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Article

Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion

10 Apr 2005

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 15821733
DOI: 10.1038/ng1548

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Related research

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Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesionPMID 15821733Read ↗

The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity.Semantic proximity Read ↗

Variations in dysfunction of sister chromatid cohesion in esco2 mutant zebrafish reflect the phenotypic diversity of Roberts syndrome.Semantic proximity Read ↗

Cohesinopathies: One ring, many obligations.Semantic proximity Read ↗

ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION.Semantic proximity Read ↗

Roberts syndrome in an Indian patient with humeroradial synostosis, congenital elbow contractures and a novel homozygous splice variant in ESCO2.Semantic proximity Read ↗

Eco1 is important for DNA damage repair in S. cerevisiae.Semantic proximity Read ↗

Expanding the mutation and clinical spectrum of Roberts syndrome.Semantic proximity Read ↗

Cohesin and human disease.Semantic proximity Read ↗

Non-Redundant Roles in Sister Chromatid Cohesion of the DNA Helicase DDX11 and the SMC3 Acetyl Transferases ESCO1/2Semantic proximity Read ↗

Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2.Semantic proximity Read ↗

The expanding universe of cohesin functions: a new genome stability caretaker involved in human disease and cancer.Semantic proximity Read ↗

Functional control of Eco1 through the MCM complex in sister chromatid cohesion.Semantic proximity Read ↗

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