Biallelic Mutations in BRCA1 Cause a New Fanconi Anemia Subtype-Reference-Cited by-同舟云学术

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Biallelic Mutations in BRCA1 Cause a New Fanconi Anemia Subtype

Published:2014-12-03 Issue:2 Volume:5 Page:135-142
ISSN:2159-8274
Container-title:Cancer Discovery
language:en
Short-container-title:Cancer Discovery

Author:

Sawyer Sarah L.,Tian Lei,Kähkönen Marketta,Schwartzentruber Jeremy,Kircher Martin,Majewski Jacek,Dyment David A.,Innes A. Micheil,Boycott Kym M.,Moreau Lisa A.,Moilanen Jukka S.,Greenberg Roger A., ,

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology

Cited by 251 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The coexistence of a BRCA2 germline and a DICER1 somatic variant in two first-degree cousins suggests their potential synergic effect;Scientific Reports;2024-09-13

2. E3 ligases: a ubiquitous link between DNA repair, DNA replication and human disease;Biochemical Journal;2024-07-10

3. Research progress on the fanconi anemia signaling pathway in non-obstructive azoospermia;Frontiers in Endocrinology;2024-05-23

4. Crosstalk between DNA Damage Repair and Metabolic Regulation in Hematopoietic Stem Cells;Cells;2024-04-24

5. A practice changing paper: biallelic inactivation of BRCA2 in Fanconi anaemia;BJC Reports;2024-04-19

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