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Olaf Riess

Showing results (71-80 of 313) with videos related to

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Human Molecular Genetics|December 22, 2018
Vulnerability of frontal brain neurons for the toxicity of expanded ataxin-3Jana Schmidt, Anja K Mayer, Daniela Bakula, et al.
Proteomics. Clinical Applications|December 8, 2010
Age-dependent gene expression profile and protein expression in a transgenic rat model of Huntington's diseaseHuu Phuc Nguyen, Silke Metzger, Carsten Holzmann, et al.
American Journal of Medical Genetics. Part A|May 29, 2012
Interstitial 9q34.11-q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palateAndreas Tzschach, Ute Grasshoff, Karin Schäferhoff, et al.
Neuropharmacology|January 23, 2018
Calpastatin ablation aggravates the molecular phenotype in cell and animal models of Huntington diseaseJonasz Jeremiasz Weber, Simon Johannes Kloock, Maike Nagel, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|July 4, 2012
Automated behavioral phenotyping reveals presymptomatic alterations in a SCA3 genetrap mouse modelJeannette Hübener, Nicolas Casadei, Peter Teismann, et al.
Fertility and Sterility|December 11, 2014
Mayer-Rokitansky-Küster-Hauser syndrome discordance in monozygotic twins: matrix metalloproteinase 14, low-density lipoprotein receptor-related protein 10, extracellular matrix, and neoangiogenesis genes identified as candidate genes in a tissue-specific mosaicismKatharina Rall, Simone Eisenbeis, Gianmaria Barresi, et al.
Genesis (New York, N.Y. : 2000)|July 22, 2009
Periphilin is strongly expressed in the murine nervous system and is indispensable for murine developmentAnne S Soehn, Thu-Trang Pham, Karin Schaeferhoff, et al.
Annals of Neurology|July 3, 2003
Do CTG expansions at the SCA8 locus cause ataxia?Ludger Schöls, Ingrid Bauer, Christine Zühlke, et al.
Neurobiology of Disease|October 13, 2009
Dysregulation of coordinated neuronal firing patterns in striatum of freely behaving transgenic rats that model Huntington's diseaseBenjamin R Miller, Adam G Walker, Stephen C Fowler, et al.
Annals of Neurology|March 14, 2002
Protein surveillance machinery in brains with spinocerebellar ataxia type 3: redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusionsThorsten Schmidt, Katrin S Lindenberg, Antje Krebs, et al.
Pageof 32

Showing results (71-80 of 313) with videos related to

Sort By:
Pageof 32
Human Molecular Genetics|December 22, 2018
Vulnerability of frontal brain neurons for the toxicity of expanded ataxin-3Jana Schmidt, Anja K Mayer, Daniela Bakula, et al.
Proteomics. Clinical Applications|December 8, 2010
Age-dependent gene expression profile and protein expression in a transgenic rat model of Huntington's diseaseHuu Phuc Nguyen, Silke Metzger, Carsten Holzmann, et al.
American Journal of Medical Genetics. Part A|May 29, 2012
Interstitial 9q34.11-q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palateAndreas Tzschach, Ute Grasshoff, Karin Schäferhoff, et al.
Neuropharmacology|January 23, 2018
Calpastatin ablation aggravates the molecular phenotype in cell and animal models of Huntington diseaseJonasz Jeremiasz Weber, Simon Johannes Kloock, Maike Nagel, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|July 4, 2012
Automated behavioral phenotyping reveals presymptomatic alterations in a SCA3 genetrap mouse modelJeannette Hübener, Nicolas Casadei, Peter Teismann, et al.
Fertility and Sterility|December 11, 2014
Mayer-Rokitansky-Küster-Hauser syndrome discordance in monozygotic twins: matrix metalloproteinase 14, low-density lipoprotein receptor-related protein 10, extracellular matrix, and neoangiogenesis genes identified as candidate genes in a tissue-specific mosaicismKatharina Rall, Simone Eisenbeis, Gianmaria Barresi, et al.
Genesis (New York, N.Y. : 2000)|July 22, 2009
Periphilin is strongly expressed in the murine nervous system and is indispensable for murine developmentAnne S Soehn, Thu-Trang Pham, Karin Schaeferhoff, et al.
Annals of Neurology|July 3, 2003
Do CTG expansions at the SCA8 locus cause ataxia?Ludger Schöls, Ingrid Bauer, Christine Zühlke, et al.
Neurobiology of Disease|October 13, 2009
Dysregulation of coordinated neuronal firing patterns in striatum of freely behaving transgenic rats that model Huntington's diseaseBenjamin R Miller, Adam G Walker, Stephen C Fowler, et al.
Annals of Neurology|March 14, 2002
Protein surveillance machinery in brains with spinocerebellar ataxia type 3: redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusionsThorsten Schmidt, Katrin S Lindenberg, Antje Krebs, et al.
Pageof 32