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Olaf Riess

Showing results (181-190 of 313) with videos related to

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Archives of Neurology|February 22, 2012
Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and YirrkalaSandra Martins, Bing-Wen Soong, Virginia C N Wong, et al.
Plos One|February 27, 2010
Reduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1Guido Krebiehl, Sabine Ruckerbauer, Lena F Burbulla, et al.
Human Molecular Genetics|October 27, 2012
Calpain-mediated ataxin-3 cleavage in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3)Jeannette Hübener, Jonasz Jeremiasz Weber, Claudia Richter, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|June 26, 2022
Host genetic loci LZTFL1 and CCL2 associated with SARS-CoV-2 infection and severity of COVID-19Jule Rüter, Srinivas Reddy Pallerla, Christian G Meyer, et al.
Cells|December 11, 2022
Evidences for Mutant Huntingtin Inducing Musculoskeletal and Brain Growth Impairments via Disturbing Testosterone Biosynthesis in Male Huntington Disease AnimalsLibo Yu-Taeger, Arianna Novati, Jonasz Jeremiasz Weber, et al.
Human Molecular Genetics|September 21, 2006
Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's diseaseHuu Phuc Nguyen, Philipp Kobbe, Henning Rahne, et al.
Neurobiology of Disease|September 6, 2011
The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effectSuzana Gispert, Alexander Kurz, Stefan Waibel, et al.
Journal of Neuropathology and Experimental Neurology|June 11, 2010
Stem cell quiescence in the hippocampal neurogenic niche is associated with elevated transforming growth factor-beta signaling in an animal model of Huntington diseaseMahesh Kandasamy, Sebastien Couillard-Despres, Kerstin A Raber, et al.
Molecular Neurobiology|October 30, 2021
A Novel SCA3 Knock-in Mouse Model Mimics the Human SCA3 Disease Phenotype Including Neuropathological, Behavioral, and Transcriptional Abnormalities Especially in OligodendrocytesEva Haas, Rana D Incebacak, Thomas Hentrich, et al.
Frontiers in Neurology|January 11, 2020
Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in DystoniaMichaela Pogoda, Franz-Joachim Hilke, Ebba Lohmann, et al.
Pageof 32

Showing results (181-190 of 313) with videos related to

Sort By:
Pageof 32
Archives of Neurology|February 22, 2012
Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and YirrkalaSandra Martins, Bing-Wen Soong, Virginia C N Wong, et al.
Plos One|February 27, 2010
Reduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1Guido Krebiehl, Sabine Ruckerbauer, Lena F Burbulla, et al.
Human Molecular Genetics|October 27, 2012
Calpain-mediated ataxin-3 cleavage in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3)Jeannette Hübener, Jonasz Jeremiasz Weber, Claudia Richter, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|June 26, 2022
Host genetic loci LZTFL1 and CCL2 associated with SARS-CoV-2 infection and severity of COVID-19Jule Rüter, Srinivas Reddy Pallerla, Christian G Meyer, et al.
Cells|December 11, 2022
Evidences for Mutant Huntingtin Inducing Musculoskeletal and Brain Growth Impairments via Disturbing Testosterone Biosynthesis in Male Huntington Disease AnimalsLibo Yu-Taeger, Arianna Novati, Jonasz Jeremiasz Weber, et al.
Human Molecular Genetics|September 21, 2006
Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's diseaseHuu Phuc Nguyen, Philipp Kobbe, Henning Rahne, et al.
Neurobiology of Disease|September 6, 2011
The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effectSuzana Gispert, Alexander Kurz, Stefan Waibel, et al.
Journal of Neuropathology and Experimental Neurology|June 11, 2010
Stem cell quiescence in the hippocampal neurogenic niche is associated with elevated transforming growth factor-beta signaling in an animal model of Huntington diseaseMahesh Kandasamy, Sebastien Couillard-Despres, Kerstin A Raber, et al.
Molecular Neurobiology|October 30, 2021
A Novel SCA3 Knock-in Mouse Model Mimics the Human SCA3 Disease Phenotype Including Neuropathological, Behavioral, and Transcriptional Abnormalities Especially in OligodendrocytesEva Haas, Rana D Incebacak, Thomas Hentrich, et al.
Frontiers in Neurology|January 11, 2020
Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in DystoniaMichaela Pogoda, Franz-Joachim Hilke, Ebba Lohmann, et al.
Pageof 32