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British Journal of Clinical Pharmacology
|
July 5, 2019
A phase I pharmacokinetic study of belinostat in patients with advanced cancers and varying degrees of liver dysfunction
Naoko Takebe, Jan H Beumer, Shivaani Kummar, et al.
American Journal of Human Genetics
|
April 9, 2022
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk
Jon A L Willcox, Joshua T Geiger, Sarah U Morton, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
December 21, 2022
Diet quality indices and changes in cognition during chemotherapy
Sylvia L Crowder, Taylor L Welniak, Aasha I Hoogland, et al.
The Journal of Clinical Investigation
|
June 3, 2024
Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypes
David M McKean, Qi Zhang, Priyanka Narayan, et al.
JACC. Basic to Translational Science
|
May 6, 2020
Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects
Jonathan J Edwards, Andrew D Rouillard, Nicolas F Fernandez, et al.
Circulation. Genomic and Precision Medicine
|
May 11, 2023
Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease
Min Young Jang, Parth N Patel, Alexandre C Pereira, et al.
Advanced Materials (Deerfield Beach, Fla.)
|
August 16, 2021
Laser-Induced Cooperative Transition in Molecular Electronic Crystal
Yong Hu, Dasharath Adhikari, Andrew Tan, et al.
JCO Precision Oncology
|
June 29, 2026
Implementing Timely Germline Genetic Testing for Patients With Pancreatic Cancer Using a Genetics Copilot for Point-of-Care Education and Health Assessment
Sophie Moravec, Laura V Barton, Revathy Suresh, et al.
Circulation. Genomic and Precision Medicine
|
August 20, 2020
De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease
Marko T Boskovski, Jason Homsy, Meena Nathan, et al.
Nature Genetics
|
July 1, 2020
Genomic analyses implicate noncoding de novo variants in congenital heart disease
Felix Richter, Sarah U Morton, Seong Won Kim, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 207) with videos related to
Sort By:
Page
of 21
British Journal of Clinical Pharmacology
|
July 5, 2019
A phase I pharmacokinetic study of belinostat in patients with advanced cancers and varying degrees of liver dysfunction
Naoko Takebe, Jan H Beumer, Shivaani Kummar, et al.
American Journal of Human Genetics
|
April 9, 2022
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk
Jon A L Willcox, Joshua T Geiger, Sarah U Morton, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer
|
December 21, 2022
Diet quality indices and changes in cognition during chemotherapy
Sylvia L Crowder, Taylor L Welniak, Aasha I Hoogland, et al.
The Journal of Clinical Investigation
|
June 3, 2024
Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypes
David M McKean, Qi Zhang, Priyanka Narayan, et al.
JACC. Basic to Translational Science
|
May 6, 2020
Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects
Jonathan J Edwards, Andrew D Rouillard, Nicolas F Fernandez, et al.
Circulation. Genomic and Precision Medicine
|
May 11, 2023
Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease
Min Young Jang, Parth N Patel, Alexandre C Pereira, et al.
Advanced Materials (Deerfield Beach, Fla.)
|
August 16, 2021
Laser-Induced Cooperative Transition in Molecular Electronic Crystal
Yong Hu, Dasharath Adhikari, Andrew Tan, et al.
JCO Precision Oncology
|
June 29, 2026
Implementing Timely Germline Genetic Testing for Patients With Pancreatic Cancer Using a Genetics Copilot for Point-of-Care Education and Health Assessment
Sophie Moravec, Laura V Barton, Revathy Suresh, et al.
Circulation. Genomic and Precision Medicine
|
August 20, 2020
De Novo Damaging Variants, Clinical Phenotypes, and Post-Operative Outcomes in Congenital Heart Disease
Marko T Boskovski, Jason Homsy, Meena Nathan, et al.
Nature Genetics
|
July 1, 2020
Genomic analyses implicate noncoding de novo variants in congenital heart disease
Felix Richter, Sarah U Morton, Seong Won Kim, et al.
Page
of 21