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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 NEFL
Poorvi 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 system
Glenn 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 polygenicity
Maria 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 Individuals
Sebastián 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 variants
Souhrid 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 Primates
Sook 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 Primates
Sook Wah Yee, Luis Ferrández-Peral, Pol Alentorn, et al.
Cell
|
September 18, 2012
Dynamic and coordinated epigenetic regulation of developmental transitions in the cardiac lineage
Joseph 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 syndrome
Gan-Xiao Chen, Hector Barajas-Martínez, Giuseppe Ciconte, et al.
Nature Communications
|
June 14, 2020
Functional annotation of rare structural variation in the human brain
Lide Han, Xuefang Zhao, Mary Lauren Benton, et al.
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of 20
Search research articles
Search
Showing results (161-170 of 196) with videos related to
Sort By:
Page
of 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 NEFL
Poorvi 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 system
Glenn 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 polygenicity
Maria 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 Individuals
Sebastián 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 variants
Souhrid 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 Primates
Sook 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 Primates
Sook Wah Yee, Luis Ferrández-Peral, Pol Alentorn, et al.
Cell
|
September 18, 2012
Dynamic and coordinated epigenetic regulation of developmental transitions in the cardiac lineage
Joseph 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 syndrome
Gan-Xiao Chen, Hector Barajas-Martínez, Giuseppe Ciconte, et al.
Nature Communications
|
June 14, 2020
Functional annotation of rare structural variation in the human brain
Lide Han, Xuefang Zhao, Mary Lauren Benton, et al.
Page
of 20