Yves Lutz

The FMR–1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

Didier Devys, Yves Lutz, N. Rouyer et al. · Nature Genetics · 1993 · 772 citations

Neurodegenerative Diseases, Molecular Neuroscience, Genetic Disorder +12

Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes

Victoria Campuzano, Laura Montermini, Yves Lutz et al. · Human Molecular Genetics · 1997 · 734 citations

Mitophagy, Pathology, Cell Death +16

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

Yvon Trottier, Yves Lutz, Giovanni Stévanin et al. · Nature · 1995 · 653 citations

Pathological Epitope, Degenerative Disease, Dominant Cerebellar Ataxias +8

The N-terminal part of TIF1, a putative mediator of the ligand-dependent activation function (AF-2) of nuclear receptors, is fused to B-raf in the oncogenic protein T18.

Bertrand Le Douarin, Christina Zechel, J.M. Garnier et al. · The EMBO Journal · 1995 · 627 citations

N-terminal Part, Signal Transduction, Signaling Pathway +11

Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form

Yvon Trottier, Didier Devys, Georges Imbert et al. · Nature Genetics · 1995 · 445 citations

Knockout Mouse, Disease Protein, Genetics +5