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Hideaki Takata et al.
CURRENT BIOLOGY (2007)
Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation
Matthew A. Deardorff et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Human Wapl is a cohesin-binding protein that promotes sister-chromatid resolution in mitotic prophase
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Wapl controls the dynamic association of cohesin with chromatin
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Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells
Jennifer L. Fish et al.
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Regulation of mitotic entry by microcephalin and its overlap with ATR signalling
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Human Scc4 is required for cohesin binding to chromatin, sister-chromatid cohesion, and mitotic progression
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CURRENT BIOLOGY (2006)
Shugoshin collaborates with protein phosphatase 2A to protect cohesin
TS Kitajima et al.
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X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations
A Musio et al.
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Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues
David Garrick et al.
PLOS GENETICS (2006)
The mammalian heterochromatin protein 1 binds diverse nuclear proteins through a common motif that targets the chromoshadow domain
MS Lechner et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)
Silencing mitosin induces misaligned chromosomes, premature chromosome decondensation before anaphase onset, and mitotic cell death
ZY Yang et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion
H Vega et al.
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A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size
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NATURE GENETICS (2005)
SMC proteins and chromosome mechanics: from bacteria to humans
T Hirano
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2005)
Shugoshin prevents dissociation of cohesin from centromeres during mitosis in vertebrate cells
BE McGuinness et al.
PLOS BIOLOGY (2005)
The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis
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JOURNAL OF CLINICAL INVESTIGATION (2005)
The RSC nucleosome-remodeling complex is required for Cohesin's association with chromosome arms
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MOLECULAR CELL (2004)
A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain
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GENE (2004)
The ctf13-30/CTF13 genomic haploinsufficiency modifier screen identifies the yeast chromatin remodeling complex RSC, which is required for the establishment of sister chromatid cohesion
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MOLECULAR AND CELLULAR BIOLOGY (2004)
Gene silencing of CENP-E by small interfering RNA in HeLa cells leads to missegregation of chromosomes after a mitotic delay
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MOLECULAR BIOLOGY OF THE CELL (2004)
ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes
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DEVELOPMENTAL BIOLOGY (2004)
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B
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NATURE GENETICS (2004)
The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies
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ASPM is a major determinant of cerebral cortical size
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NATURE GENETICS (2002)
A chromatin remodelling complex that loads cohesin onto human chromosomes
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NATURE (2002)
The dissociation of cohesin from chromosomes in prophase is regulated by polo-like kinase
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MOLECULAR CELL (2002)
Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability
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CELL (2001)
Structure-function analysis of SUV39H1 reveals a dominant role in heterochromatin organization, chromosome segregation, and mitotic progression
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MOLECULAR AND CELLULAR BIOLOGY (2000)
Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association
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HUMAN MOLECULAR GENETICS (2000)
Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins
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MOLECULAR CELL (2000)