about
The chromosome cycle: coordinating replication and segregation. Second in the cycles review series.Kinetochore-microtubule interactions: steps towards bi-orientationThree wise centromere functions: see no error, hear no break, speak no delayHigh resolution imaging reveals heterogeneity in chromatin states between cells that is not inherited through cell division.Mps1 kinase promotes sister-kinetochore bi-orientation by a tension-dependent mechanismOrdered recruitment of transcription and chromatin remodeling factors to a cell cycle- and developmentally regulated promoter.Pds5 cooperates with cohesin in maintaining sister chromatid cohesion.Cnn1 inhibits the interactions between the KMN complexes of the yeast kinetochore.Kinetochore recruitment of two nucleolar proteins is required for homolog segregation in meiosis I.Yeast kinesin-8 depolymerizes microtubules in a length-dependent manner.Modes of spindle pole body inheritance and segregation of the Bfa1p-Bub2p checkpoint protein complexEvidence that the Ipl1-Sli15 (Aurora kinase-INCENP) complex promotes chromosome bi-orientation by altering kinetochore-spindle pole connectionsTension between two kinetochores suffices for their bi-orientation on the mitotic spindle.Bi-orienting chromosomes on the mitotic spindle.Spatial regulation and organization of DNA replication within the nucleus.Mechanisms mitigating problems associated with multiple kinetochores on one microtubule in early mitosis.Molecular mechanisms facilitating the initial kinetochore encounter with spindle microtubules.Kinetochore-microtubule error correction is driven by differentially regulated interaction modes.Ipl1-dependent phosphorylation of Dam1 is reduced by tension applied on kinetochores.High-resolution replication profiles define the stochastic nature of genome replication initiation and termination.Stochastic association of neighboring replicons creates replication factories in budding yeast.The SWI/SNF complex acts to constrain distribution of the centromeric histone variant Cse4.The Ndc80 loop region facilitates formation of kinetochore attachment to the dynamic microtubule plus end.Discovery of an unconventional centromere in budding yeast redefines evolution of point centromeres.Smc3 Deacetylation by Hos1 Facilitates Efficient Dissolution of Sister Chromatid Cohesion during Early Anaphase.Molecular mechanisms of kinetochore capture by spindle microtubules.Identification of Cohesin Association Sites at Centromeres and along Chromosome ArmsAurora B-INCENP localization at centromeres/inner kinetochores is essential for chromosome bi-orientation in budding yeastLive imaging of marked chromosome regions reveals their dynamic resolution and compaction in mitosisContractile acto-myosin network on nuclear envelope remnants positions human chromosomes for mitosisKinetochore-microtubule error correction is driven by differentially regulated interaction modesZooming in on chromosome dynamics
P50
Q24537591-6B77A0C6-DBF1-40E7-8F22-F5463A9F4E49Q24602097-388E970E-A450-4423-B7C9-CE5773A902DAQ27008596-0B7DB3ED-82A6-487B-B17D-89C774BB53BDQ27318586-5ACBBB6D-98C2-42E7-B1FD-7E5A57A0C21FQ27930787-F980D86F-4FA1-4915-B6C3-DDB8CBB912E8Q27930916-459A67A6-3AF7-49AE-9C97-02240FA1D5A4Q27932492-513CFC19-3830-4EC2-B635-58A25ED4019EQ27937573-51CA1A29-D41A-4862-A272-F8BAC7D43CA5Q27939356-FD48E67E-0D83-45B7-AFE6-3C6E3FF789F3Q27939784-8C56EF9E-82BB-4D81-86AC-7AFACE80C9E1Q28364029-3D2CA3A0-4C16-4B41-B4DF-B5448A3B50E0Q29619579-DEB29DE8-95AE-4D79-B233-87800C514F95Q34298424-94AFB86C-A671-4942-A50B-FBFDCF0C5880Q34688467-78949093-EE8B-4E82-A961-44F3FA9F22F3Q37621327-75DB586E-79DE-4EDD-8CC3-AF62F634025FQ38762817-F5CD977A-4C83-4225-ADAA-AAC17D6CB16DQ38818100-375C4644-4FA4-4405-AF4F-B4911E2AED36Q41790587-921C6295-FFA4-418E-B4C8-49F4ABCD7637Q41837810-C1B1338B-0C79-46E9-86EF-3965F9AC20CCQ41885231-D8D3DA00-D84E-4358-B4DA-FBC4F317B21FQ41997371-CC8FB221-3DEC-4FF5-BBB3-67124C9E7A57Q42051038-933E8839-75D9-4321-9118-D255F08D969EQ42056835-D03D4FC3-F477-4DC5-8B4B-0C16A2468F90Q42436460-0FB087A3-EF61-4066-9D4F-9174C16AFF2AQ44076675-2486E968-2F59-4A6F-944C-1FAF8994EF0DQ48951524-D93F0783-AF82-4078-A089-942E983261E3Q57270131-C2C96A2D-3C0A-49A7-9C96-0800DB2ECB8EQ61229903-D9FEECAC-8AAB-4E43-967B-834E55488B59Q64107981-94FB8CEF-5CC3-458A-B9D9-FE19EE99C476Q83231218-4FC7777B-8F66-41B1-BCB6-BC818F9549C1Q86998659-033BA10C-1EB8-426A-8E53-F73FEB649736Q94656800-6B82601E-6C1E-49E4-8463-1C3A5013F573
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Tomoyuki U Tanaka
@ast
Tomoyuki U Tanaka
@en
Tomoyuki U Tanaka
@es
Tomoyuki U Tanaka
@nl
type
label
Tomoyuki U Tanaka
@ast
Tomoyuki U Tanaka
@en
Tomoyuki U Tanaka
@es
Tomoyuki U Tanaka
@nl
prefLabel
Tomoyuki U Tanaka
@ast
Tomoyuki U Tanaka
@en
Tomoyuki U Tanaka
@es
Tomoyuki U Tanaka
@nl
P106
P1153
7406724790
P31
P496
0000-0002-9886-5947