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J L Mandel

Showing results (41-50 of 257) with videos related to

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Human Molecular Genetics|November 11, 1999
A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) proteinB Bardoni, A Schenck, J L Mandel
Journal of Medical Genetics|May 1, 1994
Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onsetY Trottier, V Biancalana, J L Mandel
Nucleic Acids Research|December 23, 1988
Nucleotide sequence of chicken dystrophin cDNAC Lemaire, R Heilig, J L Mandel
Human Genetics|February 1, 1990
An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin geneC Oudet, R Heilig, J L Mandel
Nucleic Acids Research|December 20, 1979
DNA methylation: correlation with DNase I sensitivity of chicken ovalbumin and conalbumin chromatinM T Kuo, J L Mandel, P Chambon
American Journal of Medical Genetics|February 17, 2001
FMR1 gene and fragile X syndromeB Bardoni, J L Mandel, G S Fisch
Nucleic Acids Research|August 11, 1987
Presence of a TaqI polymorphism in the human glutamate dehydrogenase (GLUD) gene on chromosome 10A Hanauer, M G Mattei, J L Mandel
Nature Genetics|May 1, 1993
Origin of the expansion mutation in myotonic dystrophyG Imbert, C Kretz, K Johnson, et al.
Nucleic Acids Research|May 25, 1984
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long armM Koenig, G Camerino, R Heilig, et al.
Human Genetics|February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locusF Rousseau, A Vincent, I Oberlé, et al.
Pageof 26

Showing results (41-50 of 257) with videos related to

Sort By:
Pageof 26
Human Molecular Genetics|November 11, 1999
A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) proteinB Bardoni, A Schenck, J L Mandel
Journal of Medical Genetics|May 1, 1994
Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onsetY Trottier, V Biancalana, J L Mandel
Nucleic Acids Research|December 23, 1988
Nucleotide sequence of chicken dystrophin cDNAC Lemaire, R Heilig, J L Mandel
Human Genetics|February 1, 1990
An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin geneC Oudet, R Heilig, J L Mandel
Nucleic Acids Research|December 20, 1979
DNA methylation: correlation with DNase I sensitivity of chicken ovalbumin and conalbumin chromatinM T Kuo, J L Mandel, P Chambon
American Journal of Medical Genetics|February 17, 2001
FMR1 gene and fragile X syndromeB Bardoni, J L Mandel, G S Fisch
Nucleic Acids Research|August 11, 1987
Presence of a TaqI polymorphism in the human glutamate dehydrogenase (GLUD) gene on chromosome 10A Hanauer, M G Mattei, J L Mandel
Nature Genetics|May 1, 1993
Origin of the expansion mutation in myotonic dystrophyG Imbert, C Kretz, K Johnson, et al.
Nucleic Acids Research|May 25, 1984
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long armM Koenig, G Camerino, R Heilig, et al.
Human Genetics|February 1, 1990
New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locusF Rousseau, A Vincent, I Oberlé, et al.
Pageof 26