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G Mattei

Showing results (181-190 of 385) with videos related to

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Genomics|September 1, 1991
Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptorF Libert, E Passage, M Parmentier, et al.
Genomics|July 1, 1992
Assignment of the human stromelysin 3 (STMY3) gene to the q11.2 region of chromosome 22A Levy, J Zucman, O Delattre, et al.
Molecular and Cellular Biology|October 1, 1992
Characterization of Spi-B, a transcription factor related to the putative oncoprotein Spi-1/PU.1D Ray, R Bosselut, J Ghysdael, et al.
Genomics|November 1, 1989
Human laminin A chain (LAMA) gene: chromosomal mapping to locus 18p11.3T Nagayoshi, M G Mattei, E Passage, et al.
Genomics|July 15, 1994
The fibulin-1 gene (FBLN1) is located on human chromosome 22 and on mouse chromosome 15M G Mattei, T C Pan, R Z Zhang, et al.
Journal of Mental Deficiency Research|September 1, 1979
Erythrocyte copper levels in children with trisomy 21B Mallet, P Poulet, S Ayme, et al.
Materials Science & Engineering. C, Materials for Biological Applications|November 28, 2014
Bone scaffolds with homogeneous and discrete gradient mechanical propertiesC Jelen, G Mattei, F Montemurro, et al.
Human Genetics|January 1, 1987
Monosomy 21: a new case confirmed by in situ hybridizationM C Pellissier, N Philip, M A Voelckel-Baeteman, et al.
Human Genetics|December 1, 1988
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardationM A Voelckel, M G Mattei, C N'Guyen, et al.
Development (Cambridge, England)|January 1, 1987
Mapping the mouse X chromosome: possible symmetry in the location of a family of sequences on the mouse X and Y chromosomesP Avner, C Bishop, L Amar, et al.
Pageof 39

Showing results (181-190 of 385) with videos related to

Sort By:
Pageof 39
Genomics|September 1, 1991
Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptorF Libert, E Passage, M Parmentier, et al.
Genomics|July 1, 1992
Assignment of the human stromelysin 3 (STMY3) gene to the q11.2 region of chromosome 22A Levy, J Zucman, O Delattre, et al.
Molecular and Cellular Biology|October 1, 1992
Characterization of Spi-B, a transcription factor related to the putative oncoprotein Spi-1/PU.1D Ray, R Bosselut, J Ghysdael, et al.
Genomics|November 1, 1989
Human laminin A chain (LAMA) gene: chromosomal mapping to locus 18p11.3T Nagayoshi, M G Mattei, E Passage, et al.
Genomics|July 15, 1994
The fibulin-1 gene (FBLN1) is located on human chromosome 22 and on mouse chromosome 15M G Mattei, T C Pan, R Z Zhang, et al.
Journal of Mental Deficiency Research|September 1, 1979
Erythrocyte copper levels in children with trisomy 21B Mallet, P Poulet, S Ayme, et al.
Materials Science & Engineering. C, Materials for Biological Applications|November 28, 2014
Bone scaffolds with homogeneous and discrete gradient mechanical propertiesC Jelen, G Mattei, F Montemurro, et al.
Human Genetics|January 1, 1987
Monosomy 21: a new case confirmed by in situ hybridizationM C Pellissier, N Philip, M A Voelckel-Baeteman, et al.
Human Genetics|December 1, 1988
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardationM A Voelckel, M G Mattei, C N'Guyen, et al.
Development (Cambridge, England)|January 1, 1987
Mapping the mouse X chromosome: possible symmetry in the location of a family of sequences on the mouse X and Y chromosomesP Avner, C Bishop, L Amar, et al.
Pageof 39