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Nature Communications
|
November 2, 2017
Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors
Jiqiu Cheng, Jonas Demeulemeester, David C Wedge, et al.
Nature Communications
|
January 30, 2019
Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors
Jiqiu Cheng, Jonas Demeulemeester, David C Wedge, et al.
Nature
|
February 19, 2010
Signatures of mutation and selection in the cancer genome
Graham R Bignell, Chris D Greenman, Helen Davies, et al.
Nature Genetics
|
October 1, 2021
Increased somatic mutation burdens in normal human cells due to defective DNA polymerases
Philip S Robinson, Tim H H Coorens, Claire Palles, et al.
European Journal of Human Genetics : EJHG
|
December 24, 2009
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes
Anna Hackett, Patrick S Tarpey, Andrea Licata, et al.
Nature
|
April 13, 2018
Intra-tumour diversification in colorectal cancer at the single-cell level
Sophie F Roerink, Nobuo Sasaki, Henry Lee-Six, et al.
Genome Research
|
February 10, 2017
Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutations
Jonathan S Brammeld, Mia Petljak, Inigo Martincorena, et al.
Nature
|
October 25, 2019
The landscape of somatic mutation in normal colorectal epithelial cells
Henry Lee-Six, Sigurgeir Olafsson, Peter Ellis, et al.
Cancer Research
|
January 28, 2010
Novel candidate cancer genes identified by a large-scale cross-species comparative oncogenomics approach
Jenny Mattison, Jaap Kool, Anthony G Uren, et al.
Journal of Medical Genetics
|
March 21, 2007
The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene
Charles E Schwartz, Patrick S Tarpey, Herbert A Lubs, et al.
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of 27
Search research articles
Search
Showing results (111-120 of 262) with videos related to
Sort By:
Page
of 27
Nature Communications
|
November 2, 2017
Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors
Jiqiu Cheng, Jonas Demeulemeester, David C Wedge, et al.
Nature Communications
|
January 30, 2019
Author Correction: Pan-cancer analysis of homozygous deletions in primary tumours uncovers rare tumour suppressors
Jiqiu Cheng, Jonas Demeulemeester, David C Wedge, et al.
Nature
|
February 19, 2010
Signatures of mutation and selection in the cancer genome
Graham R Bignell, Chris D Greenman, Helen Davies, et al.
Nature Genetics
|
October 1, 2021
Increased somatic mutation burdens in normal human cells due to defective DNA polymerases
Philip S Robinson, Tim H H Coorens, Claire Palles, et al.
European Journal of Human Genetics : EJHG
|
December 24, 2009
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes
Anna Hackett, Patrick S Tarpey, Andrea Licata, et al.
Nature
|
April 13, 2018
Intra-tumour diversification in colorectal cancer at the single-cell level
Sophie F Roerink, Nobuo Sasaki, Henry Lee-Six, et al.
Genome Research
|
February 10, 2017
Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutations
Jonathan S Brammeld, Mia Petljak, Inigo Martincorena, et al.
Nature
|
October 25, 2019
The landscape of somatic mutation in normal colorectal epithelial cells
Henry Lee-Six, Sigurgeir Olafsson, Peter Ellis, et al.
Cancer Research
|
January 28, 2010
Novel candidate cancer genes identified by a large-scale cross-species comparative oncogenomics approach
Jenny Mattison, Jaap Kool, Anthony G Uren, et al.
Journal of Medical Genetics
|
March 21, 2007
The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene
Charles E Schwartz, Patrick S Tarpey, Herbert A Lubs, et al.
Page
of 27