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Olaf Riess

Showing results (111-120 of 313) with videos related to

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International Journal of Molecular Sciences|June 10, 2022
Mitochondrial Dysfunction in Spinocerebellar Ataxia Type 3 Is Linked to VDAC1 DeubiquitinationTina Harmuth, Jonasz J Weber, Anna J Zimmer, et al.
Acta Obstetricia Et Gynecologica Scandinavica|August 18, 2017
Sequence variants in ESR1 and OXTR are associated with Mayer-Rokitansky-Küster-Hauser syndromeSara Yvonne Brucker, Liliane Frank, Simone Eisenbeis, et al.
European Journal of Human Genetics : EJHG|May 26, 2016
The risk of re-identification versus the need to identify individuals in rare disease researchMats G Hansson, Hanns Lochmüller, Olaf Riess, et al.
Journal of Medical Genetics|November 5, 2014
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohortsJohanna Huttenlocher, Rejko Krüger, Philipp Capetian, et al.
Frontiers in Neuroscience|November 22, 2019
Enriched Environmental Conditions Modify the Gut Microbiome Composition and Fecal Markers of Inflammation in Parkinson's DiseaseYogesh Singh, Mohamed El-Hadidi, Jakob Admard, et al.
Journal of Molecular Neuroscience : MN|March 1, 2020
Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 DystoniaFubo Cheng, Michael Walter, Zinah Wassouf, et al.
Hepatology (Baltimore, Md.)|June 21, 2005
Genotype-phenotype relationships in hepatocellular tumors from mice and manSabine Stahl, Carina Ittrich, Philip Marx-Stoelting, et al.
The Journal of Biological Chemistry|November 21, 2018
Physiological and pathophysiological characteristics of ataxin-3 isoformsDaniel Weishäupl, Juliane Schneider, Barbara Peixoto Pinheiro, et al.
Scientific Reports|December 6, 2017
Reduced cell size, chromosomal aberration and altered proliferation rates are characteristics and confounding factors in the STHdh cell model of Huntington diseaseElisabeth Singer, Carolin Walter, Jonasz J Weber, et al.
Archives of Neurology|September 17, 2003
Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystoniaKathrin Grundmann, Ulrike Laubis-Herrmann, Ingrid Bauer, et al.
Pageof 32

Showing results (111-120 of 313) with videos related to

Sort By:
Pageof 32
International Journal of Molecular Sciences|June 10, 2022
Mitochondrial Dysfunction in Spinocerebellar Ataxia Type 3 Is Linked to VDAC1 DeubiquitinationTina Harmuth, Jonasz J Weber, Anna J Zimmer, et al.
Acta Obstetricia Et Gynecologica Scandinavica|August 18, 2017
Sequence variants in ESR1 and OXTR are associated with Mayer-Rokitansky-Küster-Hauser syndromeSara Yvonne Brucker, Liliane Frank, Simone Eisenbeis, et al.
European Journal of Human Genetics : EJHG|May 26, 2016
The risk of re-identification versus the need to identify individuals in rare disease researchMats G Hansson, Hanns Lochmüller, Olaf Riess, et al.
Journal of Medical Genetics|November 5, 2014
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohortsJohanna Huttenlocher, Rejko Krüger, Philipp Capetian, et al.
Frontiers in Neuroscience|November 22, 2019
Enriched Environmental Conditions Modify the Gut Microbiome Composition and Fecal Markers of Inflammation in Parkinson's DiseaseYogesh Singh, Mohamed El-Hadidi, Jakob Admard, et al.
Journal of Molecular Neuroscience : MN|March 1, 2020
Unraveling Molecular Mechanisms of THAP1 Missense Mutations in DYT6 DystoniaFubo Cheng, Michael Walter, Zinah Wassouf, et al.
Hepatology (Baltimore, Md.)|June 21, 2005
Genotype-phenotype relationships in hepatocellular tumors from mice and manSabine Stahl, Carina Ittrich, Philip Marx-Stoelting, et al.
The Journal of Biological Chemistry|November 21, 2018
Physiological and pathophysiological characteristics of ataxin-3 isoformsDaniel Weishäupl, Juliane Schneider, Barbara Peixoto Pinheiro, et al.
Scientific Reports|December 6, 2017
Reduced cell size, chromosomal aberration and altered proliferation rates are characteristics and confounding factors in the STHdh cell model of Huntington diseaseElisabeth Singer, Carolin Walter, Jonasz J Weber, et al.
Archives of Neurology|September 17, 2003
Frequency and phenotypic variability of the GAG deletion of the DYT1 gene in an unselected group of patients with dystoniaKathrin Grundmann, Ulrike Laubis-Herrmann, Ingrid Bauer, et al.
Pageof 32