a complex I analogue from
    pea thylakoid membranes. <i>PNAS</i>. National Academy of Sciences. <a href="https://doi.org/10.1073/pnas.95.3.1319">https://doi.org/10.1073/pnas.95.3.1319</a>'
  chicago: 'Sazanov, Leonid A, Paul Burrows, and Peter Nixon. “The Plastid Ndh Genes
    Code for an NADH-Specific Dehydrogenase: Isolation of a Complex I Analogue from
    Pea Thylakoid Membranes.” <i>PNAS</i>. National Academy of Sciences, 1998. <a
    href="https://doi.org/10.1073/pnas.95.3.1319">https://doi.org/10.1073/pnas.95.3.1319</a>.'
  ieee: 'L. A. Sazanov, P. Burrows, and P. Nixon, “The plastid ndh genes code for
    an NADH-specific dehydrogenase: Isolation of a complex I analogue from pea thylakoid
    membranes,” <i>PNAS</i>, vol. 95, no. 3. National Academy of Sciences, pp. 1319–1324,
    1998.'
  ista: 'Sazanov LA, Burrows P, Nixon P. 1998. The plastid ndh genes code for an NADH-specific
    dehydrogenase: Isolation of a complex I analogue from pea thylakoid membranes.
    PNAS. 95(3), 1319–1324.'
  mla: 'Sazanov, Leonid A., et al. “The Plastid Ndh Genes Code for an NADH-Specific
    Dehydrogenase: Isolation of a Complex I Analogue from Pea Thylakoid Membranes.”
    <i>PNAS</i>, vol. 95, no. 3, National Academy of Sciences, 1998, pp. 1319–24,
    doi:<a href="https://doi.org/10.1073/pnas.95.3.1319">10.1073/pnas.95.3.1319</a>.'
  short: L.A. Sazanov, P. Burrows, P. Nixon, PNAS 95 (1998) 1319–1324.
date_created: 2018-12-11T11:54:54Z
date_published: 1998-02-03T00:00:00Z
date_updated: 2022-09-01T13:47:05Z
day: '03'
doi: 10.1073/pnas.95.3.1319
extern: '1'
external_id:
  pmid:
  - '9448329 '
intvolume: '        95'
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://europepmc.org/article/pmc/18756
month: '02'
oa: 1
oa_version: None
page: 1319 - 1324
pmid: 1
publication: PNAS
publication_identifier:
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
publist_id: '5130'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'The plastid ndh genes code for an NADH-specific dehydrogenase: Isolation of
  a complex I analogue from pea thylakoid membranes'
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 95
year: '1998'
...
---
_id: '3488'
abstract:
- lang: eng
  text: We have examined gating and pharmacological characteristics of somatic K+
    channels in fast-spiking interneurons and regularly spiking principal neurons
    of hippocampal slices. In nucleated patches isolated from basket cells of the
    dentate gyrus, a fast delayed rectifier K+ current component that was highly sensitive
    to tetraethylammonium (TEA) and 4-aminopyridine (4- AP) (half-maximal inhibitory
    concentrations &lt;0.1 mM) predominated, contributing an average of 58% to the
    total K+ current in these cells. By contrast, in pyramidal neurons of the CA1
    region a rapidly inactivating A- type K+ current component that was TEA-resistant
    prevailed, contributing 61% to the total K+ current. Both types of neurons also
    showed small amounts of the K+ current component mainly found in the other type
    of neuron and, in addition, a slow delayed rectifier K+ current component with
    intermediate properties (sow inactivation, intermediate sensitivity to TEA). Single-cell
    RT-PCR analysis of mRNA revealed that Kv3 (Kv3.1, Kv3.2) subunit transcripts were
    expressed in almost all (89%) of the interneurons but only in 17% of the pyramidal
    neurons. In contrast, Kv4 (Kv4.2, Kv4.3) subunit mRNAs were present in 87% of
    pyramidal neurons but only in 55% of interneurons. Selective block of fast delayed
    rectifier K+ channels, presumably assembled from Kv3 subunits, by 4-AP reduced
    substantially the action potential frequency in interneurons. These results indicate
    that the differential expression of Kv3 and Kv4 subunits shapes the action potential
    phenotypes of principal neurons and interneurons in the cortex.
acknowledgement: Supported by German Israeli Foundation Grant I 0352–073.01/94 to
  P.J. and Deutsche Forschungsgemeinschaft Grant Mo 432/3–1 to H.M. We thank Drs.
  L. Y. Jan, D. McKinnon, O. Pongs, L. Salkoff, S. H. Snyder, and J. S. Trimmer for
  providing plasmids, Dr. D. J. Surmeier for sharing unpublished data, and Drs. J.
  Bischofberger and J. R. P. Geiger for critically reading this manuscript. M.M. and
  J.H.S. contributed equally to this work.
article_processing_charge: No
article_type: original
author:
- first_name: Marco
  full_name: Martina, Marco
  last_name: Martina
- first_name: Jobst
  full_name: Schultz, Jobst
  last_name: Schultz
- first_name: Heimo
  full_name: Ehmke, Heimo
  last_name: Ehmke
- first_name: Hannah
  full_name: Monyer, Hannah
  last_name: Monyer
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
citation:
  ama: Martina M, Schultz J, Ehmke H, Monyer H, Jonas PM. Functional and molecular
    differences between voltage-gated K+ channels of fast-spiking interneurons and
    pyramidal neurons of rat hippocampus. <i>Journal of Neuroscience</i>. 1998;18(20):8111-8125.
    doi:<a href="https://doi.org/10.1523/JNEUROSCI.18-20-08111.1998">10.1523/JNEUROSCI.18-20-08111.1998</a>
  apa: Martina, M., Schultz, J., Ehmke, H., Monyer, H., &#38; Jonas, P. M. (1998).
    Functional and molecular differences between voltage-gated K+ channels of fast-spiking
    interneurons and pyramidal neurons of rat hippocampus. <i>Journal of Neuroscience</i>.
    Society for Neuroscience. <a href="https://doi.org/10.1523/JNEUROSCI.18-20-08111.1998">https://doi.org/10.1523/JNEUROSCI.18-20-08111.1998</a>
  chicago: Martina, Marco, Jobst Schultz, Heimo Ehmke, Hannah Monyer, and Peter M
    Jonas. “Functional and Molecular Differences between Voltage-Gated K+ Channels
    of Fast-Spiking Interneurons and Pyramidal Neurons of Rat Hippocampus.” <i>Journal
    of Neuroscience</i>. Society for Neuroscience, 1998. <a href="https://doi.org/10.1523/JNEUROSCI.18-20-08111.1998">https://doi.org/10.1523/JNEUROSCI.18-20-08111.1998</a>.
  ieee: M. Martina, J. Schultz, H. Ehmke, H. Monyer, and P. M. Jonas, “Functional
    and molecular differences between voltage-gated K+ channels of fast-spiking interneurons
    and pyramidal neurons of rat hippocampus,” <i>Journal of Neuroscience</i>, vol.
    18, no. 20. Society for Neuroscience, pp. 8111–8125, 1998.
  ista: Martina M, Schultz J, Ehmke H, Monyer H, Jonas PM. 1998. Functional and molecular
    differences between voltage-gated K+ channels of fast-spiking interneurons and
    pyramidal neurons of rat hippocampus. Journal of Neuroscience. 18(20), 8111–8125.
  mla: Martina, Marco, et al. “Functional and Molecular Differences between Voltage-Gated
    K+ Channels of Fast-Spiking Interneurons and Pyramidal Neurons of Rat Hippocampus.”
    <i>Journal of Neuroscience</i>, vol. 18, no. 20, Society for Neuroscience, 1998,
    pp. 8111–25, doi:<a href="https://doi.org/10.1523/JNEUROSCI.18-20-08111.1998">10.1523/JNEUROSCI.18-20-08111.1998</a>.
  short: M. Martina, J. Schultz, H. Ehmke, H. Monyer, P.M. Jonas, Journal of Neuroscience
    18 (1998) 8111–8125.
date_created: 2018-12-11T12:03:35Z
date_published: 1998-10-15T00:00:00Z
date_updated: 2022-08-29T14:20:39Z
day: '15'
doi: 10.1523/JNEUROSCI.18-20-08111.1998
extern: '1'
external_id:
  pmid:
  - '9763458'
intvolume: '        18'
issue: '20'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792860/
month: '10'
oa: 1
oa_version: None
page: 8111 - 8125
pmid: 1
publication: Journal of Neuroscience
publication_identifier:
  issn:
  - 0270-6474
publication_status: published
publisher: Society for Neuroscience
publist_id: '2899'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Functional and molecular differences between voltage-gated K+ channels of fast-spiking
  interneurons and pyramidal neurons of rat hippocampus
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 18
year: '1998'
...
---
_id: '3506'
abstract:
- lang: eng
  text: A method of geometric morphing between a first object having a first shape
    and a second object having a second shape. The method includes the steps of generating
    a first Delaunay complex corresponding to the first shape and a second Delaunay
    complex corresponding to the second shape and generating a plurality of intermediary
    Delaunay complexes defined by a continuous family of mixed shapes corresponding
    to a mixing of the first shape and the second shape. The method further includes
    the steps of constructing a first skin corresponding to the first Delaunay complex
    and a second skin corresponding to the second Delaunay complex and constructing
    a plurality of intermediary skins corresponding to the plurality of intermediary
    Delaunay complexes. The first skin, second skin and plurality of intermediary
    skins may be visually displayed on an output device.
applicant:
- Raindrop Geomagic, Inc.
article_processing_charge: No
author:
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
- first_name: Ping
  full_name: Fu, Ping
  last_name: Fu
citation:
  ama: Edelsbrunner H, Fu P. Apparatus and method for geometric morphing. 1998.
  apa: Edelsbrunner, H., &#38; Fu, P. (1998). Apparatus and method for geometric morphing.
  chicago: Edelsbrunner, Herbert, and Ping Fu. “Apparatus and Method for Geometric
    Morphing,” 1998.
  ieee: H. Edelsbrunner and P. Fu, “Apparatus and method for geometric morphing.”
    1998.
  ista: Edelsbrunner H, Fu P. 1998. Apparatus and method for geometric morphing.
  mla: Edelsbrunner, Herbert, and Ping Fu. <i>Apparatus and Method for Geometric Morphing</i>.
    1998.
  short: H. Edelsbrunner, P. Fu, (1998).
date_created: 2018-12-11T12:03:41Z
date_published: 1998-12-15T00:00:00Z
date_updated: 2022-01-05T15:16:35Z
day: '15'
extern: '1'
ipc: G06T13/20 ; G06T2210/44
ipn: US5850229A
main_file_link:
- open_access: '1'
  url: https://patents.google.com/patent/US5850229A
month: '12'
oa: 1
oa_version: Published Version
publication_date: 1998-12-15
publist_id: '2881'
status: public
title: Apparatus and method for geometric morphing
type: patent
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
year: '1998'
...
---
_id: '3628'
abstract:
- lang: eng
  text: 'Determining the way in which deleterious mutations interact in their effects
    on fitness is crucial to numerous areas in population genetics and evolutionary
    biology. For example, if each additional mutation leads to a greater decrease
    in log fitness than the last (synergistic epistasis), then the evolution of sex
    and recombination may be favored to facilitate the elimination of deleterious
    mutations. However, there is a severe shortage of relevant data. Three relatively
    simple experimental methods to test for epistasis between deleterious mutations
    in haploid species have recently been proposed. These methods involve crossing
    individuals and examining the mean and/or skew in log fitness of the offspring
    and parents. The main aim of this paper is to formalize these methods, and determine
    the most effective way in which tests for epistasis could be carried out. We show
    that only one of these methods is likely to give useful results: crossing individuals
    that have very different numbers of deleterious mutations, and comparing the mean
    log fitness of the parents with that of their offspring. We also reconsider experimental
    data collected on Chlamydomonas moewussi using two of the three methods. Finally,
    we suggest how the test could be applied to diploid species.'
acknowledgement: We thank BRIAN  CHARLESWORTH, ANDREW  CLARK, LAURENCE  HURST, PETER  KEIGHTLEY,
  ALEXEY  KONDRASHOV, CURT  LIVELY, MARGARET  MACKINNON, KATRINA  LYTHGOE, SALLY  OTTO,
  ANDREW  READ and ARJAN DE  VISSER for useful discussion and comments on the manuscript.
  This work was supported by the Biotechnology and Biological Sciences Research Council.
article_processing_charge: No
article_type: original
author:
- first_name: Stuart
  full_name: West, Stuart
  last_name: West
- first_name: Andrew
  full_name: Peters, Andrew
  last_name: Peters
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
citation:
  ama: West S, Peters A, Barton NH. Testing for epistasis between deleterious mutations.
    <i>Genetics</i>. 1998;149(1):435-444. doi:<a href="https://doi.org/10.1093/genetics/149.1.435">10.1093/genetics/149.1.435</a>
  apa: West, S., Peters, A., &#38; Barton, N. H. (1998). Testing for epistasis between
    deleterious mutations. <i>Genetics</i>. Genetics Society of America. <a href="https://doi.org/10.1093/genetics/149.1.435">https://doi.org/10.1093/genetics/149.1.435</a>
  chicago: West, Stuart, Andrew Peters, and Nicholas H Barton. “Testing for Epistasis
    between Deleterious Mutations.” <i>Genetics</i>. Genetics Society of America,
    1998. <a href="https://doi.org/10.1093/genetics/149.1.435">https://doi.org/10.1093/genetics/149.1.435</a>.
  ieee: S. West, A. Peters, and N. H. Barton, “Testing for epistasis between deleterious
    mutations,” <i>Genetics</i>, vol. 149, no. 1. Genetics Society of America, pp.
    435–444, 1998.
  ista: West S, Peters A, Barton NH. 1998. Testing for epistasis between deleterious
    mutations. Genetics. 149(1), 435–444.
  mla: West, Stuart, et al. “Testing for Epistasis between Deleterious Mutations.”
    <i>Genetics</i>, vol. 149, no. 1, Genetics Society of America, 1998, pp. 435–44,
    doi:<a href="https://doi.org/10.1093/genetics/149.1.435">10.1093/genetics/149.1.435</a>.
  short: S. West, A. Peters, N.H. Barton, Genetics 149 (1998) 435–444.
date_created: 2018-12-11T12:04:19Z
date_published: 1998-05-01T00:00:00Z
date_updated: 2022-08-29T08:53:09Z
day: '01'
doi: 10.1093/genetics/149.1.435
extern: '1'
external_id:
  pmid:
  - '9584115'
intvolume: '       149'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://academic.oup.com/genetics/article/149/1/435/6034229
month: '05'
oa: 1
oa_version: None
page: 435 - 444
pmid: 1
publication: Genetics
publication_identifier:
  issn:
  - 0016-6731
publication_status: published
publisher: Genetics Society of America
publist_id: '2755'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Testing for epistasis between deleterious mutations
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 149
year: '1998'
...
---
_id: '4013'
abstract:
- lang: eng
  text: The shape of a protein is important for its functions, This includes the location
    and size of identifiable regions in its complement space. We formally define pockets
    as regions in the complement with limited accessibility from the outside. Pockets
    can be efficiently constructed by an algorithm based on alpha complexes. The algorithm
    is implemented and applied to proteins with known three-dimensional conformations.
    1998 Published by Elsevier Science B.V. All rights reserved.
acknowledgement: 'The authors thank Ping Fu and Ernst Miicke for their contributions
  to the alpha shapes software in which the pockets software is embedded. '
article_processing_charge: No
article_type: original
author:
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
- first_name: Michael
  full_name: Facello, Michael
  last_name: Facello
- first_name: Jie
  full_name: Liang, Jie
  last_name: Liang
citation:
  ama: Edelsbrunner H, Facello M, Liang J. On the definition and the construction
    of pockets in macromolecules. <i>Discrete Applied Mathematics</i>. 1998;88(1-3):83-102.
    doi:<a href="https://doi.org/10.1016/S0166-218X(98)00067-5">10.1016/S0166-218X(98)00067-5</a>
  apa: Edelsbrunner, H., Facello, M., &#38; Liang, J. (1998). On the definition and
    the construction of pockets in macromolecules. <i>Discrete Applied Mathematics</i>.
    Elsevier. <a href="https://doi.org/10.1016/S0166-218X(98)00067-5">https://doi.org/10.1016/S0166-218X(98)00067-5</a>
  chicago: Edelsbrunner, Herbert, Michael Facello, and Jie Liang. “On the Definition
    and the Construction of Pockets in Macromolecules.” <i>Discrete Applied Mathematics</i>.
    Elsevier, 1998. <a href="https://doi.org/10.1016/S0166-218X(98)00067-5">https://doi.org/10.1016/S0166-218X(98)00067-5</a>.
  ieee: H. Edelsbrunner, M. Facello, and J. Liang, “On the definition and the construction
    of pockets in macromolecules,” <i>Discrete Applied Mathematics</i>, vol. 88, no.
    1–3. Elsevier, pp. 83–102, 1998.
  ista: Edelsbrunner H, Facello M, Liang J. 1998. On the definition and the construction
    of pockets in macromolecules. Discrete Applied Mathematics. 88(1–3), 83–102.
  mla: Edelsbrunner, Herbert, et al. “On the Definition and the Construction of Pockets
    in Macromolecules.” <i>Discrete Applied Mathematics</i>, vol. 88, no. 1–3, Elsevier,
    1998, pp. 83–102, doi:<a href="https://doi.org/10.1016/S0166-218X(98)00067-5">10.1016/S0166-218X(98)00067-5</a>.
  short: H. Edelsbrunner, M. Facello, J. Liang, Discrete Applied Mathematics 88 (1998)
    83–102.
date_created: 2018-12-11T12:06:26Z
date_published: 1998-11-09T00:00:00Z
date_updated: 2022-08-25T15:06:30Z
day: '09'
doi: 10.1016/S0166-218X(98)00067-5
extern: '1'
external_id:
  pmid:
  - '9390238'
intvolume: '        88'
issue: 1-3
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.sciencedirect.com/science/article/pii/S0166218X98000675?via%3Dihub
month: '11'
oa: 1
oa_version: Published Version
page: 83 - 102
pmid: 1
publication: Discrete Applied Mathematics
publication_identifier:
  issn:
  - 0166-218X
publication_status: published
publisher: Elsevier
publist_id: '2114'
quality_controlled: '1'
scopus_import: '1'
status: public
title: On the definition and the construction of pockets in macromolecules
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 88
year: '1998'
...
---
_id: '4017'
abstract:
- lang: eng
  text: Identification and size characterization of surface pockets and occluded cavities
    are initial steps in protein structure-based ligand design. A new program, CAST,
    for automatically locating and measuring protein pockets and cavities, is based
    on precise computational geometry methods, including alpha shape and discrete
    flow theory. CAST identifies and measures pockets and pocket mouth openings, as
    well as cavities. The program specifies the atoms lining pockets, pocket openings.
    and buried cavities; the volume and area of pockets and cavities; and the area
    and circumference of mouth openings. CAST analysis of over 100 proteins has been
    carried out; proteins examined include a set of 51 monomeric enzyme-ligand structures,
    several elastase-inhibitor complexes, the FK506 binding protein, 30 HIV-1 protease-inhibitor
    complexes, and a number of small and large protein inhibitors, Medium-sized globular
    proteins typically have 10-20 pockets/cavities. Most often, binding sites are
    pockets with 1-2 mouth openings; much less frequently they are cavities. Ligand
    binding pockets vary widely in size, most within the range 10(2)-10(3) Angstrom(3).
    Statistical analysis reveals that the number of pockets and cavities is correlated
    with protein size, but there is no correlation between the size of the protein
    and the size of binding sites. Most frequently, the largest pocket/cavity is thp
    active site, but there are a number of instructive exceptions. Ligand volume and
    binding site volume are somewhat correlated when binding site volume is less than
    or equal to 700 Angstrom(3), but the ligand seldom occupies the entire site. Auxiliary
    pockets near the active site have been suggested as additional binding surface
    for designed ligands (Mattos C ct al., 1993, Nat Struct Biol 1:55-58). Analysis
    of elastase-inhibitor complexes suggests that CAST can identify ancillary pockets,
    suitable for recruitment in ligand design strategies. Analysis of the FK506 binding
    protein, and of compounds developed in SAR by NMR (Shuker SE et al.. 1996, Science
    274:1531-1534), indicates that CAST pocket computation may provide a priori identification
    of target proteins for Linked-fragment design. CAST analysis of 30 HIV-1 protease-inhibitor
    complexes shows that the flexible active site pocket can vary over a range of
    853-1,566 Angstrom(3), and that there are two pockets near or adjoining the active
    site that may be recruited for ligand design.
article_processing_charge: No
article_type: original
author:
- first_name: Jie
  full_name: Liang, Jie
  last_name: Liang
- first_name: Herbert
  full_name: Edelsbrunner, Herbert
  id: 3FB178DA-F248-11E8-B48F-1D18A9856A87
  last_name: Edelsbrunner
  orcid: 0000-0002-9823-6833
- first_name: Clare
  full_name: Woodward, Clare
  last_name: Woodward
citation:
  ama: 'Liang J, Edelsbrunner H, Woodward C. Anatomy of protein pockets and cavities:
    Measurement of binding site geometry and implications for ligand design. <i>Protein
    Science</i>. 1998;7(9):1884-1897. doi:<a href="https://doi.org/10.1002/pro.5560070905">10.1002/pro.5560070905</a>'
  apa: 'Liang, J., Edelsbrunner, H., &#38; Woodward, C. (1998). Anatomy of protein
    pockets and cavities: Measurement of binding site geometry and implications for
    ligand design. <i>Protein Science</i>. Wiley-Blackwell. <a href="https://doi.org/10.1002/pro.5560070905">https://doi.org/10.1002/pro.5560070905</a>'
  chicago: 'Liang, Jie, Herbert Edelsbrunner, and Clare Woodward. “Anatomy of Protein
    Pockets and Cavities: Measurement of Binding Site Geometry and Implications for
    Ligand Design.” <i>Protein Science</i>. Wiley-Blackwell, 1998. <a href="https://doi.org/10.1002/pro.5560070905">https://doi.org/10.1002/pro.5560070905</a>.'
  ieee: 'J. Liang, H. Edelsbrunner, and C. Woodward, “Anatomy of protein pockets and
    cavities: Measurement of binding site geometry and implications for ligand design,”
    <i>Protein Science</i>, vol. 7, no. 9. Wiley-Blackwell, pp. 1884–1897, 1998.'
  ista: 'Liang J, Edelsbrunner H, Woodward C. 1998. Anatomy of protein pockets and
    cavities: Measurement of binding site geometry and implications for ligand design.
    Protein Science. 7(9), 1884–1897.'
  mla: 'Liang, Jie, et al. “Anatomy of Protein Pockets and Cavities: Measurement of
    Binding Site Geometry and Implications for Ligand Design.” <i>Protein Science</i>,
    vol. 7, no. 9, Wiley-Blackwell, 1998, pp. 1884–97, doi:<a href="https://doi.org/10.1002/pro.5560070905">10.1002/pro.5560070905</a>.'
  short: J. Liang, H. Edelsbrunner, C. Woodward, Protein Science 7 (1998) 1884–1897.
date_created: 2018-12-11T12:06:27Z
date_published: 1998-09-01T00:00:00Z
date_updated: 2022-08-25T12:49:41Z
day: '01'
doi: 10.1002/pro.5560070905
extern: '1'
external_id:
  pmid:
  - '9761470 '
intvolume: '         7'
issue: '9'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2144175/
month: '09'
oa: 1
oa_version: Published Version
page: 1884 - 1897
pmid: 1
publication: Protein Science
publication_identifier:
  issn:
  - 0961-8368
publication_status: published
publisher: Wiley-Blackwell
publist_id: '2111'
quality_controlled: '1'
scopus_import: '1'
status: public
title: 'Anatomy of protein pockets and cavities: Measurement of binding site geometry
  and implications for ligand design'
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 7
year: '1998'
...
---
_id: '4492'
abstract:
- lang: eng
  text: Hybrid automata model systems with both digital and analog components, such
    as embedded control programs. Many verification tasks for such programs can be
    expressed as reachability problems for hybrid automata. By improving on previous
    decidability and undecidability results, we identify a boundary between decidability
    and undecidability for the reachability problem of hybrid automata. On the positive
    side, we give an (optimal) PSPACE reachability algorithm for the case of initialized
    rectangular automata, where all analog variables follow independent trajectories
    within piecewise-linear envelopes and are reinitialized whenever the envelope
    changes. Our algorithm is based on the construction of a timed automaton that
    contains all reachability information about a given initialized rectangular automaton.
    The translation has practical significance for verification, because it guarantees
    the termination of symbolic procedures for the reachability analysis of initialized
    rectangular automata. The translation also preserves theω-languages of initialized
    rectangular automata with bounded nondeterminism. On the negative side, we show
    that several slight generalizations of initialized rectangular automata lead to
    an undecidable reachability problem. In particular, we prove that the reachability
    problem is undecidable for timed automata augmented with a single stopwatch.
acknowledgement: This research was supported in part by the Office of Naval Research
  Young Investigator Award N00014-95-1-0520, by the National Science Foundation CAREER
  award CCR-9501708, by the National Science Foundation Grant CCR-9504469, by the
  Air Force Office of Scientific Research Contract F49620-93-1-0056, by the Army Research
  Office MURI Grant DAAH-04-96-1-0341, by the Army Research Office Contract DAAH-04-94-G-0026,
  by the Defense Advanced Research Projects Agency Grant NAG2-892, and by the California
  PATH program.
article_processing_charge: No
article_type: original
author:
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
- first_name: Peter
  full_name: Kopke, Peter
  last_name: Kopke
- first_name: Anuj
  full_name: Puri, Anuj
  last_name: Puri
- first_name: P.
  full_name: Varaiya, P.
  last_name: Varaiya
citation:
  ama: Henzinger TA, Kopke P, Puri A, Varaiya P. What’s decidable about hybrid automata?
    <i>Journal of Computer and System Sciences</i>. 1998;57(1):94-124. doi:<a href="https://doi.org/10.1006/jcss.1998.1581">10.1006/jcss.1998.1581</a>
  apa: Henzinger, T. A., Kopke, P., Puri, A., &#38; Varaiya, P. (1998). What’s decidable
    about hybrid automata? <i>Journal of Computer and System Sciences</i>. Elsevier.
    <a href="https://doi.org/10.1006/jcss.1998.1581">https://doi.org/10.1006/jcss.1998.1581</a>
  chicago: Henzinger, Thomas A, Peter Kopke, Anuj Puri, and P. Varaiya. “What’s Decidable
    about Hybrid Automata?” <i>Journal of Computer and System Sciences</i>. Elsevier,
    1998. <a href="https://doi.org/10.1006/jcss.1998.1581">https://doi.org/10.1006/jcss.1998.1581</a>.
  ieee: T. A. Henzinger, P. Kopke, A. Puri, and P. Varaiya, “What’s decidable about
    hybrid automata?,” <i>Journal of Computer and System Sciences</i>, vol. 57, no.
    1. Elsevier, pp. 94–124, 1998.
  ista: Henzinger TA, Kopke P, Puri A, Varaiya P. 1998. What’s decidable about hybrid
    automata? Journal of Computer and System Sciences. 57(1), 94–124.
  mla: Henzinger, Thomas A., et al. “What’s Decidable about Hybrid Automata?” <i>Journal
    of Computer and System Sciences</i>, vol. 57, no. 1, Elsevier, 1998, pp. 94–124,
    doi:<a href="https://doi.org/10.1006/jcss.1998.1581">10.1006/jcss.1998.1581</a>.
  short: T.A. Henzinger, P. Kopke, A. Puri, P. Varaiya, Journal of Computer and System
    Sciences 57 (1998) 94–124.
date_created: 2018-12-11T12:09:08Z
date_published: 1998-01-01T00:00:00Z
date_updated: 2022-08-23T14:29:15Z
day: '01'
doi: 10.1006/jcss.1998.1581
extern: '1'
intvolume: '        57'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.sciencedirect.com/science/article/pii/S0022000098915811
month: '01'
oa: 1
oa_version: Published Version
page: 94 - 124
publication: Journal of Computer and System Sciences
publication_identifier:
  isbn:
  - 0022-0000
publication_status: published
publisher: Elsevier
publist_id: '237'
quality_controlled: '1'
status: public
title: What's decidable about hybrid automata?
type: journal_article
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 57
year: '1998'
...
