1. A. Chojnowski, N. Ravise, C. Bachelin, C. Depienne, M. Ruberg, B. Brugg, J. Laporte, A. Baron-Van Evercooren, and E. LeGuern. Silencing of the Charcot-Marie-Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells. Neurobiol Dis, 26(2):323-31, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Animals, Animals, Newborn, Apoptosis/drug effects/genetics, Caspases/metabolism, Cell Death/drug effects/genetics, Cell Proliferation, Cells, Cultured, Charcot-Marie-Tooth Disease/*genetics/metabolism/physiopathology, Culture Media, Serum-Free/pharmacology, Down-Regulation/drug effects/genetics, Gene Expression Profiling, Gene Expression Regulation, Developmental/genetics, *Gene Silencing, Myelin Sheath/*genetics/metabolism/pathology, Peripheral Nerves/*metabolism/pathology/physiopathology, Protein Tyrosine Phosphatases/*genetics, Protein Tyrosine Phosphatases, Non-Receptor, RNA Interference, Rats, Schwann Cells/*metabolism/pathology.



2. H. Azzedine, A. Bolino, T. Taieb, N. Birouk, M. Di Duca, A. Bouhouche, S. Benamou, A. Mrabet, T. Hammadouche, T. Chkili, R. Gouider, R. Ravazzolo, A. Brice, J. Laporte, and E. LeGuern. 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. Am J Hum Genet, 72(5):1141-53, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Age of Onset, Amino Acid Sequence, Carrier Proteins/*genetics, Charcot-Marie-Tooth Disease/complications/*genetics, Child, Child, Preschool, Chromosomes, Human, Pair 11/genetics, Consanguinity, DNA Mutational Analysis, Demyelinating Diseases/complications/*genetics, Female, Genes, Recessive, Glaucoma/complications/*genetics, Humans, *Intracellular Signaling Peptides and Proteins, Male, Molecular Sequence Data, Morocco, Mutation, Phosphoric Monoester Hydrolases/genetics, Physical Chromosome Mapping, Protein-Tyrosine-Phosphatase/*genetics, Sequence Homology, Amino Acid, Syndrome, Tunisia.

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