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BRCA1 wt Allele
Known as:
BRCC1
, BRCA1
, FANCS
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Human BRCA1 wild-type allele is located within 17q21 and is approximately 81 kb in length. This allele, which encodes breast cancer type 1…
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National Institutes of Health
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Related topics
Related topics
20 relations
17q21
ATM Signaling Pathway
BARD1 Pathway
BRCA1 Protein
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Broader (1)
BRCA1 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
Bilateral Oophorectomy and Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
J. Kotsopoulos
,
T. Huzarski
,
+18 authors
S. Narod
Journal of the National Cancer Institute
2017
Corpus ID: 32623356
Background: Whether oophorectomy reduces breast cancer risk among BRCA mutation carriers is a matter of debate. We undertook a…
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Highly Cited
2014
Highly Cited
2014
PARP1-driven poly-ADP-ribosylation regulates BRCA1 function in homologous recombination-mediated DNA repair.
Yiduo Hu
,
Sarah A Petit
,
+10 authors
D. Livingston
Cancer Discovery
2014
Corpus ID: 2568946
UNLABELLED BRCA1 promotes homologous recombination-mediated DNA repair (HRR). However, HRR must be tightly regulated to prevent…
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Highly Cited
2011
Highly Cited
2011
Mild hyperthermia inhibits homologous recombination, induces BRCA2 degradation, and sensitizes cancer cells to poly (ADP-ribose) polymerase-1 inhibition
P. Krawczyk
,
Berina Eppink
,
+15 authors
J. Aten
Proceedings of the National Academy of Sciences…
2011
Corpus ID: 205252806
Defective homologous recombination (HR) DNA repair imposed by BRCA1 or BRCA2 deficiency sensitizes cells to poly (ADP-ribose…
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Review
2008
Review
2008
DNA repair deficiency as a therapeutic target in cancer.
S. Martin
,
C. Lord
,
A. Ashworth
Current Opinion in Genetics and Development
2008
Corpus ID: 205002401
Highly Cited
2004
Highly Cited
2004
Genetic Steps of Mammalian Homologous Repair with Distinct Mutagenic Consequences
Jeremy M. Stark
,
A. Pierce
,
Jin Oh
,
A. Pastink
,
M. Jasin
Molecular and Cellular Biology
2004
Corpus ID: 44913035
ABSTRACT Repair of chromosomal breaks is essential for cellular viability, but misrepair generates mutations and gross…
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Highly Cited
2004
Highly Cited
2004
Breast Cancer Risk and the DNA Double-Strand Break End-Joining Capacity of Nonhomologous End-Joining Genes Are Affected by BRCA1
D. Bau
,
Yi-Ping Fu
,
+4 authors
Chen-Yang Shen
Cancer Research
2004
Corpus ID: 14639928
A tumorigenic role of the nonhomologous end-joining (NHEJ) pathway for the repair of DNA double-strand breaks (DSBs) has been…
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Highly Cited
2000
Highly Cited
2000
Anticipated versus actual emotional reactions to disclosure of results of genetic tests for cancer susceptibility: findings from p53 and BRCA1 testing programs.
M. Dorval
,
A. Patenaude
,
+9 authors
J. Garber
Journal of Clinical Oncology
2000
Corpus ID: 34957126
PURPOSE We examined the ability of individuals undergoing genetic testing for cancer susceptibility in two structured research…
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Highly Cited
1999
Highly Cited
1999
Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response.
Q. Zhong
,
Chi Fen Chen
,
+6 authors
Wen-Hwa Lee
Science
1999
Corpus ID: 26162339
BRCA1 encodes a tumor suppressor that is mutated in familial breast and ovarian cancers. Here, it is shown that BRCA1 interacts…
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Highly Cited
1997
Highly Cited
1997
A descriptive study of BRCA1 testing and reactions to disclosure of test results
H. Lynch
,
S. Lemon
,
+12 authors
S. Narod
Cancer
1997
Corpus ID: 32124067
The identification of the BRCA1 gene is a powerful tool for predicting a patient's lifetime risk for carcinoma of the breast and…
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Highly Cited
1996
Highly Cited
1996
Cancer mortality in relatives of women with breast cancer: The OPCS study
J. Peto
,
D. Easton
,
Fiona E. Matthews
,
D. Ford
,
A. Swerdlow
International Journal of Cancer
1996
Corpus ID: 19446164
Mortality from cancer and other causes in male and female first‐degree relatives of women with breast cancer diagnosed before age…
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