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G Mattei

Showing results (311-320 of 385) with videos related to

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Genomics|September 1, 1992
Homologous chromosomal locations of the four genes for inter-alpha-inhibitor and pre-alpha-inhibitor family in human and mouse: assignment of the ancestral gene for the lipocalin superfamilyJ P Salier, D Simon, P Rouet, et al.
The Journal of Biological Chemistry|February 14, 1997
Identification and characterization of a novel human matrix metalloproteinase with unique structural characteristics, chromosomal location, and tissue distributionA M Pendás, V Knäuper, X S Puente, et al.
Human Genetics|April 1, 1989
Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridizationM G Mattei, J P Périn, P M Alliel, et al.
Genomics|June 1, 1991
Genomic analysis of the 67-kDa laminin receptor in normal and pathological tissues: circumstantial evidence for retroposon featuresC Bignon, M Roux-Dosseto, M E Zeigler, et al.
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.
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.
Pageof 39

Showing results (311-320 of 385) with videos related to

Sort By:
Pageof 39
Genomics|September 1, 1992
Homologous chromosomal locations of the four genes for inter-alpha-inhibitor and pre-alpha-inhibitor family in human and mouse: assignment of the ancestral gene for the lipocalin superfamilyJ P Salier, D Simon, P Rouet, et al.
The Journal of Biological Chemistry|February 14, 1997
Identification and characterization of a novel human matrix metalloproteinase with unique structural characteristics, chromosomal location, and tissue distributionA M Pendás, V Knäuper, X S Puente, et al.
Human Genetics|April 1, 1989
Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridizationM G Mattei, J P Périn, P M Alliel, et al.
Genomics|June 1, 1991
Genomic analysis of the 67-kDa laminin receptor in normal and pathological tissues: circumstantial evidence for retroposon featuresC Bignon, M Roux-Dosseto, M E Zeigler, et al.
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.
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.
Pageof 39