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The Journal of Clinical Endocrinology and Metabolism
|
June 1, 1992
Exercise training delineates the importance of B-cell dysfunction to the glucose intolerance of human aging
S E Kahn, V G Larson, R S Schwartz, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
November 15, 2020
Mutagenicity of 2-hydroxyamino-1-methyl-6-phenylimidazo[4,5-b]pyridine (N-OH-PhIP) in human TP53 knock-in (Hupki) mouse embryo fibroblasts
Lisa Hölzl-Armstrong, Sarah Moody, Jill E Kucab, et al.
Breast Cancer Research and Treatment
|
June 1, 2010
Mutation and association analysis of GEN1 in breast cancer susceptibility
Clare Turnbull, Sarah Hines, Anthony Renwick, et al.
Cancer Research
|
December 26, 2003
Evaluation of Fanconi Anemia genes in familial breast cancer predisposition
Sheila Seal, Rita Barfoot, Hiran Jayatilake, et al.
Biostatistics (Oxford, England)
|
October 20, 2009
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data
Chris D Greenman, Graham Bignell, Adam Butler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 30, 2008
Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencing
Peter J Campbell, Erin D Pleasance, Philip J Stephens, et al.
Plos One
|
May 10, 2014
A pathogenic mosaic TP53 mutation in two germ layers detected by next generation sequencing
Sam Behjati, Mariana Maschietto, Richard D Williams, et al.
British Journal of Cancer
|
October 9, 1998
Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients
M Shayeghi, S Seal, J Regan, et al.
Journal of Medical Genetics
|
April 5, 2005
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations
M G Butler, M J Dasouki, X-P Zhou, et al.
Journal of the National Cancer Institute
|
April 20, 2000
Penetrance of mutations in the familial Wilms tumor gene FWT1
N Rahman, L Arbour, R Houlston, et al.
Page
of 53
Search research articles
Search
Showing results (261-270 of 525) with videos related to
Sort By:
Page
of 53
The Journal of Clinical Endocrinology and Metabolism
|
June 1, 1992
Exercise training delineates the importance of B-cell dysfunction to the glucose intolerance of human aging
S E Kahn, V G Larson, R S Schwartz, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association
|
November 15, 2020
Mutagenicity of 2-hydroxyamino-1-methyl-6-phenylimidazo[4,5-b]pyridine (N-OH-PhIP) in human TP53 knock-in (Hupki) mouse embryo fibroblasts
Lisa Hölzl-Armstrong, Sarah Moody, Jill E Kucab, et al.
Breast Cancer Research and Treatment
|
June 1, 2010
Mutation and association analysis of GEN1 in breast cancer susceptibility
Clare Turnbull, Sarah Hines, Anthony Renwick, et al.
Cancer Research
|
December 26, 2003
Evaluation of Fanconi Anemia genes in familial breast cancer predisposition
Sheila Seal, Rita Barfoot, Hiran Jayatilake, et al.
Biostatistics (Oxford, England)
|
October 20, 2009
PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data
Chris D Greenman, Graham Bignell, Adam Butler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 30, 2008
Subclonal phylogenetic structures in cancer revealed by ultra-deep sequencing
Peter J Campbell, Erin D Pleasance, Philip J Stephens, et al.
Plos One
|
May 10, 2014
A pathogenic mosaic TP53 mutation in two germ layers detected by next generation sequencing
Sam Behjati, Mariana Maschietto, Richard D Williams, et al.
British Journal of Cancer
|
October 9, 1998
Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients
M Shayeghi, S Seal, J Regan, et al.
Journal of Medical Genetics
|
April 5, 2005
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations
M G Butler, M J Dasouki, X-P Zhou, et al.
Journal of the National Cancer Institute
|
April 20, 2000
Penetrance of mutations in the familial Wilms tumor gene FWT1
N Rahman, L Arbour, R Houlston, et al.
Page
of 53