Familial STAG2 germline mutation defines a new human cohesinopathy-Reference-Cited by-同舟云学术

Familial STAG2 germline mutation defines a new human cohesinopathy

Published:2017-03-20 Issue:1 Volume:2 Page:
ISSN:2056-7944
Container-title:npj Genomic Medicine
language:en
Short-container-title:npj Genomic Med

Author:

Soardi Fernanda C.,Machado-Silva Alice,Linhares Natália D.,Zheng Ge,Qu Qianhui,Pena Heloísa B.,Martins Thaís M. M.,Vieira Helaine G. S.,Pereira Núbia B.,Melo-Minardi Raquel C.,Gomes Carolina C.,Gomez Ricardo S.,Gomes Dawidson A.,Pires Douglas E. V.^ORCID,Ascher David B.,Yu Hongtao^ORCID,Pena Sérgio D. J.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

http://www.nature.com/articles/s41525-017-0009-4.pdf

Reference47 articles.

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2. Peters, J. M., Tedeschi, A. & Schmitz, J. The cohesin complex and its roles in chromosome biology. Genes Dev. 22, 3089–3114 (2008).

3. Nasmyth, K. & Haering, C. H. Cohesin: its roles and mechanisms. Annu. Rev. Genet. 43, 525–558 (2009).

4. Haarhuis, J. H., Elbatsh, A. M. & Rowland, B. D. Cohesin and its regulation: on the logic of X-shaped chromosomes. Dev. Cell 31, 7–18 (2014).

5. Wu, N. & Yu, H. The Smc complexes in DNA damage response. Cell Biosci. 2, 5 (2012).

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