---
_id: '11123'
abstract:
- lang: eng
text: The small GTPase Ran is a key regulator of nucleocytoplasmic transport during
interphase. The asymmetric distribution of the GTP-bound form of Ran across the
nuclear envelope — that is, large quantities in the nucleus compared with small
quantities in the cytoplasm — determines the directionality of many nuclear transport
processes. Recent findings that Ran also functions in spindle formation and nuclear
envelope assembly during mitosis suggest that Ran has a general role in chromatin-centred
processes. Ran functions in these events as a signal for chromosome position.
article_processing_charge: No
article_type: original
author:
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
- first_name: Oliver J.
full_name: Gruss, Oliver J.
last_name: Gruss
- first_name: Iain W.
full_name: Mattaj, Iain W.
last_name: Mattaj
citation:
ama: Hetzer M, Gruss OJ, Mattaj IW. The Ran GTPase as a marker of chromosome position
in spindle formation and nuclear envelope assembly. Nature Cell Biology.
2002;4(7):E177-E184. doi:10.1038/ncb0702-e177
apa: Hetzer, M., Gruss, O. J., & Mattaj, I. W. (2002). The Ran GTPase as a marker
of chromosome position in spindle formation and nuclear envelope assembly. Nature
Cell Biology. Springer Nature. https://doi.org/10.1038/ncb0702-e177
chicago: Hetzer, Martin, Oliver J. Gruss, and Iain W. Mattaj. “The Ran GTPase as
a Marker of Chromosome Position in Spindle Formation and Nuclear Envelope Assembly.”
Nature Cell Biology. Springer Nature, 2002. https://doi.org/10.1038/ncb0702-e177.
ieee: M. Hetzer, O. J. Gruss, and I. W. Mattaj, “The Ran GTPase as a marker of chromosome
position in spindle formation and nuclear envelope assembly,” Nature Cell Biology,
vol. 4, no. 7. Springer Nature, pp. E177–E184, 2002.
ista: Hetzer M, Gruss OJ, Mattaj IW. 2002. The Ran GTPase as a marker of chromosome
position in spindle formation and nuclear envelope assembly. Nature Cell Biology.
4(7), E177–E184.
mla: Hetzer, Martin, et al. “The Ran GTPase as a Marker of Chromosome Position in
Spindle Formation and Nuclear Envelope Assembly.” Nature Cell Biology,
vol. 4, no. 7, Springer Nature, 2002, pp. E177–84, doi:10.1038/ncb0702-e177.
short: M. Hetzer, O.J. Gruss, I.W. Mattaj, Nature Cell Biology 4 (2002) E177–E184.
date_created: 2022-04-07T07:57:19Z
date_published: 2002-07-01T00:00:00Z
date_updated: 2022-07-18T08:58:03Z
day: '01'
doi: 10.1038/ncb0702-e177
extern: '1'
external_id:
pmid:
- '12105431'
intvolume: ' 4'
issue: '7'
keyword:
- Cell Biology
language:
- iso: eng
month: '07'
oa_version: None
page: E177-E184
pmid: 1
publication: Nature Cell Biology
publication_identifier:
eissn:
- 1476-4679
issn:
- 1465-7392
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: The Ran GTPase as a marker of chromosome position in spindle formation and
nuclear envelope assembly
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 4
year: '2002'
...
---
_id: '11125'
abstract:
- lang: eng
text: Although nuclear envelope (NE) assembly is known to require the GTPase Ran,
the membrane fusion machinery involved is uncharacterized. NE assembly involves
formation of a reticular network on chromatin, fusion of this network into a closed
NE and subsequent expansion. Here we show that p97, an AAA-ATPase previously implicated
in fusion of Golgi and transitional endoplasmic reticulum (ER) membranes together
with the adaptor p47, has two discrete functions in NE assembly. Formation of
a closed NE requires the p97–Ufd1–Npl4 complex, not previously implicated in membrane
fusion. Subsequent NE growth involves a p97–p47 complex. This study provides the
first insights into the molecular mechanisms and specificity of fusion events
involved in NE formation.
article_processing_charge: No
article_type: original
author:
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
- first_name: Hemmo H.
full_name: Meyer, Hemmo H.
last_name: Meyer
- first_name: Tobias C.
full_name: Walther, Tobias C.
last_name: Walther
- first_name: Daniel
full_name: Bilbao-Cortes, Daniel
last_name: Bilbao-Cortes
- first_name: Graham
full_name: Warren, Graham
last_name: Warren
- first_name: Iain W.
full_name: Mattaj, Iain W.
last_name: Mattaj
citation:
ama: Hetzer M, Meyer HH, Walther TC, Bilbao-Cortes D, Warren G, Mattaj IW. Distinct
AAA-ATPase p97 complexes function in discrete steps of nuclear assembly. Nature
Cell Biology. 2001;3(12):1086-1091. doi:10.1038/ncb1201-1086
apa: Hetzer, M., Meyer, H. H., Walther, T. C., Bilbao-Cortes, D., Warren, G., &
Mattaj, I. W. (2001). Distinct AAA-ATPase p97 complexes function in discrete steps
of nuclear assembly. Nature Cell Biology. Springer Nature. https://doi.org/10.1038/ncb1201-1086
chicago: Hetzer, Martin, Hemmo H. Meyer, Tobias C. Walther, Daniel Bilbao-Cortes,
Graham Warren, and Iain W. Mattaj. “Distinct AAA-ATPase P97 Complexes Function
in Discrete Steps of Nuclear Assembly.” Nature Cell Biology. Springer Nature,
2001. https://doi.org/10.1038/ncb1201-1086.
ieee: M. Hetzer, H. H. Meyer, T. C. Walther, D. Bilbao-Cortes, G. Warren, and I.
W. Mattaj, “Distinct AAA-ATPase p97 complexes function in discrete steps of nuclear
assembly,” Nature Cell Biology, vol. 3, no. 12. Springer Nature, pp. 1086–1091,
2001.
ista: Hetzer M, Meyer HH, Walther TC, Bilbao-Cortes D, Warren G, Mattaj IW. 2001.
Distinct AAA-ATPase p97 complexes function in discrete steps of nuclear assembly.
Nature Cell Biology. 3(12), 1086–1091.
mla: Hetzer, Martin, et al. “Distinct AAA-ATPase P97 Complexes Function in Discrete
Steps of Nuclear Assembly.” Nature Cell Biology, vol. 3, no. 12, Springer
Nature, 2001, pp. 1086–91, doi:10.1038/ncb1201-1086.
short: M. Hetzer, H.H. Meyer, T.C. Walther, D. Bilbao-Cortes, G. Warren, I.W. Mattaj,
Nature Cell Biology 3 (2001) 1086–1091.
date_created: 2022-04-07T07:57:42Z
date_published: 2001-11-02T00:00:00Z
date_updated: 2022-07-18T08:58:07Z
day: '02'
doi: 10.1038/ncb1201-1086
extern: '1'
external_id:
pmid:
- '11781570'
intvolume: ' 3'
issue: '12'
keyword:
- Cell Biology
language:
- iso: eng
month: '11'
oa_version: None
page: 1086-1091
pmid: 1
publication: Nature Cell Biology
publication_identifier:
eissn:
- 1476-4679
issn:
- 1465-7392
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Distinct AAA-ATPase p97 complexes function in discrete steps of nuclear assembly
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 3
year: '2001'
...
---
_id: '11126'
abstract:
- lang: eng
text: Nuclear import of the two uracil-rich small nuclear ribonucleoprotein (U snRNP)
components U1A and U2B′′ is mediated by unusually long and complex nuclear localization
signals (NLSs). Here we investigate nuclear import of U1A and U2B′′ in vitro and
demonstrate that it occurs by an active, saturable process. Several lines of evidence
suggest that import of the two proteins occurs by an import mechanism different
to those characterized previously. No cross competition is seen with a variety
of previously studied NLSs. In contrast to import mediated by members of the importin-β
family of nucleocytoplasmic transport receptors, U1A/U2B′′ import is not inhibited
by either nonhydrolyzable guanosine triphosphate (GTP) analogues or by a mutant
of the GTPase Ran that is incapable of GTP hydrolysis. Adenosine triphosphate
is capable of supporting U1A and U2B′′ import, whereas neither nonhydrolyzable
adenosine triphosphate analogues nor GTP can do so. U1A and U2B′′ import in vitro
does not require the addition of soluble cytosolic proteins, but a factor or factors
required for U1A and U2B′′ import remains tightly associated with the nuclear
fraction of conventionally permeabilized cells. This activity can be solubilized
in the presence of elevated MgCl2. These data suggest that U1A and U2B′′ import
into the nucleus occurs by a hitherto uncharacterized mechanism.
article_processing_charge: No
article_type: original
author:
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
- first_name: Iain W.
full_name: Mattaj, Iain W.
last_name: Mattaj
citation:
ama: Hetzer M, Mattaj IW. An Atp-dependent, Ran-independent mechanism for nuclear
import of the U1a and U2b′′ spliceosome proteins. Journal of Cell Biology.
2000;148(2):293-304. doi:10.1083/jcb.148.2.293
apa: Hetzer, M., & Mattaj, I. W. (2000). An Atp-dependent, Ran-independent mechanism
for nuclear import of the U1a and U2b′′ spliceosome proteins. Journal of Cell
Biology. Rockefeller University Press. https://doi.org/10.1083/jcb.148.2.293
chicago: Hetzer, Martin, and Iain W. Mattaj. “An Atp-Dependent, Ran-Independent
Mechanism for Nuclear Import of the U1a and U2b′′ Spliceosome Proteins.” Journal
of Cell Biology. Rockefeller University Press, 2000. https://doi.org/10.1083/jcb.148.2.293.
ieee: M. Hetzer and I. W. Mattaj, “An Atp-dependent, Ran-independent mechanism for
nuclear import of the U1a and U2b′′ spliceosome proteins,” Journal of Cell
Biology, vol. 148, no. 2. Rockefeller University Press, pp. 293–304, 2000.
ista: Hetzer M, Mattaj IW. 2000. An Atp-dependent, Ran-independent mechanism for
nuclear import of the U1a and U2b′′ spliceosome proteins. Journal of Cell Biology.
148(2), 293–304.
mla: Hetzer, Martin, and Iain W. Mattaj. “An Atp-Dependent, Ran-Independent Mechanism
for Nuclear Import of the U1a and U2b′′ Spliceosome Proteins.” Journal of Cell
Biology, vol. 148, no. 2, Rockefeller University Press, 2000, pp. 293–304,
doi:10.1083/jcb.148.2.293.
short: M. Hetzer, I.W. Mattaj, Journal of Cell Biology 148 (2000) 293–304.
date_created: 2022-04-07T07:57:49Z
date_published: 2000-01-24T00:00:00Z
date_updated: 2022-07-18T08:58:29Z
day: '24'
doi: 10.1083/jcb.148.2.293
extern: '1'
external_id:
pmid:
- '10648562'
intvolume: ' 148'
issue: '2'
keyword:
- Cell Biology
language:
- iso: eng
month: '01'
oa_version: None
page: 293-304
pmid: 1
publication: Journal of Cell Biology
publication_identifier:
eissn:
- 1540-8140
issn:
- 0021-9525
publication_status: published
publisher: Rockefeller University Press
quality_controlled: '1'
scopus_import: '1'
status: public
title: An Atp-dependent, Ran-independent mechanism for nuclear import of the U1a and
U2b′′ spliceosome proteins
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 148
year: '2000'
...
---
_id: '11127'
abstract:
- lang: eng
text: Nuclear formation in Xenopus egg extracts requires cytosol and is inhibited
by GTPγS, indicating a requirement for GTPase activity. Nuclear envelope (NE)
vesicle fusion is extensively inhibited by GTPγS and two mutant forms of the Ran
GTPase, Q69L and T24N. Depletion of either Ran or RCC1, the exchange factor for
Ran, from the assembly reaction also inhibits this step of NE formation. Ran depletion
can be complemented by the addition of Ran loaded with either GTP or GDP but not
with GTPγS. RCC1 depletion is only complemented by RCC1 itself or by RanGTP. Thus,
generation of RanGTP by RCC1 and GTP hydrolysis by Ran are both required for the
extensive membrane fusion events that lead to NE formation.
article_processing_charge: No
article_type: original
author:
- first_name: Martin W
full_name: HETZER, Martin W
id: 86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed
last_name: HETZER
orcid: 0000-0002-2111-992X
- first_name: Daniel
full_name: Bilbao-Cortés, Daniel
last_name: Bilbao-Cortés
- first_name: Tobias C
full_name: Walther, Tobias C
last_name: Walther
- first_name: Oliver J
full_name: Gruss, Oliver J
last_name: Gruss
- first_name: Iain W
full_name: Mattaj, Iain W
last_name: Mattaj
citation:
ama: Hetzer M, Bilbao-Cortés D, Walther TC, Gruss OJ, Mattaj IW. GTP hydrolysis
by Ran is required for nuclear envelope assembly. Molecular Cell. 2000;5(6):1013-1024.
doi:10.1016/s1097-2765(00)80266-x
apa: Hetzer, M., Bilbao-Cortés, D., Walther, T. C., Gruss, O. J., & Mattaj,
I. W. (2000). GTP hydrolysis by Ran is required for nuclear envelope assembly.
Molecular Cell. Elsevier. https://doi.org/10.1016/s1097-2765(00)80266-x
chicago: Hetzer, Martin, Daniel Bilbao-Cortés, Tobias C Walther, Oliver J Gruss,
and Iain W Mattaj. “GTP Hydrolysis by Ran Is Required for Nuclear Envelope Assembly.”
Molecular Cell. Elsevier, 2000. https://doi.org/10.1016/s1097-2765(00)80266-x.
ieee: M. Hetzer, D. Bilbao-Cortés, T. C. Walther, O. J. Gruss, and I. W. Mattaj,
“GTP hydrolysis by Ran is required for nuclear envelope assembly,” Molecular
Cell, vol. 5, no. 6. Elsevier, pp. 1013–1024, 2000.
ista: Hetzer M, Bilbao-Cortés D, Walther TC, Gruss OJ, Mattaj IW. 2000. GTP hydrolysis
by Ran is required for nuclear envelope assembly. Molecular Cell. 5(6), 1013–1024.
mla: Hetzer, Martin, et al. “GTP Hydrolysis by Ran Is Required for Nuclear Envelope
Assembly.” Molecular Cell, vol. 5, no. 6, Elsevier, 2000, pp. 1013–24,
doi:10.1016/s1097-2765(00)80266-x.
short: M. Hetzer, D. Bilbao-Cortés, T.C. Walther, O.J. Gruss, I.W. Mattaj, Molecular
Cell 5 (2000) 1013–1024.
date_created: 2022-04-07T07:57:59Z
date_published: 2000-06-01T00:00:00Z
date_updated: 2022-07-18T08:58:31Z
day: '01'
doi: 10.1016/s1097-2765(00)80266-x
extern: '1'
external_id:
pmid:
- '10911995'
intvolume: ' 5'
issue: '6'
keyword:
- Cell Biology
- Molecular Biology
language:
- iso: eng
main_file_link:
- open_access: '1'
url: https://doi.org/10.1016/S1097-2765(00)80266-X
month: '06'
oa: 1
oa_version: Published Version
page: 1013-1024
pmid: 1
publication: Molecular Cell
publication_identifier:
issn:
- 1097-2765
publication_status: published
publisher: Elsevier
quality_controlled: '1'
scopus_import: '1'
status: public
title: GTP hydrolysis by Ran is required for nuclear envelope assembly
type: journal_article
user_id: 72615eeb-f1f3-11ec-aa25-d4573ddc34fd
volume: 5
year: '2000'
...
---
_id: '11681'
abstract:
- lang: eng
text: We prove lower bounds on the complexity of maintaining fully dynamic k -edge
or k -vertex connectivity in plane graphs and in (k-1) -vertex connected graphs.
We show an amortized lower bound of Ω (log n / {k (log log n} + log b)) per edge
insertion, deletion, or query operation in the cell probe model, where b is the
word size of the machine and n is the number of vertices in G . We also show an
amortized lower bound of Ω (log n /(log log n + log b)) per operation for fully
dynamic planarity testing in embedded graphs. These are the first lower bounds
for fully dynamic connectivity problems.
acknowledgement: .
article_processing_charge: No
article_type: original
author:
- first_name: Monika H
full_name: Henzinger, Monika H
id: 540c9bbd-f2de-11ec-812d-d04a5be85630
last_name: Henzinger
orcid: 0000-0002-5008-6530
- first_name: M. L.
full_name: Fredman, M. L.
last_name: Fredman
citation:
ama: Henzinger M, Fredman ML. Lower bounds for fully dynamic connectivity problems
in graphs. Algorithmica. 1998;22(3):351-362. doi:10.1007/pl00009228
apa: Henzinger, M., & Fredman, M. L. (1998). Lower bounds for fully dynamic
connectivity problems in graphs. Algorithmica. Springer Nature. https://doi.org/10.1007/pl00009228
chicago: Henzinger, Monika, and M. L. Fredman. “Lower Bounds for Fully Dynamic Connectivity
Problems in Graphs.” Algorithmica. Springer Nature, 1998. https://doi.org/10.1007/pl00009228.
ieee: M. Henzinger and M. L. Fredman, “Lower bounds for fully dynamic connectivity
problems in graphs,” Algorithmica, vol. 22, no. 3. Springer Nature, pp.
351–362, 1998.
ista: Henzinger M, Fredman ML. 1998. Lower bounds for fully dynamic connectivity
problems in graphs. Algorithmica. 22(3), 351–362.
mla: Henzinger, Monika, and M. L. Fredman. “Lower Bounds for Fully Dynamic Connectivity
Problems in Graphs.” Algorithmica, vol. 22, no. 3, Springer Nature, 1998,
pp. 351–62, doi:10.1007/pl00009228.
short: M. Henzinger, M.L. Fredman, Algorithmica 22 (1998) 351–362.
date_created: 2022-07-28T06:58:36Z
date_published: 1998-11-01T00:00:00Z
date_updated: 2024-11-06T12:08:20Z
day: '01'
doi: 10.1007/pl00009228
extern: '1'
intvolume: ' 22'
issue: '3'
keyword:
- Dynamic planarity testing
- Dynamic connectivity testing
- Lower bounds
- Cell probe model
language:
- iso: eng
month: '11'
oa_version: None
page: 351-362
publication: Algorithmica
publication_identifier:
eissn:
- 1432-0541
issn:
- 0178-4617
publication_status: published
publisher: Springer Nature
quality_controlled: '1'
scopus_import: '1'
status: public
title: Lower bounds for fully dynamic connectivity problems in graphs
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 22
year: '1998'
...
---
_id: '4097'
abstract:
- lang: eng
text: Arrangements of curves in the plane are of fundamental significance in many
problems of computational and combinatorial geometry (e.g. motion planning, algebraic
cell decomposition, etc.). In this paper we study various topological and combinatorial
properties of such arrangements under some mild assumptions on the shape of the
curves, and develop basic tools for the construction, manipulation, and analysis
of these arrangements. Our main results include a generalization of the zone theorem
of [EOS], [CGL] to arrangements of curves (in which we show that the combinatorial
complexity of the zone of a curve is nearly linear in the number of curves), and
an application of (some weaker variant of) that theorem to obtain a nearly quadratic
incremental algorithm for the construction of such arrangements.
acknowledgement: Work on this paper by the first author has been supported by Amoco
Fnd. Fac. Dev. Comput. Sci. 1-6-44862 and by the National Science Foundation under
grant CCR-8714566. Work on this paper by the third and sixth authors has been supported
by Office of Naval Research Grant N00014-82-K-0381, by National Science Foundation
Grant No. NSF-DCR-83-20085, by grants from the Digital Equipment Corporation, and
the IBM Corporation. Work by the sixth author has also been supported by a research
grant from the NCRD — the Israeli National Council for Research and Development.
Work by the fourth author has been supported by National Science Foundation Grant
DMS-8501947.
alternative_title:
- LNCS
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: Leonidas
full_name: Guibas, Leonidas
last_name: Guibas
- first_name: János
full_name: Pach, János
last_name: Pach
- first_name: Richard
full_name: Pollack, Richard
last_name: Pollack
- first_name: Raimund
full_name: Seidel, Raimund
last_name: Seidel
- first_name: Micha
full_name: Sharir, Micha
last_name: Sharir
citation:
ama: 'Edelsbrunner H, Guibas L, Pach J, Pollack R, Seidel R, Sharir M. Arrangements
of curves in the plane - topology, combinatorics, and algorithms. In: 15th
International Colloquium on Automata, Languages and Programming. Vol 317.
Springer; 1988:214-229. doi:10.1007/3-540-19488-6_118'
apa: 'Edelsbrunner, H., Guibas, L., Pach, J., Pollack, R., Seidel, R., & Sharir,
M. (1988). Arrangements of curves in the plane - topology, combinatorics, and
algorithms. In 15th International Colloquium on Automata, Languages and Programming
(Vol. 317, pp. 214–229). Tampere, Finland: Springer. https://doi.org/10.1007/3-540-19488-6_118'
chicago: Edelsbrunner, Herbert, Leonidas Guibas, János Pach, Richard Pollack, Raimund
Seidel, and Micha Sharir. “Arrangements of Curves in the Plane - Topology, Combinatorics,
and Algorithms.” In 15th International Colloquium on Automata, Languages and
Programming, 317:214–29. Springer, 1988. https://doi.org/10.1007/3-540-19488-6_118.
ieee: H. Edelsbrunner, L. Guibas, J. Pach, R. Pollack, R. Seidel, and M. Sharir,
“Arrangements of curves in the plane - topology, combinatorics, and algorithms,”
in 15th International Colloquium on Automata, Languages and Programming,
Tampere, Finland, 1988, vol. 317, pp. 214–229.
ista: 'Edelsbrunner H, Guibas L, Pach J, Pollack R, Seidel R, Sharir M. 1988. Arrangements
of curves in the plane - topology, combinatorics, and algorithms. 15th International
Colloquium on Automata, Languages and Programming. ICALP: Automata, Languages
and Programming, LNCS, vol. 317, 214–229.'
mla: Edelsbrunner, Herbert, et al. “Arrangements of Curves in the Plane - Topology,
Combinatorics, and Algorithms.” 15th International Colloquium on Automata,
Languages and Programming, vol. 317, Springer, 1988, pp. 214–29, doi:10.1007/3-540-19488-6_118.
short: H. Edelsbrunner, L. Guibas, J. Pach, R. Pollack, R. Seidel, M. Sharir, in:,
15th International Colloquium on Automata, Languages and Programming, Springer,
1988, pp. 214–229.
conference:
end_date: 1988-07-15
location: Tampere, Finland
name: 'ICALP: Automata, Languages and Programming'
start_date: 1988-07-11
date_created: 2018-12-11T12:06:55Z
date_published: 1988-01-01T00:00:00Z
date_updated: 2022-02-08T10:15:09Z
day: '01'
doi: 10.1007/3-540-19488-6_118
extern: '1'
intvolume: ' 317'
keyword:
- line segment
- computational geometry
- Jordan curve
- cell decomposition
- vertical tangency
language:
- iso: eng
main_file_link:
- url: https://link.springer.com/chapter/10.1007/3-540-19488-6_118
month: '01'
oa_version: None
page: 214 - 229
publication: 15th International Colloquium on Automata, Languages and Programming
publication_identifier:
isbn:
- 978-3-540-19488-0
publication_status: published
publisher: Springer
publist_id: '2028'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Arrangements of curves in the plane - topology, combinatorics, and algorithms
type: conference
user_id: ea97e931-d5af-11eb-85d4-e6957dddbf17
volume: 317
year: '1988'
...