FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Nacer Abbas

Research Profile

Disorders

Chemicals & Drugs

Concepts & Ideas

Age of Onset

Physiology

Anatomy

Genes & Molecular Sequences

Alleles

Procedures

Co-author Network

Publications

TOP 3
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.
Jean-Michel Itier; Pablo Ibanez; Maria Angeles Mena; Nacer Abbas; Charles Cohen-Salmon; Georg Andrees Bohme; Michel Laville; Jeremy Pratt; Olga Corti; Laurent Pradier; Gwenaëlle Ret; Chantal Joubert; Magali Periquet; Francisco Araujo; Julia Negroni; Maria José Casarejos; Santiago Canals; Rosa Maria Solano; Alba Serrano; Eva Gallego; Marina Sanchez; Patrice DENEFLE; Jesus Benavides; Günter Tremp; Thomas Rooney; Alexis Brice; Justo Garcia de Yebenes
Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse.
Frédéric Darios; Olga Corti; Christoph B Lücking; Cornelia Hampe; Marie-Paule Muriel; Nacer Abbas; Wen-Jie Gu; Etienne C Hirsch; Thomas Rooney; Merle Ruberg; Alexis Brice
Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Nacer Abbas (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

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.
Neurobiology of disease 2003;14(3):357-64.
2003: Jean-Michel Itier; Pablo Ibanez; Maria Angeles Mena; Nacer Abbas; Charles Cohen-Salmon; Georg Andrees Bohme; Michel Laville; Jeremy Pratt; Olga Corti; Laurent Pradier; Gwenaëlle Ret; Chantal Joubert; Magali Periquet; Francisco Araujo; Julia Negroni; Maria José Casarejos; Santiago Canals; Rosa Maria Solano; Alba Serrano; Eva Gallego; Marina Sanchez; Patrice DENEFLE; Jesus Benavides; Günter Tremp; Thomas Rooney; Alexis Brice; Justo Garcia de Yebenes
Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse.
Human molecular genetics 2003;12(18):2277-91.
2003: Frédéric Darios; Olga Corti; Christoph B Lücking; Cornelia Hampe; Marie-Paule Muriel; Nacer Abbas; Wen-Jie Gu; Etienne C Hirsch; Thomas Rooney; Merle Ruberg; Alexis Brice
Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death.
Human molecular genetics 2003;12(5):517-26.
2002: Andreas Hartmann; Annick Mouatt-Prigent; Miquel Vila; Nacer Abbas; Celine Perier; Baptiste A Faucheux; Sheela Vyas; Etienne C Hirsch
Increased expression and redistribution of the antiapoptotic molecule Bcl-xL in Parkinson's disease.
Neurobiology of disease 2002;10(1):28-32.
2000: Wen-Jie Gu; Nacer Abbas; M Z Lagunes; A Parent; Laurent Pradier; Georg Andrees Bohme; Yves Agid; Etienne C Hirsch; Rita Raisman-Vozari; Alexis Brice
Cloning of rat parkin cDNA and distribution of parkin in rat brain.
Journal of neurochemistry 2000;74(4):1773-6.
1999: Nacer Abbas; Christoph B Lücking; Sylvain Ricard; Alexandra Dürr; Vincenzo Bonifati; Giuseppe De Michele; S Bouley; Jenny R Vaughan; Thomas Gasser; Roberto Marconi; Emmanuel Broussolle; C Brefel-Courbon; Biswadjiet S Harhangi; Ben A Oostra; Edito Fabrizio; G A Böhme; Laurent Pradier; Nicholas W Wood; Alessandro Filla; Giuseppe Meco; Patrice DENEFLE; Yves Agid; Alexis 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.
Human molecular genetics 1999;8(4):567-74.
1998: Christoph B Lücking; Nacer Abbas; Alexandra Dürr; Vincenzo Bonifati; Anne-Marie Bonnet; T de Broucker; G De Michele; Nicholas W Wood; Yves Agid; Alexis Brice
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group.
Lancet 1998;352(9137):1355-6.
1998: JP Tassin; Alexandra Dürr; T de Broucker; Nacer Abbas; Vincenzo Bonifati; Giuseppe De Michele; Anne-Marie Bonnet; Emmanuel Broussolle; Pierre Pollak; Marie Vidailhet; Michele De Mari; Roberto Marconi; S Medjbeur; Alessandro Filla; Giuseppe Meco; Yves Agid; Alexis Brice
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
American journal of human genetics 1998;63(1):88-94.
1998: G David; Alexandra Dürr; Giovanni Stevanin; G Cancel; Nacer Abbas; Ali Benomar; Samir Belal; Anne-Sophie Lebre; M Abada-Bendib; Djamel Grid; M Holmberg; Mohamed Yahyaoui; Faycal Hentati; Taïeb Chkili; Yves Agid; Alexis Brice
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).
Human molecular genetics 1998;7(2):165-70.
1998: G Cancel; Isabelle Gourfinkel-An; Giovanni Stevanin; O Didierjean; Nacer Abbas; Etienne C Hirsch; Yves Agid; Alexis Brice
Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph disease.
Human mutation 1998;11(1):23-7.
1997: G David; Nacer Abbas; Giovanni Stevanin; Alexandra Dürr; Gaël Yvert; G Cancel; C Weber; G Imbert; Frédéric Saudou; E Antoniou; Harry A Drabkin; Robert M Gemmill; Paola Giunti; Ali Benomar; Nicholas W Wood; Merle Ruberg; Yves Agid; Jean-Louis Mandel; Alexis Brice
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion.
Nature genetics 1997;17(1):65-70.
1997: Giovanni Stevanin; Anne-Sophie Lebre; C Mathieux; G Cancel; Nacer Abbas; O Didierjean; Alexandra Dürr; Yvon Trottier; Yves Agid; Alexis Brice
Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codon.
American journal of human genetics 1997;60(6):1548-52.
1997: G Cancel; Alexandra Dürr; O Didierjean; G Imbert; Katrin Bürk; Agnes Lezin; Samir Belal; Ali Benomar; M Abada-Bendib; C Vial; J Guimarães; H Chneiweiss; Giovanni Stevanin; Gaël Yvert; Nacer Abbas; Frédéric Saudou; Anne-Sophie Lebre; Mohamed Yahyaoui; Faycal Hentati; JC Vernant; Thomas Klockgether; Jean-Louis Mandel; Yves Agid; Alexis Brice
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.
Human molecular genetics 1997;6(5):709-15.
1996: Giovanni Stevanin; Yvon Trottier; G Cancel; Alexandra Dürr; G David; O Didierjean; Katrin Bürk; G Imbert; Frédéric Saudou; M Abada-Bendib; Isabelle Gourfinkel-An; Ali Benomar; Nacer Abbas; Thomas Klockgether; Djamel Grid; Yves Agid; Jean-Louis Mandel; Alexis Brice
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.
Human molecular genetics 1996;5(12):1887-92.
1996: G David; Paola Giunti; Nacer Abbas; Philippe Coullin; Giovanni Stevanin; W Horta; Robert M Gemmill; Jean Weissenbach; Nicholas W Wood; S Cunha; Harry A Drabkin; A E Harding; Yves Agid; Alexis Brice
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.
American journal of human genetics 1996;59(6):1328-36.
1996: G Imbert; Frédéric Saudou; Gaël Yvert; Didier Devys; Yvon Trottier; J M Garnier; C Weber; Jean-Louis Mandel; G Cancel; Nacer Abbas; Alexandra Dürr; O Didierjean; Giovanni Stevanin; Yves Agid; Alexis Brice
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats.
Nature genetics 1996;14(3):285-91.
1996: Shuichi Igarashi; Yoshihisa Takiyama; G Cancel; Ekaterina Rogaeva; H Sasaki; A Wakisaka; Y X Zhou; H Takano; K Endo; K Sanpei; Mutsuo Oyake; Hajime Tanaka; Giovanni Stevanin; Nacer Abbas; Alexandra Dürr; Evgeny I Rogaev; R Sherrington; T Tsuda; Masaki Ikeda; E Cassa; Masatoyo Nishizawa; Ali Benomar; J Julien; Jean Weissenbach; G X Wang; Yves Agid; Peter St George-Hyslop; Alexis Brice; S Tsuji
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.
Human molecular genetics 1996;5(7):923-32.
1996: J Lopes; Eric LeGuern; Riadh Gouider; Sandrine Tardieu; Nacer Abbas; Nazha Birouk; M Gugenheim; Pierre Bouche; Yves Agid; Alexis Brice
Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group.
American journal of human genetics 1996;58(6):1223-30.
1996: Alexandra Dürr; Giovanni Stevanin; G Cancel; Charles Duyckaerts; Nacer Abbas; O Didierjean; H Chneiweiss; Ali Benomar; Olivier Lyon-Caen; J Julien; M Serdaru; C Penet; Yves Agid; Alexis Brice
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
Annals of neurology 1996;39(4):490-9.
1996: Eric LeGuern; Riadh Gouider; Nicole Ravisé; J Lopes; Sandrine Tardieu; M Gugenheim; Nacer Abbas; Pierre Bouche; Yves Agid; Alexis Brice
A de novo case of hereditary neuropathy with liability to pressure palsies (HNPP) of maternal origin: a new mechanism for deletion in 17p11.2?
Human molecular genetics 1996;5(1):103-6.
1995: Giovanni Stevanin; G Cancel; O Didierjean; Alexandra Dürr; Nacer Abbas; E Cassa; J Feingold; Yves Agid; Alexis Brice
Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutation.
American journal of human genetics 1995;57(5):1247-50.
1995: Giovanni Stevanin; E Cassa; G Cancel; Nacer Abbas; Alexandra Dürr; E Jardim; Yves Agid; P S Sousa; Alexis Brice
Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph disease.
Journal of medical genetics 1995;32(10):827-30.
1995: G Cancel; Nacer Abbas; Giovanni Stevanin; Alexandra Dürr; H Chneiweiss; C Néri; Charles Duyckaerts; C Penet; H M Cann; Yves Agid
Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus.
American journal of human genetics 1995;57(4):809-16.
1995: Alexandra Dürr; Giovanni Stevanin; G Cancel; Nacer Abbas; H Chneiweiss; Yves Agid; J Feingold; Alexis Brice
Gender equality in Machado-Joseph disease.
Nature genetics 1995;11(2):118-9.
1995: Eric LeGuern; Riadh Gouider; J Lopes; Nacer Abbas; M Gugenheim; Sandrine Tardieu; Nicole Ravisé; Jean-Marc Léger; Jean-Michel Vallat; Pierre Bouche
Constant rearrangement of the CMT1A-REP sequences in HNPP patients with a deletion in chromosome 17p11.2: a study of 30 unrelated cases. The French CMT Collaborative Research Group.
Human molecular genetics 1995;4(9):1673-4.