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M G Mattei

Showing results (361-370 of 427) with videos related to

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American Journal of Human Genetics|April 1, 1991
Human elastin gene: new evidence for localization to the long arm of chromosome 7M J Fazio, M G Mattei, E Passage, et al.
Human Molecular Genetics|June 1, 1994
A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and humanA I Agulnik, M J Mitchell, M G Mattei, et al.
Molecular Endocrinology (Baltimore, Md.)|January 1, 1991
Cloning and primary sequence of a mouse candidate prohormone convertase PC1 homologous to PC2, Furin, and Kex2: distinct chromosomal localization and messenger RNA distribution in brain and pituitary compared to PC2N G Seidah, M Marcinkiewicz, S Benjannet, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1993
The gene coding for the alpha 1 subunit of the skeletal dihydropyridine receptor (Cchl1a3 = mdg) maps to mouse chromosome 1 and human 1q32B Drouet, L Garcia, D Simon-Chazottes, et al.
Nature|July 25, 1991
Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genesB Lee, M Godfrey, E Vitale, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 1, 1997
Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related proteinC Taylor, R Wadey, H O'Donnell, et al.
Genomics|August 10, 1995
Identification of four novel human genes amplified and overexpressed in breast carcinoma and localized to the q11-q21.3 region of chromosome 17C Tomasetto, C Régnier, C Moog-Lutz, et al.
European Journal of Pediatrics|November 1, 1994
Clinical and molecular study of DiGeorge sequenceA Levy-Mozziconacci, F Wernert, P Scambler, et al.
European Journal of Biochemistry|February 15, 1988
Characterization of cDNA clones for human glycophorin A. Use for gene localization and for analysis of normal of glycophorin-A-deficient (Finnish type) genomic DNAC Rahuel, J London, L d'Auriol, et al.
Human Genetics|March 1, 1989
Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardationM A Voelckel, N Philip, C Piquet, et al.
Pageof 43

Showing results (361-370 of 427) with videos related to

Sort By:
Pageof 43
American Journal of Human Genetics|April 1, 1991
Human elastin gene: new evidence for localization to the long arm of chromosome 7M J Fazio, M G Mattei, E Passage, et al.
Human Molecular Genetics|June 1, 1994
A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and humanA I Agulnik, M J Mitchell, M G Mattei, et al.
Molecular Endocrinology (Baltimore, Md.)|January 1, 1991
Cloning and primary sequence of a mouse candidate prohormone convertase PC1 homologous to PC2, Furin, and Kex2: distinct chromosomal localization and messenger RNA distribution in brain and pituitary compared to PC2N G Seidah, M Marcinkiewicz, S Benjannet, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1993
The gene coding for the alpha 1 subunit of the skeletal dihydropyridine receptor (Cchl1a3 = mdg) maps to mouse chromosome 1 and human 1q32B Drouet, L Garcia, D Simon-Chazottes, et al.
Nature|July 25, 1991
Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genesB Lee, M Godfrey, E Vitale, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 1, 1997
Cloning and mapping of murine Dgcr2 and its homology to the Sez-12 seizure-related proteinC Taylor, R Wadey, H O'Donnell, et al.
Genomics|August 10, 1995
Identification of four novel human genes amplified and overexpressed in breast carcinoma and localized to the q11-q21.3 region of chromosome 17C Tomasetto, C Régnier, C Moog-Lutz, et al.
European Journal of Pediatrics|November 1, 1994
Clinical and molecular study of DiGeorge sequenceA Levy-Mozziconacci, F Wernert, P Scambler, et al.
European Journal of Biochemistry|February 15, 1988
Characterization of cDNA clones for human glycophorin A. Use for gene localization and for analysis of normal of glycophorin-A-deficient (Finnish type) genomic DNAC Rahuel, J London, L d'Auriol, et al.
Human Genetics|March 1, 1989
Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardationM A Voelckel, N Philip, C Piquet, et al.
Pageof 43