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Genetics in Medicine Open
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October 18, 2024
3-hour genome sequencing and targeted analysis to rapidly assess genetic risk
Miranda Pg Zalusky, Jonas A Gustafson, Stephanie C Bohaczuk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 9, 2012
Disruption of PH-kinase domain interactions leads to oncogenic activation of AKT in human cancers
Chaitali Parikh, Vasantharajan Janakiraman, Wen-I Wu, et al.
Nature
|
August 17, 2012
Recurrent R-spondin fusions in colon cancer
Somasekar Seshagiri, Eric W Stawiski, Steffen Durinck, et al.
Cancer Cell
|
May 18, 2013
Oncogenic ERBB3 mutations in human cancers
Bijay S Jaiswal, Noelyn M Kljavin, Eric W Stawiski, et al.
Nature Genetics
|
March 2, 2016
Comprehensive genomic analysis of malignant pleural mesothelioma identifies recurrent mutations, gene fusions and splicing alterations
Raphael Bueno, Eric W Stawiski, Leonard D Goldstein, et al.
Nature Biotechnology
|
March 29, 2022
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing
Sneha D Goenka, John E Gorzynski, Kishwar Shafin, et al.
Genome Research
|
October 4, 2012
Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events
Jinfeng Liu, William Lee, Zhaoshi Jiang, et al.
Nature Genetics
|
September 4, 2012
Comprehensive genomic analysis identifies SOX2 as a frequently amplified gene in small-cell lung cancer
Charles M Rudin, Steffen Durinck, Eric W Stawiski, et al.
Science Signaling
|
April 20, 2017
The kinase TPL2 activates ERK and p38 signaling to promote neutrophilic inflammation
Kate Senger, Victoria C Pham, Eugene Varfolomeev, et al.
Nature Genetics
|
November 18, 2014
Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes
Steffen Durinck, Eric W Stawiski, Andrea Pavía-Jiménez, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Genetics in Medicine Open
|
October 18, 2024
3-hour genome sequencing and targeted analysis to rapidly assess genetic risk
Miranda Pg Zalusky, Jonas A Gustafson, Stephanie C Bohaczuk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 9, 2012
Disruption of PH-kinase domain interactions leads to oncogenic activation of AKT in human cancers
Chaitali Parikh, Vasantharajan Janakiraman, Wen-I Wu, et al.
Nature
|
August 17, 2012
Recurrent R-spondin fusions in colon cancer
Somasekar Seshagiri, Eric W Stawiski, Steffen Durinck, et al.
Cancer Cell
|
May 18, 2013
Oncogenic ERBB3 mutations in human cancers
Bijay S Jaiswal, Noelyn M Kljavin, Eric W Stawiski, et al.
Nature Genetics
|
March 2, 2016
Comprehensive genomic analysis of malignant pleural mesothelioma identifies recurrent mutations, gene fusions and splicing alterations
Raphael Bueno, Eric W Stawiski, Leonard D Goldstein, et al.
Nature Biotechnology
|
March 29, 2022
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing
Sneha D Goenka, John E Gorzynski, Kishwar Shafin, et al.
Genome Research
|
October 4, 2012
Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events
Jinfeng Liu, William Lee, Zhaoshi Jiang, et al.
Nature Genetics
|
September 4, 2012
Comprehensive genomic analysis identifies SOX2 as a frequently amplified gene in small-cell lung cancer
Charles M Rudin, Steffen Durinck, Eric W Stawiski, et al.
Science Signaling
|
April 20, 2017
The kinase TPL2 activates ERK and p38 signaling to promote neutrophilic inflammation
Kate Senger, Victoria C Pham, Eugene Varfolomeev, et al.
Nature Genetics
|
November 18, 2014
Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes
Steffen Durinck, Eric W Stawiski, Andrea Pavía-Jiménez, et al.
Page
of 3