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Olaf Riess

Showing results (11-20 of 313) with videos related to

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World Journal of Clinical Cases|February 2, 2019
Two cases of variant late infantile ceroid lipofuscinosis in JordanOmar Nafi, Bashar Ramadan, Olaf Riess, et al.
The Lancet. Neurology|April 22, 2004
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesisLudger Schöls, Peter Bauer, Thorsten Schmidt, et al.
Aging|December 14, 2018
<i>SNCA</i> overexpression disturbs hippocampal gene expression trajectories in midlifeThomas Hentrich, Zinah Wassouf, Olaf Riess, et al.
Brain Research|January 13, 2009
Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA--a key player in the pathogenesis of Parkinson's diseaseKarina Häbig, Michael Walter, Heike Stappert, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|March 4, 2009
Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patientsClaudia Funke, Anne S Soehn, Juergen Tomiuk, et al.
Molecular Genetics & Genomic Medicine|October 30, 2023
A further case of AFG2B-related neurodevelopmental disorder with hearing loss and microcephaly allows further clarification of pathogenicity of the variant c.1313T>C, p.(Leu438Pro)Sarah Grosch, Martin Kehrer, Olaf Riess, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 29, 2009
Genetic analysis of heme oxygenase-1 (HO-1) in German Parkinson's disease patientsClaudia Funke, Juergen Tomiuk, Olaf Riess, et al.
Plos One|January 4, 2013
The Guanine nucleotide exchange factor kalirin-7 is a novel synphilin-1 interacting protein and modifies synphilin-1 aggregate transport and formationYu-Chun Tsai, Olaf Riess, Anne S Soehn, et al.
Aging|October 21, 2025
Brain region-specific and systemic transcriptomic alterations in a human alpha-synuclein overexpressing rat modelVivien Hoof, Nicolas Casadei, Olaf Riess, et al.
Plos One|August 22, 2014
Reduced motivation in the BACHD rat model of Huntington disease is dependent on the choice of food deprivation strategyErik Karl Håkan Jansson, Laura Emily Clemens, Olaf Riess, et al.
Pageof 32

Showing results (11-20 of 313) with videos related to

Sort By:
Pageof 32
World Journal of Clinical Cases|February 2, 2019
Two cases of variant late infantile ceroid lipofuscinosis in JordanOmar Nafi, Bashar Ramadan, Olaf Riess, et al.
The Lancet. Neurology|April 22, 2004
Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesisLudger Schöls, Peter Bauer, Thorsten Schmidt, et al.
Aging|December 14, 2018
<i>SNCA</i> overexpression disturbs hippocampal gene expression trajectories in midlifeThomas Hentrich, Zinah Wassouf, Olaf Riess, et al.
Brain Research|January 13, 2009
Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA--a key player in the pathogenesis of Parkinson's diseaseKarina Häbig, Michael Walter, Heike Stappert, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|March 4, 2009
Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patientsClaudia Funke, Anne S Soehn, Juergen Tomiuk, et al.
Molecular Genetics & Genomic Medicine|October 30, 2023
A further case of AFG2B-related neurodevelopmental disorder with hearing loss and microcephaly allows further clarification of pathogenicity of the variant c.1313T>C, p.(Leu438Pro)Sarah Grosch, Martin Kehrer, Olaf Riess, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 29, 2009
Genetic analysis of heme oxygenase-1 (HO-1) in German Parkinson's disease patientsClaudia Funke, Juergen Tomiuk, Olaf Riess, et al.
Plos One|January 4, 2013
The Guanine nucleotide exchange factor kalirin-7 is a novel synphilin-1 interacting protein and modifies synphilin-1 aggregate transport and formationYu-Chun Tsai, Olaf Riess, Anne S Soehn, et al.
Aging|October 21, 2025
Brain region-specific and systemic transcriptomic alterations in a human alpha-synuclein overexpressing rat modelVivien Hoof, Nicolas Casadei, Olaf Riess, et al.
Plos One|August 22, 2014
Reduced motivation in the BACHD rat model of Huntington disease is dependent on the choice of food deprivation strategyErik Karl Håkan Jansson, Laura Emily Clemens, Olaf Riess, et al.
Pageof 32