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The New England Journal of Medicine
|
September 11, 2024
Sequencing-Based Detection of Avian Influenza A(H5N1) Virus in Wastewater in Ten Cities
Michael J Tisza, Blake M Hanson, Justin R Clark, et al.
Blood Cells, Molecules & Diseases
|
November 25, 2025
Association of metabolomics measurements with blood cell phenotypes
Brian D Chen, Amanda Tapia, Eric Boerwinkle, et al.
American Journal of Hypertension
|
December 15, 2010
Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program
Jeannette Simino, Gang Shi, Rezart Kume, et al.
Journal of the American Society of Nephrology : JASN
|
November 16, 2019
<i>GSTM1</i> Deletion Exaggerates Kidney Injury in Experimental Mouse Models and Confers the Protective Effect of Cruciferous Vegetables in Mice and Humans
Joseph C Gigliotti, Adrienne Tin, Shirin Pourafshar, et al.
Atherosclerosis
|
October 26, 2007
A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease
Themistocles L Assimes, Joshua W Knowles, James R Priest, et al.
Journal of Transcultural Nursing : Official Journal of the Transcultural Nursing Society
|
November 18, 2022
Achieving a Representative Sample of Asian Americans in Biomedical Research Through Community-Based Approaches: Comparing Demographic Data in the <i>All of Us</i> Research Program With the American Community Survey
Fornessa T Randal, Paula Lozano, Siya Qi, et al.
Hypertension (Dallas, Tex. : 1979)
|
September 7, 2021
Epidemiologic and Genetic Associations of Erythropoietin With Blood Pressure, Hypertension, and Coronary Artery Disease
Pengfei Sun, Nitin Kumar, Adrienne Tin, et al.
Nucleic Acids Research
|
December 17, 2016
Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort
Tomasz Gambin, Zeynep C Akdemir, Bo Yuan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 28, 2024
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
American Journal of Human Genetics
|
June 21, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
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Showing results (661-670 of 1,215) with videos related to
Sort By:
Page
of 122
The New England Journal of Medicine
|
September 11, 2024
Sequencing-Based Detection of Avian Influenza A(H5N1) Virus in Wastewater in Ten Cities
Michael J Tisza, Blake M Hanson, Justin R Clark, et al.
Blood Cells, Molecules & Diseases
|
November 25, 2025
Association of metabolomics measurements with blood cell phenotypes
Brian D Chen, Amanda Tapia, Eric Boerwinkle, et al.
American Journal of Hypertension
|
December 15, 2010
Five blood pressure loci identified by an updated genome-wide linkage scan: meta-analysis of the Family Blood Pressure Program
Jeannette Simino, Gang Shi, Rezart Kume, et al.
Journal of the American Society of Nephrology : JASN
|
November 16, 2019
<i>GSTM1</i> Deletion Exaggerates Kidney Injury in Experimental Mouse Models and Confers the Protective Effect of Cruciferous Vegetables in Mice and Humans
Joseph C Gigliotti, Adrienne Tin, Shirin Pourafshar, et al.
Atherosclerosis
|
October 26, 2007
A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease
Themistocles L Assimes, Joshua W Knowles, James R Priest, et al.
Journal of Transcultural Nursing : Official Journal of the Transcultural Nursing Society
|
November 18, 2022
Achieving a Representative Sample of Asian Americans in Biomedical Research Through Community-Based Approaches: Comparing Demographic Data in the <i>All of Us</i> Research Program With the American Community Survey
Fornessa T Randal, Paula Lozano, Siya Qi, et al.
Hypertension (Dallas, Tex. : 1979)
|
September 7, 2021
Epidemiologic and Genetic Associations of Erythropoietin With Blood Pressure, Hypertension, and Coronary Artery Disease
Pengfei Sun, Nitin Kumar, Adrienne Tin, et al.
Nucleic Acids Research
|
December 17, 2016
Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort
Tomasz Gambin, Zeynep C Akdemir, Bo Yuan, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 28, 2024
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
American Journal of Human Genetics
|
June 21, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
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of 122