Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe-Reference-Cited by-同舟云学术

Analysis of a RECQL splicing mutation, c.1667_1667+3delAGTA, in breast cancer patients and controls from Central Europe

Published:2016-11-10 Issue:2 Volume:16 Page:181-186
ISSN:1389-9600
Container-title:Familial Cancer
language:en
Short-container-title:Familial Cancer

Author:

Bogdanova Natalia,Pfeifer Katja,Schürmann Peter,Antonenkova Natalia,Siggelkow Wulf,Christiansen Hans,Hillemanns Peter,Park-Simon Tjoung-Won,Dörk Thilo

Funder

Claudia von Schilling Foundation for Breast Cancer Research

Rudolf Bartling Foundation

Lower Saxonian Cancer Society

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics(clinical),Oncology,Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10689-016-9944-y.pdf

Reference30 articles.

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2. Bogdanova N, Helbig S, Dörk T (2013) Hereditary breast cancer: ever more pieces to the polygenic puzzle. Hered Cancer Clin Pract 11(1):12

3. Ghoussaini M, Pharoah PD, Easton DF (2013) Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning? Am J Pathol 183(4):1038–1051

4. Croteau DL, Popuri V, Opresko PL, Bohr VA (2014) Human RecQ helicases in DNA repair, recombination, and replication. Annu Rev Biochem 83:519–552

5. Bernstein KA, Gangloff S, Rothstein R (2010) The RecQ DNA helicases in DNA repair. Annu Rev Genet 44:393–417

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