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Judith Eschbach

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Biochimica Et Biophysica Acta|October 5, 2010
Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissuesJudith Eschbach, Anissa Fergani, Hugues Oudart, et al.
Human Molecular Genetics|May 15, 2013
PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosisJudith Eschbach, Birgit Schwalenstöcker, Selma M Soyal, et al.
Neurobiology of Disease|June 8, 2013
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with ageJudith Eschbach, Jérôme Sinniger, Jamal Bouitbir, et al.
Annals of Neurology|November 4, 2014
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerizationJudith Eschbach, Björn von Einem, Kathrin Müller, et al.
Human Molecular Genetics|September 3, 2010
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neuronsKerstin E Braunstein, Judith Eschbach, Krisztina Ròna-Vörös, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Biochimica Et Biophysica Acta|October 5, 2010
Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissuesJudith Eschbach, Anissa Fergani, Hugues Oudart, et al.
Human Molecular Genetics|May 15, 2013
PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosisJudith Eschbach, Birgit Schwalenstöcker, Selma M Soyal, et al.
Neurobiology of Disease|June 8, 2013
Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with ageJudith Eschbach, Jérôme Sinniger, Jamal Bouitbir, et al.
Annals of Neurology|November 4, 2014
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerizationJudith Eschbach, Björn von Einem, Kathrin Müller, et al.
Human Molecular Genetics|September 3, 2010
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neuronsKerstin E Braunstein, Judith Eschbach, Krisztina Ròna-Vörös, et al.
Pageof 2