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Thomas Hays

Showing results (31-40 of 40) with videos related to

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Chemical Research in Toxicology|February 21, 2006
Genomic identification of potential risk factors during acetaminophen-induced liver disease in susceptible and resistant strains of miceKevin D Welch, Timothy P Reilly, Mohammed Bourdi, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|May 4, 2022
Learning the Language of Medical Device Innovation: A Longitudinal Interdisciplinary Elective for Medical StudentsLauren M Maloney, Mathew Hakimi, Thomas Hays, et al.
Prenatal Diagnosis|January 29, 2024
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart diseaseEmily Zhao, Miles Bomback, Atlas Khan, et al.
Plos One|June 21, 2014
Proteomics analysis of the non-muscle myosin heavy chain IIa-enriched actin-myosin complex reveals multiple functions within the podocyteThomas Hays, Avi Ma'ayan, Neil R Clark, et al.
Prenatal Diagnosis|August 18, 2023
The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstructionBobby K Brar, Karin Blakemore, Christine Hertenstein, et al.
Circulation. Genomic and Precision Medicine|July 7, 2023
Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart DiseaseThomas Hays, Rebecca Hernan, Michele Disco, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 11, 2024
A Deep Intronic PKHD1 Variant Identified by SpliceAI in a Deceased Neonate With Autosomal Recessive Polycystic Kidney DiseaseFelix Richter, Kayleigh D Rutherford, Anisha J Cooke, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2023
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic DiagnosisDina F Ahram, Tze Y Lim, Juntao Ke, et al.
Nature Communications|October 9, 2025
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.
Nature Communications|August 7, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Chemical Research in Toxicology|February 21, 2006
Genomic identification of potential risk factors during acetaminophen-induced liver disease in susceptible and resistant strains of miceKevin D Welch, Timothy P Reilly, Mohammed Bourdi, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|May 4, 2022
Learning the Language of Medical Device Innovation: A Longitudinal Interdisciplinary Elective for Medical StudentsLauren M Maloney, Mathew Hakimi, Thomas Hays, et al.
Prenatal Diagnosis|January 29, 2024
The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart diseaseEmily Zhao, Miles Bomback, Atlas Khan, et al.
Plos One|June 21, 2014
Proteomics analysis of the non-muscle myosin heavy chain IIa-enriched actin-myosin complex reveals multiple functions within the podocyteThomas Hays, Avi Ma'ayan, Neil R Clark, et al.
Prenatal Diagnosis|August 18, 2023
The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstructionBobby K Brar, Karin Blakemore, Christine Hertenstein, et al.
Circulation. Genomic and Precision Medicine|July 7, 2023
Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart DiseaseThomas Hays, Rebecca Hernan, Michele Disco, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 11, 2024
A Deep Intronic PKHD1 Variant Identified by SpliceAI in a Deceased Neonate With Autosomal Recessive Polycystic Kidney DiseaseFelix Richter, Kayleigh D Rutherford, Anisha J Cooke, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2023
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic DiagnosisDina F Ahram, Tze Y Lim, Juntao Ke, et al.
Nature Communications|October 9, 2025
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.
Nature Communications|August 7, 2025
Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.
Pageof 4