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Showing results (131-140 of 140) with videos related to

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Gastroenterology|October 22, 2022
G9a Modulates Lipid Metabolism in CD4 T Cells to Regulate Intestinal InflammationGuilherme Piovezani Ramos, Adebowale O Bamidele, Emily E Klatt, et al.
European Heart Journal|July 2, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohortLea Lippert, Tobias Burkard, Franziska Markel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2019
Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patientsChristian Staufner, Bianca Peters, Matias Wagner, et al.
Nature Cardiovascular Research|April 23, 2025
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathyNadine Spielmann, Gregor Miller, Tudor I Oprea, et al.
Nature Cardiovascular Research|August 28, 2024
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathyNadine Spielmann, Gregor Miller, Tudor I Oprea, et al.
The Lancet. Neurology|October 25, 2020
Monogenic variants in dystonia: an exome-wide sequencing studyMichael Zech, Robert Jech, Sylvia Boesch, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
American Journal of Human Genetics|July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Nature Genetics|July 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Nature Genetics|June 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Pageof 14

Showing results (131-140 of 140) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 140 results.
Gastroenterology|October 22, 2022
G9a Modulates Lipid Metabolism in CD4 T Cells to Regulate Intestinal InflammationGuilherme Piovezani Ramos, Adebowale O Bamidele, Emily E Klatt, et al.
European Heart Journal|July 2, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohortLea Lippert, Tobias Burkard, Franziska Markel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2019
Defining clinical subgroups and genotype-phenotype correlations in NBAS-associated disease across 110 patientsChristian Staufner, Bianca Peters, Matias Wagner, et al.
Nature Cardiovascular Research|April 23, 2025
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathyNadine Spielmann, Gregor Miller, Tudor I Oprea, et al.
Nature Cardiovascular Research|August 28, 2024
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathyNadine Spielmann, Gregor Miller, Tudor I Oprea, et al.
The Lancet. Neurology|October 25, 2020
Monogenic variants in dystonia: an exome-wide sequencing studyMichael Zech, Robert Jech, Sylvia Boesch, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
American Journal of Human Genetics|July 10, 2026
Clinical, in vitro, and in vivo evidence of WAPL as a cohesinopathy-associated gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Nature Genetics|July 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
Nature Genetics|June 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findingsAxel Schmidt, Magdalena Danyel, Kathrin Grundmann, et al.
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