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Michael Wigler

Showing results (61-70 of 71) with videos related to

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Elife|May 14, 2020
Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencingTimour Baslan, Jude Kendall, Konstantin Volyanskyy, et al.
Cancer Research|November 29, 2017
Utility of Single-Cell Genomics in Diagnostic Evaluation of Prostate CancerJoan Alexander, Jude Kendall, Jean McIndoo, et al.
Molecular Oncology|December 21, 2010
DNA methylation patterns in luminal breast cancers differ from non-luminal subtypes and can identify relapse risk independent of other clinical variablesSitharthan Kamalakaran, Vinay Varadan, Hege E Giercksky Russnes, et al.
American Journal of Human Genetics|August 7, 2012
Rare de novo germline copy-number variation in testicular cancerZsofia K Stadler, Diane Esposito, Sohela Shah, et al.
Science Translational Medicine|July 2, 2010
Genomic architecture characterizes tumor progression paths and fate in breast cancer patientsHege G Russnes, Hans Kristian Moen Vollan, Ole Christian Lingjærde, et al.
Cancer Discovery|July 25, 2020
Intraductal Transplantation Models of Human Pancreatic Ductal Adenocarcinoma Reveal Progressive Transition of Molecular SubtypesKoji Miyabayashi, Lindsey A Baker, Astrid Deschênes, et al.
Science (New York, N.Y.)|March 17, 2007
Strong association of de novo copy number mutations with autismJonathan Sebat, B Lakshmi, Dheeraj Malhotra, et al.
Omics : a Journal of Integrative Biology|October 30, 2003
A sense of life: computational and experimental investigations with models of biochemical and evolutionary processesBud Mishra, Raoul-Sam Daruwala, Yi Zhou, et al.
Neuron|May 1, 2012
De novo gene disruptions in children on the autistic spectrumIvan Iossifov, Michael Ronemus, Dan Levy, et al.
Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Elife|May 14, 2020
Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencingTimour Baslan, Jude Kendall, Konstantin Volyanskyy, et al.
Cancer Research|November 29, 2017
Utility of Single-Cell Genomics in Diagnostic Evaluation of Prostate CancerJoan Alexander, Jude Kendall, Jean McIndoo, et al.
Molecular Oncology|December 21, 2010
DNA methylation patterns in luminal breast cancers differ from non-luminal subtypes and can identify relapse risk independent of other clinical variablesSitharthan Kamalakaran, Vinay Varadan, Hege E Giercksky Russnes, et al.
American Journal of Human Genetics|August 7, 2012
Rare de novo germline copy-number variation in testicular cancerZsofia K Stadler, Diane Esposito, Sohela Shah, et al.
Science Translational Medicine|July 2, 2010
Genomic architecture characterizes tumor progression paths and fate in breast cancer patientsHege G Russnes, Hans Kristian Moen Vollan, Ole Christian Lingjærde, et al.
Cancer Discovery|July 25, 2020
Intraductal Transplantation Models of Human Pancreatic Ductal Adenocarcinoma Reveal Progressive Transition of Molecular SubtypesKoji Miyabayashi, Lindsey A Baker, Astrid Deschênes, et al.
Science (New York, N.Y.)|March 17, 2007
Strong association of de novo copy number mutations with autismJonathan Sebat, B Lakshmi, Dheeraj Malhotra, et al.
Omics : a Journal of Integrative Biology|October 30, 2003
A sense of life: computational and experimental investigations with models of biochemical and evolutionary processesBud Mishra, Raoul-Sam Daruwala, Yi Zhou, et al.
Neuron|May 1, 2012
De novo gene disruptions in children on the autistic spectrumIvan Iossifov, Michael Ronemus, Dan Levy, et al.
Nature|November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorderIvan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
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