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J L Mandel

Showing results (201-210 of 257) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 1, 1984
Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus)G Camerino, K H Grzeschik, M Jaye, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Genomic organization of the MTM1 gene implicated in X-linked myotubular myopathyJ Laporte, C Guiraud-Chaumeil, S M Tanner, et al.
Nature|February 25, 1993
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transportersJ Mosser, A M Douar, C O Sarde, et al.
Nature Genetics|June 1, 1996
A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeastJ Laporte, L J Hu, C Kretz, et al.
Science (New York, N.Y.)|October 2, 1992
Genome maps III. 1992. Wall ChartJ L Mandel, A P Monaco, D L Nelson, et al.
Human Molecular Genetics|February 1, 1994
The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane proteinJ Mosser, Y Lutz, M E Stoeckel, et al.
American Journal of Medical Genetics|April 1, 1992
Methylation and mutation patterns in the fragile X syndromeH Malmgren, M L Steén-Bondeson, K H Gustavson, et al.
Nature Genetics|May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated formY Trottier, D Devys, G Imbert, et al.
Nature Genetics|February 1, 1995
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer proteinK Ouahchi, M Arita, H Kayden, et al.
Nature Genetics|May 13, 1999
A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardationK Merienne, S Jacquot, S Pannetier, et al.
Pageof 26

Showing results (201-210 of 257) with videos related to

Sort By:
Pageof 26
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1984
Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus)G Camerino, K H Grzeschik, M Jaye, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Genomic organization of the MTM1 gene implicated in X-linked myotubular myopathyJ Laporte, C Guiraud-Chaumeil, S M Tanner, et al.
Nature|February 25, 1993
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transportersJ Mosser, A M Douar, C O Sarde, et al.
Nature Genetics|June 1, 1996
A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeastJ Laporte, L J Hu, C Kretz, et al.
Science (New York, N.Y.)|October 2, 1992
Genome maps III. 1992. Wall ChartJ L Mandel, A P Monaco, D L Nelson, et al.
Human Molecular Genetics|February 1, 1994
The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane proteinJ Mosser, Y Lutz, M E Stoeckel, et al.
American Journal of Medical Genetics|April 1, 1992
Methylation and mutation patterns in the fragile X syndromeH Malmgren, M L Steén-Bondeson, K H Gustavson, et al.
Nature Genetics|May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated formY Trottier, D Devys, G Imbert, et al.
Nature Genetics|February 1, 1995
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer proteinK Ouahchi, M Arita, H Kayden, et al.
Nature Genetics|May 13, 1999
A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardationK Merienne, S Jacquot, S Pannetier, et al.
Pageof 26