(Q31936221)

English

The frequency of founder mutations in the BRCA1, BRCA2, and APC genes in Australian Ashkenazi Jews: implications for the generality of U.S. population data

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scholarly article

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Europe PubMed Central

PubMed publication ID

5 July 2017

The frequency of founder mutations in the BRCA1, BRCA2, and APC genes in Australian Ashkenazi Jews: implications for the generality of U.S. population data (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

author name string

Bahar AY

1

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

Taylor PJ

2

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

Andrews L

3

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

Proos A

4

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

Burnett L

5

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

Tucker K

6

1 reference

Europe PubMed Central

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5 July 2017

Friedlander M

7

1 reference

Europe PubMed Central

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5 July 2017

Buckley MF

8

1 reference

Europe PubMed Central

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5 July 2017

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publication date

1 July 2001

1 reference

Europe PubMed Central

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5 July 2017

1 reference

Europe PubMed Central

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5 July 2017

92

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Europe PubMed Central

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5 July 2017

2

1 reference

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5 July 2017

440-445

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

Linkage of early-onset familial breast cancer to chromosome 17q21

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

BRCA1 required for transcription-coupled repair of oxidative DNA damage

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

Association of BRCA1 with Rad51 in mitotic and meiotic cells

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

Identification of the breast cancer susceptibility gene BRCA2

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

Lessons from hereditary colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

The APC variants I1307K and E1317Q are associated with colorectal tumors, but not always with a family history.

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

The I1307K polymorphism of the APC gene in colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

I1307K APC and hMLH1 mutations in a non-Jewish family with hereditary non-polyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2F1097-0142%2820010715%2992%3A2%3C440%3A%3AAID-CNCR1340%3E3.0.CO%3B2-O

21 January 2018

Identifiers

10.1002/1097-0142(20010715)92:2<440::AID-CNCR1340>3.0.CO;2-O

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 July 2017

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