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D Devys

Showing results (1-10 of 26) with videos related to

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Current Biology : CB|November 1, 1993
An expanding storyY Trottier, D Devys, J L Mandel
The Journal of Biological Chemistry|March 28, 1997
SH3 domain-dependent association of huntingtin with epidermal growth factor receptor signaling complexesY F Liu, R C Deth, D Devys
Human Molecular Genetics|January 1, 1996
Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoformsA Sittler, D Devys, C Weber, et al.
Cell|October 20, 1998
Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusionsF Saudou, S Finkbeiner, D Devys, et al.
American Journal of Human Genetics|January 1, 1995
Quantitative comparison of FMR1 gene expression in normal and premutation allelesY Feng, L Lakkis, D Devys, et al.
Journal of Medical Genetics|November 1, 1992
Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutationD Heitz, D Devys, G Imbert, et al.
Advances in Experimental Medicine and Biology|June 14, 2001
Pathological mechanisms in polyglutamine expansion diseasesD Devys, G Yvert, A Lunkes, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Mental retardation in fragile X syndrome]J L Mandel, V Biancalana, M Cossée, et al.
Nature Genetics|August 1, 1993
The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutationD Devys, Y Lutz, N Rouyer, et al.
EXS|January 1, 1993
Microsatellites and disease: a new paradigmK Wrogemann, V Biancalana, D Devys, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Current Biology : CB|November 1, 1993
An expanding storyY Trottier, D Devys, J L Mandel
The Journal of Biological Chemistry|March 28, 1997
SH3 domain-dependent association of huntingtin with epidermal growth factor receptor signaling complexesY F Liu, R C Deth, D Devys
Human Molecular Genetics|January 1, 1996
Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoformsA Sittler, D Devys, C Weber, et al.
Cell|October 20, 1998
Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusionsF Saudou, S Finkbeiner, D Devys, et al.
American Journal of Human Genetics|January 1, 1995
Quantitative comparison of FMR1 gene expression in normal and premutation allelesY Feng, L Lakkis, D Devys, et al.
Journal of Medical Genetics|November 1, 1992
Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutationD Heitz, D Devys, G Imbert, et al.
Advances in Experimental Medicine and Biology|June 14, 2001
Pathological mechanisms in polyglutamine expansion diseasesD Devys, G Yvert, A Lunkes, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 1, 1996
[Mental retardation in fragile X syndrome]J L Mandel, V Biancalana, M Cossée, et al.
Nature Genetics|August 1, 1993
The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutationD Devys, Y Lutz, N Rouyer, et al.
EXS|January 1, 1993
Microsatellites and disease: a new paradigmK Wrogemann, V Biancalana, D Devys, et al.
Pageof 3