CCAN makes multiple contacts with centromeric DNA to provide distinct pathways to the outer kinetochore (Q24324027)

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18 January 2020

title

CCAN makes multiple contacts with centromeric DNA to provide distinct pathways to the outer kinetochore (English)

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18 January 2020

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5

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18 January 2020

Iain M Cheeseman

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18 January 2020

author name string

Tetsuya Hori

1

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18 January 2020

Miho Amano

2

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18 January 2020

Aussie Suzuki

3

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18 January 2020

Chelsea B Backer

4

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18 January 2020

Yimin Dong

6

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18 January 2020

Bruce F McEwen

7

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18 January 2020

Wei-Hao Shang

8

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18 January 2020

Emiko Suzuki

9

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18 January 2020

Katsuya Okawa

10

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18 January 2020

Tatsuo Fukagawa

12

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18 January 2020

language of work or name

English

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publication date

1 December 2008

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18 January 2020

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18 January 2020

volume

135

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18 January 2020

issue

6

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18 January 2020

page(s)

1039-1052

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On the positions of centromeres in chicken lampbrush chromosomes

18 January 2020

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CENP-C, an autoantigen in scleroderma, is a component of the human inner kinetochore plate

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Mislocalization of the Drosophila centromere-specific histone CID promotes formation of functional ectopic kinetochores

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Priming of centromere for CENP-A recruitment by human hMis18alpha, hMis18beta, and M18BP1

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Human Blinkin/AF15q14 is required for chromosome alignment and the mitotic checkpoint through direct interaction with Bub1 and BubR1

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Conserved organization of centromeric chromatin in flies and humans

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CENP-I is essential for centromere function in vertebrate cells

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Structural determinants for generating centromeric chromatin

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The CENP-H-I complex is required for the efficient incorporation of newly synthesized CENP-A into centromeres

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Molecular architecture of the kinetochore-microtubule interface

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Human centromeric chromatin is a dynamic chromosomal domain that can spread over noncentromeric DNA

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A 17-kD centromere protein (CENP-A) copurifies with nucleosome core particles and with histones

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CENP-C is required for maintaining proper kinetochore size and for a timely transition to anaphase.

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The human Mis12 complex is required for kinetochore assembly and proper chromosome segregation.

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Mapping the assembly pathways that specify formation of the trilaminar kinetochore plates in human cells

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7 January 2021

Functional genomics identifies a Myb domain-containing protein family required for assembly of CENP-A chromatin

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7 January 2021

Propagation of centromeric chromatin requires exit from mitosis.

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Molecular architecture of the kinetochore-microtubule attachment site is conserved between point and regional centromeres

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Hec1 and nuf2 are core components of the kinetochore outer plate essential for organizing microtubule attachment sites

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CENP-C is involved in chromosome segregation, mitotic checkpoint function, and kinetochore assembly

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7 January 2021

CENP-O class proteins form a stable complex and are required for proper kinetochore function

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7 January 2021

ESPript: analysis of multiple sequence alignments in PostScript

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7 January 2021

CENP-C is necessary but not sufficient to induce formation of a functional centromere

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7 January 2021

CENP-H, a constitutive centromere component, is required for centromere targeting of CENP-C in vertebrate cells.

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7 January 2021

A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension

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Proteomics analysis of the centromere complex from HeLa interphase cells: UV-damaged DNA binding protein 1 (DDB-1) is a component of the CEN-complex, while BMI-1 is transiently co-localized with the centromeric region in interphase

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CENP-A, -B, and -C chromatin complex that contains the I-type alpha-satellite array constitutes the prekinetochore in HeLa cells

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Consolidated OpenCitations Corpus – April 2017

2325713

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18 January 2020

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Consolidated OpenCitations Corpus – April 2017

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