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List of works by J. Eschbach

A mutation in the dynein heavy chain gene compensates for energy deficit of mutant SOD1 mice and increases potentially neuroprotective IGF-1 ⬇️

scientific article published on April 26, 2011

A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons ⬇️

scientific article published on August 31, 2010

Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age ⬇️

scientific article published on 04 June 2013

Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation ⬇️

scientific article published on July 29, 2013

Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease

scientific article published on 8 October 2008

Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons

scientific article published on 30 April 2009

Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues

scientific article published on 29 September 2010

Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization

scientific article

PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis ⬇️

scientific article published on May 12, 2013

The Golgi-localized, gamma ear-containing, ARF-binding (GGA) protein family alters alpha synuclein (α-syn) oligomerization and secretion

scientific article published on 15 July 2017

α-Synuclein in Parkinson's disease: pathogenic function and translation into animal models

scientific article published on 24 September 2013

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