Oscillatory movements of monooriented chromosomes and their position relative to the spindle pole result from the ejection properties of the aster and half-spindle
about
A delay in the Saccharomyces cerevisiae cell cycle that is induced by a dicentric chromosome and dependent upon mitotic checkpointsThe checkpoint delaying anaphase in response to chromosome monoorientation is mediated by an inhibitory signal produced by unattached kinetochoresThe kinesin-8 motor Kif18A suppresses kinetochore movements to control mitotic chromosome alignmentAberrantly segregating centromeres activate the spindle assembly checkpoint in budding yeastMotile kinetochores and polar ejection forces dictate chromosome position on the vertebrate mitotic spindleDirectional instability of kinetochore motility during chromosome congression and segregation in mitotic newt lung cells: a push-pull mechanismThe small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore-microtubule attachment and in maintaining the spindle assembly checkpointKinetochores capture astral microtubules during chromosome attachment to the mitotic spindle: direct visualization in live newt lung cellsThe chromokinesin Kid is necessary for chromosome arm orientation and oscillation, but not congression, on mitotic spindlesRole of the Number of Microtubules in Chromosome Segregation during Cell DivisionNuSAP governs chromosome oscillation by facilitating the Kid-generated polar ejection forceA Brief History of Research on Mitotic MechanismsPolar Ejection Forces Promote the Conversion from Lateral to End-on Kinetochore-Microtubule Attachments on Mono-oriented ChromosomesKinetochore alignment within the metaphase plate is regulated by centromere stiffness and microtubule depolymerasesReal-time observations of microtubule dynamic instability in living cellsKinetochore chemistry is sensitive to tension and may link mitotic forces to a cell cycle checkpoint.The kinetochore microtubule minus-end disassembly associated with poleward flux produces a force that can do work.Microtubules in the metaphase-arrested mouse oocyte turn over rapidlyEvidence that replication fork components catalyze establishment of cohesion between sister chromatids.Microtubule movements on the arms of mitotic chromosomes: polar ejection forces quantified in vitro.A functional relationship between NuMA and kid is involved in both spindle organization and chromosome alignment in vertebrate cellsTension applied through the Dam1 complex promotes microtubule elongation providing a direct mechanism for length control in mitosisThe distribution of polar ejection forces determines the amplitude of chromosome directional instability.Mechanisms of chromosome behaviour during mitosisAnalysis of DNA double-strand break response and chromatin structure in mitosis using laser microirradiation."Artificial mitotic spindle" generated by dielectrophoresis and protein micropatterning supports bidirectional transport of kinesin-coated beadsThe coupling between sister kinetochore directional instability and oscillations in centromere stretch in metaphase PtK1 cells.Human chromokinesins promote chromosome congression and spindle microtubule dynamics during mitosisElevated polar ejection forces stabilize kinetochore-microtubule attachmentsDeformations within moving kinetochores reveal different sites of active and passive force generation.Chromosome position at the spindle equator is regulated by chromokinesin and a bipolar microtubule array.Microtubule depolymerization promotes particle and chromosome movement in vitro.Meiotic spindle assembly in Drosophila females: behavior of nonexchange chromosomes and the effects of mutations in the nod kinesin-like protein.Laser microsurgery in the GFP era: a cell biologist's perspectiveMicrotubule composition: cryptography of dynamic polymers.Finding the middle ground: how kinetochores power chromosome congression.CENP-E is essential for reliable bioriented spindle attachment, but chromosome alignment can be achieved via redundant mechanisms in mammalian cellsDrosophila Nod protein binds preferentially to the plus ends of microtubules and promotes microtubule polymerization in vitro.Mechanisms of microtubule-based kinetochore positioning in the yeast metaphase spindle.Poleward force at the kinetochore in metaphase depends on the number of kinetochore microtubules.
P2860
Q24601605-C61541A8-68AC-458E-9DB8-82A0C6185FC2Q24651512-B32CCE9A-AB3F-4E99-B543-F944929F3785Q24653914-AC70B8D5-1B51-4653-990C-3DDE4A493D47Q24672009-45D417B9-7DBA-40AE-8723-157D0B70A91AQ24673532-954B103E-4E90-4418-93E3-188880BAD45FQ24674852-AF633A30-FF2B-4C39-B3BD-EA7A5618F3A9Q24675117-3E53A0AA-3C2C-4A31-A57C-5FEE6508DEB4Q24678769-2CAF28BC-9195-425C-AFAF-3B9A283FD9F8Q24685481-DF4BE4B9-CBB7-4F0F-95EE-18A7CA8AB756Q27311999-563909C8-39EC-42BE-A5BE-78FE11D568D8Q27333708-43A812C9-4AEC-495C-8C58-99EB53CEE886Q28074607-27AF695F-6D0A-4C6E-B4C7-7E59BA92D0A4Q28268443-C62B35E1-642C-4C7E-9424-8EC3D6327C54Q28275327-CD4B9027-BCA2-4217-B220-0967AF9874E8Q28760164-682F5BE9-F364-4504-A171-1850FAADC1F5Q30442219-5F6B62B8-8397-4AA0-993E-80EA9DA3D077Q30450974-0D150A54-608D-4A4E-81DE-73BAEDEFEE3CQ30454177-41EC2D8F-7079-46D1-8470-33B58BF8FAB3Q30454198-4D55ADFB-59FF-4A27-BC27-CC6F87A99DB0Q30476206-DEFC5733-1536-4541-A66F-77661957078DQ30480022-D1C1B7A1-75EC-427D-BC92-9941AE9FCCE3Q30487581-69408D85-94EA-4221-A259-73D042014AAFQ30488889-65771F64-22ED-49B2-A571-E38674A6F661Q30495185-82A9BA76-353B-4626-98F2-C6F5B3F8A3BAQ30497641-CEE13B39-C62B-4B29-AD26-661ACE1DEAE1Q30499368-BF58F86D-3872-4F50-8600-46217A66F0FBQ30510172-57D9F0D5-8E21-4DD7-80F3-589707A17217Q30524669-CA3F649D-AC7B-467A-9A9A-148723C86EEEQ30532728-51F638A3-E483-4B40-9332-BA60ADAA7A89Q30540291-AB6C314F-2E07-4859-8C3D-78824A09BE65Q30547575-575E896D-3167-46AC-B478-53EADD7A980AQ30966793-94723DDD-20DC-4330-849C-785DBD835BA6Q33280889-D9AC60C2-AC3D-413A-96DD-D7511D3C43BCQ33288550-AAE52D90-EA23-4C0F-BEB1-B393F39B0F2CQ33780919-C6D82FD7-1C96-45EB-BF43-95F620B7CB39Q33903518-21AF467C-C040-4844-A0B8-55365DB9A0B6Q33946743-2BBAFB21-025E-4A57-8170-A1B9C2DEE79CQ34099603-C1E89505-85A8-4E8F-A08B-6844E90643E3Q34181361-D9F8C1C8-B55B-4013-B3E5-DF6295CF932EQ34417496-6DE2E448-1E24-47B0-9E76-AF4FCB81D953
P2860
Oscillatory movements of monooriented chromosomes and their position relative to the spindle pole result from the ejection properties of the aster and half-spindle
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Oscillatory movements of monoo ...... of the aster and half-spindle
@ast
Oscillatory movements of monoo ...... of the aster and half-spindle
@en
type
label
Oscillatory movements of monoo ...... of the aster and half-spindle
@ast
Oscillatory movements of monoo ...... of the aster and half-spindle
@en
prefLabel
Oscillatory movements of monoo ...... of the aster and half-spindle
@ast
Oscillatory movements of monoo ...... of the aster and half-spindle
@en
P2093
P2860
P356
P1476
Oscillatory movements of monoo ...... of the aster and half-spindle
@en
P2093
C L Rieder
E A Davison
E D Salmon
L C Jensen
L Cassimeris
P2860
P304
P356
10.1083/JCB.103.2.581
P407
P577
1986-08-01T00:00:00Z