Published in Biochim Biophys Acta on November 22, 2013
Complex elaboration: making sense of meiotic cohesin dynamics. FEBS J (2015) 0.93
Cohesin mutations in myeloid malignancies: underlying mechanisms. Exp Hematol Oncol (2014) 0.90
Drosophila Nipped-B Mutants Model Cornelia de Lange Syndrome in Growth and Behavior. PLoS Genet (2015) 0.84
Drosophila TDP-43 RNA-Binding Protein Facilitates Association of Sister Chromatid Cohesion Proteins with Genes, Enhancers and Polycomb Response Elements. PLoS Genet (2016) 0.82
Double SMCHD1 variants in FSHD2: the synergistic effect of two SMCHD1 variants on D4Z4 hypomethylation and disease penetrance in FSHD2. Eur J Hum Genet (2015) 0.79
Disorders of Transcriptional Regulation: An Emerging Category of Multiple Malformation Syndromes. Mol Syndromol (2016) 0.78
Measuring Sister Chromatid Cohesion Protein Genome Occupancy in Drosophila melanogaster by ChIP-seq. Methods Mol Biol (2017) 0.77
A neural crest origin for cohesinopathy heart defects. Hum Mol Genet (2015) 0.77
The Opposing Actions of Arabidopsis CHROMOSOME TRANSMISSION FIDELITY7 and WINGS APART-LIKE1 and 2 Differ in Mitotic and Meiotic Cells. Plant Cell (2016) 0.75
Emancipation from transcriptional latency: unphosphorylated STAT5 as guardian of hematopoietic differentiation. EMBO J (2016) 0.75
The cohesin complex prevents Myc-induced replication stress. Cell Death Dis (2017) 0.75
DNA Topoisomerase II modulates acetyl-regulation of cohesin-mediated chromosome dynamics. Curr Genet (2017) 0.75
Role of histone H3 lysine 27 methylation in Polycomb-group silencing. Science (2002) 24.31
Mediator and cohesin connect gene expression and chromatin architecture. Nature (2010) 14.34
Cohesins: chromosomal proteins that prevent premature separation of sister chromatids. Cell (1997) 12.90
Cohesin mediates transcriptional insulation by CCCTC-binding factor. Nature (2008) 12.01
A direct link between sister chromatid cohesion and chromosome condensation revealed through the analysis of MCD1 in S. cerevisiae. Cell (1997) 9.79
Cohesins functionally associate with CTCF on mammalian chromosome arms. Cell (2008) 7.80
Long-range chromatin regulatory interactions in vivo. Nat Genet (2002) 6.55
Architectural protein subclasses shape 3D organization of genomes during lineage commitment. Cell (2013) 6.37
Role of Bmi-1 and Ring1A in H2A ubiquitylation and Hox gene silencing. Mol Cell (2005) 6.29
Cohesin: its roles and mechanisms. Annu Rev Genet (2009) 6.19
Cohesins form chromosomal cis-interactions at the developmentally regulated IFNG locus. Nature (2009) 5.96
Identification of Xenopus SMC protein complexes required for sister chromatid cohesion. Genes Dev (1998) 5.78
Proximity among distant regulatory elements at the beta-globin locus requires GATA-1 and FOG-1. Mol Cell (2005) 5.77
The beta-globin nuclear compartment in development and erythroid differentiation. Nat Genet (2003) 5.54
CTCF-promoted RNA polymerase II pausing links DNA methylation to splicing. Nature (2011) 5.50
Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins. Mol Cell (2000) 5.49
At the heart of the chromosome: SMC proteins in action. Nat Rev Mol Cell Biol (2006) 5.45
The structure and function of SMC and kleisin complexes. Annu Rev Biochem (2005) 5.38
Molecular architecture of SMC proteins and the yeast cohesin complex. Mol Cell (2002) 5.36
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B. Nat Genet (2004) 5.19
Two distinct pathways remove mammalian cohesin from chromosome arms in prophase and from centromeres in anaphase. Cell (2000) 5.10
Mutational inactivation of STAG2 causes aneuploidy in human cancer. Science (2011) 5.04
Requirement of heterochromatin for cohesion at centromeres. Science (2001) 5.02
Cohesin relocation from sites of chromosomal loading to places of convergent transcription. Nature (2004) 5.00
NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome. Nat Genet (2004) 4.90
CTCF physically links cohesin to chromatin. Proc Natl Acad Sci U S A (2008) 4.89
A unifying genetic model for facioscapulohumeral muscular dystrophy. Science (2010) 4.87
Chromosomal cohesin forms a ring. Cell (2003) 4.38
Cohesins localize with CTCF at the KSHV latency control region and at cellular c-myc and H19/Igf2 insulators. EMBO J (2008) 4.28
Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation. Am J Hum Genet (2007) 4.20
Involvement of the cohesin protein, Smc1, in Atm-dependent and independent responses to DNA damage. Genes Dev (2002) 4.12
SMC1: an essential yeast gene encoding a putative head-rod-tail protein is required for nuclear division and defines a new ubiquitous protein family. J Cell Biol (1993) 4.08
The active spatial organization of the beta-globin locus requires the transcription factor EKLF. Genes Dev (2004) 4.04
Genome-wide mapping of the cohesin complex in the yeast Saccharomyces cerevisiae. PLoS Biol (2004) 4.03
Functional roles of enhancer RNAs for oestrogen-dependent transcriptional activation. Nature (2013) 3.93
A CTCF-independent role for cohesin in tissue-specific transcription. Genome Res (2010) 3.89
X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations. Nat Genet (2006) 3.89
Recruitment of cohesin to heterochromatic regions by Swi6/HP1 in fission yeast. Nat Cell Biol (2002) 3.85
Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair. Mol Cell (2004) 3.83
Saccharomyces cerevisiae CTF18 and CTF4 are required for sister chromatid cohesion. Mol Cell Biol (2001) 3.79
Phosphorylation of SMC1 is a critical downstream event in the ATM-NBS1-BRCA1 pathway. Genes Dev (2004) 3.76
Eco1-dependent cohesin acetylation during establishment of sister chromatid cohesion. Science (2008) 3.72
Characterization of vertebrate cohesin complexes and their regulation in prophase. J Cell Biol (2000) 3.70
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy. Nat Genet (2003) 3.60
The cohesin ring concatenates sister DNA molecules. Nature (2008) 3.58
SMC1 is a downstream effector in the ATM/NBS1 branch of the human S-phase checkpoint. Genes Dev (2002) 3.49
Identification of RFC(Ctf18p, Ctf8p, Dcc1p): an alternative RFC complex required for sister chromatid cohesion in S. cerevisiae. Mol Cell (2001) 3.40
A molecular determinant for the establishment of sister chromatid cohesion. Science (2008) 3.39
Sister chromatid cohesion is required for postreplicative double-strand break repair in Saccharomyces cerevisiae. Curr Biol (2001) 3.35
The cohesin complex and its roles in chromosome biology. Genes Dev (2008) 3.33
Dynamic molecular linkers of the genome: the first decade of SMC proteins. Genes Dev (2005) 3.29
Cohesin is required for higher-order chromatin conformation at the imprinted IGF2-H19 locus. PLoS Genet (2009) 3.25
Condensin and cohesin display different arm conformations with characteristic hinge angles. J Cell Biol (2002) 3.09
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle. Nature (2012) 3.08
Cell type specificity of chromatin organization mediated by CTCF and cohesin. Proc Natl Acad Sci U S A (2010) 3.03
Acetylation of Smc3 by Eco1 is required for S phase sister chromatid cohesion in both human and yeast. Mol Cell (2008) 3.01
Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element. Gene (1999) 3.00
Sister chromatid cohesion: a simple concept with a complex reality. Annu Rev Cell Dev Biol (2008) 2.99
Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene. PLoS Genet (2010) 2.95
Pol kappa: A DNA polymerase required for sister chromatid cohesion. Science (2000) 2.92
Identification and characterization of SA/Scc3p subunits in the Xenopus and human cohesin complexes. J Cell Biol (2000) 2.91
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD). PLoS Genet (2009) 2.90
Transcriptional dysregulation in NIPBL and cohesin mutant human cells. PLoS Biol (2009) 2.89
Identification of cis-acting sites for condensin loading onto budding yeast chromosomes. Genes Dev (2008) 2.87
Controlling long-range genomic interactions at a native locus by targeted tethering of a looping factor. Cell (2012) 2.87
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2. Nat Genet (2012) 2.82
Structure and stability of cohesin's Smc1-kleisin interaction. Mol Cell (2004) 2.81
Drosophila nipped-B protein supports sister chromatid cohesion and opposes the stromalin/Scc3 cohesion factor to facilitate long-range activation of the cut gene. Mol Cell Biol (2004) 2.79
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion. Nat Genet (2005) 2.77
An isogenetic myoblast expression screen identifies DUX4-mediated FSHD-associated molecular pathologies. EMBO J (2008) 2.74
Association of cohesin and Nipped-B with transcriptionally active regions of the Drosophila melanogaster genome. Chromosoma (2007) 2.73
ATP hydrolysis is required for cohesin's association with chromosomes. Curr Biol (2003) 2.69
NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations. Am J Hum Genet (2004) 2.67
MIX-1: an essential component of the C. elegans mitotic machinery executes X chromosome dosage compensation. Cell (1998) 2.65
Evidence that loading of cohesin onto chromosomes involves opening of its SMC hinge. Cell (2006) 2.58
A role for cohesin in T-cell-receptor rearrangement and thymocyte differentiation. Nature (2011) 2.58
Chromosomal addresses of the cohesin component Mcd1p. J Cell Biol (2000) 2.56
Architectural roles of multiple chromatin insulators at the human apolipoprotein gene cluster. EMBO J (2009) 2.56
A chromatin remodelling complex that loads cohesin onto human chromosomes. Nature (2002) 2.53
CTCF and cohesin: linking gene regulatory elements with their targets. Cell (2013) 2.53
The insulator factor CTCF controls MHC class II gene expression and is required for the formation of long-distance chromatin interactions. J Exp Med (2008) 2.50
Condensin and cohesin complexity: the expanding repertoire of functions. Nat Rev Genet (2010) 2.49
Recruitment of Xenopus Scc2 and cohesin to chromatin requires the pre-replication complex. Nat Cell Biol (2004) 2.45
A positive role for NLI/Ldb1 in long-range beta-globin locus control region function. Mol Cell (2007) 2.43
Condensins: universal organizers of chromosomes with diverse functions. Genes Dev (2012) 2.40
A model for ATP hydrolysis-dependent binding of cohesin to DNA. Curr Biol (2003) 2.40
Establishment of sister chromatid cohesion at the S. cerevisiae replication fork. Mol Cell (2006) 2.39
A topological interaction between cohesin rings and a circular minichromosome. Cell (2005) 2.35
Scc2 couples replication licensing to sister chromatid cohesion in Xenopus egg extracts. Curr Biol (2004) 2.24
Cohesin acetylation speeds the replication fork. Nature (2009) 2.23
An Smc3 acetylation cycle is essential for establishment of sister chromatid cohesion. Mol Cell (2010) 2.23
CCCTC-binding factor (CTCF) and cohesin influence the genomic architecture of the Igh locus and antisense transcription in pro-B cells. Proc Natl Acad Sci U S A (2011) 2.23
SmcHD1, containing a structural-maintenance-of-chromosomes hinge domain, has a critical role in X inactivation. Nat Genet (2008) 2.19
DUX4 activates germline genes, retroelements, and immune mediators: implications for facioscapulohumeral dystrophy. Dev Cell (2011) 2.17
Roles of the sister chromatid cohesion apparatus in gene expression, development, and human syndromes. Chromosoma (2006) 2.15
Conserved, developmentally regulated mechanism couples chromosomal looping and heterochromatin barrier activity at the homeobox gene A locus. Proc Natl Acad Sci U S A (2011) 2.15
Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome. PLoS Genet (2009) 2.14
Chromosomal association of the Smc5/6 complex reveals that it functions in differently regulated pathways. Mol Cell (2006) 2.13
Human SMC5/6 complex promotes sister chromatid homologous recombination by recruiting the SMC1/3 cohesin complex to double-strand breaks. EMBO J (2006) 2.13
Sororin mediates sister chromatid cohesion by antagonizing Wapl. Cell (2010) 2.12
Damage site chromatin: open or closed? Curr Opin Cell Biol (2011) 0.92
Damage-induced reactivation of cohesin in postreplicative DNA repair. Bioessays (2008) 0.78