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Single-cell analysis of somatic mutation burden in mammary epithelial cells of pathogenic BRCA1/2 mu...

Single-cell analysis of somatic mutation burden in mammary epithelial cells of pathogenic BRCA1/2 mu...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_88f073b576eb4d2d946165cf1fe3a4e1

Single-cell analysis of somatic mutation burden in mammary epithelial cells of pathogenic BRCA1/2 mutation carriers

About this item

Full title

Single-cell analysis of somatic mutation burden in mammary epithelial cells of pathogenic BRCA1/2 mutation carriers

Publisher

United States: American Society for Clinical Investigation

Journal title

The Journal of clinical investigation, 2022-03, Vol.132 (5), p.1-6

Language

English

Formats

Publication information

Publisher

United States: American Society for Clinical Investigation

More information

Scope and Contents

Contents

Inherited germline mutations in the breast cancer gene 1 (BRCA1) or BRCA2 genes (herein BRCA1/2) greatly increase the risk of breast and ovarian cancer, presumably by elevating somatic mutational errors as a consequence of deficient DNA repair. However, this has never been directly demonstrated by a comprehensive analysis of the somatic mutational...

Alternative Titles

Full title

Single-cell analysis of somatic mutation burden in mammary epithelial cells of pathogenic BRCA1/2 mutation carriers

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_88f073b576eb4d2d946165cf1fe3a4e1

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_88f073b576eb4d2d946165cf1fe3a4e1

Other Identifiers

ISSN

1558-8238,0021-9738

E-ISSN

1558-8238

DOI

10.1172/JCI148113

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