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Valerie K Jordan

Showing results (1-10 of 12) with videos related to

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The Application of Clinical Genetics|September 9, 2015
1p36 deletion syndrome: an updateValerie K Jordan, Hitisha P Zaveri, Daryl A Scott
American Journal of Medical Genetics. Part A|April 3, 2015
Duplication of HEY2 in cardiac and neurologic developmentValerie K Jordan, Jill A Rosenfeld, Seema R Lalani, et al.
Human Molecular Genetics|March 27, 2021
RERE deficiency contributes to the development of orofacial clefts in humans and miceBum Jun Kim, Hitisha P Zaveri, Peter N Kundert, et al.
Disease Models & Mechanisms|August 1, 2018
RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defectsBum Jun Kim, Hitisha P Zaveri, Valerie K Jordan, et al.
Human Molecular Genetics|March 31, 2023
SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2Andrés Hernández-García, Katherine E Pendleton, Sangbae Kim, et al.
Circulation|January 9, 2014
Ryanodine receptor-mediated calcium leak drives progressive development of an atrial fibrillation substrate in a transgenic mouse modelNa Li, David Y Chiang, Sufen Wang, et al.
Journal of Cellular Physiology|March 11, 2024
Running a successful STEMM summer program: A week-by-week guideHeather K Beasley, Zer Vue, Melanie R McReynolds, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
FBN1 contributing to familial congenital diaphragmatic herniaTyler F Beck, Philippe M Campeau, Shalini N Jhangiani, et al.
Journal of Medical Genetics|August 24, 2016
Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONODaryl A Scott, Andres Hernandez-Garcia, Mahshid S Azamian, et al.
Human Molecular Genetics|April 5, 2018
The role of FREM2 and FRAS1 in the development of congenital diaphragmatic herniaValerie K Jordan, Tyler F Beck, Andres Hernandez-Garcia, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The Application of Clinical Genetics|September 9, 2015
1p36 deletion syndrome: an updateValerie K Jordan, Hitisha P Zaveri, Daryl A Scott
American Journal of Medical Genetics. Part A|April 3, 2015
Duplication of HEY2 in cardiac and neurologic developmentValerie K Jordan, Jill A Rosenfeld, Seema R Lalani, et al.
Human Molecular Genetics|March 27, 2021
RERE deficiency contributes to the development of orofacial clefts in humans and miceBum Jun Kim, Hitisha P Zaveri, Peter N Kundert, et al.
Disease Models & Mechanisms|August 1, 2018
RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defectsBum Jun Kim, Hitisha P Zaveri, Valerie K Jordan, et al.
Human Molecular Genetics|March 31, 2023
SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2Andrés Hernández-García, Katherine E Pendleton, Sangbae Kim, et al.
Circulation|January 9, 2014
Ryanodine receptor-mediated calcium leak drives progressive development of an atrial fibrillation substrate in a transgenic mouse modelNa Li, David Y Chiang, Sufen Wang, et al.
Journal of Cellular Physiology|March 11, 2024
Running a successful STEMM summer program: A week-by-week guideHeather K Beasley, Zer Vue, Melanie R McReynolds, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
FBN1 contributing to familial congenital diaphragmatic herniaTyler F Beck, Philippe M Campeau, Shalini N Jhangiani, et al.
Journal of Medical Genetics|August 24, 2016
Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONODaryl A Scott, Andres Hernandez-Garcia, Mahshid S Azamian, et al.
Human Molecular Genetics|April 5, 2018
The role of FREM2 and FRAS1 in the development of congenital diaphragmatic herniaValerie K Jordan, Tyler F Beck, Andres Hernandez-Garcia, et al.
Pageof 2