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Anuj Goel

Showing results (31-40 of 120) with videos related to

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Journal of Molecular and Cellular Cardiology|July 27, 2018
Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletionMehroz Ehsan, Matthew Kelly, Charlotte Hooper, et al.
Molecular Medicine (Cambridge, Mass.)|July 18, 2014
Human genetic evidence for involvement of CD137 in atherosclerosisLeif Å Söderström, Karl Gertow, Lasse Folkersen, et al.
Nature Genetics|January 26, 2021
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivityAndrew R Harper, Anuj Goel, Christopher Grace, et al.
Hypertension (Dallas, Tex. : 1979)|October 6, 2018
Neonatal Micro-RNA Profile Determines Endothelial Function in Offspring of Hypertensive PregnanciesGrace Z Yu, Svetlana Reilly, Adam J Lewandowski, et al.
Circulation. Genomic and Precision Medicine|March 13, 2020
Reevaluation of the South Asian <i>MYBPC3</i><sup>Δ25bp</sup> Intronic Deletion in Hypertrophic CardiomyopathyAndrew R Harper, Michael Bowman, Jesse B G Hayesmoore, et al.
Nature Genetics|December 17, 2013
Meta-analysis of gene-level tests for rare variant associationDajiang J Liu, Gina M Peloso, Xiaowei Zhan, et al.
The New England Journal of Medicine|December 25, 2009
Genetic variants associated with Lp(a) lipoprotein level and coronary diseaseRobert Clarke, John F Peden, Jemma C Hopewell, et al.
Scientific Reports|May 16, 2019
Genetic variation in CADM2 as a link between psychological traits and obesityJulia Morris, Mark E S Bailey, Damiano Baldassarre, et al.
Scientific Reports|February 23, 2018
Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targetsHarri Lempiäinen, Ingrid Brænne, Tom Michoel, et al.
Human Molecular Genetics|February 10, 2024
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in NigeriaOyesola O Ojewunmi, Titilope A Adeyemo, Ajoke I Oyetunji, et al.
Pageof 12

Showing results (31-40 of 120) with videos related to

Sort By:
Pageof 12
Journal of Molecular and Cellular Cardiology|July 27, 2018
Mutant Muscle LIM Protein C58G causes cardiomyopathy through protein depletionMehroz Ehsan, Matthew Kelly, Charlotte Hooper, et al.
Molecular Medicine (Cambridge, Mass.)|July 18, 2014
Human genetic evidence for involvement of CD137 in atherosclerosisLeif Å Söderström, Karl Gertow, Lasse Folkersen, et al.
Nature Genetics|January 26, 2021
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivityAndrew R Harper, Anuj Goel, Christopher Grace, et al.
Hypertension (Dallas, Tex. : 1979)|October 6, 2018
Neonatal Micro-RNA Profile Determines Endothelial Function in Offspring of Hypertensive PregnanciesGrace Z Yu, Svetlana Reilly, Adam J Lewandowski, et al.
Circulation. Genomic and Precision Medicine|March 13, 2020
Reevaluation of the South Asian <i>MYBPC3</i><sup>Δ25bp</sup> Intronic Deletion in Hypertrophic CardiomyopathyAndrew R Harper, Michael Bowman, Jesse B G Hayesmoore, et al.
Nature Genetics|December 17, 2013
Meta-analysis of gene-level tests for rare variant associationDajiang J Liu, Gina M Peloso, Xiaowei Zhan, et al.
The New England Journal of Medicine|December 25, 2009
Genetic variants associated with Lp(a) lipoprotein level and coronary diseaseRobert Clarke, John F Peden, Jemma C Hopewell, et al.
Scientific Reports|May 16, 2019
Genetic variation in CADM2 as a link between psychological traits and obesityJulia Morris, Mark E S Bailey, Damiano Baldassarre, et al.
Scientific Reports|February 23, 2018
Network analysis of coronary artery disease risk genes elucidates disease mechanisms and druggable targetsHarri Lempiäinen, Ingrid Brænne, Tom Michoel, et al.
Human Molecular Genetics|February 10, 2024
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in NigeriaOyesola O Ojewunmi, Titilope A Adeyemo, Ajoke I Oyetunji, et al.
Pageof 12