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M G Mattei

Showing results (251-260 of 427) with videos related to

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Genomics|September 11, 2001
Identification of MAL2, a novel member of the mal proteolipid family, though interactions with TPD52-like proteins in the yeast two-hybrid systemS H Wilson, A M Bailey, C R Nourse, et al.
The Journal of Biological Chemistry|February 7, 1998
A novel, secreted form of human ADAM 12 (meltrin alpha) provokes myogenesis in vivoB J Gilpin, F Loechel, M G Mattei, et al.
Journal De Genetique Humaine|December 1, 1984
[Reciprocal translocation at the origin of a Robertsonian translocation 15;22 by the loss of a metacentric chromosome. Genetic counseling]H Pison, M G Mattei, H Jalbert, et al.
DNA and Cell Biology|December 1, 1994
The mouse homeoprotein mLIM-3 is expressed early in cells derived from the neuroepithelium and persists in adult pituitaryN G Seidah, J C Barale, M Marcinkiewicz, et al.
Human Genetics|November 1, 1988
Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridizationM C Pellissier, M Laffage, N Philip, et al.
Journal of Medical Genetics|September 1, 1991
Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new casesA Moncla, M O Livet, M Auger, et al.
Gene|December 29, 1995
Cloning of the mouse gene encoding plasma glutathione peroxidase: organization, sequence and chromosomal localizationV Schwaab, E Baud, N Ghyselinck, et al.
Human Genetics|December 1, 1986
Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14-q21M G Mattei, Y Colin, C Le Van Kim, et al.
FEBS Letters|July 14, 1997
Tissue-specific expression of the human laminin alpha5-chain, and mapping of the gene to human chromosome 20q13.2-13.3 and to distal mouse chromosome 2 near the locus for the ragged (Ra) mutationM E Durkin, F Loechel, M G Mattei, et al.
Human Genetics|January 1, 1990
In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13J Castella-Escola, M G Mattei, D M Ojcius, et al.
Pageof 43

Showing results (251-260 of 427) with videos related to

Sort By:
Pageof 43
Genomics|September 11, 2001
Identification of MAL2, a novel member of the mal proteolipid family, though interactions with TPD52-like proteins in the yeast two-hybrid systemS H Wilson, A M Bailey, C R Nourse, et al.
The Journal of Biological Chemistry|February 7, 1998
A novel, secreted form of human ADAM 12 (meltrin alpha) provokes myogenesis in vivoB J Gilpin, F Loechel, M G Mattei, et al.
Journal De Genetique Humaine|December 1, 1984
[Reciprocal translocation at the origin of a Robertsonian translocation 15;22 by the loss of a metacentric chromosome. Genetic counseling]H Pison, M G Mattei, H Jalbert, et al.
DNA and Cell Biology|December 1, 1994
The mouse homeoprotein mLIM-3 is expressed early in cells derived from the neuroepithelium and persists in adult pituitaryN G Seidah, J C Barale, M Marcinkiewicz, et al.
Human Genetics|November 1, 1988
Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridizationM C Pellissier, M Laffage, N Philip, et al.
Journal of Medical Genetics|September 1, 1991
Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new casesA Moncla, M O Livet, M Auger, et al.
Gene|December 29, 1995
Cloning of the mouse gene encoding plasma glutathione peroxidase: organization, sequence and chromosomal localizationV Schwaab, E Baud, N Ghyselinck, et al.
Human Genetics|December 1, 1986
Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14-q21M G Mattei, Y Colin, C Le Van Kim, et al.
FEBS Letters|July 14, 1997
Tissue-specific expression of the human laminin alpha5-chain, and mapping of the gene to human chromosome 20q13.2-13.3 and to distal mouse chromosome 2 near the locus for the ragged (Ra) mutationM E Durkin, F Loechel, M G Mattei, et al.
Human Genetics|January 1, 1990
In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13J Castella-Escola, M G Mattei, D M Ojcius, et al.
Pageof 43