1. Morwena Latouche, Christelle Lasbleiz, Elodie Martin, Veronique Monnier, Thomas Debeir, Annick Mouatt-Prigent, Marie-Paule Muriel, Lydie Morel, Merle Ruberg, Alexis Brice, Giovanni Stevanin, and Herve Tricoire. A Conditional Pan-Neuronal Drosophila Model of Spinocerebellar Ataxia 7 with a Reversible Adult Phenotype Suitable for Identifying Modifier Genes. J Neurosci, 27(10):2483-2492, 2007. [WWW] [doi:10.1523/jneurosci.5453-06.2007]



2. M. Latouche, C. Lasbleiz, E. Martin, V. Monnier, T. Debeir, A. Mouatt-Prigent, M. P. Muriel, L. Morel, M. Ruberg, A. Brice, G. Stevanin, and H. Tricoire. A conditional pan-neuronal Drosophila model of spinocerebellar ataxia 7 with a reversible adult phenotype suitable for identifying modifier genes. J Neurosci, 27(10):2483-92, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesthe official journal of the Society for Neuroscience. [WWW] Keyword(s): Animals, Animals, Genetically Modified, Cell Death, Cells, Cultured, *Disease Models, Animal, *Drosophila, Dyskinesias/genetics, Glutamine, Humans, Intranuclear Inclusion Bodies/ultrastructure, Longevity, Male, Mutation, Nerve Tissue Proteins/genetics/metabolism, Neurons/metabolism, Peptides/genetics, Phenotype, Rats, Spinocerebellar Ataxias/*genetics/metabolism/pathology/physiopathology, Threonine.



3. M. Namekawa, M. P. Muriel, A. Janer, M. Latouche, A. Dauphin, T. Debeir, E. Martin, C. Duyckaerts, A. Prigent, C. Depienne, A. Sittler, A. Brice, and M. Ruberg. Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis. Mol Cell Neurosci, 35(1):1-13, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adult, Cell Line, Cytoplasmic Vesicles/*enzymology/ultrastructure, Endoplasmic Reticulum/*enzymology/ultrastructure, Epitopes, GTP Phosphohydrolases/*genetics/*metabolism, Golgi Apparatus/*enzymology/ultrastructure, Humans, Kidney/cytology, Microscopy, Electron, Motor Cortex/cytology, Motor Neurons/*enzymology, Paraplegia/genetics/metabolism, Point Mutation, Protein Transport/physiology, Spinal Cord/cytology.



4. A. Janer, E. Martin, M. P. Muriel, M. Latouche, H. Fujigasaki, M. Ruberg, A. Brice, Y. Trottier, and A. Sittler. PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteins. J Cell Biol, 174(1):65-76, 2006. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Animals, COS Cells, Cadmium Chloride/pharmacology, Cell Nucleus/*metabolism, Cells, Cultured, Cercopithecus aethiops, Humans, Interferon-beta/pharmacology, Mice, Mice, Transgenic, Multiprotein Complexes/drug effects/*metabolism, Mutation, Neoplasm Proteins/drug effects/*metabolism, Nerve Tissue Proteins/genetics/*metabolism, Nuclear Proteins/drug effects/*metabolism, Peptides/genetics, Proteasome Endopeptidase Complex/drug effects/*metabolism, Protein Isoforms/drug effects/metabolism, Transcription Factors/drug effects/*metabolism, Tumor Suppressor Proteins/drug effects/*metabolism.



5. M. Latouche, P. Fragner, E. Martin, K. H. El Hachimi, C. Zander, A. Sittler, M. Ruberg, A. Brice, and G. Stevanin. Polyglutamine and polyalanine expansions in ataxin7 result in different types of aggregation and levels of toxicity. Mol Cell Neurosci, 31(3):438-45, 2006. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Animals, Brain/*metabolism/pathology/physiopathology, Cell Line, Cells, Cultured, Humans, Intranuclear Inclusion Bodies/genetics/*metabolism/pathology, Molecular Chaperones/genetics/metabolism, Nerve Tissue Proteins/genetics/*metabolism/toxicity, Neurofibrils/genetics/metabolism/pathology, Neurons/*metabolism/pathology, Peptides/*metabolism, Proteasome Endopeptidase Complex/genetics/metabolism, Protein Folding, Rats, Spinocerebellar Ataxias/genetics/metabolism/physiopathology.



6. M. Periquet, M. Latouche, E. Lohmann, N. Rawal, G. De Michele, S. Ricard, H. Teive, V. Fraix, M. Vidailhet, D. Nicholl, P. Barone, N. W. Wood, S. Raskin, J. F. Deleuze, Y. Agid, A. Durr, and A. Brice. Parkin mutations are frequent in patients with isolated early-onset parkinsonism. Brain, 126(Pt 6):1271-8, 2003. Note: French Parkinson's Disease Genetics Study GroupEuropean Consortium on Genetic Susceptibility in Parkinson's DiseaseNs41723-01a1/ns/nindsJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.Englanda journal of neurology. [WWW] Keyword(s): Adolescent, Adult, Age of Onset, Base Sequence, Child, DNA, Complementary/genetics, Female, *Genetic Predisposition to Disease, Humans, Ligases/*genetics, Male, Middle Aged, Molecular Sequence Data, *Mutation, Parkinsonian Disorders/*genetics, Point Mutation, Polymerase Chain Reaction, *Ubiquitin-Protein Ligases.

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