Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1-Reference-Cited by-同舟云学术

Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1

Published:2010-02 Issue:2 Volume:86 Page:262-266
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

van der Lelij Petra,Chrzanowska Krystyna H.,Godthelp Barbara C.,Rooimans Martin A.,Oostra Anneke B.,Stumm Markus,Zdzienicka Małgorzata Z.,Joenje Hans,de Winter Johan P.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference8 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;Vega;Nat. Genet.,2005

2. Chl1p, a DNA helicase-like protein in budding yeast, functions in sister-chromatid cohesion;Skibbens;Genetics,2004

3. The DNA helicase ChlR1 is required for sister chromatid cohesion in mammalian cells;Parish;J. Cell Sci.,2006

4. Loss of ChlR1 helicase in mouse causes lethality due to the accumulation of aneuploid cells generated by cohesion defects and placental malformation;Inoue;Cell Cycle,2007

5. ChlR1 is required for loading papillomavirus E2 onto mitotic chromosomes and viral genome maintenance;Parish;Mol. Cell,2006

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