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Showing results (161-170 of 196) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|November 21, 2025
Haplotype editing with CRISPR-Cas9 as a therapeutic approach for dominant-negative missense mutations in NEFLPoorvi H Dua, Bazilco M J Simon, Chiara B E Marley, et al.
Neuroinformatics|March 27, 2004
Informatics center for mouse genomics: the dissection of complex traits of the nervous systemGlenn D Rosen, Nathan T La Porte, Boris Diechtiareff, et al.
Nature Human Behaviour|June 16, 2022
Genome-wide association study of musical beat synchronization demonstrates high polygenicityMaria Niarchou, Daniel E Gustavson, J Fah Sathirapongsasuti, et al.
Biorxiv : the Preprint Server for Biology|October 28, 2024
Methylation Clocks Do Not Predict Age or Alzheimer's Disease Risk Across Genetically Admixed IndividualsSebastián Cruz-González, Esther Gu, Lissette Gomez, et al.
HGG Advances|August 29, 2022
Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by <i>de novo</i> KCNC2 variantsSouhrid Mukherjee, Thomas A Cassini, Ningning Hu, et al.
Research Square|October 4, 2023
Illuminating the Function of the Orphan Transporter, SLC22A10 in Humans and Other PrimatesSook Wah Yee, Luis Ferrández-Peral, Pol Alentorn, et al.
Biorxiv : the Preprint Server for Biology|August 23, 2023
Illuminating the Function of the Orphan Transporter, SLC22A10 in Humans and Other PrimatesSook Wah Yee, Luis Ferrández-Peral, Pol Alentorn, et al.
Cell|September 18, 2012
Dynamic and coordinated epigenetic regulation of developmental transitions in the cardiac lineageJoseph A Wamstad, Jeffrey M Alexander, Rebecca M Truty, et al.
Ebiomedicine|December 14, 2022
Clinical characteristics and electrophysiologic properties of SCN5A variants in fever-induced Brugada syndromeGan-Xiao Chen, Hector Barajas-Martínez, Giuseppe Ciconte, et al.
Nature Communications|June 14, 2020
Functional annotation of rare structural variation in the human brainLide Han, Xuefang Zhao, Mary Lauren Benton, et al.
Pageof 20

Showing results (161-170 of 196) with videos related to

Sort By:
Pageof 20
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 21, 2025
Haplotype editing with CRISPR-Cas9 as a therapeutic approach for dominant-negative missense mutations in NEFLPoorvi H Dua, Bazilco M J Simon, Chiara B E Marley, et al.
Neuroinformatics|March 27, 2004
Informatics center for mouse genomics: the dissection of complex traits of the nervous systemGlenn D Rosen, Nathan T La Porte, Boris Diechtiareff, et al.
Nature Human Behaviour|June 16, 2022
Genome-wide association study of musical beat synchronization demonstrates high polygenicityMaria Niarchou, Daniel E Gustavson, J Fah Sathirapongsasuti, et al.
Biorxiv : the Preprint Server for Biology|October 28, 2024
Methylation Clocks Do Not Predict Age or Alzheimer's Disease Risk Across Genetically Admixed IndividualsSebastián Cruz-González, Esther Gu, Lissette Gomez, et al.
HGG Advances|August 29, 2022
Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by <i>de novo</i> KCNC2 variantsSouhrid Mukherjee, Thomas A Cassini, Ningning Hu, et al.
Research Square|October 4, 2023
Illuminating the Function of the Orphan Transporter, SLC22A10 in Humans and Other PrimatesSook Wah Yee, Luis Ferrández-Peral, Pol Alentorn, et al.
Biorxiv : the Preprint Server for Biology|August 23, 2023
Illuminating the Function of the Orphan Transporter, SLC22A10 in Humans and Other PrimatesSook Wah Yee, Luis Ferrández-Peral, Pol Alentorn, et al.
Cell|September 18, 2012
Dynamic and coordinated epigenetic regulation of developmental transitions in the cardiac lineageJoseph A Wamstad, Jeffrey M Alexander, Rebecca M Truty, et al.
Ebiomedicine|December 14, 2022
Clinical characteristics and electrophysiologic properties of SCN5A variants in fever-induced Brugada syndromeGan-Xiao Chen, Hector Barajas-Martínez, Giuseppe Ciconte, et al.
Nature Communications|June 14, 2020
Functional annotation of rare structural variation in the human brainLide Han, Xuefang Zhao, Mary Lauren Benton, et al.
Pageof 20