1. F. Gros-Louis, J. Kriz, E. Kabashi, J. McDearmid, S. Millecamps, M. Urushitani, L. Lin, P. Dion, Q. Zhu, P. Drapeau, J. P. Julien, and G. A. Rouleau. Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish. Hum Mol Genet, 17(17):2691-702, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Amyotrophic Lateral Sclerosis/*genetics/*physiopathology, Animals, Disease Models, Animal, Guanine Nucleotide Exchange Factors/*genetics/*metabolism, Mice, Mice, Inbred C57BL, Mice, Knockout, Motor Neurons/*physiology, Nerve Tissue Proteins/*genetics/*metabolism, Protein Isoforms/genetics/metabolism, Zebrafish/genetics, Zebrafish Proteins/*genetics/*metabolism.



2. S. Millecamps and J. P. Julien. [Dysfunction of axonal transport in neuropathies and motor neuron diseases]. Med Sci (Paris), 24(1):65-71, 2008. Note: English AbstractJournal ArticleReviewFranceM/s. [WWW] Keyword(s): Axonal Transport/*physiology, Biological Transport, Humans, Motor Neuron Disease/*physiopathology, Nerve Tissue Proteins/physiology, Nervous System Diseases/*physiopathology.



3. S. Millecamps, G. Gowing, O. Corti, J. Mallet, and J. P. Julien. Conditional NF-L transgene expression in mice for in vivo analysis of turnover and transport rate of neurofilaments. J Neurosci, 27(18):4947-56, 2007. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited Statesthe official journal of the Society for Neuroscience. [WWW] Keyword(s): Animals, Axonal Transport/*genetics, Gene Expression Regulation/*physiology, Half-Life, Humans, Mice, Mice, Inbred C3H, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Neurofilament Proteins/*biosynthesis/*genetics/metabolism/physiology, Protein Transport/genetics.



4. S. Millecamps, J. Robertson, R. Lariviere, J. Mallet, and J. P. Julien. Defective axonal transport of neurofilament proteins in neurons overexpressing peripherin. J Neurochem, 98(3):926-38, 2006. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Amyotrophic Lateral Sclerosis/metabolism/pathology, Animals, *Axonal Transport/genetics, Cell Line, Cell Line, Tumor, Ganglia, Spinal/cytology/metabolism, Humans, Intermediate Filament Proteins/*biosynthesis/*genetics/physiology, Membrane Glycoproteins/*biosynthesis/*genetics/physiology, Mice, Mice, Transgenic, Nerve Tissue Proteins/*biosynthesis/*genetics/physiology, Neurofilament Proteins/antagonists &, inhibitors/classification/genetics/*metabolism, Neurons/*metabolism/pathology, Organ Culture Techniques, Spheroids, Cellular/pathology, Up-Regulation/genetics.



5. S. Millecamps, B. J. Gentil, F. Gros-Louis, G. Rouleau, and J. P. Julien. Alsin is partially associated with centrosome in human cells. Biochimica Et Biophysica Acta-Molecular Cell Research, 1745(1):84-100, 2005. Note: 958EYTimes Cited:7Cited References Count:59. [WWW] Keyword(s): amyotrophic lateral sclerosis, als2, alsin, endosome, centrosome, microtubule, amyotrophic-lateral-sclerosis, guanine-nucleotide exchange, hereditary spastic paralysis, heavy neurofilament subunit, gdp dissociation inhibitor, human neuroblastoma-cells, small gtpase rab5, gamma-tubulin, superoxide-dismutase, mammalian-cells.



6. A. M. Clement, M. D. Nguyen, E. A. Roberts, M. L. Garcia, S. Boillee, M. Rule, A. P. McMahon, W. Doucette, D. Siwek, R. J. Ferrante, R. H. Jr Brown, J. P. Julien, L. S. Goldstein, and D. W. Cleveland. Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice. Science, 302(5642):113-7, 2003. Note: Ag 12992/ag/niaAg 13846/ag/niaHd 30249/hd/nichdNs 27036/ns/nindsNs 31248/ns/nindsNs 37912/ns/nindsJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.Research Support, U.S. Gov't, P.H.S.United States. [WWW] Keyword(s): Amyotrophic Lateral Sclerosis/*pathology, Animals, Axons/pathology, Cell Survival, Chimera, Humans, Mice, Mice, Inbred C57BL, Mice, Inbred Strains, Mice, Transgenic, Motor Neurons/metabolism/pathology/*physiology, Mutation, Nerve Degeneration, Neurofilament Proteins/metabolism, Spinal Cord/metabolism/*pathology, Superoxide Dismutase/*genetics/metabolism, Survival Rate, Ubiquitin/analysis.

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