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Caleb Webber

Showing results (41-50 of 76) with videos related to

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Genome Medicine|November 17, 2022
Universal clinical Parkinson's disease axes identify a major influence of neuroinflammationCynthia Sandor, Stephanie Millin, Andrew Dahl, et al.
American Journal of Human Genetics|January 11, 2016
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent ModulesKorinna Kochinke, Christiane Zweier, Bonnie Nijhof, et al.
Genome Research|May 20, 2021
Targeted single-cell RNA sequencing of transcription factors enhances the identification of cell types and trajectoriesAlexandra Pokhilko, Adam E Handel, Fabiola Curion, et al.
Genome Research|April 5, 2011
Natural genetic variation caused by small insertions and deletions in the human genomeRyan E Mills, W Stephen Pittard, Julienne M Mullaney, et al.
JCI Insight|July 8, 2021
Combining multiomics and drug perturbation profiles to identify muscle-specific treatments for spinal muscular atrophyKatharina E Meijboom, Viola Volpato, Jimena Monzón-Sandoval, et al.
Brain : a Journal of Neurology|September 5, 2020
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disordersNiccolò E Mencacci, Regina Reynolds, Sonia Garcia Ruiz, et al.
Stem Cell Reports|June 25, 2026
A highly efficient method to differentiate CGRP-expressing peptidergic nociceptors from human induced pluripotent stem cellsGalbha Duggal, Xinyu Li, Philippa Pettingill, et al.
Bioinformatics Advances|June 24, 2024
Demultiplexing of single-cell RNA-sequencing data using interindividual variation in gene expressionIsar Nassiri, Andrew J Kwok, Aneesha Bhandari, et al.
Cell Stem Cell|December 4, 2018
Single-Cell Sequencing of iPSC-Dopamine Neurons Reconstructs Disease Progression and Identifies HDAC4 as a Regulator of Parkinson Cell PhenotypesCharmaine Lang, Kieran R Campbell, Brent J Ryan, et al.
Scientific Reports|January 25, 2017
Whole-exome sequencing of 228 patients with sporadic Parkinson's diseaseCynthia Sandor, Frantisek Honti, Wilfried Haerty, et al.
Pageof 8

Showing results (41-50 of 76) with videos related to

Sort By:
Pageof 8
Genome Medicine|November 17, 2022
Universal clinical Parkinson's disease axes identify a major influence of neuroinflammationCynthia Sandor, Stephanie Millin, Andrew Dahl, et al.
American Journal of Human Genetics|January 11, 2016
Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent ModulesKorinna Kochinke, Christiane Zweier, Bonnie Nijhof, et al.
Genome Research|May 20, 2021
Targeted single-cell RNA sequencing of transcription factors enhances the identification of cell types and trajectoriesAlexandra Pokhilko, Adam E Handel, Fabiola Curion, et al.
Genome Research|April 5, 2011
Natural genetic variation caused by small insertions and deletions in the human genomeRyan E Mills, W Stephen Pittard, Julienne M Mullaney, et al.
JCI Insight|July 8, 2021
Combining multiomics and drug perturbation profiles to identify muscle-specific treatments for spinal muscular atrophyKatharina E Meijboom, Viola Volpato, Jimena Monzón-Sandoval, et al.
Brain : a Journal of Neurology|September 5, 2020
Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disordersNiccolò E Mencacci, Regina Reynolds, Sonia Garcia Ruiz, et al.
Stem Cell Reports|June 25, 2026
A highly efficient method to differentiate CGRP-expressing peptidergic nociceptors from human induced pluripotent stem cellsGalbha Duggal, Xinyu Li, Philippa Pettingill, et al.
Bioinformatics Advances|June 24, 2024
Demultiplexing of single-cell RNA-sequencing data using interindividual variation in gene expressionIsar Nassiri, Andrew J Kwok, Aneesha Bhandari, et al.
Cell Stem Cell|December 4, 2018
Single-Cell Sequencing of iPSC-Dopamine Neurons Reconstructs Disease Progression and Identifies HDAC4 as a Regulator of Parkinson Cell PhenotypesCharmaine Lang, Kieran R Campbell, Brent J Ryan, et al.
Scientific Reports|January 25, 2017
Whole-exome sequencing of 228 patients with sporadic Parkinson's diseaseCynthia Sandor, Frantisek Honti, Wilfried Haerty, et al.
Pageof 8