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Peter Heutink

Showing results (181-190 of 240) with videos related to

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Nature Cell Biology|June 4, 2021
Non-invasive and high-throughput interrogation of exon-specific isoform expressionDong-Jiunn Jeffery Truong, Teeradon Phlairaharn, Bianca Eßwein, et al.
Brain : a Journal of Neurology|February 4, 2012
The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansionsJavier Simón-Sánchez, Elise G P Dopper, Petra E Cohn-Hokke, et al.
Nature Biomedical Engineering|December 5, 2024
Arrayed CRISPR libraries for the genome-wide activation, deletion and silencing of human protein-coding genesJiang-An Yin, Lukas Frick, Manuel C Scheidmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.
JAMA Neurology|August 8, 2013
Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic riskValentina Moskvina, Denise Harold, GianCarlo Russo, et al.
Neurobiology of Aging|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.
Neuron|December 23, 2025
The Alzheimer's disease risk genes MS4A4A and MS4A6A cooperate to negatively regulate TREM2 and microglia statesDalya Rosner, Jiahong Sun, Rita Cacace, et al.
Neurobiology of Aging|December 3, 2014
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesMike A Nalls, Jose Bras, Dena G Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 8, 2004
Novel parkin mutations detected in patients with early-onset Parkinson's diseaseAida M Bertoli-Avella, José L Giroud-Benitez, Ali Akyol, et al.
Medrxiv : the Preprint Server for Health Sciences|March 26, 2024
Understanding monogenic Parkinson's disease at a global scaleJohanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
Pageof 24

Showing results (181-190 of 240) with videos related to

Sort By:
Pageof 24
Nature Cell Biology|June 4, 2021
Non-invasive and high-throughput interrogation of exon-specific isoform expressionDong-Jiunn Jeffery Truong, Teeradon Phlairaharn, Bianca Eßwein, et al.
Brain : a Journal of Neurology|February 4, 2012
The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansionsJavier Simón-Sánchez, Elise G P Dopper, Petra E Cohn-Hokke, et al.
Nature Biomedical Engineering|December 5, 2024
Arrayed CRISPR libraries for the genome-wide activation, deletion and silencing of human protein-coding genesJiang-An Yin, Lukas Frick, Manuel C Scheidmann, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2013
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphismStephan Klebe, Jean-Louis Golmard, Michael A Nalls, et al.
JAMA Neurology|August 8, 2013
Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic riskValentina Moskvina, Denise Harold, GianCarlo Russo, et al.
Neurobiology of Aging|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.
Neuron|December 23, 2025
The Alzheimer's disease risk genes MS4A4A and MS4A6A cooperate to negatively regulate TREM2 and microglia statesDalya Rosner, Jiahong Sun, Rita Cacace, et al.
Neurobiology of Aging|December 3, 2014
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesMike A Nalls, Jose Bras, Dena G Hernandez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 8, 2004
Novel parkin mutations detected in patients with early-onset Parkinson's diseaseAida M Bertoli-Avella, José L Giroud-Benitez, Ali Akyol, et al.
Medrxiv : the Preprint Server for Health Sciences|March 26, 2024
Understanding monogenic Parkinson's disease at a global scaleJohanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
Pageof 24