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J L Mandel

Showing results (51-60 of 257) with videos related to

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Nucleic Acids Research|July 24, 1982
The ovalbumin gene family: complete sequence and structure of the Y geneR Heilig, R Muraskowsky, C Kloepfer, et al.
Nucleic Acids Research|July 11, 1988
A PstI RFLP for the human retinoic acid receptor in 17q21B Arveiler, M Petkovich, J L Mandel, et al.
Journal of Medical Genetics|December 1, 1991
Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutationF Rousseau, D Heitz, I Oberlé, et al.
Nucleic Acids Research|March 11, 1983
Repetitive satellite-like sequences are present within or upstream from 3 avian protein-coding genesL Maroteaux, R Heilig, D Dupret, et al.
Genomics|February 1, 1990
A 195-kb cosmid walk encompassing the human Xq28 color vision pigment genesR Feil, P Aubourg, R Heilig, et al.
Neurobiology of Disease|January 1, 1997
Analysis of domains affecting intracellular localization of the FMRP proteinB Bardoni, A Sittler, Y Shen, et al.
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.
Genomics|June 1, 1994
The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27G Imbert, Y Trottier, J Beckmann, et al.
Human Genetics|January 1, 1985
A new MspI restriction fragment length polymorphism in the hemophilia B locusG Camerino, I Oberlé, D Drayna, et al.
Human Genetics|April 1, 1989
A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosomeA Vincent, C Kretz, I Oberlé, et al.
Pageof 26

Showing results (51-60 of 257) with videos related to

Sort By:
Pageof 26
Nucleic Acids Research|July 24, 1982
The ovalbumin gene family: complete sequence and structure of the Y geneR Heilig, R Muraskowsky, C Kloepfer, et al.
Nucleic Acids Research|July 11, 1988
A PstI RFLP for the human retinoic acid receptor in 17q21B Arveiler, M Petkovich, J L Mandel, et al.
Journal of Medical Genetics|December 1, 1991
Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutationF Rousseau, D Heitz, I Oberlé, et al.
Nucleic Acids Research|March 11, 1983
Repetitive satellite-like sequences are present within or upstream from 3 avian protein-coding genesL Maroteaux, R Heilig, D Dupret, et al.
Genomics|February 1, 1990
A 195-kb cosmid walk encompassing the human Xq28 color vision pigment genesR Feil, P Aubourg, R Heilig, et al.
Neurobiology of Disease|January 1, 1997
Analysis of domains affecting intracellular localization of the FMRP proteinB Bardoni, A Sittler, Y Shen, et al.
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.
Genomics|June 1, 1994
The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27G Imbert, Y Trottier, J Beckmann, et al.
Human Genetics|January 1, 1985
A new MspI restriction fragment length polymorphism in the hemophilia B locusG Camerino, I Oberlé, D Drayna, et al.
Human Genetics|April 1, 1989
A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosomeA Vincent, C Kretz, I Oberlé, et al.
Pageof 26