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Gavin Chapman

Showing results (21-30 of 41) with videos related to

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International Journal of Cardiology|December 20, 2016
The promises and challenges of exome sequencing in familial, non-syndromic congenital heart diseaseGillian M Blue, David Humphreys, Justin Szot, et al.
Differentiation; Research in Biological Diversity|February 1, 2026
Comprehensive defect detection in mouse embryos and the heart by combining automated phenotyping with novel population averages and atlasesElla M M A Martin, Kyle Drover, Anton Shpak, et al.
Differentiation; Research in Biological Diversity|October 4, 2022
Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factorsDimuthu Alankarage, Annabelle Enriquez, Robert D Steiner, et al.
Developmental Biology|March 25, 2014
Gene-environment interaction demonstrates the vulnerability of the embryonic heartVictoria C O'Reilly, Kylie Lopes Floro, Hongjun Shi, et al.
Development (Cambridge, England)|July 21, 2016
Gestational stress induces the unfolded protein response, resulting in heart defectsHongjun Shi, Victoria C O'Reilly, Julie L M Moreau, et al.
Cell|April 10, 2012
A mechanism for gene-environment interaction in the etiology of congenital scoliosisDuncan B Sparrow, Gavin Chapman, Allanceson J Smith, et al.
American Journal of Human Genetics|December 30, 2019
Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency DisordersJustin O Szot, Carla Campagnolo, Ye Cao, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
A three generation family with VACTERL association is found to have a rare form of diamond-blackfan anaemiaIryna Leshchynska, Debjani Das, Victoria O'Reilly, et al.
Development (Cambridge, England)|February 22, 2019
Gene-environment interaction impacts on heart development and embryo survivalJulie L M Moreau, Scott Kesteven, Ella M M A Martin, et al.
Elife|July 7, 2015
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targetsRomaric Bouveret, Ashley J Waardenberg, Nicole Schonrock, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
International Journal of Cardiology|December 20, 2016
The promises and challenges of exome sequencing in familial, non-syndromic congenital heart diseaseGillian M Blue, David Humphreys, Justin Szot, et al.
Differentiation; Research in Biological Diversity|February 1, 2026
Comprehensive defect detection in mouse embryos and the heart by combining automated phenotyping with novel population averages and atlasesElla M M A Martin, Kyle Drover, Anton Shpak, et al.
Differentiation; Research in Biological Diversity|October 4, 2022
Myhre syndrome is caused by dominant-negative dysregulation of SMAD4 and other co-factorsDimuthu Alankarage, Annabelle Enriquez, Robert D Steiner, et al.
Developmental Biology|March 25, 2014
Gene-environment interaction demonstrates the vulnerability of the embryonic heartVictoria C O'Reilly, Kylie Lopes Floro, Hongjun Shi, et al.
Development (Cambridge, England)|July 21, 2016
Gestational stress induces the unfolded protein response, resulting in heart defectsHongjun Shi, Victoria C O'Reilly, Julie L M Moreau, et al.
Cell|April 10, 2012
A mechanism for gene-environment interaction in the etiology of congenital scoliosisDuncan B Sparrow, Gavin Chapman, Allanceson J Smith, et al.
American Journal of Human Genetics|December 30, 2019
Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency DisordersJustin O Szot, Carla Campagnolo, Ye Cao, et al.
European Journal of Human Genetics : EJHG|March 19, 2026
A three generation family with VACTERL association is found to have a rare form of diamond-blackfan anaemiaIryna Leshchynska, Debjani Das, Victoria O'Reilly, et al.
Development (Cambridge, England)|February 22, 2019
Gene-environment interaction impacts on heart development and embryo survivalJulie L M Moreau, Scott Kesteven, Ella M M A Martin, et al.
Elife|July 7, 2015
NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targetsRomaric Bouveret, Ashley J Waardenberg, Nicole Schonrock, et al.
Pageof 5