Jocelyn Laporte
Centre National de la Recherche Scientifique(FR)Inserm(FR)Institut de génétique et de biologie moléculaire et cellulaire(FR)
Publications by Year
Research Areas
Cellular transport and secretion, Muscle Physiology and Disorders, Cardiomyopathy and Myosin Studies, Genetic Neurodegenerative Diseases, Ubiquitin and proteasome pathways
Most-Cited Works
- → A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast(1996)624 cited
- → Mutations in dynamin 2 cause dominant centronuclear myopathy(2005)456 cited
- → Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy(2007)431 cited
- → Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy(2011)326 cited
- → Centronuclear (myotubular) myopathy(2008)307 cited
- → Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma(2003)302 cited