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Proceedings of the National Academy of Sciences of the United States of America
|
April 27, 2022
Genomewide CRISPR knockout screen identified PLAC8 as an essential factor for SADS-CoVs infection
Longping V Tse, Rita M Meganck, Kenza C Araba, et al.
Cellular and Molecular Gastroenterology and Hepatology
|
December 11, 2023
IGF2BP1/IMP1 Deletion Enhances a Facultative Stem Cell State via Regulation of MAP1LC3B
Louis R Parham, Patrick A Williams, Kay Katada, et al.
Immunity, Inflammation and Disease
|
January 7, 2016
CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroids
Amber Dahlin, Joshua Denny, Dan M Roden, et al.
Thrombosis and Haemostasis
|
December 16, 2014
A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record
Jason H Karnes, Robert M Cronin, Jerome Rollin, et al.
Cell Metabolism
|
July 31, 2024
Development of a functional beige fat cell line uncovers independent subclasses of cells expressing UCP1 and the futile creatine cycle
Ariana Vargas-Castillo, Yizhi Sun, Amanda L Smythers, et al.
Magnetic Resonance in Medicine
|
April 16, 2016
Multisite, multivendor validation of the accuracy and reproducibility of proton-density fat-fraction quantification at 1.5T and 3T using a fat-water phantom
Diego Hernando, Samir D Sharma, Mounes Aliyari Ghasabeh, et al.
The Journal of Allergy and Clinical Immunology
|
June 16, 2015
CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studies
Michael J McGeachie, Ann C Wu, Sze Man Tse, et al.
JAMA Internal Medicine
|
June 28, 2021
Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients
Sara L Van Driest, Noura S Abul-Husn, Joseph T Glessner, et al.
Kidney International
|
April 6, 2020
Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways
Archna Bajaj, Andrea Ihegword, Chengxiang Qiu, et al.
JAMA Cardiology
|
September 8, 2021
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes
Zachary T Yoneda, Katherine C Anderson, Joseph A Quintana, et al.
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of 52
Search research articles
Search
Showing results (461-470 of 520) with videos related to
Sort By:
Page
of 52
Proceedings of the National Academy of Sciences of the United States of America
|
April 27, 2022
Genomewide CRISPR knockout screen identified PLAC8 as an essential factor for SADS-CoVs infection
Longping V Tse, Rita M Meganck, Kenza C Araba, et al.
Cellular and Molecular Gastroenterology and Hepatology
|
December 11, 2023
IGF2BP1/IMP1 Deletion Enhances a Facultative Stem Cell State via Regulation of MAP1LC3B
Louis R Parham, Patrick A Williams, Kay Katada, et al.
Immunity, Inflammation and Disease
|
January 7, 2016
CMTR1 is associated with increased asthma exacerbations in patients taking inhaled corticosteroids
Amber Dahlin, Joshua Denny, Dan M Roden, et al.
Thrombosis and Haemostasis
|
December 16, 2014
A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record
Jason H Karnes, Robert M Cronin, Jerome Rollin, et al.
Cell Metabolism
|
July 31, 2024
Development of a functional beige fat cell line uncovers independent subclasses of cells expressing UCP1 and the futile creatine cycle
Ariana Vargas-Castillo, Yizhi Sun, Amanda L Smythers, et al.
Magnetic Resonance in Medicine
|
April 16, 2016
Multisite, multivendor validation of the accuracy and reproducibility of proton-density fat-fraction quantification at 1.5T and 3T using a fat-water phantom
Diego Hernando, Samir D Sharma, Mounes Aliyari Ghasabeh, et al.
The Journal of Allergy and Clinical Immunology
|
June 16, 2015
CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studies
Michael J McGeachie, Ann C Wu, Sze Man Tse, et al.
JAMA Internal Medicine
|
June 28, 2021
Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients
Sara L Van Driest, Noura S Abul-Husn, Joseph T Glessner, et al.
Kidney International
|
April 6, 2020
Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways
Archna Bajaj, Andrea Ihegword, Chengxiang Qiu, et al.
JAMA Cardiology
|
September 8, 2021
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes
Zachary T Yoneda, Katherine C Anderson, Joseph A Quintana, et al.
Page
of 52