1. N. Rawal, O. Corti, P. Sacchetti, H. Ardilla-Osorio, B. Sehat, A. Brice, and E. Arenas. Parkin protects dopaminergic neurons from excessive Wnt/beta-catenin signaling. Biochem Biophys Res Commun, 388(3):473-8, 2009. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



2. S. N. Illarioshkin, M. Periquet, N. Rawal, C. B. Lucking, T. B. Zagorovskaya, P. A. Slominsky, O. V. Miloserdova, E. D. Markova, S. A. Limborska, I. A. Ivanova-Smolenskaya, and A. Brice. Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism. Mov Disord, 18(8):914-9, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society. [WWW] Keyword(s): Adult, Antiparkinson Agents/therapeutic use, DNA Mutational Analysis, GTP Cyclohydrolase/genetics, Humans, Levodopa/therapeutic use, Middle Aged, Parkinsonian Disorders/drug therapy/*ethnology/*genetics, Pedigree, Point Mutation/*genetics, Severity of Illness Index, Ubiquitin-Protein Ligases/*genetics.



3. 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.



4. N. Rawal, M. Periquet, E. Lohmann, C. B. Lucking, H. A. Teive, G. Ambrosio, S. Raskin, S. Lincoln, N. Hattori, J. Guimaraes, M. W. Horstink, W. Dos Santos Bele, E. Brousolle, A. Destee, Y. Mizuno, M. Farrer, J. F. Deleuze, G. De Michele, Y. Agid, A. Durr, and A. Brice. New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism. Neurology, 60(8):1378-81, 2003. Note: French Parkinson's Disease Genetics Study GroupEuropean Consortium on Genetic Susceptibility in Parkinson's Disease1 r01 ns41723â\texteuro``01a1/ns/nindsJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.United States. [WWW] Keyword(s): Adult, Codon, Nonsense, DNA Mutational Analysis, Exons/genetics, Female, Genes, Recessive, Humans, Male, Middle Aged, Phenotype, Point Mutation, Polymerase Chain Reaction, RNA Splice Sites/genetics, Ubiquitin-Protein Ligases/*genetics.

This material is presented to ensure timely dissemination of scholarly and technical work. Copyright and all rights therein are retained by authors or by other copyright holders. All person copying this information are expected to adhere to the terms and constraints invoked by each author's copyright. In most cases, these works may not be reposted without the explicit permission of the copyright holder.

Les documents contenus dans ces répertoires sont rendus disponibles par les auteurs qui y ont contribué en vue d'assurer la diffusion à temps de travaux savants et techniques sur une base non-commerciale. Les droits de copie et autres droits sont gardés par les auteurs et par les détenteurs du copyright, en dépit du fait qu'ils présentent ici leurs travaux sous forme électronique. Les personnes copiant ces informations doivent adhérer aux termes et contraintes couverts par le copyright de chaque auteur. Ces travaux ne peuvent pas être rendus disponibles ailleurs sans la permission explicite du détenteur du copyright.

This document was translated from BibT_EX by bibtex2html