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Nicholas J. Severs et al.
CARDIOVASCULAR RESEARCH (2008)
Connexin43 (GJA1) is required in the population of dividing cells during fin regeneration
Angela D. Hoptak-Solga et al.
DEVELOPMENTAL BIOLOGY (2008)
Loss of both GATA4 and GATA6 blocks cardiac myocyte differentiation and results in acardia in mice
Roong Zhao et al.
DEVELOPMENTAL BIOLOGY (2008)
Cohesins localize with CTCF at the KSHV latency control region and at cellular c-myc and H19/Igf2 insulators
William Stedman et al.
EMBO JOURNAL (2008)
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity
Miriam Gordillo et al.
HUMAN MOLECULAR GENETICS (2008)
ODDD-Linked Cx43 mutants reduce endogenous Cx43 expression and function in osteoblasts and inhibit late stage differentiation
Elizabeth McLachlan et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2008)
A handcuff model for the cohesin complex
Nenggang Zhang et al.
JOURNAL OF CELL BIOLOGY (2008)
Acetylation of Smc3 by Eco1 is required for S phase sister chromatid cohesion in both human and yeast
Jinglan Zhang et al.
MOLECULAR CELL (2008)
Cohesin mediates transcriptional insulation by CCCTC-binding factor
Kerstin S. Wendt et al.
NATURE (2008)
A molecular determinant for the establishment of sister chromatid cohesion
Elcin Unal et al.
SCIENCE (2008)
Eco1-dependent cohesin acetylation during establishment of sister chromatid cohesion
Tom Rolef Ben-Shahar et al.
SCIENCE (2008)
A new GJA1 (Connexin 43) mutation causing oculodentodigital dysplasia associated to uncommon features
David Rivera de la Parra et al.
OPHTHALMIC GENETICS (2007)
Cohesin-dependent regulation of Runx genes
Julia A. Horsfield et al.
DEVELOPMENT (2007)
Postreplicative formation of cohesion is required for repair and induced by a single DNA break
Lena Stroem et al.
SCIENCE (2007)
DNA double-strand breaks trigger genome-wide sister-chromatid cohesion through Eco1 (Ctf7)
Elcin Uenal et al.
SCIENCE (2007)
Comprehensive Expression Profiling of Tumor Cell Lines Identifies Molecular Signatures of Melanoma Progression
Byungwoo Ryu et al.
PLOS ONE (2007)
Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair
Mischa G. Vrouwe et al.
HUMAN MOLECULAR GENETICS (2007)
Chromosome segregation and double-strand break repair -: a complex connection
Lena Strom et al.
CURRENT OPINION IN CELL BIOLOGY (2007)
Sox17 is essential for the specification of cardiac mesoderm in embryonic stem cells
Yu Liu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (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)
Impaired ribosome biogenesis in Diamond-Blackfan anemia
Valerie Choesmel et al.
BLOOD (2007)
Wapl controls the dynamic association of cohesin with chromatin
Stephanie Kueng et al.
CELL (2006)
Functional characterization of a GJA1 frameshift mutation causing oculodentodigital dysplasia and palmoplantar keratoderma
Xiang-Qun Gong et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Semaphorin3D regulates invasion of cardiac neural crest cells into the primary heart field
Mariko Sato et al.
DEVELOPMENTAL BIOLOGY (2006)
Gene regulatory networks in the evolution and development of the heart
Eric N. Olson
SCIENCE (2006)
Making or breaking the heart: From lineage determination to morphogenesis
Deepak Srivastava
CELL (2006)
Establishment of sister chromatid cohesion at the S-cerevisiae replication fork
Armelle Lengronne et al.
MOLECULAR CELL (2006)
Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesis
Alessandro D. Mori et al.
DEVELOPMENTAL BIOLOGY (2006)
PCNA controls establishment of sister chromatid cohesion during S phase
George-Lucian Moldovan et al.
MOLECULAR CELL (2006)
X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations
A Musio et al.
NATURE GENETICS (2006)
Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart
K Koshiba-Takeuchi et al.
NATURE GENETICS (2006)
Sema3D, Sema3F, and Sema5A are expressed in overlapping and distinct patterns in chick embryonic heart
Z Jin et al.
DEVELOPMENTAL DYNAMICS (2006)
Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome:: No phenotype-genotype correlation
B Schüle et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
A novel mutation in the GJA1 gene in a family with oculodentodigital dysplasia
JPC Vasconcellos et al.
ARCHIVES OF OPHTHALMOLOGY (2005)
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia
AM Flenniken et al.
DEVELOPMENT (2005)
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD)
P Debeer et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2005)
Functional characterization of oculodentodigital dysplasia-associated Cx43 mutants
E McLachlan et al.
CELL COMMUNICATION AND ADHESION (2005)
Two human orthologues of Eco1/Ctf7 acetyltransferases are both required for proper sister-chromatid cohesion
FJ Hou et al.
MOLECULAR BIOLOGY OF THE CELL (2005)
Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasia
J Shibayama et al.
CIRCULATION RESEARCH (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.
NATURE GENETICS (2005)
Mutation of the cohesin related gene PDS5 causes cell death with predominant apoptotic features in Saccharomyces cerevisiae during early meiosis
Q Ren et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2005)
Mutations in connexin43 (GJA1) perturb bone growth in zebrafish fins
MK Iovine et al.
DEVELOPMENTAL BIOLOGY (2005)
NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations
LA Gillis et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair
L Ström et al.
MOLECULAR CELL (2004)
DNA damage response pathway uses histone modification to assemble a double-strand break-specific cohesin domain
E Ünal et al.
MOLECULAR CELL (2004)
Transcriptional regulation of the murine Connexin40 promoter by cardiac factors Nkx2-5, GATA4 and Tbx5
VLF Linhares et al.
CARDIOVASCULAR RESEARCH (2004)
In vivo requirements for rDNA chromosome condensation reveal two cell-cycle-regulated pathways for mitotic chromosome folding
BD Lavoie et al.
GENES & DEVELOPMENT (2004)
Baf60c is essential for function of BAF chromatin remodelling complexes in heart development
H Lickert et al.
NATURE (2004)
NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome
ET Tonkin et al.
NATURE GENETICS (2004)
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B
ID Krantz et al.
NATURE GENETICS (2004)
Gap junctions and the connexin protein family
G Söhl et al.
CARDIOVASCULAR RESEARCH (2004)
Gap junction alterations in human cardiac disease
NJ Severs et al.
CARDIOVASCULAR RESEARCH (2004)
Human EFO1p exhibits acetyltransferase activity and is a unique combination of linker histone and Ctf7p/Eco1p chromatid cohesion establishment domains
AM Bellows et al.
NUCLEIC ACIDS RESEARCH (2003)
Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy
J Kohlhase et al.
JOURNAL OF MEDICAL GENETICS (2003)
Cardiac electrophysiological phenotypes in postnatal expression of Nkx2.5 transgenic mice
H Wakimoto et al.
GENESIS (2003)
Developmentally modulated cardiac conduction failure in transgenic mice with fetal or postnatal overexpression of DNA nonbinding mutant Nkx2.5
H Wakimoto et al.
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY (2002)
Cardiac gap junctions and connexins: their role in atrial fibrillation and potential as therapeutic targets
HMW van der Velden et al.
CARDIOVASCULAR RESEARCH (2002)
In vivo dissection of the chromosome condensation machinery: reversibility of condensation distinguishes contributions of condensin and cohesin
BD Lavoie et al.
JOURNAL OF CELL BIOLOGY (2002)
Eco1 is a novel acetyltransferase that can acetylate proteins involved in cohesion
D Ivanov et al.
CURRENT BIOLOGY (2002)
Regulation of the epithelial-mesenchymal transformation through gap junction channels in heart development
K Nishii et al.
TRENDS IN CARDIOVASCULAR MEDICINE (2001)
Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation
Y Hiroi et al.
NATURE GENETICS (2001)
Characterization of homo- and heterodimerization of cardiac Csx/Nkx2.5 homeoprotein
H Kasahara et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Pds5p is an essential chromosomal protein required for both sister chromatid cohesion and condensation in Saccharomyces cerevisiae
T Hartman et al.
JOURNAL OF CELL BIOLOGY (2000)
Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins
R Ciosk et al.
MOLECULAR CELL (2000)