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Olaf Riess

Showing results (51-60 of 313) with videos related to

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Human Genetics|August 11, 2010
Age at onset in Huntington's disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7Silke Metzger, Meiju Saukko, Hong Van Che, et al.
Neurobiology of Aging|February 19, 2008
Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's diseaseManu Sharma, Peter Lichtner, Rejko Kruger, et al.
American Journal of Medical Genetics. Part A|May 27, 2021
New euchromatic variant dup(11)(p15.3p15.1) transmitted through two generations defined by low coverage whole genome sequencingSylke Singer, Anastasia Gazou, Marc Sturm, et al.
Frontiers in Neuroscience|January 29, 2019
Distinct Stress Response and Altered Striatal Transcriptome in Alpha-Synuclein Overexpressing MiceZinah Wassouf, Thomas Hentrich, Nicolas Casadei, et al.
Journal of Neurochemistry|March 19, 2016
In vivo assessment of riluzole as a potential therapeutic drug for spinocerebellar ataxia type 3Jana Schmidt, Thorsten Schmidt, Matthias Golla, et al.
Frontiers in Integrative Neuroscience|June 6, 2018
The Alteration of Emotion Regulation Precedes the Deficits in Interval Timing in the BACHD Rat Model for Huntington DiseaseDaniel Garces, Nicole El Massioui, Charlotte Lamirault, et al.
Functional & Integrative Genomics|May 9, 2025
sc-MULTI-omics approach in nano-rare diseases: understanding the pathophysiological mechanism of Mulvihill-Smith SyndromeAngelika Riess, Cristiana Roggia, Antje Schulze Selting, et al.
Bioinformatics (Oxford, England)|April 17, 2013
UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarraysChristopher Schroeder, Marc Sturm, Andreas Dufke, et al.
Journal of Psychopharmacology (Oxford, England)|November 19, 2016
Capturing schizophrenia-like prodromal symptoms in a spinocerebellar ataxia-17 transgenic ratDavide Amato, Fabio Canneva, Huu Phuc Nguyen, et al.
Annals of Neurology|September 4, 2003
Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)Arndt Rolfs, Arnulf H Koeppen, Ingrid Bauer, et al.
Pageof 32

Showing results (51-60 of 313) with videos related to

Sort By:
Pageof 32
Human Genetics|August 11, 2010
Age at onset in Huntington's disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7Silke Metzger, Meiju Saukko, Hong Van Che, et al.
Neurobiology of Aging|February 19, 2008
Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's diseaseManu Sharma, Peter Lichtner, Rejko Kruger, et al.
American Journal of Medical Genetics. Part A|May 27, 2021
New euchromatic variant dup(11)(p15.3p15.1) transmitted through two generations defined by low coverage whole genome sequencingSylke Singer, Anastasia Gazou, Marc Sturm, et al.
Frontiers in Neuroscience|January 29, 2019
Distinct Stress Response and Altered Striatal Transcriptome in Alpha-Synuclein Overexpressing MiceZinah Wassouf, Thomas Hentrich, Nicolas Casadei, et al.
Journal of Neurochemistry|March 19, 2016
In vivo assessment of riluzole as a potential therapeutic drug for spinocerebellar ataxia type 3Jana Schmidt, Thorsten Schmidt, Matthias Golla, et al.
Frontiers in Integrative Neuroscience|June 6, 2018
The Alteration of Emotion Regulation Precedes the Deficits in Interval Timing in the BACHD Rat Model for Huntington DiseaseDaniel Garces, Nicole El Massioui, Charlotte Lamirault, et al.
Functional & Integrative Genomics|May 9, 2025
sc-MULTI-omics approach in nano-rare diseases: understanding the pathophysiological mechanism of Mulvihill-Smith SyndromeAngelika Riess, Cristiana Roggia, Antje Schulze Selting, et al.
Bioinformatics (Oxford, England)|April 17, 2013
UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarraysChristopher Schroeder, Marc Sturm, Andreas Dufke, et al.
Journal of Psychopharmacology (Oxford, England)|November 19, 2016
Capturing schizophrenia-like prodromal symptoms in a spinocerebellar ataxia-17 transgenic ratDavide Amato, Fabio Canneva, Huu Phuc Nguyen, et al.
Annals of Neurology|September 4, 2003
Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)Arndt Rolfs, Arnulf H Koeppen, Ingrid Bauer, et al.
Pageof 32