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R Stratton

Showing results (371-380 of 525) with videos related to

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European Journal of Human Genetics : EJHG|December 24, 2009
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypesAnna Hackett, Patrick S Tarpey, Andrea Licata, et al.
Nature|April 13, 2018
Intra-tumour diversification in colorectal cancer at the single-cell levelSophie 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 mutationsJonathan S Brammeld, Mia Petljak, Inigo Martincorena, et al.
Life Science Alliance|September 12, 2024
Crosstalk between bone metastatic cancer cells and sensory nerves in bone metastatic progressionSun H Park, Shunsuke Tsuzuki, Kelly F Contino, et al.
Nature|October 25, 2019
The landscape of somatic mutation in normal colorectal epithelial cellsHenry 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 approachJenny 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 geneCharles E Schwartz, Patrick S Tarpey, Herbert A Lubs, et al.
Nature|August 26, 2021
Extensive phylogenies of human development inferred from somatic mutationsTim H H Coorens, Luiza Moore, Philip S Robinson, et al.
Nature Communications|June 3, 2018
Recurrent rearrangements of FOS and FOSB define osteoblastomaMatthew W Fittall, William Mifsud, Nischalan Pillay, et al.
Familial Cancer|July 18, 2009
Younger age-at-diagnosis for familial malignant testicular germ cell tumorPhuong L Mai, Bingshu E Chen, Kathy Tucker, et al.
Pageof 53

Showing results (371-380 of 525) with videos related to

Sort By:
Pageof 53
European Journal of Human Genetics : EJHG|December 24, 2009
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypesAnna Hackett, Patrick S Tarpey, Andrea Licata, et al.
Nature|April 13, 2018
Intra-tumour diversification in colorectal cancer at the single-cell levelSophie 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 mutationsJonathan S Brammeld, Mia Petljak, Inigo Martincorena, et al.
Life Science Alliance|September 12, 2024
Crosstalk between bone metastatic cancer cells and sensory nerves in bone metastatic progressionSun H Park, Shunsuke Tsuzuki, Kelly F Contino, et al.
Nature|October 25, 2019
The landscape of somatic mutation in normal colorectal epithelial cellsHenry 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 approachJenny 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 geneCharles E Schwartz, Patrick S Tarpey, Herbert A Lubs, et al.
Nature|August 26, 2021
Extensive phylogenies of human development inferred from somatic mutationsTim H H Coorens, Luiza Moore, Philip S Robinson, et al.
Nature Communications|June 3, 2018
Recurrent rearrangements of FOS and FOSB define osteoblastomaMatthew W Fittall, William Mifsud, Nischalan Pillay, et al.
Familial Cancer|July 18, 2009
Younger age-at-diagnosis for familial malignant testicular germ cell tumorPhuong L Mai, Bingshu E Chen, Kathy Tucker, et al.
Pageof 53