Ubiquitin Thiolesterase < Ubiquitin-Protein Ligases < Ubiquitination

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List of bibliographic references

Number of relevant bibliographic references: 39.
[20-40] [0 - 20][0 - 39]

Ident.	Authors (with country if any)	Title
000C05 (2009)	A. Destée ; E. Mutez ; A. Kreisler ; C. Vanbesien-Maillot ; M C Chartier-Harlin	[Parkinson disease: genetics and neuronal death].
000C28 (2009)	E. Lohmann ; S. Thobois ; S. Lesage ; E. Broussolle ; S Tezenas Du Montcel ; M-J Ribeiro ; P. Remy ; A. Pelissolo ; B. Dubois ; L. Mallet ; P. Pollak ; Y. Agid ; A. Brice	A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
000C35 (2009)	Olga Corti ; Margot Fournier ; Alexis Brice	Neurodegeneration in Parkinson's disease: genetics enlightens physiopathology.
000D27 (2008)	S. Lesage ; E. Lohmann ; F. Tison ; F. Durif ; A. Dürr ; A. Brice	Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls.
000E14 (2007)	Suzanne Lesage ; Periquet Magali ; Ebba Lohmann ; Lucette Lacomblez ; Helio Teive ; Sabine Janin ; Pierre-Yves Cousin ; Alexandra Dürr ; Alexis Brice	Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism.
000E58 (2006)	Cornelia Hampe ; Hector Ardila-Osorio ; Margot Fournier ; Alexis Brice ; Olga Corti	Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity.
000F65 (2005)	Olga Corti ; Cornelia Hampe ; Frédéric Darios ; Pablo Ibanez ; Merle Ruberg ; Alexis Brice	Parkinson's disease: from causes to mechanisms.
001051 (2004)	Pierre Pollak	Movement disorders: Parkinson's disease dominates.
001065 (2003)	Wen-Jie Gu ; Olga Corti ; Francisco Araujo ; Cornelia Hampe ; Sandrine Jacquier ; Christoph B. Lücking ; Nacer Abbas ; Charles Duyckaerts ; Thomas Rooney ; Laurent Pradier ; Merle Ruberg ; Alexis Brice	The C289G and C418R missense mutations cause rapid sequestration of human Parkin into insoluble aggregates.
001079 (2003)	Christoph-Burkhard Lücking ; Véronique Chesneau ; Ebba Lohmann ; Patrice Verpillat ; Cyprien Dulac ; Anne-Marie Bonnet ; Francesca Gasparini ; Yves Agid ; Alexandra Dürr ; Alexis Brice	Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.
001086 (2003)	Ebba Lohmann ; Magali Periquet ; Vincenzo Bonifati ; Nick W. Wood ; Giuseppe De Michele ; Anne-Marie Bonnet ; Valérie Fraix ; Emmanuel Broussolle ; Martin W I M. Horstink ; Marie Vidailhet ; Patrice Verpillat ; Thomas Gasser ; David Nicholl ; Hélio Teive ; Salmo Raskin ; Olivier Rascol ; Alain Destée ; Merle Ruberg ; Francesca Gasparini ; Giuseppe Meco ; Yves Agid ; Alexandra Durr ; Alexis Brice	How much phenotypic variation can be attributed to parkin genotype?
001098 (2003)	Olga Corti ; Cornelia Hampe ; Hana Koutnikova ; Frédéric Darios ; Sandrine Jacquier ; Annick Prigent ; Jean-Charles Robinson ; Laurent Pradier ; Merle Ruberg ; Marc Mirande ; Etienne Hirsch ; Thomas Rooney ; Alain Fournier ; Alexis Brice	The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration.
001102 (2003)	Stéphane Thobois ; Maria-Joao Ribeiro ; Ebba Lohmann ; Alexandra Dürr ; Pierre Pollak ; Olivier Rascol ; Stéphane Guillouet ; Elizabeth Chapoy ; Nicolas Costes ; Yves Agid ; Philippe Remy ; Alexis Brice ; Emmanuel Broussolle	Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography study.
001108 (2003)	Olga Corti ; Alexis Brice	[Parkinson's disease: what have we learned from the genes responsible for familial forms?].
001255 (2001)	M. Periquet ; C. Lücking ; J. Vaughan ; V. Bonifati ; A. Dürr ; G. De Michele ; M. Horstink ; M. Farrer ; S N Illarioshkin ; P. Pollak ; M. Borg ; C. Brefel-Courbon ; P. Denefle ; G. Meco ; T. Gasser ; M M Breteler ; N. Wood ; Y. Agid ; A. Brice	Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects.
001289 (2000)	M. Farrer ; T. Destée ; E. Becquet ; F. Wavrant-De Vrièze ; V. Mouroux ; F. Richard ; L. Defebvre ; S. Lincoln ; J. Hardy ; P. Amouyel ; M C Chartier-Harlin	Linkage exclusion in French families with probable Parkinson' s disease.
001331 (2000)	W J Gu ; N. Abbas ; M Z Lagunes ; A. Parent ; L. Pradier ; G A Bohme ; Y. Agid ; E C Hirsch ; R. Raisman-Vozari ; A. Brice	Cloning of rat parkin cDNA and distribution of parkin in rat brain.
001387 (1999)	D. Brassat ; A. Durr ; Y. Agid ; A. Brice	[Genetics of Parkinson disease].
001408 (1999)	N. Abbas ; C B Lücking ; S. Ricard ; A. Dürr ; V. Bonifati ; G. De Michele ; S. Bouley ; J R Vaughan ; T. Gasser ; R. Marconi ; E. Broussolle ; C. Brefel-Courbon ; B S Harhangi ; B A Oostra ; E. Fabrizio ; G A Böhme ; L. Pradier ; N W Wood ; A. Filla ; G. Meco ; P. Denefle ; Y. Agid ; A. Brice	A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.

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