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D Devys

Showing results (11-20 of 26) with videos related to

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American Journal of Medical Genetics|April 1, 1992
Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in developmentD Devys, V Biancalana, F Rousseau, et al.
American Journal of Medical Genetics|April 1, 1992
Prenatally detected fragile X females: long-term follow-up studies show high risk of mental impairmentW T Brown, E C Jenkins, P Goonewardena, et al.
Human Molecular Genetics|August 7, 2001
SCA7 mouse models show selective stabilization of mutant ataxin-7 and similar cellular responses in different neuronal cell typesG Yvert, K S Lindenberg, D Devys, et al.
Cell and Tissue Research|April 16, 2021
BBS4 protein has basal body/ciliary localization in sensory organs but extra-ciliary localization in oligodendrocytes during human developmentK Bénardais, G Delfino, B Samama, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Polyglutamine expansions and neurodegenerative diseasesF Saudou, D Devys, Y Trottier, et al.
Human Molecular Genetics|May 1, 1995
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell cultureE W Khandjian, A Fortin, A Thibodeau, et al.
Lancet (London, England)|May 6, 1995
Rapid antibody test for fragile X syndromeR Willemsen, S Mohkamsing, B de Vries, et al.
Nature|November 23, 1995
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxiasY Trottier, Y Lutz, G Stevanin, et al.
Science (New York, N.Y.)|May 24, 1991
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndromeI Oberlé, F Rousseau, D Heitz, et al.
Science (New York, N.Y.)|March 8, 1991
Isolation of sequences that span the fragile X and identification of a fragile X-related CpG islandD Heitz, F Rousseau, D Devys, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics|April 1, 1992
Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in developmentD Devys, V Biancalana, F Rousseau, et al.
American Journal of Medical Genetics|April 1, 1992
Prenatally detected fragile X females: long-term follow-up studies show high risk of mental impairmentW T Brown, E C Jenkins, P Goonewardena, et al.
Human Molecular Genetics|August 7, 2001
SCA7 mouse models show selective stabilization of mutant ataxin-7 and similar cellular responses in different neuronal cell typesG Yvert, K S Lindenberg, D Devys, et al.
Cell and Tissue Research|April 16, 2021
BBS4 protein has basal body/ciliary localization in sensory organs but extra-ciliary localization in oligodendrocytes during human developmentK Bénardais, G Delfino, B Samama, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Polyglutamine expansions and neurodegenerative diseasesF Saudou, D Devys, Y Trottier, et al.
Human Molecular Genetics|May 1, 1995
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell cultureE W Khandjian, A Fortin, A Thibodeau, et al.
Lancet (London, England)|May 6, 1995
Rapid antibody test for fragile X syndromeR Willemsen, S Mohkamsing, B de Vries, et al.
Nature|November 23, 1995
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxiasY Trottier, Y Lutz, G Stevanin, et al.
Science (New York, N.Y.)|May 24, 1991
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndromeI Oberlé, F Rousseau, D Heitz, et al.
Science (New York, N.Y.)|March 8, 1991
Isolation of sequences that span the fragile X and identification of a fragile X-related CpG islandD Heitz, F Rousseau, D Devys, et al.
Pageof 3