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Results:
1-16
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Results: 16
Authors:
SAUDOU F
FINKBEINER S
DEVYS D
GREENBERG ME
Citation: F. Saudou et al., HUNTINGTIN ACTS IN THE NUCLEUS TO INDUCE APOPTOSIS BUT DEATH DOES NOTCORRELATE WITH THE FORMATION OF INTRANUCLEAR INCLUSIONS, Cell (Cambridge), 95(1), 1998, pp. 55-66
Authors:
GOURFINKELAN I
CANCEL G
TROTTIER Y
DEVYS D
TORA L
LUTZ Y
IMBERT G
SAUDOU F
STEVANIN G
AGID Y
BRICE A
MANDEL JL
HIRSCH EC
Citation: I. Gourfinkelan et al., DIFFERENTIAL DISTRIBUTION OF THE NORMAL AND MUTATED FORMS OF HUNTINGTIN IN THE HUMAN BRAIN, Annals of neurology, 42(5), 1997, pp. 712-719
Authors:
LIU YF
DETH RC
DEVYS D
Citation: Yf. Liu et al., SH3 DOMAIN-DEPENDENT ASSOCIATION OF HUNTINGTON WITH EPIDERMAL GROWTH-FACTOR RECEPTOR SIGNALING COMPLEXES, The Journal of biological chemistry, 272(13), 1997, pp. 8121-8124
Authors:
IMBERT G
SAUDOU F
YVERT G
DEVYS D
TROTTIER Y
GARNIER JM
WEBER C
MANDEL JL
CANCEL G
ABBAS N
DURR A
DIDIERJEAN O
STEVANIN G
AGID Y
BRICE A
Citation: G. Imbert et al., CLONING OF THE GENE FOR SPINOCEREBELLAR ATAXIA-2 REVEALS A LOCUS WITHHIGH-SENSITIVITY TO EXPANDED CAG GLUTAMINE REPEATS/, Nature genetics, 14(3), 1996, pp. 285-291
Authors:
SITTLER A
DEVYS D
WEBER C
MANDEL JL
Citation: A. Sittler et al., ALTERNATIVE SPLICING OF EXON-14 DETERMINES NUCLEAR OR CYTOPLASMIC LOCALIZATION OF FMR1 PROTEIN ISOFORMS, Human molecular genetics, 5(1), 1996, pp. 95-102
Authors:
OOSTRA BA
WILLEMSEN R
MANDEL JL
DEVRIES B
DEVYS D
Citation: Ba. Oostra et al., RAPID SCREENING-TEST FOR FRAGILE-X SYNDROME, American journal of medical genetics, 64(1), 1996, pp. 18-18
Authors:
SAUDOU F
DEVYS D
TROTTIER Y
IMBERT G
STOECKEL ME
BRICE A
MANDEL JL
Citation: F. Saudou et al., POLYGLUTAMINE EXPANSIONS AND NEURODEGENERATIVE DISEASES, Cold Spring Harbor Symposia on Quantitative Biology, 61, 1996, pp. 639-647
Authors:
TROTTIER Y
DEVYS D
IMBERT G
SAUDOU F
AN I
LUTZ Y
WEBER C
AGID Y
HIRSCH EC
MANDEL JL
Citation: Y. Trottier et al., CELLULAR-LOCALIZATION OF THE HUNTINGTONS-DISEASE PROTEIN AND DISCRIMINATION OF THE NORMAL AND MUTATED FORM, Nature genetics, 10(1), 1995, pp. 104-110
Authors:
KHANDJIAN EW
FORTIN A
THIBODEAU A
TREMBLAY S
COTE F
DEVYS D
MANDEL JL
ROUSSEAU F
Citation: Ew. Khandjian et al., A HETEROGENEOUS SET OF FMR1 PROTEINS IS WIDELY DISTRIBUTED IN MOUSE-TISSUES AND IS MODULATED IN CELL-CULTURE, Human molecular genetics, 4(5), 1995, pp. 783-789
Authors:
WILLEMSEN R
MOHKAMSING S
DEVRIES B
DEVYS D
VANDENOUWELAND A
MANDEL JL
GALJAARD H
OOSTRA B
Citation: R. Willemsen et al., RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME, Lancet, 345(8958), 1995, pp. 1147-1148
Authors:
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
Citation: Y. Trottier et al., POLYGLUTAMINE EXPANSION AS A PATHOLOGICAL EPITOPE IN HUNTINGTONS-DISEASE AND 4 DOMINANT CEREBELLAR ATAXIAS, Nature, 378(6555), 1995, pp. 403-406
Authors:
WILLEMSEN R
BAKKER C
MANDEL JL
DEVRIES B
DEVYS D
OOSTRA BA
Citation: R. Willemsen et al., RAPID SCREENING-TEST FOR FRAGILE-X SYNDROME, American journal of human genetics, 57(4), 1995, pp. 1344-1344
Authors:
IMBERT G
SAUDOU F
DEVYS D
TROTTIER Y
WEBER C
LEMEUR M
MANDEL JL
Citation: G. Imbert et al., TRANSGENIC MICE AND NEUROBLASTOMA CELL-LINES CARRYING THE MUTATED HUNTINGTONS-DISEASE CDNA, American journal of human genetics, 57(4), 1995, pp. 1403-1403
Authors:
FENG Y
LAKKIS L
DEVYS D
WARREN ST
Citation: Y. Feng et al., QUANTITATIVE COMPARISON OF FMRI GENE-EXPRESSION IN NORMAL AND PREMUTATION ALLELES, American journal of human genetics, 56(1), 1995, pp. 106-113
Authors:
DEVYS D
LUTZ Y
ROUYER N
BELLOCQ JP
MANDEL JL
Citation: D. Devys et al., THE FMR-1 PROTEIN IS CYTOPLASMIC, MOST ABUNDANT IN NEURONS AND APPEARS NORMAL IN CARRIERS OF A FRAGILE X PREMUTATION, Nature genetics, 4(4), 1993, pp. 335-340
Authors:
TROTTIER Y
DEVYS D
MANDEL JL
Citation: Y. Trottier et al., FRAGILE-X SYNDROME - AN EXPANDING STORY, Current biology, 3(11), 1993, pp. 783-786
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1-16
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