A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers (Q28387138)

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author name string

A Lahad

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S Eisenberg

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E Dagan

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T Paperna

5

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L Kasinetz

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R Catane

7

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U Beller

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P Renbaum

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R Gershoni-Baruch

Proceedings of the National Academy of Sciences of the United States of America

11

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language of work or name

English

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publication date

13 March 2001

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published in

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volume

98

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page(s)

3232-6

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issue

6

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cites work

Over-expression of wild-type Rad51 correlates with histological grading of invasive ductal breast cancer

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Abnormal expression of BRCA1 and BRCA1-interactive DNA-repair proteins in breast carcinomas

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Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study

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Frequency and carrier risk associated with common BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer patients

20 March 2017

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The BRC repeats in BRCA2 are critical for RAD51 binding and resistance to methyl methanesulfonate treatment

20 March 2017

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RAD51 interacts with the evolutionarily conserved BRC motifs in the human breast cancer susceptibility gene brca2

20 March 2017

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Association of BRCA1 with Rad51 in mitotic and meiotic cells

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A simple salting out procedure for extracting DNA from human nucleated cells

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Abnormal expression of BRCA1 and BRCA1-interactive DNA-repair proteins in breast carcinomas

20 March 2017

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Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

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The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

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BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer

29 September 2017

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Detection of loss of heterozygosity at RAD51, RAD52, RAD54 and BRCA1 and BRCA2 loci in breast cancer: pathological correlations.

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Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families

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The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women

29 September 2017

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Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.

2 June 2018

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Efficacy of Bilateral Prophylactic Mastectomy in Women with a Family History of Breast Cancer

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Population-based study of risk of breast cancer in carriers of BRCA2 mutation

21 January 2018

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Prevalence and Penetrance of BRCA1 and BRCA2 Gene Mutations in Unselected Ashkenazi Jewish Women With Breast Cancer

21 January 2018

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BRCA1 and BRCA2 founder mutations in patients with bilateral breast cancer

21 January 2018

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12 December 2020

Identification of Rad51 alteration in patients with bilateral breast cancer

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12 December 2020

Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2

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12 December 2020

Breast cancer risk after bilateral prophylactic oophorectomy in BRCA1 mutation carriers

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release_fuo2l4b4jnahlarsonfb37dupa

Identifiers

DOI

10.1073/PNAS.051624098

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ADS bibcode

2001PNAS...98.3232L

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Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fuo2l4b4jnahlarsonfb37dupa

24 November 2022