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Thorsten Schmidt

Showing results (71-80 of 119) with videos related to

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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.
Molecular Brain|March 20, 2021
Neurodegenerative phosphoprotein signaling landscape in models of SCA3Anna S Sowa, Taissia G Popova, Tina Harmuth, et al.
Proteomics|February 20, 2008
An approach to handling and interpretation of ambiguous data in transcriptome and proteome comparisonsMartin Irmler, Daniela Hartl, Thorsten Schmidt, et al.
Peptides|November 30, 2020
Transcriptomic changes in pancreatic islets, adipose and liver after Roux-en-Y gastric bypass in a diet-induced obese rat modelChen Zhang, Lise Christine Biehl Rudkjær, Marisa Fernández Cachón, et al.
AJR. American Journal of Roentgenology|December 24, 2004
Radiation dose reduction to the male gonads during MDCT: the effectiveness of a lead shieldChristian Hohl, Andreas H Mahnken, Ernst Klotz, et al.
Neurochemistry International|November 8, 2017
Mass spectrometry analyses of normal and polyglutamine expanded ataxin-3 reveal novel interaction partners involved in mitochondrial functionLine V Kristensen, Felix S Oppermann, Matthias J Rauen, 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 Personalized Medicine|March 25, 2022
A Holistic Approach for the Identification of Success Factors in Secondary Cleft OsteoplastyTom A Schröder, Martin Maiwald, Axel Reinicke, 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.
Neurobiology of Disease|August 25, 2009
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeatsJana Boy, Thorsten Schmidt, Ulrike Schumann, et al.
Pageof 12

Showing results (71-80 of 119) with videos related to

Sort By:
Pageof 12
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.
Molecular Brain|March 20, 2021
Neurodegenerative phosphoprotein signaling landscape in models of SCA3Anna S Sowa, Taissia G Popova, Tina Harmuth, et al.
Proteomics|February 20, 2008
An approach to handling and interpretation of ambiguous data in transcriptome and proteome comparisonsMartin Irmler, Daniela Hartl, Thorsten Schmidt, et al.
Peptides|November 30, 2020
Transcriptomic changes in pancreatic islets, adipose and liver after Roux-en-Y gastric bypass in a diet-induced obese rat modelChen Zhang, Lise Christine Biehl Rudkjær, Marisa Fernández Cachón, et al.
AJR. American Journal of Roentgenology|December 24, 2004
Radiation dose reduction to the male gonads during MDCT: the effectiveness of a lead shieldChristian Hohl, Andreas H Mahnken, Ernst Klotz, et al.
Neurochemistry International|November 8, 2017
Mass spectrometry analyses of normal and polyglutamine expanded ataxin-3 reveal novel interaction partners involved in mitochondrial functionLine V Kristensen, Felix S Oppermann, Matthias J Rauen, 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 Personalized Medicine|March 25, 2022
A Holistic Approach for the Identification of Success Factors in Secondary Cleft OsteoplastyTom A Schröder, Martin Maiwald, Axel Reinicke, 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.
Neurobiology of Disease|August 25, 2009
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeatsJana Boy, Thorsten Schmidt, Ulrike Schumann, et al.
Pageof 12