Mitochondrial defect in Huntington's disease caudate nucleus
Muxin Gu(Wellcome/MRC Cambridge Stem Cell Institute), Anthony H.V. Schapira(National Hospital for Neurology and Neurosurgery), Jonathan M. Cooper(University of Glasgow), M. T. Gash(The Royal Free Hospital), V. M. Mann(The Royal Free Hospital), F. Javoy‐Agid(Inserm)
Cited by 738
Related Papers
Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy
|Human Molecular Genetics|2010|896
Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking Palsy
|Movement Disorders|2017|846
Priorities in Parkinson's disease research
|Nature Reviews Drug Discovery|2011|430
METTL1-mediated m7G modification of Arg-TCT tRNA drives oncogenic transformation
|Molecular Cell|2021|359