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Genome Medicine
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November 17, 2022
Universal clinical Parkinson's disease axes identify a major influence of neuroinflammation
Cynthia 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 Modules
Korinna 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 trajectories
Alexandra 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 genome
Ryan 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 atrophy
Katharina 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 disorders
Niccolò 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 cells
Galbha Duggal, Xinyu Li, Philippa Pettingill, et al.
Bioinformatics Advances
|
June 24, 2024
Demultiplexing of single-cell RNA-sequencing data using interindividual variation in gene expression
Isar 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 Phenotypes
Charmaine Lang, Kieran R Campbell, Brent J Ryan, et al.
Scientific Reports
|
January 25, 2017
Whole-exome sequencing of 228 patients with sporadic Parkinson's disease
Cynthia Sandor, Frantisek Honti, Wilfried Haerty, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 76) with videos related to
Sort By:
Page
of 8
Genome Medicine
|
November 17, 2022
Universal clinical Parkinson's disease axes identify a major influence of neuroinflammation
Cynthia 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 Modules
Korinna 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 trajectories
Alexandra 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 genome
Ryan 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 atrophy
Katharina 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 disorders
Niccolò 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 cells
Galbha Duggal, Xinyu Li, Philippa Pettingill, et al.
Bioinformatics Advances
|
June 24, 2024
Demultiplexing of single-cell RNA-sequencing data using interindividual variation in gene expression
Isar 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 Phenotypes
Charmaine Lang, Kieran R Campbell, Brent J Ryan, et al.
Scientific Reports
|
January 25, 2017
Whole-exome sequencing of 228 patients with sporadic Parkinson's disease
Cynthia Sandor, Frantisek Honti, Wilfried Haerty, et al.
Page
of 8