---
_id: '8015'
abstract:
- lang: eng
  text: 'The neural code of cortical processing remains uncracked; however, it must
    necessarily rely on faithful signal propagation between cortical areas. In this
    issue of Neuron, Joglekar et al. (2018) show that strong inter-areal excitation
    balanced by local inhibition can enable reliable signal propagation in data-constrained
    network models of macaque cortex. '
article_processing_charge: No
article_type: original
author:
- first_name: Jake P.
  full_name: Stroud, Jake P.
  last_name: Stroud
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
citation:
  ama: 'Stroud JP, Vogels TP. Cortical signal propagation: Balance, amplify, transmit.
    <i>Neuron</i>. 2018;98(1):8-9. doi:<a href="https://doi.org/10.1016/j.neuron.2018.03.028">10.1016/j.neuron.2018.03.028</a>'
  apa: 'Stroud, J. P., &#38; Vogels, T. P. (2018). Cortical signal propagation: Balance,
    amplify, transmit. <i>Neuron</i>. Elsevier. <a href="https://doi.org/10.1016/j.neuron.2018.03.028">https://doi.org/10.1016/j.neuron.2018.03.028</a>'
  chicago: 'Stroud, Jake P., and Tim P Vogels. “Cortical Signal Propagation: Balance,
    Amplify, Transmit.” <i>Neuron</i>. Elsevier, 2018. <a href="https://doi.org/10.1016/j.neuron.2018.03.028">https://doi.org/10.1016/j.neuron.2018.03.028</a>.'
  ieee: 'J. P. Stroud and T. P. Vogels, “Cortical signal propagation: Balance, amplify,
    transmit,” <i>Neuron</i>, vol. 98, no. 1. Elsevier, pp. 8–9, 2018.'
  ista: 'Stroud JP, Vogels TP. 2018. Cortical signal propagation: Balance, amplify,
    transmit. Neuron. 98(1), 8–9.'
  mla: 'Stroud, Jake P., and Tim P. Vogels. “Cortical Signal Propagation: Balance,
    Amplify, Transmit.” <i>Neuron</i>, vol. 98, no. 1, Elsevier, 2018, pp. 8–9, doi:<a
    href="https://doi.org/10.1016/j.neuron.2018.03.028">10.1016/j.neuron.2018.03.028</a>.'
  short: J.P. Stroud, T.P. Vogels, Neuron 98 (2018) 8–9.
date_created: 2020-06-25T12:53:39Z
date_published: 2018-04-04T00:00:00Z
date_updated: 2021-01-12T08:16:31Z
day: '04'
doi: 10.1016/j.neuron.2018.03.028
extern: '1'
external_id:
  pmid:
  - '29621492'
fulldoi: https://doi.org/10.1016/j.neuron.2018.03.028
intvolume: '        98'
issue: '1'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.neuron.2018.03.028
month: '04'
oa: 1
oa_version: Published Version
page: 8-9
pmid: 1
publication: Neuron
publication_identifier:
  issn:
  - 0896-6273
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: 'Cortical signal propagation: Balance, amplify, transmit'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 98
year: '2018'
...
---
_id: '806'
abstract:
- lang: eng
  text: Social insect colonies have evolved many collectively performed adaptations
    that reduce the impact of infectious disease and that are expected to maximize
    their fitness. This colony-level protection is termed social immunity, and it
    enhances the health and survival of the colony. In this review, we address how
    social immunity emerges from its mechanistic components to produce colony-level
    disease avoidance, resistance, and tolerance. To understand the evolutionary causes
    and consequences of social immunity, we highlight the need for studies that evaluate
    the effects of social immunity on colony fitness. We discuss the role that host
    life history and ecology have on predicted eco-evolutionary dynamics, which differ
    among the social insect lineages. Throughout the review, we highlight current
    gaps in our knowledge and promising avenues for future research, which we hope
    will bring us closer to an integrated understanding of socio-eco-evo-immunology.
article_processing_charge: No
author:
- first_name: Sylvia
  full_name: Cremer, Sylvia
  id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
  last_name: Cremer
  orcid: 0000-0002-2193-3868
- first_name: Christopher
  full_name: Pull, Christopher
  id: 3C7F4840-F248-11E8-B48F-1D18A9856A87
  last_name: Pull
  orcid: 0000-0003-1122-3982
- first_name: Matthias
  full_name: Fürst, Matthias
  id: 393B1196-F248-11E8-B48F-1D18A9856A87
  last_name: Fürst
  orcid: 0000-0002-3712-925X
citation:
  ama: 'Cremer S, Pull C, Fürst M. Social immunity: Emergence and evolution of colony-level
    disease protection. <i>Annual Review of Entomology</i>. 2018;63:105-123. doi:<a
    href="https://doi.org/10.1146/annurev-ento-020117-043110">10.1146/annurev-ento-020117-043110</a>'
  apa: 'Cremer, S., Pull, C., &#38; Fürst, M. (2018). Social immunity: Emergence and
    evolution of colony-level disease protection. <i>Annual Review of Entomology</i>.
    Annual Reviews. <a href="https://doi.org/10.1146/annurev-ento-020117-043110">https://doi.org/10.1146/annurev-ento-020117-043110</a>'
  chicago: 'Cremer, Sylvia, Christopher Pull, and Matthias Fürst. “Social Immunity:
    Emergence and Evolution of Colony-Level Disease Protection.” <i>Annual Review
    of Entomology</i>. Annual Reviews, 2018. <a href="https://doi.org/10.1146/annurev-ento-020117-043110">https://doi.org/10.1146/annurev-ento-020117-043110</a>.'
  ieee: 'S. Cremer, C. Pull, and M. Fürst, “Social immunity: Emergence and evolution
    of colony-level disease protection,” <i>Annual Review of Entomology</i>, vol.
    63. Annual Reviews, pp. 105–123, 2018.'
  ista: 'Cremer S, Pull C, Fürst M. 2018. Social immunity: Emergence and evolution
    of colony-level disease protection. Annual Review of Entomology. 63, 105–123.'
  mla: 'Cremer, Sylvia, et al. “Social Immunity: Emergence and Evolution of Colony-Level
    Disease Protection.” <i>Annual Review of Entomology</i>, vol. 63, Annual Reviews,
    2018, pp. 105–23, doi:<a href="https://doi.org/10.1146/annurev-ento-020117-043110">10.1146/annurev-ento-020117-043110</a>.'
  short: S. Cremer, C. Pull, M. Fürst, Annual Review of Entomology 63 (2018) 105–123.
corr_author: '1'
date_created: 2018-12-11T11:48:36Z
date_published: 2018-01-07T00:00:00Z
date_updated: 2026-04-08T14:19:10Z
day: '07'
department:
- _id: SyCr
doi: 10.1146/annurev-ento-020117-043110
external_id:
  isi:
  - '000424633700008'
fulldoi: https://doi.org/10.1146/annurev-ento-020117-043110
intvolume: '        63'
isi: 1
language:
- iso: eng
month: '01'
oa_version: None
page: 105 - 123
publication: Annual Review of Entomology
publication_identifier:
  issn:
  - 1545-4487
publication_status: published
publisher: Annual Reviews
publist_id: '6844'
quality_controlled: '1'
related_material:
  record:
  - id: '819'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: 'Social immunity: Emergence and evolution of colony-level disease protection'
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 63
year: '2018'
...
---
_id: '8073'
abstract:
- lang: eng
  text: Motor cortex (M1) exhibits a rich repertoire of neuronal activities to support
    the generation of complex movements. Although recent neuronal-network models capture
    many qualitative aspects of M1 dynamics, they can generate only a few distinct
    movements. Additionally, it is unclear how M1 efficiently controls movements over
    a wide range of shapes and speeds. We demonstrate that modulation of neuronal
    input–output gains in recurrent neuronal-network models with a fixed architecture
    can dramatically reorganize neuronal activity and thus downstream muscle outputs.
    Consistent with the observation of diffuse neuromodulatory projections to M1,
    a relatively small number of modulatory control units provide sufficient flexibility
    to adjust high-dimensional network activity using a simple reward-based learning
    rule. Furthermore, it is possible to assemble novel movements from previously
    learned primitives, and one can separately change movement speed while preserving
    movement shape. Our results provide a new perspective on the role of modulatory
    systems in controlling recurrent cortical activity.
article_processing_charge: No
article_type: original
author:
- first_name: Jake P.
  full_name: Stroud, Jake P.
  last_name: Stroud
- first_name: Mason A.
  full_name: Porter, Mason A.
  last_name: Porter
- first_name: Guillaume
  full_name: Hennequin, Guillaume
  last_name: Hennequin
- first_name: Tim P
  full_name: Vogels, Tim P
  id: CB6FF8D2-008F-11EA-8E08-2637E6697425
  last_name: Vogels
  orcid: 0000-0003-3295-6181
citation:
  ama: Stroud JP, Porter MA, Hennequin G, Vogels TP. Motor primitives in space and
    time via targeted gain modulation in cortical networks. <i>Nature Neuroscience</i>.
    2018;21(12):1774-1783. doi:<a href="https://doi.org/10.1038/s41593-018-0276-0">10.1038/s41593-018-0276-0</a>
  apa: Stroud, J. P., Porter, M. A., Hennequin, G., &#38; Vogels, T. P. (2018). Motor
    primitives in space and time via targeted gain modulation in cortical networks.
    <i>Nature Neuroscience</i>. Springer Nature. <a href="https://doi.org/10.1038/s41593-018-0276-0">https://doi.org/10.1038/s41593-018-0276-0</a>
  chicago: Stroud, Jake P., Mason A. Porter, Guillaume Hennequin, and Tim P Vogels.
    “Motor Primitives in Space and Time via Targeted Gain Modulation in Cortical Networks.”
    <i>Nature Neuroscience</i>. Springer Nature, 2018. <a href="https://doi.org/10.1038/s41593-018-0276-0">https://doi.org/10.1038/s41593-018-0276-0</a>.
  ieee: J. P. Stroud, M. A. Porter, G. Hennequin, and T. P. Vogels, “Motor primitives
    in space and time via targeted gain modulation in cortical networks,” <i>Nature
    Neuroscience</i>, vol. 21, no. 12. Springer Nature, pp. 1774–1783, 2018.
  ista: Stroud JP, Porter MA, Hennequin G, Vogels TP. 2018. Motor primitives in space
    and time via targeted gain modulation in cortical networks. Nature Neuroscience.
    21(12), 1774–1783.
  mla: Stroud, Jake P., et al. “Motor Primitives in Space and Time via Targeted Gain
    Modulation in Cortical Networks.” <i>Nature Neuroscience</i>, vol. 21, no. 12,
    Springer Nature, 2018, pp. 1774–83, doi:<a href="https://doi.org/10.1038/s41593-018-0276-0">10.1038/s41593-018-0276-0</a>.
  short: J.P. Stroud, M.A. Porter, G. Hennequin, T.P. Vogels, Nature Neuroscience
    21 (2018) 1774–1783.
date_created: 2020-06-30T13:18:02Z
date_published: 2018-12-01T00:00:00Z
date_updated: 2021-01-12T08:16:46Z
day: '01'
doi: 10.1038/s41593-018-0276-0
extern: '1'
external_id:
  pmid:
  - '30482949'
fulldoi: https://doi.org/10.1038/s41593-018-0276-0
intvolume: '        21'
issue: '12'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276991/
month: '12'
oa: 1
oa_version: Submitted Version
page: 1774-1783
pmid: 1
publication: Nature Neuroscience
publication_identifier:
  issn:
  - 1097-6256
  - 1546-1726
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
related_material:
  link:
  - relation: erratum
    url: https://doi.org/10.1038/s41593-018-0307-x
status: public
title: Motor primitives in space and time via targeted gain modulation in cortical
  networks
type: journal_article
user_id: D865714E-FA4E-11E9-B85B-F5C5E5697425
volume: 21
year: '2018'
...
---
_id: '81'
abstract:
- lang: eng
  text: We solve the offline monitoring problem for timed propositional temporal logic
    (TPTL), interpreted over dense-time Boolean signals. The variant of TPTL we consider
    extends linear temporal logic (LTL) with clock variables and reset quantifiers,
    providing a mechanism to specify real-time constraints. We first describe a general
    monitoring algorithm based on an exhaustive computation of the set of satisfying
    clock assignments as a finite union of zones. We then propose a specialized monitoring
    algorithm for the one-variable case using a partition of the time domain based
    on the notion of region equivalence, whose complexity is linear in the length
    of the signal, thereby generalizing a known result regarding the monitoring of
    metric temporal logic (MTL). The region and zone representations of time constraints
    are known from timed automata verification and can also be used in the discrete-time
    case. Our prototype implementation appears to outperform previous discrete-time
    implementations of TPTL monitoring,
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Adrian
  full_name: Elgyütt, Adrian
  id: 4A2E9DBA-F248-11E8-B48F-1D18A9856A87
  last_name: Elgyütt
- first_name: Thomas
  full_name: Ferrere, Thomas
  id: 40960E6E-F248-11E8-B48F-1D18A9856A87
  last_name: Ferrere
  orcid: 0000-0001-5199-3143
- first_name: Thomas A
  full_name: Henzinger, Thomas A
  id: 40876CD8-F248-11E8-B48F-1D18A9856A87
  last_name: Henzinger
  orcid: 0000−0002−2985−7724
citation:
  ama: 'Elgyütt A, Ferrere T, Henzinger TA. Monitoring temporal logic with clock variables.
    In: Vol 11022. Springer; 2018:53-70. doi:<a href="https://doi.org/10.1007/978-3-030-00151-3_4">10.1007/978-3-030-00151-3_4</a>'
  apa: 'Elgyütt, A., Ferrere, T., &#38; Henzinger, T. A. (2018). Monitoring temporal
    logic with clock variables (Vol. 11022, pp. 53–70). Presented at the FORMATS:
    Formal Modeling and Analysis of Timed Systems, Beijing, China: Springer. <a href="https://doi.org/10.1007/978-3-030-00151-3_4">https://doi.org/10.1007/978-3-030-00151-3_4</a>'
  chicago: Elgyütt, Adrian, Thomas Ferrere, and Thomas A Henzinger. “Monitoring Temporal
    Logic with Clock Variables,” 11022:53–70. Springer, 2018. <a href="https://doi.org/10.1007/978-3-030-00151-3_4">https://doi.org/10.1007/978-3-030-00151-3_4</a>.
  ieee: 'A. Elgyütt, T. Ferrere, and T. A. Henzinger, “Monitoring temporal logic with
    clock variables,” presented at the FORMATS: Formal Modeling and Analysis of Timed
    Systems, Beijing, China, 2018, vol. 11022, pp. 53–70.'
  ista: 'Elgyütt A, Ferrere T, Henzinger TA. 2018. Monitoring temporal logic with
    clock variables. FORMATS: Formal Modeling and Analysis of Timed Systems, LNCS,
    vol. 11022, 53–70.'
  mla: Elgyütt, Adrian, et al. <i>Monitoring Temporal Logic with Clock Variables</i>.
    Vol. 11022, Springer, 2018, pp. 53–70, doi:<a href="https://doi.org/10.1007/978-3-030-00151-3_4">10.1007/978-3-030-00151-3_4</a>.
  short: A. Elgyütt, T. Ferrere, T.A. Henzinger, in:, Springer, 2018, pp. 53–70.
conference:
  end_date: 2018-09-06
  location: Beijing, China
  name: 'FORMATS: Formal Modeling and Analysis of Timed Systems'
  start_date: 2018-09-04
date_created: 2018-12-11T11:44:31Z
date_published: 2018-08-26T00:00:00Z
date_updated: 2025-04-15T06:26:03Z
day: '26'
ddc:
- '000'
department:
- _id: ToHe
doi: 10.1007/978-3-030-00151-3_4
external_id:
  isi:
  - '000884993200004'
file:
- access_level: open_access
  checksum: e5d81c9b50a6bd9d8a2c16953aad7e23
  content_type: application/pdf
  creator: dernst
  date_created: 2020-10-09T06:24:21Z
  date_updated: 2020-10-09T06:24:21Z
  file_id: '8638'
  file_name: 2018_LNCS_Elgyuett.pdf
  file_size: 537219
  relation: main_file
  success: 1
file_date_updated: 2020-10-09T06:24:21Z
fulldoi: https://doi.org/10.1007/978-3-030-00151-3_4
has_accepted_license: '1'
intvolume: '     11022'
isi: 1
language:
- iso: eng
month: '08'
oa: 1
oa_version: Submitted Version
page: 53 - 70
project:
- _id: 25F5A88A-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: S11402-N23
  name: Moderne Concurrency Paradigms
- _id: 25F42A32-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z211
  name: Formal methods for the design and analysis of complex systems
publication_status: published
publisher: Springer
publist_id: '7973'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Monitoring temporal logic with clock variables
type: conference
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 11022
year: '2018'
...
---
_id: '82'
abstract:
- lang: eng
  text: In experimental cultures, when bacteria are mixed with lytic (virulent) bacteriophage,
    bacterial cells resistant to the phage commonly emerge and become the dominant
    population of bacteria. Following the ascent of resistant mutants, the densities
    of bacteria in these simple communities become limited by resources rather than
    the phage. Despite the evolution of resistant hosts, upon which the phage cannot
    replicate, the lytic phage population is most commonly maintained in an apparently
    stable state with the resistant bacteria. Several mechanisms have been put forward
    to account for this result. Here we report the results of population dynamic/evolution
    experiments with a virulent mutant of phage Lambda, λVIR, and Escherichia coli
    in serial transfer cultures. We show that, following the ascent of λVIR-resistant
    bacteria, λVIRis maintained in the majority of cases in maltose-limited minimal
    media and in all cases in nutrient-rich broth. Using mathematical models and experiments,
    we show that the dominant mechanism responsible for maintenance of λVIRin these
    resource-limited populations dominated by resistant E. coli is a high rate of
    either phenotypic or genetic transition from resistance to susceptibility—a hitherto
    undemonstrated mechanism we term &quot;leaky resistance.&quot; We discuss the
    implications of leaky resistance to our understanding of the conditions for the
    maintenance of phage in populations of bacteria—their “existence conditions.”.
article_number: '2005971'
article_processing_charge: Yes
author:
- first_name: Waqas
  full_name: Chaudhry, Waqas
  last_name: Chaudhry
- first_name: Maros
  full_name: Pleska, Maros
  id: 4569785E-F248-11E8-B48F-1D18A9856A87
  last_name: Pleska
  orcid: 0000-0001-7460-7479
- first_name: Nilang
  full_name: Shah, Nilang
  last_name: Shah
- first_name: Howard
  full_name: Weiss, Howard
  last_name: Weiss
- first_name: Ingrid
  full_name: Mccall, Ingrid
  last_name: Mccall
- first_name: Justin
  full_name: Meyer, Justin
  last_name: Meyer
- first_name: Animesh
  full_name: Gupta, Animesh
  last_name: Gupta
- first_name: Calin C
  full_name: Guet, Calin C
  id: 47F8433E-F248-11E8-B48F-1D18A9856A87
  last_name: Guet
  orcid: 0000-0001-6220-2052
- first_name: Bruce
  full_name: Levin, Bruce
  last_name: Levin
citation:
  ama: Chaudhry W, Pleska M, Shah N, et al. Leaky resistance and the conditions for
    the existence of lytic bacteriophage. <i>PLoS Biology</i>. 2018;16(8). doi:<a
    href="https://doi.org/10.1371/journal.pbio.2005971">10.1371/journal.pbio.2005971</a>
  apa: Chaudhry, W., Pleska, M., Shah, N., Weiss, H., Mccall, I., Meyer, J., … Levin,
    B. (2018). Leaky resistance and the conditions for the existence of lytic bacteriophage.
    <i>PLoS Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.2005971">https://doi.org/10.1371/journal.pbio.2005971</a>
  chicago: Chaudhry, Waqas, Maros Pleska, Nilang Shah, Howard Weiss, Ingrid Mccall,
    Justin Meyer, Animesh Gupta, Calin C Guet, and Bruce Levin. “Leaky Resistance
    and the Conditions for the Existence of Lytic Bacteriophage.” <i>PLoS Biology</i>.
    Public Library of Science, 2018. <a href="https://doi.org/10.1371/journal.pbio.2005971">https://doi.org/10.1371/journal.pbio.2005971</a>.
  ieee: W. Chaudhry <i>et al.</i>, “Leaky resistance and the conditions for the existence
    of lytic bacteriophage,” <i>PLoS Biology</i>, vol. 16, no. 8. Public Library of
    Science, 2018.
  ista: Chaudhry W, Pleska M, Shah N, Weiss H, Mccall I, Meyer J, Gupta A, Guet CC,
    Levin B. 2018. Leaky resistance and the conditions for the existence of lytic
    bacteriophage. PLoS Biology. 16(8), 2005971.
  mla: Chaudhry, Waqas, et al. “Leaky Resistance and the Conditions for the Existence
    of Lytic Bacteriophage.” <i>PLoS Biology</i>, vol. 16, no. 8, 2005971, Public
    Library of Science, 2018, doi:<a href="https://doi.org/10.1371/journal.pbio.2005971">10.1371/journal.pbio.2005971</a>.
  short: W. Chaudhry, M. Pleska, N. Shah, H. Weiss, I. Mccall, J. Meyer, A. Gupta,
    C.C. Guet, B. Levin, PLoS Biology 16 (2018).
date_created: 2018-12-11T11:44:32Z
date_published: 2018-08-16T00:00:00Z
date_updated: 2023-09-13T08:45:41Z
day: '16'
ddc:
- '570'
department:
- _id: CaGu
doi: 10.1371/journal.pbio.2005971
external_id:
  isi:
  - '000443383300024'
file:
- access_level: open_access
  checksum: 527076f78265cd4ea192cd1569851587
  content_type: application/pdf
  creator: dernst
  date_created: 2018-12-17T12:55:31Z
  date_updated: 2020-07-14T12:48:10Z
  file_id: '5706'
  file_name: 2018_Plos_Chaudhry.pdf
  file_size: 4007095
  relation: main_file
file_date_updated: 2020-07-14T12:48:10Z
fulldoi: https://doi.org/10.1371/journal.pbio.2005971
has_accepted_license: '1'
intvolume: '        16'
isi: 1
issue: '8'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
publication: PLoS Biology
publication_status: published
publisher: Public Library of Science
publist_id: '7972'
quality_controlled: '1'
related_material:
  record:
  - id: '9810'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Leaky resistance and the conditions for the existence of lytic bacteriophage
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: c635000d-4b10-11ee-a964-aac5a93f6ac1
volume: 16
year: '2018'
...
---
_id: '8231'
article_processing_charge: No
article_type: letter_note
author:
- first_name: Judit
  full_name: Fazekas-Singer, Judit
  id: 36432834-F248-11E8-B48F-1D18A9856A87
  last_name: Fazekas-Singer
  orcid: 0000-0002-8777-3502
- first_name: Josef
  full_name: Singer, Josef
  last_name: Singer
- first_name: Kristina M.
  full_name: Ilieva, Kristina M.
  last_name: Ilieva
- first_name: Miroslawa
  full_name: Matz, Miroslawa
  last_name: Matz
- first_name: Ina
  full_name: Herrmann, Ina
  last_name: Herrmann
- first_name: Edzard
  full_name: Spillner, Edzard
  last_name: Spillner
- first_name: Sophia N.
  full_name: Karagiannis, Sophia N.
  last_name: Karagiannis
- first_name: Erika
  full_name: Jensen-Jarolim, Erika
  last_name: Jensen-Jarolim
citation:
  ama: 'Singer J, Singer J, Ilieva KM, et al. AllergoOncology: Generating a canine
    anticancer IgE against the epidermal growth factor receptor. <i>Journal of Allergy
    and Clinical Immunology</i>. 2018;142(3):973-976.e11. doi:<a href="https://doi.org/10.1016/j.jaci.2018.04.021">10.1016/j.jaci.2018.04.021</a>'
  apa: 'Singer, J., Singer, J., Ilieva, K. M., Matz, M., Herrmann, I., Spillner, E.,
    … Jensen-Jarolim, E. (2018). AllergoOncology: Generating a canine anticancer IgE
    against the epidermal growth factor receptor. <i>Journal of Allergy and Clinical
    Immunology</i>. Elsevier. <a href="https://doi.org/10.1016/j.jaci.2018.04.021">https://doi.org/10.1016/j.jaci.2018.04.021</a>'
  chicago: 'Singer, Judit, Josef Singer, Kristina M. Ilieva, Miroslawa Matz, Ina Herrmann,
    Edzard Spillner, Sophia N. Karagiannis, and Erika Jensen-Jarolim. “AllergoOncology:
    Generating a Canine Anticancer IgE against the Epidermal Growth Factor Receptor.”
    <i>Journal of Allergy and Clinical Immunology</i>. Elsevier, 2018. <a href="https://doi.org/10.1016/j.jaci.2018.04.021">https://doi.org/10.1016/j.jaci.2018.04.021</a>.'
  ieee: 'J. Singer <i>et al.</i>, “AllergoOncology: Generating a canine anticancer
    IgE against the epidermal growth factor receptor,” <i>Journal of Allergy and Clinical
    Immunology</i>, vol. 142, no. 3. Elsevier, p. 973–976.e11, 2018.'
  ista: 'Singer J, Singer J, Ilieva KM, Matz M, Herrmann I, Spillner E, Karagiannis
    SN, Jensen-Jarolim E. 2018. AllergoOncology: Generating a canine anticancer IgE
    against the epidermal growth factor receptor. Journal of Allergy and Clinical
    Immunology. 142(3), 973–976.e11.'
  mla: 'Singer, Judit, et al. “AllergoOncology: Generating a Canine Anticancer IgE
    against the Epidermal Growth Factor Receptor.” <i>Journal of Allergy and Clinical
    Immunology</i>, vol. 142, no. 3, Elsevier, 2018, p. 973–976.e11, doi:<a href="https://doi.org/10.1016/j.jaci.2018.04.021">10.1016/j.jaci.2018.04.021</a>.'
  short: J. Singer, J. Singer, K.M. Ilieva, M. Matz, I. Herrmann, E. Spillner, S.N.
    Karagiannis, E. Jensen-Jarolim, Journal of Allergy and Clinical Immunology 142
    (2018) 973–976.e11.
date_created: 2020-08-10T11:51:36Z
date_published: 2018-09-01T00:00:00Z
date_updated: 2021-01-12T08:17:37Z
day: '01'
doi: 10.1016/j.jaci.2018.04.021
extern: '1'
fulldoi: https://doi.org/10.1016/j.jaci.2018.04.021
intvolume: '       142'
issue: '3'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.jaci.2018.04.021
month: '09'
oa: 1
oa_version: Published Version
page: 973-976.e11
publication: Journal of Allergy and Clinical Immunology
publication_identifier:
  issn:
  - 0091-6749
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: 'AllergoOncology: Generating a canine anticancer IgE against the epidermal
  growth factor receptor'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 142
year: '2018'
...
---
_id: '8232'
abstract:
- lang: eng
  text: 'Anti-epidermal growth factor receptor (EGFR) antibody therapy is used in
    EGFR expressing cancers including lung, colon, head and neck, and bladder cancers,
    however results have been modest. Near infrared photoimmunotherapy (NIR-PIT) is
    a highly selective tumor treatment that employs an antibody-photo-absorber conjugate
    which is activated by NIR light. NIR-PIT is in clinical trials in patients with
    recurrent head and neck cancers using cetuximab-IR700 as the conjugate. However,
    its use has otherwise been restricted to mouse models. This is an effort to explore
    larger animal models with NIR-PIT. We describe the use of a recombinant canine
    anti-EGFR monoclonal antibody (mAb), can225IgG, conjugated to the photo-absorber,
    IR700DX, in three EGFR expressing canine transitional cell carcinoma (TCC) cell
    lines as a prelude to possible canine clinical studies. Can225-IR700 conjugate
    showed specific binding and cell-specific killing after NIR-PIT on EGFR expressing
    cells in vitro. In the in vivo study, can225-IR700 conjugate demonstrated accumulation
    of the fluorescent conjugate with high tumor-to-background ratio. Tumor-bearing
    mice were separated into 4 groups: (1) no treatment; (2) 100 μg of can225-IR700
    i.v. only; (3) NIR light exposure only; (4) 100 μg of can225-IR700 i.v., NIR light
    exposure. Tumor growth was significantly inhibited by NIR-PIT treatment compared
    with the other groups (p < 0.001), and significantly prolonged survival was achieved
    (p < 0.001 vs. other groups) in the treatment groups. In conclusion, NIR-PIT with
    can225-IR700 is a promising treatment for canine EGFR-expressing cancers, including
    invasive transitional cell carcinoma in pet dogs, that could provide a pathway
    to translation to humans.'
article_processing_charge: No
article_type: original
author:
- first_name: Tadanobu
  full_name: Nagaya, Tadanobu
  last_name: Nagaya
- first_name: Shuhei
  full_name: Okuyama, Shuhei
  last_name: Okuyama
- first_name: Fusa
  full_name: Ogata, Fusa
  last_name: Ogata
- first_name: Yasuhiro
  full_name: Maruoka, Yasuhiro
  last_name: Maruoka
- first_name: Deborah W.
  full_name: Knapp, Deborah W.
  last_name: Knapp
- first_name: Sophia N.
  full_name: Karagiannis, Sophia N.
  last_name: Karagiannis
- first_name: Judit
  full_name: Fazekas-Singer, Judit
  id: 36432834-F248-11E8-B48F-1D18A9856A87
  last_name: Fazekas-Singer
  orcid: 0000-0002-8777-3502
- first_name: Peter L.
  full_name: Choyke, Peter L.
  last_name: Choyke
- first_name: Amy K.
  full_name: LeBlanc, Amy K.
  last_name: LeBlanc
- first_name: Erika
  full_name: Jensen-Jarolim, Erika
  last_name: Jensen-Jarolim
- first_name: Hisataka
  full_name: Kobayashi, Hisataka
  last_name: Kobayashi
citation:
  ama: Nagaya T, Okuyama S, Ogata F, et al. Near infrared photoimmunotherapy targeting
    bladder cancer with a canine anti-epidermal growth factor receptor (EGFR) antibody.
    <i>Oncotarget</i>. 2018;9:19026-19038. doi:<a href="https://doi.org/10.18632/oncotarget.24876">10.18632/oncotarget.24876</a>
  apa: Nagaya, T., Okuyama, S., Ogata, F., Maruoka, Y., Knapp, D. W., Karagiannis,
    S. N., … Kobayashi, H. (2018). Near infrared photoimmunotherapy targeting bladder
    cancer with a canine anti-epidermal growth factor receptor (EGFR) antibody. <i>Oncotarget</i>.
    Impact Journals. <a href="https://doi.org/10.18632/oncotarget.24876">https://doi.org/10.18632/oncotarget.24876</a>
  chicago: Nagaya, Tadanobu, Shuhei Okuyama, Fusa Ogata, Yasuhiro Maruoka, Deborah
    W. Knapp, Sophia N. Karagiannis, Judit Singer, et al. “Near Infrared Photoimmunotherapy
    Targeting Bladder Cancer with a Canine Anti-Epidermal Growth Factor Receptor (EGFR)
    Antibody.” <i>Oncotarget</i>. Impact Journals, 2018. <a href="https://doi.org/10.18632/oncotarget.24876">https://doi.org/10.18632/oncotarget.24876</a>.
  ieee: T. Nagaya <i>et al.</i>, “Near infrared photoimmunotherapy targeting bladder
    cancer with a canine anti-epidermal growth factor receptor (EGFR) antibody,” <i>Oncotarget</i>,
    vol. 9. Impact Journals, pp. 19026–19038, 2018.
  ista: Nagaya T, Okuyama S, Ogata F, Maruoka Y, Knapp DW, Karagiannis SN, Singer
    J, Choyke PL, LeBlanc AK, Jensen-Jarolim E, Kobayashi H. 2018. Near infrared photoimmunotherapy
    targeting bladder cancer with a canine anti-epidermal growth factor receptor (EGFR)
    antibody. Oncotarget. 9, 19026–19038.
  mla: Nagaya, Tadanobu, et al. “Near Infrared Photoimmunotherapy Targeting Bladder
    Cancer with a Canine Anti-Epidermal Growth Factor Receptor (EGFR) Antibody.” <i>Oncotarget</i>,
    vol. 9, Impact Journals, 2018, pp. 19026–38, doi:<a href="https://doi.org/10.18632/oncotarget.24876">10.18632/oncotarget.24876</a>.
  short: T. Nagaya, S. Okuyama, F. Ogata, Y. Maruoka, D.W. Knapp, S.N. Karagiannis,
    J. Singer, P.L. Choyke, A.K. LeBlanc, E. Jensen-Jarolim, H. Kobayashi, Oncotarget
    9 (2018) 19026–19038.
date_created: 2020-08-10T11:52:54Z
date_published: 2018-04-10T00:00:00Z
date_updated: 2021-01-12T08:17:37Z
day: '10'
doi: 10.18632/oncotarget.24876
extern: '1'
fulldoi: https://doi.org/10.18632/oncotarget.24876
intvolume: '         9'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.18632/oncotarget.24876
month: '04'
oa: 1
oa_version: Published Version
page: 19026-19038
publication: Oncotarget
publication_identifier:
  eissn:
  - 1949-2553
publication_status: published
publisher: Impact Journals
quality_controlled: '1'
status: public
title: Near infrared photoimmunotherapy targeting bladder cancer with a canine anti-epidermal
  growth factor receptor (EGFR) antibody
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 9
year: '2018'
...
---
_id: '8233'
abstract:
- lang: eng
  text: The M2a subtype of macrophages plays an important role in human immunoglobulin
    E (IgE-mediated allergies) and other Th2 type immune reactions. In contrast, very
    little is known about these cells in the dog. Here we describe an in vitro method
    to activate canine histiocytic DH82 cells and primary canine monocyte-derived
    macrophages (MDMs) toward the M2a macrophages using human cytokines. For a side-by-side
    comparison, we compared the canine cells to human MDMs, and the human monocytic
    cell line U937 activated towards M1 and M2a cells on the cellular and molecular
    level. In analogy to activated human M2a cells, canine M2a, differentiated from
    both DH82 and MDMs, showed an increase in CD206 surface receptor expression compared
    to M1. Interestingly, canine M2a, but not M1 derived from MDM, upregulated the
    high-affinity IgE receptor (FcεRI). Transcription levels of M2a-associated genes
    (IL10, CCL22, TGFβ, CD163) showed a diverse pattern between the human and dog
    species, whereas M1 genes (IDO1, CXCL11, IL6, TNF-α) were similarly upregulated
    in canine and human M1 cells (cell lines and MDMs). We suggest that our novel
    in vitro method will be suitable in comparative allergology studies focussing
    on macrophages.
article_processing_charge: No
article_type: original
author:
- first_name: Ina
  full_name: Herrmann, Ina
  last_name: Herrmann
- first_name: Jelena
  full_name: Gotovina, Jelena
  last_name: Gotovina
- first_name: Judit
  full_name: Fazekas-Singer, Judit
  id: 36432834-F248-11E8-B48F-1D18A9856A87
  last_name: Fazekas-Singer
  orcid: 0000-0002-8777-3502
- first_name: Michael B.
  full_name: Fischer, Michael B.
  last_name: Fischer
- first_name: Karin
  full_name: Hufnagl, Karin
  last_name: Hufnagl
- first_name: Rodolfo
  full_name: Bianchini, Rodolfo
  last_name: Bianchini
- first_name: Erika
  full_name: Jensen-Jarolim, Erika
  last_name: Jensen-Jarolim
citation:
  ama: Herrmann I, Gotovina J, Singer J, et al. Canine macrophages can like human
    macrophages be in vitro activated toward the M2a subtype relevant in allergy.
    <i>Developmental &#38; Comparative Immunology</i>. 2018;82(5):118-127. doi:<a
    href="https://doi.org/10.1016/j.dci.2018.01.005">10.1016/j.dci.2018.01.005</a>
  apa: Herrmann, I., Gotovina, J., Singer, J., Fischer, M. B., Hufnagl, K., Bianchini,
    R., &#38; Jensen-Jarolim, E. (2018). Canine macrophages can like human macrophages
    be in vitro activated toward the M2a subtype relevant in allergy. <i>Developmental
    &#38; Comparative Immunology</i>. Elsevier. <a href="https://doi.org/10.1016/j.dci.2018.01.005">https://doi.org/10.1016/j.dci.2018.01.005</a>
  chicago: Herrmann, Ina, Jelena Gotovina, Judit Singer, Michael B. Fischer, Karin
    Hufnagl, Rodolfo Bianchini, and Erika Jensen-Jarolim. “Canine Macrophages Can
    like Human Macrophages Be in Vitro Activated toward the M2a Subtype Relevant in
    Allergy.” <i>Developmental &#38; Comparative Immunology</i>. Elsevier, 2018. <a
    href="https://doi.org/10.1016/j.dci.2018.01.005">https://doi.org/10.1016/j.dci.2018.01.005</a>.
  ieee: I. Herrmann <i>et al.</i>, “Canine macrophages can like human macrophages
    be in vitro activated toward the M2a subtype relevant in allergy,” <i>Developmental
    &#38; Comparative Immunology</i>, vol. 82, no. 5. Elsevier, pp. 118–127, 2018.
  ista: Herrmann I, Gotovina J, Singer J, Fischer MB, Hufnagl K, Bianchini R, Jensen-Jarolim
    E. 2018. Canine macrophages can like human macrophages be in vitro activated toward
    the M2a subtype relevant in allergy. Developmental &#38; Comparative Immunology.
    82(5), 118–127.
  mla: Herrmann, Ina, et al. “Canine Macrophages Can like Human Macrophages Be in Vitro
    Activated toward the M2a Subtype Relevant in Allergy.” <i>Developmental &#38;
    Comparative Immunology</i>, vol. 82, no. 5, Elsevier, 2018, pp. 118–27, doi:<a
    href="https://doi.org/10.1016/j.dci.2018.01.005">10.1016/j.dci.2018.01.005</a>.
  short: I. Herrmann, J. Gotovina, J. Singer, M.B. Fischer, K. Hufnagl, R. Bianchini,
    E. Jensen-Jarolim, Developmental &#38; Comparative Immunology 82 (2018) 118–127.
date_created: 2020-08-10T11:53:01Z
date_published: 2018-05-01T00:00:00Z
date_updated: 2021-01-12T08:17:38Z
day: '01'
doi: 10.1016/j.dci.2018.01.005
extern: '1'
fulldoi: https://doi.org/10.1016/j.dci.2018.01.005
intvolume: '        82'
issue: '5'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1016/j.dci.2018.01.005
month: '05'
oa: 1
oa_version: Published Version
page: 118-127
publication: Developmental & Comparative Immunology
publication_identifier:
  issn:
  - 0145-305X
publication_status: published
publisher: Elsevier
quality_controlled: '1'
status: public
title: Canine macrophages can like human macrophages be in vitro activated toward
  the M2a subtype relevant in allergy
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 82
year: '2018'
...
---
_id: '8234'
abstract:
- lang: eng
  text: Molecular imaging probes such as PET-tracers have the potential to improve
    the accuracy of tumor characterization by directly visualizing the biochemical
    situation. Thus, molecular changes can be detected early before morphological
    manifestation. The A3 adenosine receptor (A3AR) is described to be highly expressed
    in colon cancer cell lines and human colorectal cancer (CRC), suggesting this
    receptor as a tumor marker. The aim of this preclinical study was the evaluation
    of FE@SUPPY as a PET-tracer for CRC using in vitro imaging and in vivo PET imaging.
    First, affinity and selectivity of FE@SUPPY and its metabolites were determined,
    proving the favorable binding profile of FE@SUPPY. The human adenocarcinoma cell
    line HT-29 was characterized regarding its hA3AR expression and was subsequently
    chosen as tumor graft. Promising results regarding the potential of FE@SUPPY as
    a PET-tracer for CRC imaging were obtained by autoradiography as ≥2.3-fold higher
    accumulation of FE@SUPPY was found in CRC tissue compared to adjacent healthy
    colon tissue from the same patient. Nevertheless, first in vivo studies using
    HT-29 xenografts showed insufficient tumor uptake due to (1) poor conservation
    of target expression in xenografts and (2) unfavorable pharmacokinetics of FE@SUPPY
    in mice. We therefore conclude that HT-29 xenografts are not adequate to visualize
    hA3ARs using FE@SUPPY.
article_number: '1269830'
article_processing_charge: No
article_type: original
author:
- first_name: T.
  full_name: Balber, T.
  last_name: Balber
- first_name: Judit
  full_name: Singer, Judit
  id: 36432834-F248-11E8-B48F-1D18A9856A87
  last_name: Singer
  orcid: 0000-0002-8777-3502
- first_name: N.
  full_name: Berroterán-Infante, N.
  last_name: Berroterán-Infante
- first_name: M.
  full_name: Dumanic, M.
  last_name: Dumanic
- first_name: L.
  full_name: Fetty, L.
  last_name: Fetty
- first_name: J.
  full_name: Fazekas-Singer, J.
  last_name: Fazekas-Singer
  orcid: 0000-0002-8777-3502
- first_name: C.
  full_name: Vraka, C.
  last_name: Vraka
- first_name: L.
  full_name: Nics, L.
  last_name: Nics
- first_name: M.
  full_name: Bergmann, M.
  last_name: Bergmann
- first_name: K.
  full_name: Pallitsch, K.
  last_name: Pallitsch
- first_name: H.
  full_name: Spreitzer, H.
  last_name: Spreitzer
- first_name: W.
  full_name: Wadsak, W.
  last_name: Wadsak
  orcid: 0000-0003-4479-8053
- first_name: M.
  full_name: Hacker, M.
  last_name: Hacker
- first_name: E.
  full_name: Jensen-Jarolim, E.
  last_name: Jensen-Jarolim
- first_name: H.
  full_name: Viernstein, H.
  last_name: Viernstein
- first_name: M.
  full_name: Mitterhauser, M.
  last_name: Mitterhauser
  orcid: 0000-0003-3173-5272
citation:
  ama: 'Balber T, Singer J, Berroterán-Infante N, et al. Preclinical in vitro and
    in vivo evaluation of [18F]FE@SUPPY for cancer PET imaging: Limitations of a xenograft
    model for colorectal cancer. <i>Contrast Media &#38; Molecular Imaging</i>. 2018;2018.
    doi:<a href="https://doi.org/10.1155/2018/1269830">10.1155/2018/1269830</a>'
  apa: 'Balber, T., Singer, J., Berroterán-Infante, N., Dumanic, M., Fetty, L., Fazekas-Singer,
    J., … Mitterhauser, M. (2018). Preclinical in vitro and in vivo evaluation of
    [18F]FE@SUPPY for cancer PET imaging: Limitations of a xenograft model for colorectal
    cancer. <i>Contrast Media &#38; Molecular Imaging</i>. Hindawi. <a href="https://doi.org/10.1155/2018/1269830">https://doi.org/10.1155/2018/1269830</a>'
  chicago: 'Balber, T., Judit Singer, N. Berroterán-Infante, M. Dumanic, L. Fetty,
    J. Fazekas-Singer, C. Vraka, et al. “Preclinical in Vitro and in Vivo Evaluation
    of [18F]FE@SUPPY for Cancer PET Imaging: Limitations of a Xenograft Model for
    Colorectal Cancer.” <i>Contrast Media &#38; Molecular Imaging</i>. Hindawi, 2018.
    <a href="https://doi.org/10.1155/2018/1269830">https://doi.org/10.1155/2018/1269830</a>.'
  ieee: 'T. Balber <i>et al.</i>, “Preclinical in vitro and in vivo evaluation of
    [18F]FE@SUPPY for cancer PET imaging: Limitations of a xenograft model for colorectal
    cancer,” <i>Contrast Media &#38; Molecular Imaging</i>, vol. 2018. Hindawi, 2018.'
  ista: 'Balber T, Singer J, Berroterán-Infante N, Dumanic M, Fetty L, Fazekas-Singer
    J, Vraka C, Nics L, Bergmann M, Pallitsch K, Spreitzer H, Wadsak W, Hacker M,
    Jensen-Jarolim E, Viernstein H, Mitterhauser M. 2018. Preclinical in vitro and
    in vivo evaluation of [18F]FE@SUPPY for cancer PET imaging: Limitations of a xenograft
    model for colorectal cancer. Contrast Media &#38; Molecular Imaging. 2018, 1269830.'
  mla: 'Balber, T., et al. “Preclinical in Vitro and in Vivo Evaluation of [18F]FE@SUPPY
    for Cancer PET Imaging: Limitations of a Xenograft Model for Colorectal Cancer.”
    <i>Contrast Media &#38; Molecular Imaging</i>, vol. 2018, 1269830, Hindawi, 2018,
    doi:<a href="https://doi.org/10.1155/2018/1269830">10.1155/2018/1269830</a>.'
  short: T. Balber, J. Singer, N. Berroterán-Infante, M. Dumanic, L. Fetty, J. Fazekas-Singer,
    C. Vraka, L. Nics, M. Bergmann, K. Pallitsch, H. Spreitzer, W. Wadsak, M. Hacker,
    E. Jensen-Jarolim, H. Viernstein, M. Mitterhauser, Contrast Media &#38; Molecular
    Imaging 2018 (2018).
date_created: 2020-08-10T11:53:07Z
date_published: 2018-02-13T00:00:00Z
date_updated: 2021-01-12T08:17:38Z
day: '13'
doi: 10.1155/2018/1269830
extern: '1'
fulldoi: https://doi.org/10.1155/2018/1269830
intvolume: '      2018'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1155/2018/1269830
month: '02'
oa: 1
oa_version: Published Version
publication: Contrast Media & Molecular Imaging
publication_identifier:
  issn:
  - 1555-4309
  - 1555-4317
publication_status: published
publisher: Hindawi
quality_controlled: '1'
status: public
title: 'Preclinical in vitro and in vivo evaluation of [18F]FE@SUPPY for cancer PET
  imaging: Limitations of a xenograft model for colorectal cancer'
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 2018
year: '2018'
...
---
_id: '8262'
abstract:
- lang: eng
  text: "Background: The genus Burkholderia consists of species that occupy remarkably
    diverse ecological niches. Its best known members are important pathogens, B.
    mallei and B. pseudomallei, which cause glanders and melioidosis, respectively.
    Burkholderia genomes are unusual due to their multichromosomal organization, generally
    comprised of 2-3 chromosomes.\r\n\r\nResults: We performed integrated genomic
    analysis of 127 Burkholderia strains. The pan-genome is open with the saturation
    to be reached between 86,000 and 88,000 genes. The reconstructed rearrangements
    indicate a strong avoidance of intra-replichore inversions that is likely caused
    by selection against the transfer of large groups of genes between the leading
    and the lagging strands. Translocated genes also tend to retain their position
    in the leading or the lagging strand, and this selection is stronger for large
    syntenies. Integrated reconstruction of chromosome rearrangements in the context
    of strains phylogeny reveals parallel rearrangements that may indicate inversion-based
    phase variation and integration of new genomic islands. In particular, we detected
    parallel inversions in the second chromosomes of B. pseudomallei with breakpoints
    formed by genes encoding membrane components of multidrug resistance complex,
    that may be linked to a phase variation mechanism. Two genomic islands, spreading
    horizontally between chromosomes, were detected in the B. cepacia group.\r\n\r\nConclusions:
    This study demonstrates the power of integrated analysis of pan-genomes, chromosome
    rearrangements, and selection regimes. Non-random inversion patterns indicate
    selective pressure, inversions are particularly frequent in a recent pathogen
    B. mallei, and, together with periods of positive selection at other branches,
    may indicate adaptation to new niches. One such adaptation could be a possible
    phase variation mechanism in B. pseudomallei."
article_number: '965'
article_processing_charge: No
article_type: original
author:
- first_name: Olga
  full_name: Bochkareva, Olga
  id: C4558D3C-6102-11E9-A62E-F418E6697425
  last_name: Bochkareva
  orcid: 0000-0003-1006-6639
- first_name: Elena V.
  full_name: Moroz, Elena V.
  last_name: Moroz
- first_name: Iakov I.
  full_name: Davydov, Iakov I.
  last_name: Davydov
- first_name: Mikhail S.
  full_name: Gelfand, Mikhail S.
  last_name: Gelfand
citation:
  ama: Bochkareva O, Moroz EV, Davydov II, Gelfand MS. Genome rearrangements and selection
    in multi-chromosome bacteria Burkholderia spp. <i>BMC Genomics</i>. 2018;19. doi:<a
    href="https://doi.org/10.1186/s12864-018-5245-1">10.1186/s12864-018-5245-1</a>
  apa: Bochkareva, O., Moroz, E. V., Davydov, I. I., &#38; Gelfand, M. S. (2018).
    Genome rearrangements and selection in multi-chromosome bacteria Burkholderia
    spp. <i>BMC Genomics</i>. Springer Nature. <a href="https://doi.org/10.1186/s12864-018-5245-1">https://doi.org/10.1186/s12864-018-5245-1</a>
  chicago: Bochkareva, Olga, Elena V. Moroz, Iakov I. Davydov, and Mikhail S. Gelfand.
    “Genome Rearrangements and Selection in Multi-Chromosome Bacteria Burkholderia
    Spp.” <i>BMC Genomics</i>. Springer Nature, 2018. <a href="https://doi.org/10.1186/s12864-018-5245-1">https://doi.org/10.1186/s12864-018-5245-1</a>.
  ieee: O. Bochkareva, E. V. Moroz, I. I. Davydov, and M. S. Gelfand, “Genome rearrangements
    and selection in multi-chromosome bacteria Burkholderia spp.,” <i>BMC Genomics</i>,
    vol. 19. Springer Nature, 2018.
  ista: Bochkareva O, Moroz EV, Davydov II, Gelfand MS. 2018. Genome rearrangements
    and selection in multi-chromosome bacteria Burkholderia spp. BMC Genomics. 19,
    965.
  mla: Bochkareva, Olga, et al. “Genome Rearrangements and Selection in Multi-Chromosome
    Bacteria Burkholderia Spp.” <i>BMC Genomics</i>, vol. 19, 965, Springer Nature,
    2018, doi:<a href="https://doi.org/10.1186/s12864-018-5245-1">10.1186/s12864-018-5245-1</a>.
  short: O. Bochkareva, E.V. Moroz, I.I. Davydov, M.S. Gelfand, BMC Genomics 19 (2018).
date_created: 2020-08-15T11:02:08Z
date_published: 2018-12-27T00:00:00Z
date_updated: 2023-02-23T13:28:52Z
day: '27'
doi: 10.1186/s12864-018-5245-1
extern: '1'
fulldoi: https://doi.org/10.1186/s12864-018-5245-1
intvolume: '        19'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1186/s12864-018-5245-1
month: '12'
oa: 1
oa_version: Published Version
publication: BMC Genomics
publication_identifier:
  issn:
  - 1471-2164
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Genome rearrangements and selection in multi-chromosome bacteria Burkholderia
  spp.
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 19
year: '2018'
...
---
_id: '8265'
abstract:
- lang: eng
  text: Genome rearrangements have played an important role in the evolution of Yersinia
    pestis from its progenitor Yersinia pseudotuberculosis. Traditional phylogenetic
    trees for Y. pestis based on sequence comparison have short internal branches
    and low bootstrap supports as only a small number of nucleotide substitutions
    have occurred. On the other hand, even a small number of genome rearrangements
    may resolve topological ambiguities in a phylogenetic tree. We reconstructed phylogenetic
    trees based on genome rearrangements using several popular approaches such as
    Maximum likelihood for Gene Order and the Bayesian model of genome rearrangements
    by inversions. We also reconciled phylogenetic trees for each of the three CRISPR
    loci to obtain an integrated scenario of the CRISPR cassette evolution. Analysis
    of contradictions between the obtained evolutionary trees yielded numerous parallel
    inversions and gain/loss events. Our data indicate that an integrated analysis
    of sequence-based and inversion-based trees enhances the resolution of phylogenetic
    reconstruction. In contrast, reconstructions of strain relationships based on
    solely CRISPR loci may not be reliable, as the history is obscured by large deletions,
    obliterating the order of spacer gains. Similarly, numerous parallel gene losses
    preclude reconstruction of phylogeny based on gene content.
article_number: e4545
article_processing_charge: No
article_type: original
author:
- first_name: Olga
  full_name: Bochkareva, Olga
  id: C4558D3C-6102-11E9-A62E-F418E6697425
  last_name: Bochkareva
  orcid: 0000-0003-1006-6639
- first_name: Natalia O.
  full_name: Dranenko, Natalia O.
  last_name: Dranenko
- first_name: Elena S.
  full_name: Ocheredko, Elena S.
  last_name: Ocheredko
- first_name: German M.
  full_name: Kanevsky, German M.
  last_name: Kanevsky
- first_name: Yaroslav N.
  full_name: Lozinsky, Yaroslav N.
  last_name: Lozinsky
- first_name: Vera A.
  full_name: Khalaycheva, Vera A.
  last_name: Khalaycheva
- first_name: Irena I.
  full_name: Artamonova, Irena I.
  last_name: Artamonova
- first_name: Mikhail S.
  full_name: Gelfand, Mikhail S.
  last_name: Gelfand
citation:
  ama: Bochkareva O, Dranenko NO, Ocheredko ES, et al. Genome rearrangements and phylogeny
    reconstruction in Yersinia pestis. <i>PeerJ</i>. 2018;6. doi:<a href="https://doi.org/10.7717/peerj.4545">10.7717/peerj.4545</a>
  apa: Bochkareva, O., Dranenko, N. O., Ocheredko, E. S., Kanevsky, G. M., Lozinsky,
    Y. N., Khalaycheva, V. A., … Gelfand, M. S. (2018). Genome rearrangements and
    phylogeny reconstruction in Yersinia pestis. <i>PeerJ</i>. PeerJ. <a href="https://doi.org/10.7717/peerj.4545">https://doi.org/10.7717/peerj.4545</a>
  chicago: Bochkareva, Olga, Natalia O. Dranenko, Elena S. Ocheredko, German M. Kanevsky,
    Yaroslav N. Lozinsky, Vera A. Khalaycheva, Irena I. Artamonova, and Mikhail S.
    Gelfand. “Genome Rearrangements and Phylogeny Reconstruction in Yersinia Pestis.”
    <i>PeerJ</i>. PeerJ, 2018. <a href="https://doi.org/10.7717/peerj.4545">https://doi.org/10.7717/peerj.4545</a>.
  ieee: O. Bochkareva <i>et al.</i>, “Genome rearrangements and phylogeny reconstruction
    in Yersinia pestis,” <i>PeerJ</i>, vol. 6. PeerJ, 2018.
  ista: Bochkareva O, Dranenko NO, Ocheredko ES, Kanevsky GM, Lozinsky YN, Khalaycheva
    VA, Artamonova II, Gelfand MS. 2018. Genome rearrangements and phylogeny reconstruction
    in Yersinia pestis. PeerJ. 6, e4545.
  mla: Bochkareva, Olga, et al. “Genome Rearrangements and Phylogeny Reconstruction
    in Yersinia Pestis.” <i>PeerJ</i>, vol. 6, e4545, PeerJ, 2018, doi:<a href="https://doi.org/10.7717/peerj.4545">10.7717/peerj.4545</a>.
  short: O. Bochkareva, N.O. Dranenko, E.S. Ocheredko, G.M. Kanevsky, Y.N. Lozinsky,
    V.A. Khalaycheva, I.I. Artamonova, M.S. Gelfand, PeerJ 6 (2018).
date_created: 2020-08-15T11:08:23Z
date_published: 2018-03-27T00:00:00Z
date_updated: 2023-02-23T13:28:57Z
day: '27'
doi: 10.7717/peerj.4545
extern: '1'
external_id:
  pmid:
  - '29607260'
fulldoi: https://doi.org/10.7717/peerj.4545
intvolume: '         6'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.7717/peerj.4545
month: '03'
oa: 1
oa_version: Published Version
pmid: 1
publication: PeerJ
publication_identifier:
  issn:
  - 2167-8359
publication_status: published
publisher: PeerJ
quality_controlled: '1'
status: public
title: Genome rearrangements and phylogeny reconstruction in Yersinia pestis
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 6
year: '2018'
...
---
_id: '8274'
abstract:
- lang: eng
  text: 'Background/Aim: Our aim was to investigate the crosstalk between tumor and
    immune cells (M2 macrophages) and its effects on cyclo-oxygenase-2 (COX2) regulation
    in canine mammary tumors (CMT). Materials and Methods: Sh1b CMT cells and human
    BT474 mammary or HT29 colon cancer cells were co-cultured with canine peripheral
    blood mononuclear cells (PBMCs) or with macrophage-like differentiated THP1 monocytes
    (dTHP1). Intracellular COX2 expression by PBMCs, dTHP1 and cancer cells was evaluated
    by flow cytometry. Results: Co-culturing of Sh1b and canine PBMCs induced COX2
    overexpression in CMT cells. In turn, COX2 expression by PBMCs, mostly CD68+ macrophages,
    was attenuated by co-culture with Sh1b (p=0.0001). In accordance, co-culture with
    dTHP1 prompted intracellular production of COX2 in both Sh1b CMT cells and HT29
    human colon cancer cells and reduced production of COX2 in BT474 human mammary
    cancer cells. The intracellular COX2 expression from dTHP1 decreased when treated
    with conditioned medium from cultured Sh1b and HT29 cancer cells. Conclusion:
    Bidirectional COX2 regulation between cancer and monocytes/macrophages might shape
    a tolerogenic tumor microenvironment in CMT.'
article_processing_charge: No
article_type: original
author:
- first_name: Maria Isabel
  full_name: Carvalho, Maria Isabel
  last_name: Carvalho
- first_name: Rodolfo
  full_name: Bianchini, Rodolfo
  last_name: Bianchini
- first_name: Judit
  full_name: Fazekas-Singer, Judit
  id: 36432834-F248-11E8-B48F-1D18A9856A87
  last_name: Fazekas-Singer
  orcid: 0000-0002-8777-3502
- first_name: Ina
  full_name: Herrmann, Ina
  last_name: Herrmann
- first_name: Irene
  full_name: Flickinger, Irene
  last_name: Flickinger
- first_name: Johann G.
  full_name: Thalhammer, Johann G.
  last_name: Thalhammer
- first_name: Isabel
  full_name: Pires, Isabel
  last_name: Pires
- first_name: Erika
  full_name: Jensen-Jarolim, Erika
  last_name: Jensen-Jarolim
- first_name: Felisbina L.
  full_name: Queiroga, Felisbina L.
  last_name: Queiroga
citation:
  ama: Carvalho MI, Bianchini R, Singer J, et al. Bidirectional regulation of COX-2
    expression between cancer cells and macrophages. <i>Anticancer Research</i>. 2018;38(5):2811-2817.
    doi:<a href="https://doi.org/10.21873/anticanres.12525">10.21873/anticanres.12525</a>
  apa: Carvalho, M. I., Bianchini, R., Singer, J., Herrmann, I., Flickinger, I., Thalhammer,
    J. G., … Queiroga, F. L. (2018). Bidirectional regulation of COX-2 expression
    between cancer cells and macrophages. <i>Anticancer Research</i>. International
    Institute of Anticancer Research. <a href="https://doi.org/10.21873/anticanres.12525">https://doi.org/10.21873/anticanres.12525</a>
  chicago: Carvalho, Maria Isabel, Rodolfo Bianchini, Judit Singer, Ina Herrmann,
    Irene Flickinger, Johann G. Thalhammer, Isabel Pires, Erika Jensen-Jarolim, and
    Felisbina L. Queiroga. “Bidirectional Regulation of COX-2 Expression between Cancer
    Cells and Macrophages.” <i>Anticancer Research</i>. International Institute of
    Anticancer Research, 2018. <a href="https://doi.org/10.21873/anticanres.12525">https://doi.org/10.21873/anticanres.12525</a>.
  ieee: M. I. Carvalho <i>et al.</i>, “Bidirectional regulation of COX-2 expression
    between cancer cells and macrophages,” <i>Anticancer Research</i>, vol. 38, no.
    5. International Institute of Anticancer Research, pp. 2811–2817, 2018.
  ista: Carvalho MI, Bianchini R, Singer J, Herrmann I, Flickinger I, Thalhammer JG,
    Pires I, Jensen-Jarolim E, Queiroga FL. 2018. Bidirectional regulation of COX-2
    expression between cancer cells and macrophages. Anticancer Research. 38(5), 2811–2817.
  mla: Carvalho, Maria Isabel, et al. “Bidirectional Regulation of COX-2 Expression
    between Cancer Cells and Macrophages.” <i>Anticancer Research</i>, vol. 38, no.
    5, International Institute of Anticancer Research, 2018, pp. 2811–17, doi:<a href="https://doi.org/10.21873/anticanres.12525">10.21873/anticanres.12525</a>.
  short: M.I. Carvalho, R. Bianchini, J. Singer, I. Herrmann, I. Flickinger, J.G.
    Thalhammer, I. Pires, E. Jensen-Jarolim, F.L. Queiroga, Anticancer Research 38
    (2018) 2811–2817.
date_created: 2020-08-17T07:13:55Z
date_published: 2018-05-01T00:00:00Z
date_updated: 2021-01-12T08:17:52Z
day: '01'
doi: 10.21873/anticanres.12525
extern: '1'
fulldoi: https://doi.org/10.21873/anticanres.12525
intvolume: '        38'
issue: '5'
language:
- iso: eng
month: '05'
oa_version: None
page: 2811-2817
publication: Anticancer Research
publication_identifier:
  eissn:
  - 1791-7530
  issn:
  - 0250-7005
publication_status: published
publisher: International Institute of Anticancer Research
quality_controlled: '1'
status: public
title: Bidirectional regulation of COX-2 expression between cancer cells and macrophages
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 38
year: '2018'
...
---
_id: '8297'
abstract:
- lang: eng
  text: "Designing a secure permissionless distributed ledger (blockchain) that performs
    on par with centralized payment\r\nprocessors, such as Visa, is a challenging
    task. Most existing distributed ledgers are unable to scale-out, i.e., to grow
    their totalprocessing capacity with the number of validators; and those that do,
    compromise security or decentralization. We present OmniLedger, a novel scale-out
    distributed ledger that preserves longterm security under permissionless operation.
    It ensures security and correctness by using a bias-resistant public-randomness
    protocol for choosing large, statistically representative shards that process
    transactions, and by introducing an efficient crossshard commit protocol that
    atomically handles transactions affecting multiple shards. OmniLedger also optimizes
    performance via parallel intra-shard transaction processing, ledger pruning via
    collectively-signed state blocks, and low-latency “trust-butverify” \r\nvalidation
    for low-value transactions. An evaluation ofour experimental prototype shows that
    OmniLedger’s throughput\r\nscales linearly in the number of active validators,
    supporting Visa-level workloads and beyond, while confirming typical transactions
    in under two seconds."
article_processing_charge: No
author:
- first_name: Eleftherios
  full_name: Kokoris Kogias, Eleftherios
  id: f5983044-d7ef-11ea-ac6d-fd1430a26d30
  last_name: Kokoris Kogias
- first_name: Philipp
  full_name: Jovanovic, Philipp
  last_name: Jovanovic
- first_name: Linus
  full_name: Gasser, Linus
  last_name: Gasser
- first_name: Nicolas
  full_name: Gailly, Nicolas
  last_name: Gailly
- first_name: Ewa
  full_name: Syta, Ewa
  last_name: Syta
- first_name: Bryan
  full_name: Ford, Bryan
  last_name: Ford
citation:
  ama: 'Kokoris Kogias E, Jovanovic P, Gasser L, Gailly N, Syta E, Ford B. OmniLedger:
    A secure, scale-out, decentralized ledger via sharding. In: <i>2018 IEEE Symposium
    on Security and Privacy</i>. IEEE; 2018:583-598. doi:<a href="https://doi.org/10.1109/sp.2018.000-5">10.1109/sp.2018.000-5</a>'
  apa: 'Kokoris Kogias, E., Jovanovic, P., Gasser, L., Gailly, N., Syta, E., &#38;
    Ford, B. (2018). OmniLedger: A secure, scale-out, decentralized ledger via sharding.
    In <i>2018 IEEE Symposium on Security and Privacy</i> (pp. 583–598). San Francisco,
    CA, United States: IEEE. <a href="https://doi.org/10.1109/sp.2018.000-5">https://doi.org/10.1109/sp.2018.000-5</a>'
  chicago: 'Kokoris Kogias, Eleftherios, Philipp Jovanovic, Linus Gasser, Nicolas
    Gailly, Ewa Syta, and Bryan Ford. “OmniLedger: A Secure, Scale-out, Decentralized
    Ledger via Sharding.” In <i>2018 IEEE Symposium on Security and Privacy</i>, 583–98.
    IEEE, 2018. <a href="https://doi.org/10.1109/sp.2018.000-5">https://doi.org/10.1109/sp.2018.000-5</a>.'
  ieee: 'E. Kokoris Kogias, P. Jovanovic, L. Gasser, N. Gailly, E. Syta, and B. Ford,
    “OmniLedger: A secure, scale-out, decentralized ledger via sharding,” in <i>2018
    IEEE Symposium on Security and Privacy</i>, San Francisco, CA, United States,
    2018, pp. 583–598.'
  ista: 'Kokoris Kogias E, Jovanovic P, Gasser L, Gailly N, Syta E, Ford B. 2018.
    OmniLedger: A secure, scale-out, decentralized ledger via sharding. 2018 IEEE
    Symposium on Security and Privacy. SP: Symposium on Security and Privacy, 583–598.'
  mla: 'Kokoris Kogias, Eleftherios, et al. “OmniLedger: A Secure, Scale-out, Decentralized
    Ledger via Sharding.” <i>2018 IEEE Symposium on Security and Privacy</i>, IEEE,
    2018, pp. 583–98, doi:<a href="https://doi.org/10.1109/sp.2018.000-5">10.1109/sp.2018.000-5</a>.'
  short: E. Kokoris Kogias, P. Jovanovic, L. Gasser, N. Gailly, E. Syta, B. Ford,
    in:, 2018 IEEE Symposium on Security and Privacy, IEEE, 2018, pp. 583–598.
conference:
  end_date: 2018-05-24
  location: San Francisco, CA, United States
  name: 'SP: Symposium on Security and Privacy'
  start_date: 2018-05-20
date_created: 2020-08-26T11:46:35Z
date_published: 2018-07-26T00:00:00Z
date_updated: 2021-01-12T08:17:56Z
day: '26'
doi: 10.1109/sp.2018.000-5
extern: '1'
fulldoi: https://doi.org/10.1109/sp.2018.000-5
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://eprint.iacr.org/2017/406
month: '07'
oa: 1
oa_version: Preprint
page: 583-598
publication: 2018 IEEE Symposium on Security and Privacy
publication_identifier:
  isbn:
  - '9781538643532'
  issn:
  - 2375-1207
publication_status: published
publisher: IEEE
quality_controlled: '1'
status: public
title: 'OmniLedger: A secure, scale-out, decentralized ledger via sharding'
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
year: '2018'
...
---
_id: '8298'
abstract:
- lang: eng
  text: Sharding, or partitioning the system’s state so that different subsets of
    participants handle it, is a proven approach to building distributed systems whose
    total capacity scales horizontally with the number of participants. Many distributed
    ledgers have adopted this approach to increase their performance, however, they
    focus on the permissionless setting that assumes the existence of a strong adversary.
    In this paper, we deploy channels for permissioned blockchains. Our first contribution
    is to adapt sharding on asset-management applications for the permissioned setting,
    while preserving liveness and safety even on transactions spanning across-channels.
    Our second contribution is to leverage channels as a confidentiality boundary,
    enabling different organizations and consortia to preserve their privacy within
    their channels and still be part of a bigger collaborative ecosystem. To make
    our system concrete we map it on top of Hyperledger Fabric.
alternative_title:
- LNCS
article_processing_charge: No
author:
- first_name: Elli
  full_name: Androulaki, Elli
  last_name: Androulaki
- first_name: Christian
  full_name: Cachin, Christian
  last_name: Cachin
- first_name: Angelo
  full_name: De Caro, Angelo
  last_name: De Caro
- first_name: Eleftherios
  full_name: Kokoris Kogias, Eleftherios
  id: f5983044-d7ef-11ea-ac6d-fd1430a26d30
  last_name: Kokoris Kogias
citation:
  ama: 'Androulaki E, Cachin C, De Caro A, Kokoris Kogias E. Channels: Horizontal
    scaling and confidentiality on permissioned blockchains. In: <i>Computer Security</i>.
    Vol 11098. Springer Nature; 2018:111-131. doi:<a href="https://doi.org/10.1007/978-3-319-99073-6_6">10.1007/978-3-319-99073-6_6</a>'
  apa: 'Androulaki, E., Cachin, C., De Caro, A., &#38; Kokoris Kogias, E. (2018).
    Channels: Horizontal scaling and confidentiality on permissioned blockchains.
    In <i>Computer Security</i> (Vol. 11098, pp. 111–131). Barcelona, Spain: Springer
    Nature. <a href="https://doi.org/10.1007/978-3-319-99073-6_6">https://doi.org/10.1007/978-3-319-99073-6_6</a>'
  chicago: 'Androulaki, Elli, Christian Cachin, Angelo De Caro, and Eleftherios Kokoris
    Kogias. “Channels: Horizontal Scaling and Confidentiality on Permissioned Blockchains.”
    In <i>Computer Security</i>, 11098:111–31. Springer Nature, 2018. <a href="https://doi.org/10.1007/978-3-319-99073-6_6">https://doi.org/10.1007/978-3-319-99073-6_6</a>.'
  ieee: 'E. Androulaki, C. Cachin, A. De Caro, and E. Kokoris Kogias, “Channels: Horizontal
    scaling and confidentiality on permissioned blockchains,” in <i>Computer Security</i>,
    Barcelona, Spain, 2018, vol. 11098, pp. 111–131.'
  ista: 'Androulaki E, Cachin C, De Caro A, Kokoris Kogias E. 2018. Channels: Horizontal
    scaling and confidentiality on permissioned blockchains. Computer Security. ESORICS:
    European Symposium on Research in Computer Security, LNCS, vol. 11098, 111–131.'
  mla: 'Androulaki, Elli, et al. “Channels: Horizontal Scaling and Confidentiality
    on Permissioned Blockchains.” <i>Computer Security</i>, vol. 11098, Springer Nature,
    2018, pp. 111–31, doi:<a href="https://doi.org/10.1007/978-3-319-99073-6_6">10.1007/978-3-319-99073-6_6</a>.'
  short: E. Androulaki, C. Cachin, A. De Caro, E. Kokoris Kogias, in:, Computer Security,
    Springer Nature, 2018, pp. 111–131.
conference:
  end_date: 2018-09-07
  location: Barcelona, Spain
  name: 'ESORICS: European Symposium on Research in Computer Security'
  start_date: 2018-09-03
date_created: 2020-08-26T11:47:34Z
date_published: 2018-08-08T00:00:00Z
date_updated: 2021-01-12T08:17:57Z
day: '08'
doi: 10.1007/978-3-319-99073-6_6
extern: '1'
fulldoi: https://doi.org/10.1007/978-3-319-99073-6_6
intvolume: '     11098'
language:
- iso: eng
month: '08'
oa_version: None
page: 111-131
publication: Computer Security
publication_identifier:
  eisbn:
  - '9783319990736'
  isbn:
  - '9783319990729'
  issn:
  - 0302-9743
  - 1611-3349
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: 'Channels: Horizontal scaling and confidentiality on permissioned blockchains'
type: conference
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 11098
year: '2018'
...
---
_id: '8417'
abstract:
- lang: eng
  text: The restricted planar elliptic three body problem (RPETBP) describes the motion
    of a massless particle (a comet or an asteroid) under the gravitational field
    of two massive bodies (the primaries, say the Sun and Jupiter) revolving around
    their center of mass on elliptic orbits with some positive eccentricity. The aim
    of this paper is to show the existence of orbits whose angular momentum performs
    arbitrary excursions in a large region. In particular, there exist diffusive orbits,
    that is, with a large variation of angular momentum. The leading idea of the proof
    consists in analyzing parabolic motions of the comet. By a well-known result of
    McGehee, the union of future (resp. past) parabolic orbits is an analytic manifold
    P+ (resp. P−). In a properly chosen coordinate system these manifolds are stable
    (resp. unstable) manifolds of a manifold at infinity P∞, which we call the manifold
    at parabolic infinity. On P∞ it is possible to define two scattering maps, which
    contain the map structure of the homoclinic trajectories to it, i.e. orbits parabolic
    both in the future and the past. Since the inner dynamics inside P∞ is trivial,
    two different scattering maps are used. The combination of these two scattering
    maps permits the design of the desired diffusive pseudo-orbits. Using shadowing
    techniques and these pseudo orbits we show the existence of true trajectories
    of the RPETBP whose angular momentum varies in any predetermined fashion.
article_processing_charge: No
article_type: original
author:
- first_name: Amadeu
  full_name: Delshams, Amadeu
  last_name: Delshams
- first_name: Vadim
  full_name: Kaloshin, Vadim
  id: FE553552-CDE8-11E9-B324-C0EBE5697425
  last_name: Kaloshin
  orcid: 0000-0002-6051-2628
- first_name: Abraham
  full_name: de la Rosa, Abraham
  last_name: de la Rosa
- first_name: Tere M.
  full_name: Seara, Tere M.
  last_name: Seara
citation:
  ama: Delshams A, Kaloshin V, de la Rosa A, Seara TM. Global instability in the restricted
    planar elliptic three body problem. <i>Communications in Mathematical Physics</i>.
    2018;366(3):1173-1228. doi:<a href="https://doi.org/10.1007/s00220-018-3248-z">10.1007/s00220-018-3248-z</a>
  apa: Delshams, A., Kaloshin, V., de la Rosa, A., &#38; Seara, T. M. (2018). Global
    instability in the restricted planar elliptic three body problem. <i>Communications
    in Mathematical Physics</i>. Springer Nature. <a href="https://doi.org/10.1007/s00220-018-3248-z">https://doi.org/10.1007/s00220-018-3248-z</a>
  chicago: Delshams, Amadeu, Vadim Kaloshin, Abraham de la Rosa, and Tere M. Seara.
    “Global Instability in the Restricted Planar Elliptic Three Body Problem.” <i>Communications
    in Mathematical Physics</i>. Springer Nature, 2018. <a href="https://doi.org/10.1007/s00220-018-3248-z">https://doi.org/10.1007/s00220-018-3248-z</a>.
  ieee: A. Delshams, V. Kaloshin, A. de la Rosa, and T. M. Seara, “Global instability
    in the restricted planar elliptic three body problem,” <i>Communications in Mathematical
    Physics</i>, vol. 366, no. 3. Springer Nature, pp. 1173–1228, 2018.
  ista: Delshams A, Kaloshin V, de la Rosa A, Seara TM. 2018. Global instability in
    the restricted planar elliptic three body problem. Communications in Mathematical
    Physics. 366(3), 1173–1228.
  mla: Delshams, Amadeu, et al. “Global Instability in the Restricted Planar Elliptic
    Three Body Problem.” <i>Communications in Mathematical Physics</i>, vol. 366,
    no. 3, Springer Nature, 2018, pp. 1173–228, doi:<a href="https://doi.org/10.1007/s00220-018-3248-z">10.1007/s00220-018-3248-z</a>.
  short: A. Delshams, V. Kaloshin, A. de la Rosa, T.M. Seara, Communications in Mathematical
    Physics 366 (2018) 1173–1228.
date_created: 2020-09-17T10:41:43Z
date_published: 2018-09-05T00:00:00Z
date_updated: 2021-01-12T08:19:08Z
day: '05'
doi: 10.1007/s00220-018-3248-z
extern: '1'
fulldoi: https://doi.org/10.1007/s00220-018-3248-z
intvolume: '       366'
issue: '3'
keyword:
- Mathematical Physics
- Statistical and Nonlinear Physics
language:
- iso: eng
month: '09'
oa_version: None
page: 1173-1228
publication: Communications in Mathematical Physics
publication_identifier:
  issn:
  - 0010-3616
  - 1432-0916
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Global instability in the restricted planar elliptic three body problem
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 366
year: '2018'
...
---
_id: '8419'
abstract:
- lang: eng
  text: "In this survey, we provide a concise introduction to convex billiards and
    describe some recent results, obtained by the authors and collaborators, on the
    classification of integrable billiards, namely the so-called Birkhoff conjecture.\r\n\r\nThis
    article is part of the theme issue ‘Finite dimensional integrable systems: new
    trends and methods’."
article_number: '20170419'
article_processing_charge: No
article_type: original
author:
- first_name: Vadim
  full_name: Kaloshin, Vadim
  id: FE553552-CDE8-11E9-B324-C0EBE5697425
  last_name: Kaloshin
  orcid: 0000-0002-6051-2628
- first_name: Alfonso
  full_name: Sorrentino, Alfonso
  last_name: Sorrentino
citation:
  ama: 'Kaloshin V, Sorrentino A. On the integrability of Birkhoff billiards. <i>Philosophical
    Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences</i>.
    2018;376(2131). doi:<a href="https://doi.org/10.1098/rsta.2017.0419">10.1098/rsta.2017.0419</a>'
  apa: 'Kaloshin, V., &#38; Sorrentino, A. (2018). On the integrability of Birkhoff
    billiards. <i>Philosophical Transactions of the Royal Society A: Mathematical,
    Physical and Engineering Sciences</i>. The Royal Society. <a href="https://doi.org/10.1098/rsta.2017.0419">https://doi.org/10.1098/rsta.2017.0419</a>'
  chicago: 'Kaloshin, Vadim, and Alfonso Sorrentino. “On the Integrability of Birkhoff
    Billiards.” <i>Philosophical Transactions of the Royal Society A: Mathematical,
    Physical and Engineering Sciences</i>. The Royal Society, 2018. <a href="https://doi.org/10.1098/rsta.2017.0419">https://doi.org/10.1098/rsta.2017.0419</a>.'
  ieee: 'V. Kaloshin and A. Sorrentino, “On the integrability of Birkhoff billiards,”
    <i>Philosophical Transactions of the Royal Society A: Mathematical, Physical and
    Engineering Sciences</i>, vol. 376, no. 2131. The Royal Society, 2018.'
  ista: 'Kaloshin V, Sorrentino A. 2018. On the integrability of Birkhoff billiards.
    Philosophical Transactions of the Royal Society A: Mathematical, Physical and
    Engineering Sciences. 376(2131), 20170419.'
  mla: 'Kaloshin, Vadim, and Alfonso Sorrentino. “On the Integrability of Birkhoff
    Billiards.” <i>Philosophical Transactions of the Royal Society A: Mathematical,
    Physical and Engineering Sciences</i>, vol. 376, no. 2131, 20170419, The Royal
    Society, 2018, doi:<a href="https://doi.org/10.1098/rsta.2017.0419">10.1098/rsta.2017.0419</a>.'
  short: 'V. Kaloshin, A. Sorrentino, Philosophical Transactions of the Royal Society
    A: Mathematical, Physical and Engineering Sciences 376 (2018).'
date_created: 2020-09-17T10:42:01Z
date_published: 2018-10-28T00:00:00Z
date_updated: 2021-01-12T08:19:09Z
day: '28'
doi: 10.1098/rsta.2017.0419
extern: '1'
fulldoi: https://doi.org/10.1098/rsta.2017.0419
intvolume: '       376'
issue: '2131'
keyword:
- General Engineering
- General Physics and Astronomy
- General Mathematics
language:
- iso: eng
month: '10'
oa_version: None
publication: 'Philosophical Transactions of the Royal Society A: Mathematical, Physical
  and Engineering Sciences'
publication_identifier:
  issn:
  - 1364-503X
  - 1471-2962
publication_status: published
publisher: The Royal Society
quality_controlled: '1'
status: public
title: On the integrability of Birkhoff billiards
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 376
year: '2018'
...
---
_id: '8420'
abstract:
- lang: eng
  text: We show that in the space of all convex billiard boundaries, the set of boundaries
    with rational caustics is dense. More precisely, the set of billiard boundaries
    with caustics of rotation number 1/q is polynomially sense in the smooth case,
    and exponentially dense in the analytic case.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Vadim
  full_name: Kaloshin, Vadim
  id: FE553552-CDE8-11E9-B324-C0EBE5697425
  last_name: Kaloshin
  orcid: 0000-0002-6051-2628
- first_name: Ke
  full_name: Zhang, Ke
  last_name: Zhang
citation:
  ama: Kaloshin V, Zhang K. Density of convex billiards with rational caustics. <i>Nonlinearity</i>.
    2018;31(11):5214-5234. doi:<a href="https://doi.org/10.1088/1361-6544/aadc12">10.1088/1361-6544/aadc12</a>
  apa: Kaloshin, V., &#38; Zhang, K. (2018). Density of convex billiards with rational
    caustics. <i>Nonlinearity</i>. IOP Publishing. <a href="https://doi.org/10.1088/1361-6544/aadc12">https://doi.org/10.1088/1361-6544/aadc12</a>
  chicago: Kaloshin, Vadim, and Ke Zhang. “Density of Convex Billiards with Rational
    Caustics.” <i>Nonlinearity</i>. IOP Publishing, 2018. <a href="https://doi.org/10.1088/1361-6544/aadc12">https://doi.org/10.1088/1361-6544/aadc12</a>.
  ieee: V. Kaloshin and K. Zhang, “Density of convex billiards with rational caustics,”
    <i>Nonlinearity</i>, vol. 31, no. 11. IOP Publishing, pp. 5214–5234, 2018.
  ista: Kaloshin V, Zhang K. 2018. Density of convex billiards with rational caustics.
    Nonlinearity. 31(11), 5214–5234.
  mla: Kaloshin, Vadim, and Ke Zhang. “Density of Convex Billiards with Rational Caustics.”
    <i>Nonlinearity</i>, vol. 31, no. 11, IOP Publishing, 2018, pp. 5214–34, doi:<a
    href="https://doi.org/10.1088/1361-6544/aadc12">10.1088/1361-6544/aadc12</a>.
  short: V. Kaloshin, K. Zhang, Nonlinearity 31 (2018) 5214–5234.
date_created: 2020-09-17T10:42:09Z
date_published: 2018-10-15T00:00:00Z
date_updated: 2021-01-12T08:19:10Z
day: '15'
doi: 10.1088/1361-6544/aadc12
extern: '1'
external_id:
  arxiv:
  - '1706.07968'
fulldoi: https://doi.org/10.1088/1361-6544/aadc12
intvolume: '        31'
issue: '11'
keyword:
- Mathematical Physics
- General Physics and Astronomy
- Applied Mathematics
- Statistical and Nonlinear Physics
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1706.07968
month: '10'
oa: 1
oa_version: Preprint
page: 5214-5234
publication: Nonlinearity
publication_identifier:
  issn:
  - 0951-7715
  - 1361-6544
publication_status: published
publisher: IOP Publishing
quality_controlled: '1'
status: public
title: Density of convex billiards with rational caustics
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 31
year: '2018'
...
---
_id: '8421'
abstract:
- lang: eng
  text: 'The classical Birkhoff conjecture claims that the boundary of a strictly
    convex integrable billiard table is necessarily an ellipse (or a circle as a special
    case). In this article we prove a complete local version of this conjecture: a
    small integrable perturbation of an ellipse must be an ellipse. This extends and
    completes the result in Avila-De Simoi-Kaloshin, where nearly circular domains
    were considered. One of the crucial ideas in the proof is to extend action-angle
    coordinates for elliptic billiards into complex domains (with respect to the angle),
    and to thoroughly analyze the nature of their complex singularities. As an application,
    we are able to prove some spectral rigidity results for elliptic domains.'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Vadim
  full_name: Kaloshin, Vadim
  id: FE553552-CDE8-11E9-B324-C0EBE5697425
  last_name: Kaloshin
  orcid: 0000-0002-6051-2628
- first_name: Alfonso
  full_name: Sorrentino, Alfonso
  last_name: Sorrentino
citation:
  ama: Kaloshin V, Sorrentino A. On the local Birkhoff conjecture for convex billiards.
    <i>Annals of Mathematics</i>. 2018;188(1):315-380. doi:<a href="https://doi.org/10.4007/annals.2018.188.1.6">10.4007/annals.2018.188.1.6</a>
  apa: Kaloshin, V., &#38; Sorrentino, A. (2018). On the local Birkhoff conjecture
    for convex billiards. <i>Annals of Mathematics</i>. Annals of Mathematics, Princeton
    U. <a href="https://doi.org/10.4007/annals.2018.188.1.6">https://doi.org/10.4007/annals.2018.188.1.6</a>
  chicago: Kaloshin, Vadim, and Alfonso Sorrentino. “On the Local Birkhoff Conjecture
    for Convex Billiards.” <i>Annals of Mathematics</i>. Annals of Mathematics, Princeton
    U, 2018. <a href="https://doi.org/10.4007/annals.2018.188.1.6">https://doi.org/10.4007/annals.2018.188.1.6</a>.
  ieee: V. Kaloshin and A. Sorrentino, “On the local Birkhoff conjecture for convex
    billiards,” <i>Annals of Mathematics</i>, vol. 188, no. 1. Annals of Mathematics,
    Princeton U, pp. 315–380, 2018.
  ista: Kaloshin V, Sorrentino A. 2018. On the local Birkhoff conjecture for convex
    billiards. Annals of Mathematics. 188(1), 315–380.
  mla: Kaloshin, Vadim, and Alfonso Sorrentino. “On the Local Birkhoff Conjecture
    for Convex Billiards.” <i>Annals of Mathematics</i>, vol. 188, no. 1, Annals of
    Mathematics, Princeton U, 2018, pp. 315–80, doi:<a href="https://doi.org/10.4007/annals.2018.188.1.6">10.4007/annals.2018.188.1.6</a>.
  short: V. Kaloshin, A. Sorrentino, Annals of Mathematics 188 (2018) 315–380.
date_created: 2020-09-17T10:42:22Z
date_published: 2018-07-01T00:00:00Z
date_updated: 2021-01-12T08:19:10Z
day: '01'
doi: 10.4007/annals.2018.188.1.6
extern: '1'
external_id:
  arxiv:
  - '1612.09194'
fulldoi: https://doi.org/10.4007/annals.2018.188.1.6
intvolume: '       188'
issue: '1'
keyword:
- Statistics
- Probability and Uncertainty
- Statistics and Probability
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1612.09194
month: '07'
oa: 1
oa_version: Preprint
page: 315-380
publication: Annals of Mathematics
publication_identifier:
  issn:
  - 0003-486X
publication_status: published
publisher: Annals of Mathematics, Princeton U
quality_controlled: '1'
status: public
title: On the local Birkhoff conjecture for convex billiards
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 188
year: '2018'
...
---
_id: '8422'
abstract:
- lang: eng
  text: 'The Birkhoff conjecture says that the boundary of a strictly convex integrable
    billiard table is necessarily an ellipse. In this article, we consider a stronger
    notion of integrability, namely integrability close to the boundary, and prove
    a local version of this conjecture: a small perturbation of an ellipse of small
    eccentricity which preserves integrability near the boundary, is itself an ellipse.
    This extends the result in Avila et al. (Ann Math 184:527–558, ADK16), where integrability
    was assumed on a larger set. In particular, it shows that (local) integrability
    near the boundary implies global integrability. One of the crucial ideas in the
    proof consists in analyzing Taylor expansion of the corresponding action-angle
    coordinates with respect to the eccentricity parameter, deriving and studying
    higher order conditions for the preservation of integrable rational caustics.'
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Guan
  full_name: Huang, Guan
  last_name: Huang
- first_name: Vadim
  full_name: Kaloshin, Vadim
  id: FE553552-CDE8-11E9-B324-C0EBE5697425
  last_name: Kaloshin
  orcid: 0000-0002-6051-2628
- first_name: Alfonso
  full_name: Sorrentino, Alfonso
  last_name: Sorrentino
citation:
  ama: Huang G, Kaloshin V, Sorrentino A. Nearly circular domains which are integrable
    close to the boundary are ellipses. <i>Geometric and Functional Analysis</i>.
    2018;28(2):334-392. doi:<a href="https://doi.org/10.1007/s00039-018-0440-4">10.1007/s00039-018-0440-4</a>
  apa: Huang, G., Kaloshin, V., &#38; Sorrentino, A. (2018). Nearly circular domains
    which are integrable close to the boundary are ellipses. <i>Geometric and Functional
    Analysis</i>. Springer Nature. <a href="https://doi.org/10.1007/s00039-018-0440-4">https://doi.org/10.1007/s00039-018-0440-4</a>
  chicago: Huang, Guan, Vadim Kaloshin, and Alfonso Sorrentino. “Nearly Circular Domains
    Which Are Integrable Close to the Boundary Are Ellipses.” <i>Geometric and Functional
    Analysis</i>. Springer Nature, 2018. <a href="https://doi.org/10.1007/s00039-018-0440-4">https://doi.org/10.1007/s00039-018-0440-4</a>.
  ieee: G. Huang, V. Kaloshin, and A. Sorrentino, “Nearly circular domains which are
    integrable close to the boundary are ellipses,” <i>Geometric and Functional Analysis</i>,
    vol. 28, no. 2. Springer Nature, pp. 334–392, 2018.
  ista: Huang G, Kaloshin V, Sorrentino A. 2018. Nearly circular domains which are
    integrable close to the boundary are ellipses. Geometric and Functional Analysis.
    28(2), 334–392.
  mla: Huang, Guan, et al. “Nearly Circular Domains Which Are Integrable Close to
    the Boundary Are Ellipses.” <i>Geometric and Functional Analysis</i>, vol. 28,
    no. 2, Springer Nature, 2018, pp. 334–92, doi:<a href="https://doi.org/10.1007/s00039-018-0440-4">10.1007/s00039-018-0440-4</a>.
  short: G. Huang, V. Kaloshin, A. Sorrentino, Geometric and Functional Analysis 28
    (2018) 334–392.
date_created: 2020-09-17T10:42:30Z
date_published: 2018-03-18T00:00:00Z
date_updated: 2021-01-12T08:19:11Z
day: '18'
doi: 10.1007/s00039-018-0440-4
extern: '1'
external_id:
  arxiv:
  - '1705.10601'
fulldoi: https://doi.org/10.1007/s00039-018-0440-4
intvolume: '        28'
issue: '2'
keyword:
- Geometry and Topology
- Analysis
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1705.10601
month: '03'
oa: 1
oa_version: Preprint
page: 334-392
publication: Geometric and Functional Analysis
publication_identifier:
  issn:
  - 1016-443X
  - 1420-8970
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Nearly circular domains which are integrable close to the boundary are ellipses
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 28
year: '2018'
...
---
_id: '8426'
abstract:
- lang: eng
  text: For any strictly convex planar domain Ω ⊂ R2 with a C∞ boundary one can associate
    an infinite sequence of spectral invariants introduced by Marvizi–Merlose [5].
    These invariants can generically be determined using the spectrum of the Dirichlet
    problem of the Laplace operator. A natural question asks if this collection is
    sufficient to determine Ω up to isometry. In this paper we give a counterexample,
    namely, we present two nonisometric domains Ω and Ω¯ with the same collection
    of Marvizi–Melrose invariants. Moreover, each domain has countably many periodic
    orbits {Sn}n≥1 (resp. {S¯n}n⩾1) of period going to infinity such that Sn and S¯n
    have the same period and perimeter for each n.
article_processing_charge: No
article_type: original
arxiv: 1
author:
- first_name: Lev
  full_name: Buhovsky, Lev
  last_name: Buhovsky
- first_name: Vadim
  full_name: Kaloshin, Vadim
  id: FE553552-CDE8-11E9-B324-C0EBE5697425
  last_name: Kaloshin
  orcid: 0000-0002-6051-2628
citation:
  ama: Buhovsky L, Kaloshin V. Nonisometric domains with the same Marvizi-Melrose
    invariants. <i>Regular and Chaotic Dynamics</i>. 2018;23:54-59. doi:<a href="https://doi.org/10.1134/s1560354718010057">10.1134/s1560354718010057</a>
  apa: Buhovsky, L., &#38; Kaloshin, V. (2018). Nonisometric domains with the same
    Marvizi-Melrose invariants. <i>Regular and Chaotic Dynamics</i>. Springer Nature.
    <a href="https://doi.org/10.1134/s1560354718010057">https://doi.org/10.1134/s1560354718010057</a>
  chicago: Buhovsky, Lev, and Vadim Kaloshin. “Nonisometric Domains with the Same
    Marvizi-Melrose Invariants.” <i>Regular and Chaotic Dynamics</i>. Springer Nature,
    2018. <a href="https://doi.org/10.1134/s1560354718010057">https://doi.org/10.1134/s1560354718010057</a>.
  ieee: L. Buhovsky and V. Kaloshin, “Nonisometric domains with the same Marvizi-Melrose
    invariants,” <i>Regular and Chaotic Dynamics</i>, vol. 23. Springer Nature, pp.
    54–59, 2018.
  ista: Buhovsky L, Kaloshin V. 2018. Nonisometric domains with the same Marvizi-Melrose
    invariants. Regular and Chaotic Dynamics. 23, 54–59.
  mla: Buhovsky, Lev, and Vadim Kaloshin. “Nonisometric Domains with the Same Marvizi-Melrose
    Invariants.” <i>Regular and Chaotic Dynamics</i>, vol. 23, Springer Nature, 2018,
    pp. 54–59, doi:<a href="https://doi.org/10.1134/s1560354718010057">10.1134/s1560354718010057</a>.
  short: L. Buhovsky, V. Kaloshin, Regular and Chaotic Dynamics 23 (2018) 54–59.
date_created: 2020-09-17T10:43:21Z
date_published: 2018-02-05T00:00:00Z
date_updated: 2021-01-12T08:19:11Z
day: '05'
doi: 10.1134/s1560354718010057
extern: '1'
external_id:
  arxiv:
  - '1801.00952'
fulldoi: https://doi.org/10.1134/s1560354718010057
intvolume: '        23'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://arxiv.org/abs/1801.00952
month: '02'
oa: 1
oa_version: Preprint
page: 54-59
publication: Regular and Chaotic Dynamics
publication_identifier:
  issn:
  - 1560-3547
  - 1468-4845
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
status: public
title: Nonisometric domains with the same Marvizi-Melrose invariants
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 23
year: '2018'
...
