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Shankaracharya

Showing results (11-20 of 23) with videos related to

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Brain : a Journal of Neurology|May 6, 2022
ATXN2 intermediate expansions in amyotrophic lateral sclerosisJonathan D Glass, Ramita Dewan, Jinhui Ding, et al.
Human Gene Therapy|November 8, 2019
<i>Ly6a</i> Differential Expression in Blood-Brain Barrier Is Responsible for Strain Specific Central Nervous System Transduction Profile of AAV-PHP.BAna Rita Batista, Oliver D King, Christopher P Reardon, et al.
Plos Genetics|February 6, 2014
Relationship estimation from whole-genome sequence dataHong Li, Gustavo Glusman, Hao Hu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 9, 2022
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease RiskLetizia Straniero, Valeria Rimoldi, Edoardo Monfrini, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microgliaSalome Funes, Del Hayden Gadd, Michelle Mosqueda, et al.
Nature Biotechnology|May 20, 2014
A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence dataHao Hu, Jared C Roach, Hilary Coon, et al.
Cell Reports|April 6, 2022
ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of functionDesiree M Baron, Adam R Fenton, Sara Saez-Atienzar, et al.
Nature Genetics|June 10, 2024
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's diseasePaul J Hop, Dongbing Lai, Pamela J Keagle, et al.
Nature Communications|March 21, 2024
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microgliaSalome Funes, Jonathan Jung, Del Hayden Gadd, et al.
Cancer Discovery|July 23, 2014
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancersDaniel J Park, Kayoko Tao, Florence Le Calvez-Kelm, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Brain : a Journal of Neurology|May 6, 2022
ATXN2 intermediate expansions in amyotrophic lateral sclerosisJonathan D Glass, Ramita Dewan, Jinhui Ding, et al.
Human Gene Therapy|November 8, 2019
<i>Ly6a</i> Differential Expression in Blood-Brain Barrier Is Responsible for Strain Specific Central Nervous System Transduction Profile of AAV-PHP.BAna Rita Batista, Oliver D King, Christopher P Reardon, et al.
Plos Genetics|February 6, 2014
Relationship estimation from whole-genome sequence dataHong Li, Gustavo Glusman, Hao Hu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 9, 2022
Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease RiskLetizia Straniero, Valeria Rimoldi, Edoardo Monfrini, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microgliaSalome Funes, Del Hayden Gadd, Michelle Mosqueda, et al.
Nature Biotechnology|May 20, 2014
A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence dataHao Hu, Jared C Roach, Hilary Coon, et al.
Cell Reports|April 6, 2022
ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of functionDesiree M Baron, Adam R Fenton, Sara Saez-Atienzar, et al.
Nature Genetics|June 10, 2024
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's diseasePaul J Hop, Dongbing Lai, Pamela J Keagle, et al.
Nature Communications|March 21, 2024
Expression of ALS-PFN1 impairs vesicular degradation in iPSC-derived microgliaSalome Funes, Jonathan Jung, Del Hayden Gadd, et al.
Cancer Discovery|July 23, 2014
Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancersDaniel J Park, Kayoko Tao, Florence Le Calvez-Kelm, et al.
Pageof 3