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G Imbert

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Chemicals & Drugs

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Publications

TOP 3
C Delluc; Nathalie Costedoat-Chalumeau; G Leroux; G Imbert; D Boutin Le Thi Huong; D Vauthier-Brouzes; Jean-Charles Piette; O Chazouilleres; Patrice Cacoub
[Liver disease and pregnancy].
Oliver H Wittekindt; Anna Jauch; Edgar Burgert; Lars O Schärer; Heidi Holtgreve-Grez; Gaël Yvert; G Imbert; J Zimmer; Margret R Hoehe; Jean-Paul Macher; P Chiaroni; Dietrich van Calker; Marc-Antoine Crocq; Deborah J Morris-Rosendahl
The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia.
Isabelle Gourfinkel-An; G Cancel; Yvon Trottier; Didier Devys; Làszlò Tora; Yves Lutz; G Imbert; Frédéric Saudou; Giovanni Stevanin; Yves Agid; Alexis Brice; Jean-Louis Mandel; Etienne C Hirsch
Differential distribution of the normal and mutated forms of huntingtin in the human brain.

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All Publications

2009: C Delluc; Nathalie Costedoat-Chalumeau; G Leroux; G Imbert; D Boutin Le Thi Huong; D Vauthier-Brouzes; Jean-Charles Piette; O Chazouilleres; Patrice Cacoub
[Liver disease and pregnancy].
La Revue de médecine interne / fondée ... par la Société nationale francaise de médecine interne 2009;30(6):508-15.
1998: Oliver H Wittekindt; Anna Jauch; Edgar Burgert; Lars O Schärer; Heidi Holtgreve-Grez; Gaël Yvert; G Imbert; J Zimmer; Margret R Hoehe; Jean-Paul Macher; P Chiaroni; Dietrich van Calker; Marc-Antoine Crocq; Deborah J Morris-Rosendahl
The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia.
Neurogenetics 1998;1(4):259-65.
1997: Isabelle Gourfinkel-An; G Cancel; Yvon Trottier; Didier Devys; Làszlò Tora; Yves Lutz; G Imbert; Frédéric Saudou; Giovanni Stevanin; Yves Agid; Alexis Brice; Jean-Louis Mandel; Etienne C Hirsch
Differential distribution of the normal and mutated forms of huntingtin in the human brain.
Annals of neurology 1997;42(5):712-9.
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: 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 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: Frédéric Saudou; Didier Devys; Yvon Trottier; G Imbert; M E Stoeckel; Alexis Brice; Jean-Louis Mandel
Polyglutamine expansions and neurodegenerative diseases.
Cold Spring Harbor symposia on quantitative biology 1996;61():639-47.
1995: Yvon Trottier; Yves Lutz; Giovanni Stevanin; G Imbert; Didier Devys; G Cancel; Frédéric Saudou; C Weber; G David; Làszlò Tora
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias.
Nature 1995;378(6555):403-6.
1995: Yvon Trottier; Didier Devys; G Imbert; Frédéric Saudou; I An; Yves Lutz; C Weber; Yves Agid; Etienne C Hirsch; Jean-Louis Mandel
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated form.
Nature genetics 1995;10(1):104-10.
1994: Yvon Trottier; G Imbert; A Poustka; J P Fryns; Jean-Louis Mandel
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region.
American journal of medical genetics 1994;51(4):454-7.
1994: G Imbert; Yvon Trottier; Jacques Beckmann; Jean-Louis Mandel
The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27.
Genomics 1994;21(3):667-8.
1993: G Imbert; Christine Kretz; keith jack johnson; Jean-Louis Mandel
Origin of the expansion mutation in myotonic dystrophy.
Nature genetics 1993;4(1):72-6.
1993: K Wrogemann; Valérie Biancalana; Didier Devys; G Imbert; Yvon Trottier; Jean-Louis Mandel
Microsatellites and disease: a new paradigm.
EXS 1993;67():141-52.
1992: D Heitz; Didier Devys; G Imbert; Christine Kretz; Jean-Louis Mandel
Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.
Journal of medical genetics 1992;29(11):794-801.