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Stacey B Gabriel

Showing results (91-100 of 133) with videos related to

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Nature Genetics|May 22, 2012
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancerChristopher E Barbieri, Sylvan C Baca, Michael S Lawrence, et al.
Nature Genetics|April 8, 2015
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunctionNaiara Akizu, Vincent Cantagrel, Maha S Zaki, et al.
Science Translational Medicine|January 16, 2015
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and diseaseAngharad M Roberts, James S Ware, Daniel S Herman, et al.
Nature|March 25, 2011
Initial genome sequencing and analysis of multiple myelomaMichael A Chapman, Michael S Lawrence, Jonathan J Keats, et al.
Nature|June 23, 2012
Sequence analysis of mutations and translocations across breast cancer subtypesShantanu Banerji, Kristian Cibulskis, Claudia Rangel-Escareno, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>Wenhan Lu, Robert J Carroll, Matthew Solomonson, et al.
Nature Medicine|February 7, 2022
Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variantsNicole L Welch, Meilin Zhu, Catherine Hua, et al.
Cancer Discovery|March 8, 2018
Genetic Mechanisms of Immune Evasion in Colorectal CancerCatherine S Grasso, Marios Giannakis, Daniel K Wells, et al.
Nature|March 31, 2012
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivityJordi Barretina, Giordano Caponigro, Nicolas Stransky, et al.
Pageof 14

Showing results (91-100 of 133) with videos related to

Sort By:
Pageof 14
Nature Genetics|May 22, 2012
Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancerChristopher E Barbieri, Sylvan C Baca, Michael S Lawrence, et al.
Nature Genetics|April 8, 2015
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunctionNaiara Akizu, Vincent Cantagrel, Maha S Zaki, et al.
Science Translational Medicine|January 16, 2015
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and diseaseAngharad M Roberts, James S Ware, Daniel S Herman, et al.
Nature|March 25, 2011
Initial genome sequencing and analysis of multiple myelomaMichael A Chapman, Michael S Lawrence, Jonathan J Keats, et al.
Nature|June 23, 2012
Sequence analysis of mutations and translocations across breast cancer subtypesShantanu Banerji, Kristian Cibulskis, Claudia Rangel-Escareno, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>Wenhan Lu, Robert J Carroll, Matthew Solomonson, et al.
Nature Medicine|February 7, 2022
Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variantsNicole L Welch, Meilin Zhu, Catherine Hua, et al.
Cancer Discovery|March 8, 2018
Genetic Mechanisms of Immune Evasion in Colorectal CancerCatherine S Grasso, Marios Giannakis, Daniel K Wells, et al.
Nature|March 31, 2012
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivityJordi Barretina, Giordano Caponigro, Nicolas Stransky, et al.
Pageof 14