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J L Mandel

Showing results (91-100 of 257) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxiaR Fujita, A Hanauer, G Sirugo, et al.
Biochemical and Biophysical Research Communications|January 6, 1970
Alpha-amanitin: a specific inhibitor of one of two DNA-pendent RNA polymerase activities from calf thymusC Kedinger, M Gniazdowski, J L Mandel, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasiaM C Vincent, V Biancalana, D Ginisty, et al.
Cytogenetics and Cell Genetics|January 1, 1985
Report of the Committee on Human Gene Mapping by Recombinant DNA TechniquesH F Willard, M H Skolnick, P L Pearson, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)C Broccardo, N Troffer-Charlier, S Savary, et al.
Human Mutation|September 30, 1999
Identification of novel mutations in the MTM1 gene causing severe and mild forms of X-linked myotubular myopathyA Buj-Bello, V Biancalana, C Moutou, et al.
Genomics|November 23, 2000
Characterization of the adrenoleukodystrophy-related (ALDR, ABCD2) gene promoter: inductibility by retinoic acid and forskolinA Pujol, N Troffer-Charlier, E Metzger, 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.
American Journal of Medical Genetics|July 15, 1994
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream regionY Trottier, G Imbert, A Poustka, et al.
Human Genetics|October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal markerA Hanauer, Y Alembik, B Arveiler, et al.
Pageof 26

Showing results (91-100 of 257) with videos related to

Sort By:
Pageof 26
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxiaR Fujita, A Hanauer, G Sirugo, et al.
Biochemical and Biophysical Research Communications|January 6, 1970
Alpha-amanitin: a specific inhibitor of one of two DNA-pendent RNA polymerase activities from calf thymusC Kedinger, M Gniazdowski, J L Mandel, et al.
European Journal of Human Genetics : EJHG|May 30, 2001
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasiaM C Vincent, V Biancalana, D Ginisty, et al.
Cytogenetics and Cell Genetics|January 1, 1985
Report of the Committee on Human Gene Mapping by Recombinant DNA TechniquesH F Willard, M H Skolnick, P L Pearson, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Exon organisation of the mouse gene encoding the Adrenoleukodystrophy related protein (ALDRP)C Broccardo, N Troffer-Charlier, S Savary, et al.
Human Mutation|September 30, 1999
Identification of novel mutations in the MTM1 gene causing severe and mild forms of X-linked myotubular myopathyA Buj-Bello, V Biancalana, C Moutou, et al.
Genomics|November 23, 2000
Characterization of the adrenoleukodystrophy-related (ALDR, ABCD2) gene promoter: inductibility by retinoic acid and forskolinA Pujol, N Troffer-Charlier, E Metzger, 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.
American Journal of Medical Genetics|July 15, 1994
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream regionY Trottier, G Imbert, A Poustka, et al.
Human Genetics|October 1, 1988
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal markerA Hanauer, Y Alembik, B Arveiler, et al.
Pageof 26