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Circulation Research
|
January 1, 2014
Increased burden of cardiovascular disease in carriers of APOL1 genetic variants
Kaoru Ito, Alexander G Bick, Jason Flannick, et al.
Cancer Cell
|
March 12, 2015
A functional landscape of resistance to ALK inhibition in lung cancer
Frederick H Wilson, Cory M Johannessen, Federica Piccioni, et al.
Cell
|
March 12, 2017
Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation
Ah Ram Kim, Jacob C Ulirsch, Stephan Wilmes, et al.
The Journal of Experimental Medicine
|
March 28, 2019
Impaired human hematopoiesis due to a cryptic intronic <i>GATA1</i> splicing mutation
Nour J Abdulhay, Claudia Fiorini, Jeffrey M Verboon, et al.
Journal of Clinical Immunology
|
April 19, 2020
Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction
Jeffrey M Verboon, Dilnar Mahmut, Ah Ram Kim, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 30, 2016
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms
Michael H Guo, Satish K Nandakumar, Jacob C Ulirsch, et al.
American Journal of Human Genetics
|
December 7, 2014
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability
Rosalind Law, Tracy Dixon-Salazar, Julie Jerber, et al.
The New England Journal of Medicine
|
July 31, 2007
Risk alleles for multiple sclerosis identified by a genomewide study
, David A Hafler, Alastair Compston, et al.
The New England Journal of Medicine
|
November 27, 2014
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
Giulio Genovese, Anna K Kähler, Robert E Handsaker, et al.
Plos One
|
June 9, 2017
Systematic genomic and translational efficiency studies of uveal melanoma
Chelsea Place Johnson, Ivana K Kim, Bita Esmaeli, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 133) with videos related to
Sort By:
Page
of 14
Circulation Research
|
January 1, 2014
Increased burden of cardiovascular disease in carriers of APOL1 genetic variants
Kaoru Ito, Alexander G Bick, Jason Flannick, et al.
Cancer Cell
|
March 12, 2015
A functional landscape of resistance to ALK inhibition in lung cancer
Frederick H Wilson, Cory M Johannessen, Federica Piccioni, et al.
Cell
|
March 12, 2017
Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation
Ah Ram Kim, Jacob C Ulirsch, Stephan Wilmes, et al.
The Journal of Experimental Medicine
|
March 28, 2019
Impaired human hematopoiesis due to a cryptic intronic <i>GATA1</i> splicing mutation
Nour J Abdulhay, Claudia Fiorini, Jeffrey M Verboon, et al.
Journal of Clinical Immunology
|
April 19, 2020
Infantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction
Jeffrey M Verboon, Dilnar Mahmut, Ah Ram Kim, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 30, 2016
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms
Michael H Guo, Satish K Nandakumar, Jacob C Ulirsch, et al.
American Journal of Human Genetics
|
December 7, 2014
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability
Rosalind Law, Tracy Dixon-Salazar, Julie Jerber, et al.
The New England Journal of Medicine
|
July 31, 2007
Risk alleles for multiple sclerosis identified by a genomewide study
, David A Hafler, Alastair Compston, et al.
The New England Journal of Medicine
|
November 27, 2014
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
Giulio Genovese, Anna K Kähler, Robert E Handsaker, et al.
Plos One
|
June 9, 2017
Systematic genomic and translational efficiency studies of uveal melanoma
Chelsea Place Johnson, Ivana K Kim, Bita Esmaeli, et al.
Page
of 14