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Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3030920

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Renal-carcinoma-inducing oncogene
Using large-scale exome sequencing, Andrew Futreal and colleagues have identified a second frequently mutated gene (after
VHL
) in clear cell renal cell carcinomas, the most frequent type of kidney cancer.
PBRM1
, a member of the SWI/SNF complex involved in transcriptional regulation, is mutated in a...

Alternative Titles

Full title

Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3030920

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3030920

Other Identifiers

ISSN

0028-0836

E-ISSN

1476-4687

DOI

10.1038/nature09639

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