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Auteur Cancel G

Documents disponibles écrits par cet auteur (22)

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Article

Journal of medical genetics, 36, 5. Linkage disequilibrium at the SCA2 locus

Didierjean O ; Cancel G ; Stevanin G ; Durr A ; Burk K ; Benomar A ; Lezin A ; Belal S ; Abada-Bendid M ; Klockgether T ; Brice A | 1999

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Nature genetics, 17, 1. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

David G ; Abbas N ; Stevanin G ; Durr A ; Yvert G ; Cancel G ; Weber C ; Imbert G ; Saudou F ; Antoniou E ; Drabkin H ; Gemmill R ; Giunti P ; Benomar A ; Wood N ; Ruberg M ; Agid Y ; Mandel JL ; Brice A | 1997

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Article

Annals of neurology, 39, 4. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features

Durr A ; Stevanin G ; Cancel G ; Duyckaerts C ; Abbas N ; Didierjean O ; Chneiweiss H ; Benomar A ; Lyon-Caen O ; Julien J ; Serdaru M ; Penet C ; Agid Y ; Brice A | 1996

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Article

Human genetics, 97, 5. Autosomal dominant cerebellar ataxia type 1 in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families

Lezin A ; Cancel G ; Stevanin G ; Smadja D ; Vernant JC ; Durr A ; Martial J ; Buisson GG ; Bellance R ; Chneiweiss H ; Agid Y ; Brice A | 1996

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Article

Human molecular genetics, 5, 7. 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

Igarashi S ; Takiyama Y ; Cancel G ; Rogaeva EA ; Sasaki H ; Wakisaka A ; Zhou YX ; Takano H ; Endo K ; Sanpei K ; Oyake M ; Tanaka H ; Stevanin G ; Abbas N ; Durr A ; Rogaev EI ; Sherrington R ; Tsuda T ; Ikeda M ; Cassa E ; Nishizawa M ; Benomar A ; Julien J ; Weissenbach J ; Wang GX ; Agid Y ; Saint-George-Hyslop PH ; Brice A ; Tsuji S | 1996

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Article

Revue neurologique, 151, 11. La forme ataxo-choréique de DRPLA existe-t-elle en Europe ? Recherche de la mutation dans 120 familles : Does the ataxo-choreic form of DRPLA exist in Europe? Search of mutation in 120 families

Dubourg O ; Durr A ; Chneiweiss H ; Stevanin G ; Cancel G ; Penet C ; Agid Y ; Brice A | 1995

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Article

American journal of human genetics (The), 57, 4. Localization of the candidate gene D-amino acid oxidase outside the refined I-cM region of spinocerebellar ataxia 2

Gispert S ; Lunkes A ; Santos N ; Orozco G ; Ha-Hao D ; Ratzlaff T ; Aguiar J ; Torrens I ; Heredero L ; Brice A ; Cancel G ; Stevanin G ; Vernant JC ; Durr A ; Lepage-Lezin A ; Belal S ; Ben Hamida M ; Pulst S ; Rouleau G ; Weissenbach J ; Le Paslier D ; Kucherlapati R ; Montgomery K ; Fukui K ; Auburger G | 1995

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Article

American journal of human genetics (The), 57, 4. Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locus

Cancel G ; Abbas N ; Stevanin G ; Durr A ; Chneiweiss H ; Néri C ; Duyckaerts C ; Penet C ; Cann HM ; Agid Y ; Brice A | 1995

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Article

American journal of human genetics (The), 57, 5. 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

Stevanin G ; Cancel G ; Didierjean O ; Durr A ; Abbas N ; Cassa E ; Feingold J ; Agid Y ; Brice A | 1995

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Article

American Journal of Medical Genetics, 60, 5. SCA2 is not a major locus for ADCA type 1 in French families

Cancel G ; Stevanin G ; Durr A ; Chneiweiss H ; Penet C ; Pothin Y ; Agid Y ; Brice A | 1995

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Article

Annals of neurology, 37, 2. Analysis of the SCA1 CAG repeat in a large number of families with dominant ataxia: clinical and molecular correlations

Dubourg O ; Durr A ; Cancel G ; Stevanin G ; Chneiweiss H ; Penet C ; Agid Y ; Brice A | 1995

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Article

Brain, 118, 6. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families

Durr A ; Smadja D ; Cancel G ; Lezin A ; Stevanin G ; Mikol J ; Bellance R ; Buisson GG ; Chneiweiss H ; Dellanave J ; Agid Y ; Brice A ; Vernant JC | 1995

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Article

Journal of medical genetics, 32, 10. Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph disease

Stevanin G ; Cassa E ; Cancel G ; Abbas N ; Durr A ; Jardim E ; Agid Y ; Sousa PS ; Brice A | 1995

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Article

Nature, 378, 403-406. Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

Trottier Y ; Lutz Y ; Stevanin G ; Imbert G ; Devys D ; Cancel G ; Saudou F ; Weber C ; David G ; Tora L ; Agid Y ; Brice A ; Mandel JL | 1995

Accès au résumé PubMed / to PubMed abstract

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Nature, 378. Poluglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

Trottier Y ; Lutz Y ; Stevanin G ; Imbert G ; Devys D ; Cancel G ; Saudou F ; Weber C ; David G ; Tora L ; Agid Y ; Brice A ; Mandel JL | 1995

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Article

Nature genetics, 10. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1

Benomar A ; Krols L ; Cancel G ; Stevanin G ; Le Guern E ; David G ; Ouhabi H ; Martin JJ ; Durr A ; Zaim A ; Ravisé N ; Busque C ; Penet C ; van Regemorter N ; Weissenbach J ; Yahyaoui M ; Chkili T ; Agid Y ; Brice A | 1995

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Article

Nature genetics, 11, 2. Gender equality in Machado-Joseph disease

Durr A ; Stevanin G ; Cancel G ; Abbas N ; Chneiweiss H ; Agid Y ; Feingold J ; Brice A | 1995

Comment on: Unique features of the CAG repeats in Machado-Joseph disease. Kawakami H, Maruyama H, Nakamura S, Kawaguchi Y, Kakizuka A, Doyu M, Sobue G. Nat Genet. 1995 Apr;9(4):344-5.

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Article

American journal of human genetics (The), 54, 1. A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus

Stevanin G ; Le Guern E ; Ravisé N ; Chneiweiss H ; Durr A ; Cancel G ; Vignal A ; Boch AL ; Ruberg M ; Penet C ; Pothin Y ; Lagroua I ; Haguenau M ; Rancurel G ; Weissenbach J ; Agid Y ; Brice A | 1994

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Article

Nature genetics, 6, 1. Is DRPLA also linked to 14q?

Cancel G ; Durr A ; Stevanin G ; Chneiweiss H ; Duyckaerts C ; Serdaru M ; de Toffol B ; Agid Y ; Brice A | 1994

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Article

Neurology, 44, 8. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus

Belal S ; Cancel G ; Stevanin G ; Hentati F ; Khati C ; Ben Hamida C ; Auburger G ; Agid Y ; Ben Hamida M | 1994

Accès au résumé PubMed / to PubMed abstract

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Article

Brain, 116, 6. Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity

Durr A ; Chneiweiss H ; Khati C ; Stevanin G ; Cancel G ; Feingold J ; Agid Y ; Brice A | 1993

Accès au résumé PubMed / to PubMed abstract

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Article

Human molecular genetics, 2, 9. Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1

Cancel G ; Khati C ; Stevanin G ; Pages JC ; Agid Y ; Brice A ; Cann HM | 1993

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Auteur Cancel G

Documents disponibles écrits par cet auteur (22)

Journal of medical genetics, 36, 5. Linkage disequilibrium at the SCA2 locus

Nature genetics, 17, 1. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

Annals of neurology, 39, 4. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features

Human genetics, 97, 5. Autosomal dominant cerebellar ataxia type 1 in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families

Human molecular genetics, 5, 7. 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

Revue neurologique, 151, 11. La forme ataxo-choréique de DRPLA existe-t-elle en Europe ? Recherche de la mutation dans 120 familles : Does the ataxo-choreic form of DRPLA exist in Europe? Search of mutation in 120 families

American journal of human genetics (The), 57, 4. Localization of the candidate gene D-amino acid oxidase outside the refined I-cM region of spinocerebellar ataxia 2

American journal of human genetics (The), 57, 4. 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 (The), 57, 5. 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 Medical Genetics, 60, 5. SCA2 is not a major locus for ADCA type 1 in French families

Annals of neurology, 37, 2. Analysis of the SCA1 CAG repeat in a large number of families with dominant ataxia: clinical and molecular correlations

Brain, 118, 6. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families

Journal of medical genetics, 32, 10. Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph disease

Nature, 378, 403-406. Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

Nature, 378. Poluglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

Nature genetics, 10. The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1

Nature genetics, 11, 2. Gender equality in Machado-Joseph disease

American journal of human genetics (The), 54, 1. A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus

Nature genetics, 6, 1. Is DRPLA also linked to 14q?

Neurology, 44, 8. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus

Brain, 116, 6. Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity

Human molecular genetics, 2, 9. Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1