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M G Mattei

Showing results (331-340 of 427) with videos related to

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Nature|July 16, 1987
A new member of the immunoglobulin superfamily--CTLA-4J F Brunet, F Denizot, M F Luciani, et al.
Carcinogenesis|August 30, 2000
Molecular cloning and characterization of the human KIN17 cDNA encoding a component of the UVC response that is conserved among metazoansP Kannouche, P Mauffrey, G Pinon-Lataillade, et al.
Molecular Pharmacology|March 1, 1993
Mouse 5-hydroxytryptamine5A and 5-hydroxytryptamine5B receptors define a new family of serotonin receptors: cloning, functional expression, and chromosomal localizationH Matthes, U Boschert, N Amlaiky, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
Characterization of cDNAs encoding human leukosialin and localization of the leukosialin gene to chromosome 16A Pallant, A Eskenazi, M G Mattei, et al.
Human Genetics|April 1, 1986
The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosomeM G Mattei, P M Alliel, A Dautigny, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
Intrachromosomal triplication for the distal part of chromosome 15qC Schluth, M G Mattei, C Mignon-Ravix, et al.
Oncogene|October 1, 1993
Characterization of the murine Mpl proto-oncogene, a member of the hematopoietic cytokine receptor family: molecular cloning, chromosomal location and evidence for a function in cell growthI Vigon, C Florindo, S Fichelson, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.
American Journal of Medical Genetics. Part A|February 26, 2005
Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocationN Philip, L Colleaux, S Sigaudy, et al.
Human Genetics|January 1, 1985
Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X siteM G Mattei, M A Baeteman, R Heilig, et al.
Pageof 43

Showing results (331-340 of 427) with videos related to

Sort By:
Pageof 43
Nature|July 16, 1987
A new member of the immunoglobulin superfamily--CTLA-4J F Brunet, F Denizot, M F Luciani, et al.
Carcinogenesis|August 30, 2000
Molecular cloning and characterization of the human KIN17 cDNA encoding a component of the UVC response that is conserved among metazoansP Kannouche, P Mauffrey, G Pinon-Lataillade, et al.
Molecular Pharmacology|March 1, 1993
Mouse 5-hydroxytryptamine5A and 5-hydroxytryptamine5B receptors define a new family of serotonin receptors: cloning, functional expression, and chromosomal localizationH Matthes, U Boschert, N Amlaiky, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1989
Characterization of cDNAs encoding human leukosialin and localization of the leukosialin gene to chromosome 16A Pallant, A Eskenazi, M G Mattei, et al.
Human Genetics|April 1, 1986
The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosomeM G Mattei, P M Alliel, A Dautigny, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
Intrachromosomal triplication for the distal part of chromosome 15qC Schluth, M G Mattei, C Mignon-Ravix, et al.
Oncogene|October 1, 1993
Characterization of the murine Mpl proto-oncogene, a member of the hematopoietic cytokine receptor family: molecular cloning, chromosomal location and evidence for a function in cell growthI Vigon, C Florindo, S Fichelson, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approachP Malzac, A Moncla, M A Voelckel, et al.
American Journal of Medical Genetics. Part A|February 26, 2005
Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocationN Philip, L Colleaux, S Sigaudy, et al.
Human Genetics|January 1, 1985
Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X siteM G Mattei, M A Baeteman, R Heilig, et al.
Pageof 43