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Judith Eschbach

Showing results (1-10 of 15) with videos related to

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Pharmacology & Therapeutics|March 23, 2011
Cytoplasmic dynein in neurodegenerationJudith Eschbach, Luc Dupuis
Neuro-Degenerative Diseases|October 2, 2013
α-Synuclein in Parkinson's disease: pathogenic function and translation into animal modelsJudith Eschbach, Karin M Danzer
Molecular Neurodegeneration|April 28, 2011
A mutation in the dynein heavy chain gene compensates for energy deficit of mutant SOD1 mice and increases potentially neuroprotective IGF-1Anissa Fergani, Judith Eschbach, Hugues Oudart, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 19, 2024
Energy Metabolism in Residents in the Low- and Moderate Altitude Regions of Central Asia with MAFLD and Type 2 Diabetes MellitusNurgul Toktogulova, Matthias Breidert, Judith Eschbach, et al.
Drug Development Research|February 13, 2024
Drug upgrade: A complete methodology from old drug to new chemical entities using Nematic Protein Organization TechniqueJudith Eschbach, Alain Wagner, Corinne Beahr, et al.
Biochemistry and Molecular Biology Education : a Bimonthly Publication of the International Union of Biochemistry and Molecular Biology|May 14, 2011
"OpenLAB": A 2-hour PCR-based practical for high school studentsCaroline Bouakaze, Judith Eschbach, Elise Fouquerel, et al.
Plos One|May 1, 2009
Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neuronsLuc Dupuis, Jose-Luis Gonzalez de Aguilar, Andoni Echaniz-Laguna, et al.
Experimental Neurology|October 28, 2008
Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron diseaseLuc Dupuis, Anissa Fergani, Kerstin E Braunstein, et al.
Aging|July 20, 2017
The Golgi-localized, gamma ear-containing, ARF-binding (GGA) protein family alters alpha synuclein (α-syn) oligomerization and secretionBjoern von Einem, Judith Eschbach, Martin Kiechle, et al.
Human Molecular Genetics|August 1, 2013
Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferationKrisztina Rona-Voros, Judith Eschbach, Aurélia Vernay, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Pharmacology & Therapeutics|March 23, 2011
Cytoplasmic dynein in neurodegenerationJudith Eschbach, Luc Dupuis
Neuro-Degenerative Diseases|October 2, 2013
α-Synuclein in Parkinson's disease: pathogenic function and translation into animal modelsJudith Eschbach, Karin M Danzer
Molecular Neurodegeneration|April 28, 2011
A mutation in the dynein heavy chain gene compensates for energy deficit of mutant SOD1 mice and increases potentially neuroprotective IGF-1Anissa Fergani, Judith Eschbach, Hugues Oudart, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 19, 2024
Energy Metabolism in Residents in the Low- and Moderate Altitude Regions of Central Asia with MAFLD and Type 2 Diabetes MellitusNurgul Toktogulova, Matthias Breidert, Judith Eschbach, et al.
Drug Development Research|February 13, 2024
Drug upgrade: A complete methodology from old drug to new chemical entities using Nematic Protein Organization TechniqueJudith Eschbach, Alain Wagner, Corinne Beahr, et al.
Biochemistry and Molecular Biology Education : a Bimonthly Publication of the International Union of Biochemistry and Molecular Biology|May 14, 2011
"OpenLAB": A 2-hour PCR-based practical for high school studentsCaroline Bouakaze, Judith Eschbach, Elise Fouquerel, et al.
Plos One|May 1, 2009
Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neuronsLuc Dupuis, Jose-Luis Gonzalez de Aguilar, Andoni Echaniz-Laguna, et al.
Experimental Neurology|October 28, 2008
Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron diseaseLuc Dupuis, Anissa Fergani, Kerstin E Braunstein, et al.
Aging|July 20, 2017
The Golgi-localized, gamma ear-containing, ARF-binding (GGA) protein family alters alpha synuclein (α-syn) oligomerization and secretionBjoern von Einem, Judith Eschbach, Martin Kiechle, et al.
Human Molecular Genetics|August 1, 2013
Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferationKrisztina Rona-Voros, Judith Eschbach, Aurélia Vernay, et al.
Pageof 2