Further Confirmation of Germline Glioma Risk Variant rs78378222 in TP53 and Its Implication in Tumor Tissues via Integrative Analysis of TCGA Data. Issue 7 (18th May 2015)
- Record Type:
- Journal Article
- Title:
- Further Confirmation of Germline Glioma Risk Variant rs78378222 in TP53 and Its Implication in Tumor Tissues via Integrative Analysis of TCGA Data. Issue 7 (18th May 2015)
- Main Title:
- Further Confirmation of Germline Glioma Risk Variant rs78378222 in TP53 and Its Implication in Tumor Tissues via Integrative Analysis of TCGA Data
- Authors:
- Wang, Zhaoming
Rajaraman, Preetha
Melin, Beatrice S.
Chung, Charles C.
Zhang, Weijia
McKean‐Cowdin, Roberta
Michaud, Dominique
Yeager, Meredith
Ahlbom, Anders
Albanes, Demetrius
Andersson, Ulrika
Freeman, Laura E. Beane
Buring, Julie E.
Butler, Mary Ann
Carreón, Tania
Feychting, Maria
Gapstur, Susan M.
Gaziano, J. Michael
Giles, Graham G.
Hallmans, Goran
Henriksson, Roger
Hoffman‐Bolton, Judith
Inskip, Peter D.
Kitahara, Cari M.
Marchand, Loic Le
Linet, Martha S.
Li, Shengchao
Peters, Ulrike
Purdue, Mark P.
Rothman, Nathaniel
Ruder, Avima M.
Sesso, Howard D.
Severi, Gianluca
Stampfer, Meir
Stevens, Victoria L.
Visvanathan, Kala
Wang, Sophia S.
White, Emily
Zeleniuch‐Jacquotte, Anne
Hoover, Robert
Fraumeni, Joseph F.
Chatterjee, Nilanjan
Hartge, Patricia
Chanock, Stephen J.
… (more) - Abstract:
- <abstract abstract-type="graphical" xml:lang="en" id="humu22799-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Imputation analysis of a genome‐wide association study (GWAS) of glioma confirmed a strong association of the germline risk variant: rs78378222 in 3′‐UTR of <italic>TP53</italic>. Further integrative analyses based on the Cancer Genome Atlas (TCGA) multi‐dimensional data suggest the rare risk allele (C) disrupts proper mRNA termination and an allelic loss of a genomic region encapsulating common protective allele (A) occurs during tumor initiation or progression for glioma. <graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgj11pwmwtn" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></p> </abstract>
- Is Part Of:
- Human mutation. Volume 36:Issue 7(2015:Jul.)
- Journal:
- Human mutation
- Issue:
- Volume 36:Issue 7(2015:Jul.)
- Issue Display:
- Volume 36, Issue 7 (2015)
- Year:
- 2015
- Volume:
- 36
- Issue:
- 7
- Issue Sort Value:
- 2015-0036-0007-0000
- Page Start:
- 684
- Page End:
- 688
- Publication Date:
- 2015-05-18
- Subjects:
- Human chromosome abnormalities -- Periodicals
Mutation (Biology) -- Periodicals
616.04205 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1004 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/humu.22799 ↗
- Languages:
- English
- ISSNs:
- 1059-7794
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4336.217000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3382.xml