(Q54432969)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20383589%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

title

Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20383589%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

1 reference

1 reference

1

1 reference

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30 January 2020

Pawel Blecharz

5

1 reference

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30 January 2020

author name string

Elzbieta Skasko

2

1 reference

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30 January 2020

Dorota Nowakowska

3

1 reference

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30 January 2020

Anna Niwinska

4

1 reference

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30 January 2020

publication date

1 September 2010

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30 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20383589%20AND%20SRC:MED&resulttype=core&format=json

30 January 2020

volume

9

1 reference

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30 January 2020

issue

3

1 reference

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30 January 2020

page(s)

267-274

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https://scigraph.springernature.com/pub.10.1007/s10689-010-9338-5

30 January 2020

exact match

0 references

cites work

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

1 reference

12 December 2020

Role of BRCA2 in control of the RAD51 recombination and DNA repair protein.

1 reference

12 December 2020

T-Coffee: A novel method for fast and accurate multiple sequence alignment

1 reference

12 December 2020

Variation in cancer risks, by mutation position, in BRCA2 mutation carriers

1 reference

12 December 2020

BRCA2 germline mutations in male breast cancer patients in the Polish population

1 reference

12 December 2020

The prevalence of BRCA2 mutations in familial pancreatic cancer

1 reference

12 December 2020

The BRC repeats are conserved in mammalian BRCA2 proteins

1 reference

12 December 2020

High frequency of germ-line BRCA2 mutations among Hungarian male breast cancer patients without family history

1 reference

12 December 2020

BRCA2 germ-line mutations are frequent in male breast cancer patients without a family history of the disease

1 reference

12 December 2020

Functional evaluation and cancer risk assessment of BRCA2 unclassified variants

1 reference

12 December 2020

BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer.

1 reference

12 December 2020

A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability

1 reference

12 December 2020

Denaturing high-performance liquid chromatography detects reliably BRCA1 and BRCA2 mutations

1 reference

12 December 2020

BRCA2 gene mutations in families with aggregations of breast and stomach cancers

1 reference

12 December 2020

The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years.

1 reference

12 December 2020

Association between the BRCA2 N372H variant and male breast cancer risk: a population-based case-control study in Tuscany, Central Italy

1 reference

12 December 2020

A common missense variant in BRCA2 predisposes to early onset breast cancer

1 reference

12 December 2020

Analysis of BRCA1/BRCA2 genes' contribution to breast cancer susceptibility in high risk Jewish Ashkenazi women

1 reference

12 December 2020

Structure-based assessment of BRCA1 and BRCA2 mutations in a small Spanish population

1 reference

12 December 2020

Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2

1 reference

12 December 2020

A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes

1 reference

12 December 2020

High frequency of recurrent mutations in BRCA1 and BRCA2 genes in Polish families with breast and ovarian cancer.

1 reference

12 December 2020

Novel de novo BRCA2 mutation in a patient with a family history of breast cancer

1 reference

12 December 2020

1 reference

12 December 2020

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

1 reference

12 December 2020

10.1007/S10689-010-9338-5

Identifiers

DOI

1 reference

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30 January 2020

1 reference