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Elife
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May 14, 2020
Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing
Timour Baslan, Jude Kendall, Konstantin Volyanskyy, et al.
Cancer Research
|
November 29, 2017
Utility of Single-Cell Genomics in Diagnostic Evaluation of Prostate Cancer
Joan 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 variables
Sitharthan 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 cancer
Zsofia 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 patients
Hege 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 Subtypes
Koji 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 autism
Jonathan 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 processes
Bud Mishra, Raoul-Sam Daruwala, Yi Zhou, et al.
Neuron
|
May 1, 2012
De novo gene disruptions in children on the autistic spectrum
Ivan Iossifov, Michael Ronemus, Dan Levy, et al.
Nature
|
November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorder
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 71) with videos related to
Sort By:
Page
of 8
Elife
|
May 14, 2020
Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing
Timour Baslan, Jude Kendall, Konstantin Volyanskyy, et al.
Cancer Research
|
November 29, 2017
Utility of Single-Cell Genomics in Diagnostic Evaluation of Prostate Cancer
Joan 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 variables
Sitharthan 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 cancer
Zsofia 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 patients
Hege 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 Subtypes
Koji 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 autism
Jonathan 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 processes
Bud Mishra, Raoul-Sam Daruwala, Yi Zhou, et al.
Neuron
|
May 1, 2012
De novo gene disruptions in children on the autistic spectrum
Ivan Iossifov, Michael Ronemus, Dan Levy, et al.
Nature
|
November 4, 2014
The contribution of de novo coding mutations to autism spectrum disorder
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, et al.
Page
of 8