(Q59548973)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25154786%20AND%20SRC:MED&resulttype=core&format=json

13 March 2020

title

Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations (English)

1 reference

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13 March 2020

1

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13 March 2020

Anne-Marie Gerdes

6

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13 March 2020

5

Finn C Nielsen

1 reference

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13 March 2020

author name string

Lars Jønson

3

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13 March 2020

Malene Djursby

4

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13 March 2020

Ane Y Steffensen

2

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13 March 2020

Thomas V O Hansen

7

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13 March 2020

publication date

1 March 2015

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13 March 2020

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13 March 2020

volume

14

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13 March 2020

issue

1

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13 March 2020

page(s)

129-133

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Functional characterization of BRCA1 gene variants by mini-gene splicing assay

13 March 2020

cites work

1 reference

12 December 2020

BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure

1 reference

12 December 2020

Mutation of the RAD51C gene in a Fanconi anemia-like disorder

1 reference

12 December 2020

Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair

1 reference

12 December 2020

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

1 reference

12 December 2020

Familial breast cancer: double heterozygosity for BRCA1 and BRCA2 mutations with differing phenotypes

1 reference

12 December 2020

Role of RAD51C and XRCC3 in genetic recombination and DNA repair.

1 reference

12 December 2020

Phenotypic expression of double heterozygosity for BRCA1 and BRCA2 germline mutations.

1 reference

12 December 2020

Mammalian Rad51C contributes to DNA cross-link resistance, sister chromatid cohesion and genomic stability

1 reference

12 December 2020

Next-generation sequencing for inherited breast cancer risk: counseling through the complexity

1 reference

12 December 2020

Germline mutations in RAD51C in Jewish high cancer risk families

1 reference

12 December 2020

Pathology of hereditary breast cancer.

1 reference

12 December 2020

Identification of functional domains in the RAD51L2 (RAD51C) protein and its requirement for gene conversion

1 reference

12 December 2020

Contribution of bioinformatics predictions and functional splicing assays to the interpretation of unclassified variants of the BRCA genes

1 reference

12 December 2020

A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity

1 reference

12 December 2020

Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2

1 reference

12 December 2020

Molecular pathogenesis and clinical management of Fanconi anemia

1 reference

12 December 2020

‘Indirect’ BRCA1/2 testing. A useful approach in hereditary breast and ovarian cancer families without a living affected relative

1 reference

12 December 2020

Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients.

1 reference

12 December 2020

Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations

1 reference

12 December 2020

The breast cancer information core: database design, structure, and scope

1 reference

12 December 2020

A breast cancer family from Spain with germline mutations in both the BRCA1 and BRCA2 genes.

1 reference

12 December 2020

Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families

1 reference

12 December 2020

Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications.

1 reference

12 December 2020

Intronic variants in BRCA1 and BRCA2 that affect RNA splicing can be reliably selected by splice-site prediction programs

1 reference

12 December 2020

10.1007/S10689-014-9747-Y

Identifiers

DOI

1 reference

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13 March 2020

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