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Olaf Riess

Showing results (61-70 of 313) with videos related to

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Neurobiology of Disease|August 8, 2009
Identification and functional dissection of localization signals within ataxin-3Paul Michel Aloyse Antony, Simone Mäntele, Phillip Mollenkopf, et al.
Human Molecular Genetics|July 19, 2015
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's diseaseJohanna Huttenlocher, Hreinn Stefansson, Stacy Steinberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 11, 2006
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown causePeter Bauer, Friedmar R Kreuz, Katrin Bürk, et al.
CNS Neuroscience & Therapeutics|January 11, 2018
Divalproex sodium modulates nuclear localization of ataxin-3 and prevents cellular toxicity caused by expanded ataxin-3Zi-Jian Wang, Aoife Hanet, Daniel Weishäupl, et al.
Plos One|July 30, 2013
The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patientsSilke Metzger, Carolin Walter, Olaf Riess, et al.
Neuroscience Letters|August 29, 2006
Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigraNilgün Akbas, Helmine Hochstrasser, Joelle Deplazes, et al.
Plos One|March 9, 2017
Further investigation of phenotypes and confounding factors of progressive ratio performance and feeding behavior in the BACHD rat model of Huntington diseaseErik Karl Håkan Clemensson, Laura Emily Clemensson, Benedikt Fabry, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 10, 2005
Functional relevance of ceruloplasmin mutations in Parkinson's diseaseHelmine Hochstrasser, Jürgen Tomiuk, Uwe Walter, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 1, 2008
A comprehensive genetic study of the proteasomal subunit S6 ATPase in German Parkinson's disease patientsClaudia Wahl, Sabine Kautzmann, Guido Krebiehl, et al.
The Journal of Molecular Diagnostics : JMD|April 12, 2008
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's diseaseChristopher Schroeder, Michael Walter, Daniela Berg, et al.
Pageof 32

Showing results (61-70 of 313) with videos related to

Sort By:
Pageof 32
Neurobiology of Disease|August 8, 2009
Identification and functional dissection of localization signals within ataxin-3Paul Michel Aloyse Antony, Simone Mäntele, Phillip Mollenkopf, et al.
Human Molecular Genetics|July 19, 2015
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's diseaseJohanna Huttenlocher, Hreinn Stefansson, Stacy Steinberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 11, 2006
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown causePeter Bauer, Friedmar R Kreuz, Katrin Bürk, et al.
CNS Neuroscience & Therapeutics|January 11, 2018
Divalproex sodium modulates nuclear localization of ataxin-3 and prevents cellular toxicity caused by expanded ataxin-3Zi-Jian Wang, Aoife Hanet, Daniel Weishäupl, et al.
Plos One|July 30, 2013
The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patientsSilke Metzger, Carolin Walter, Olaf Riess, et al.
Neuroscience Letters|August 29, 2006
Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigraNilgün Akbas, Helmine Hochstrasser, Joelle Deplazes, et al.
Plos One|March 9, 2017
Further investigation of phenotypes and confounding factors of progressive ratio performance and feeding behavior in the BACHD rat model of Huntington diseaseErik Karl Håkan Clemensson, Laura Emily Clemensson, Benedikt Fabry, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 10, 2005
Functional relevance of ceruloplasmin mutations in Parkinson's diseaseHelmine Hochstrasser, Jürgen Tomiuk, Uwe Walter, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 1, 2008
A comprehensive genetic study of the proteasomal subunit S6 ATPase in German Parkinson's disease patientsClaudia Wahl, Sabine Kautzmann, Guido Krebiehl, et al.
The Journal of Molecular Diagnostics : JMD|April 12, 2008
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's diseaseChristopher Schroeder, Michael Walter, Daniela Berg, et al.
Pageof 32