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Olaf Riess

Showing results (101-110 of 313) with videos related to

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Neuroscience Letters|November 15, 2003
Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigraBettina Felletschin, Peter Bauer, Uwe Walter, et al.
Neurogenetics|February 1, 2012
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) Peter Bauer, Esther Leshinsky-Silver, Lubov Blumkin, et al.
Proteomics. Clinical Applications|December 8, 2010
Gene expression changes in a transgenic mouse model overexpressing human wildtype and mutant torsinAKathrin Grundmann, Jeannette Hübener, Karina Häbig, et al.
Orphanet Journal of Rare Diseases|May 31, 2011
A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patientsKatharina Rall, Gianmaria Barresi, Michael Walter, et al.
Human Molecular Genetics|August 12, 2009
Reversibility of symptoms in a conditional mouse model of spinocerebellar ataxia type 3Jana Boy, Thorsten Schmidt, Hartwig Wolburg, et al.
Journal of Neurology|October 27, 2004
Mutation at the SCA17 locus is not a common cause of primary dystoniaKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
European Journal of Human Genetics : EJHG|October 13, 2006
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approachJürgen Tomiuk, Lutz Bachmann, Claudia Bauer, et al.
Caries Research|May 23, 2015
Lactotransferrin Gene Polymorphism Associated with Caries ExperienceAndrea D Doetzer, João A Brancher, Giovana D Pecharki, et al.
Neurology|July 17, 2023
Frequency and Phenotype of <i>RFC1</i> Repeat Expansions in Bilateral VestibulopathyAndreas Traschütz, Felix Heindl, Muhammad Bilal, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 6, 2004
Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's diseaseEsti Liani, Allon Eyal, Eyal Avraham, et al.
Pageof 32

Showing results (101-110 of 313) with videos related to

Sort By:
Pageof 32
Neuroscience Letters|November 15, 2003
Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigraBettina Felletschin, Peter Bauer, Uwe Walter, et al.
Neurogenetics|February 1, 2012
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) Peter Bauer, Esther Leshinsky-Silver, Lubov Blumkin, et al.
Proteomics. Clinical Applications|December 8, 2010
Gene expression changes in a transgenic mouse model overexpressing human wildtype and mutant torsinAKathrin Grundmann, Jeannette Hübener, Karina Häbig, et al.
Orphanet Journal of Rare Diseases|May 31, 2011
A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patientsKatharina Rall, Gianmaria Barresi, Michael Walter, et al.
Human Molecular Genetics|August 12, 2009
Reversibility of symptoms in a conditional mouse model of spinocerebellar ataxia type 3Jana Boy, Thorsten Schmidt, Hartwig Wolburg, et al.
Journal of Neurology|October 27, 2004
Mutation at the SCA17 locus is not a common cause of primary dystoniaKathrin Grundmann, Ulrike Laubis-Herrmann, Dirk Dressler, et al.
European Journal of Human Genetics : EJHG|October 13, 2006
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approachJürgen Tomiuk, Lutz Bachmann, Claudia Bauer, et al.
Caries Research|May 23, 2015
Lactotransferrin Gene Polymorphism Associated with Caries ExperienceAndrea D Doetzer, João A Brancher, Giovana D Pecharki, et al.
Neurology|July 17, 2023
Frequency and Phenotype of <i>RFC1</i> Repeat Expansions in Bilateral VestibulopathyAndreas Traschütz, Felix Heindl, Muhammad Bilal, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 6, 2004
Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's diseaseEsti Liani, Allon Eyal, Eyal Avraham, et al.
Pageof 32