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Nature Communications
|
August 10, 2016
Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers
Christopher A Miller, Yevgeniy Gindin, Charles Lu, et al.
Nature Communications
|
October 4, 2018
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects
Allison A Regier, Yossi Farjoun, David E Larson, et al.
Nature
|
May 28, 2020
Mapping and characterization of structural variation in 17,795 human genomes
Haley J Abel, David E Larson, Allison A Regier, et al.
Cell Reports
|
September 30, 2016
Truncating Prolactin Receptor Mutations Promote Tumor Growth in Murine Estrogen Receptor-Alpha Mammary Carcinomas
Obi L Griffith, Szeman Ruby Chan, Malachi Griffith, et al.
JAMA
|
April 21, 2011
Use of whole-genome sequencing to diagnose a cryptic fusion oncogene
John S Welch, Peter Westervelt, Li Ding, et al.
Cell Stem Cell
|
May 1, 2012
Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells
Margaret A Young, David E Larson, Chiao-Wang Sun, et al.
Experimental Hematology
|
August 2, 2017
Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes
Jin Zhang, Malachi Griffith, Christopher A Miller, et al.
Nature Methods
|
October 15, 2013
DGIdb: mining the druggable genome
Malachi Griffith, Obi L Griffith, Adam C Coffman, et al.
American Journal of Human Genetics
|
April 2, 2021
Association of structural variation with cardiometabolic traits in Finns
Lei Chen, Haley J Abel, Indraniel Das, et al.
The New England Journal of Medicine
|
March 16, 2012
Clonal architecture of secondary acute myeloid leukemia
Matthew J Walter, Dong Shen, Li Ding, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 57) with videos related to
Sort By:
Page
of 6
Nature Communications
|
August 10, 2016
Aromatase inhibition remodels the clonal architecture of estrogen-receptor-positive breast cancers
Christopher A Miller, Yevgeniy Gindin, Charles Lu, et al.
Nature Communications
|
October 4, 2018
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects
Allison A Regier, Yossi Farjoun, David E Larson, et al.
Nature
|
May 28, 2020
Mapping and characterization of structural variation in 17,795 human genomes
Haley J Abel, David E Larson, Allison A Regier, et al.
Cell Reports
|
September 30, 2016
Truncating Prolactin Receptor Mutations Promote Tumor Growth in Murine Estrogen Receptor-Alpha Mammary Carcinomas
Obi L Griffith, Szeman Ruby Chan, Malachi Griffith, et al.
JAMA
|
April 21, 2011
Use of whole-genome sequencing to diagnose a cryptic fusion oncogene
John S Welch, Peter Westervelt, Li Ding, et al.
Cell Stem Cell
|
May 1, 2012
Background mutations in parental cells account for most of the genetic heterogeneity of induced pluripotent stem cells
Margaret A Young, David E Larson, Chiao-Wang Sun, et al.
Experimental Hematology
|
August 2, 2017
Comprehensive discovery of noncoding RNAs in acute myeloid leukemia cell transcriptomes
Jin Zhang, Malachi Griffith, Christopher A Miller, et al.
Nature Methods
|
October 15, 2013
DGIdb: mining the druggable genome
Malachi Griffith, Obi L Griffith, Adam C Coffman, et al.
American Journal of Human Genetics
|
April 2, 2021
Association of structural variation with cardiometabolic traits in Finns
Lei Chen, Haley J Abel, Indraniel Das, et al.
The New England Journal of Medicine
|
March 16, 2012
Clonal architecture of secondary acute myeloid leukemia
Matthew J Walter, Dong Shen, Li Ding, et al.
Page
of 6