Cohesinopathies of a Feather Flock Together-Reference-Cited by-同舟云学术

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Cohesinopathies of a Feather Flock Together

Published:2013-12-19 Issue:12 Volume:9 Page:e1004036
ISSN:1553-7404
Container-title:PLoS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Skibbens Robert V.,Colquhoun Jennifer M.,Green Megan J.,Molnar Cody A.,Sin Danielle N.,Sullivan Brian J.,Tanzosh Eden E.

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference79 articles.

1. 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;Nat Genet,2005

2. Inactivation mutations in ESCO2 cause SC phocomelia and Roberts Syndrome: No phenotype-genotype correlation;B Schule;Am J Hum Genet,2005

3. The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity;M Gordillo;Hum Mol Genet,2008

4. Cohesin codes – interpreting chromatin architecture and the many facets of cohesin function;S Rudra;J Cell Science,2013

5. X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations;A Musio;Nat Genet,2006

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1. Limb reduction in an Esco2 cohesinopathy mouse model is mediated by p53-dependent apoptosis and vascular disruption;Nature Communications;2024-08-21

2. Mosaic variegated aneuploidy in development, ageing and cancer;Nature Reviews Genetics;2024-08-21

3. Genetic determinants of micronucleus formation in vivo;Nature;2024-02-14

4. Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases;The Journal of Pediatrics;2022-07

5. Cohesin-Mediated Chromatin Interactions and Autoimmunity;Frontiers in Immunology;2022-02-10

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