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A Ballabio

Showing results (171-180 of 200) with videos related to

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Human Gene Therapy|September 12, 2007
Safety of arylsulfatase A overexpression for gene therapy of metachromatic leukodystrophyA Capotondo, M Cesani, S Pepe, et al.
Genomics|March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)I Wang, B Franco, G B Ferrero, et al.
Cell|July 11, 1998
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloproteaseG Casari, M De Fusco, S Ciarmatori, et al.
Genomics|February 14, 2004
Molecular cloning and characterization of NEU4, the fourth member of the human sialidase gene familyE Monti, M T Bassi, R Bresciani, et al.
Nature|May 23, 1991
Characterization of a murine gene expressed from the inactive X chromosomeG Borsani, R Tonlorenzi, M C Simmler, et al.
The EMBO Journal|May 2, 2001
The tripartite motif family identifies cell compartmentsA Reymond, G Meroni, A Fantozzi, et al.
American Journal of Human Genetics|July 25, 2000
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationM Fukami, S Kirsch, S Schiller, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1997
Comparative mapping of Xp22 genes in hominoids--evolutionary linear instability of their Y homologuesB Gläser, F Grützner, K Taylor, et al.
Human Molecular Genetics|April 1, 1994
A gene from the Xp22.3 region shares homology with voltage-gated chloride channelsM A van Slegtenhorst, M T Bassi, G Borsani, et al.
Nature Genetics|July 1, 1993
A high resolution deletion map of human chromosome Xp22L Schaefer, G B Ferrero, A Grillo, et al.
Pageof 20

Showing results (171-180 of 200) with videos related to

Sort By:
Pageof 20
Human Gene Therapy|September 12, 2007
Safety of arylsulfatase A overexpression for gene therapy of metachromatic leukodystrophyA Capotondo, M Cesani, S Pepe, et al.
Genomics|March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)I Wang, B Franco, G B Ferrero, et al.
Cell|July 11, 1998
Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloproteaseG Casari, M De Fusco, S Ciarmatori, et al.
Genomics|February 14, 2004
Molecular cloning and characterization of NEU4, the fourth member of the human sialidase gene familyE Monti, M T Bassi, R Bresciani, et al.
Nature|May 23, 1991
Characterization of a murine gene expressed from the inactive X chromosomeG Borsani, R Tonlorenzi, M C Simmler, et al.
The EMBO Journal|May 2, 2001
The tripartite motif family identifies cell compartmentsA Reymond, G Meroni, A Fantozzi, et al.
American Journal of Human Genetics|July 25, 2000
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardationM Fukami, S Kirsch, S Schiller, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|May 1, 1997
Comparative mapping of Xp22 genes in hominoids--evolutionary linear instability of their Y homologuesB Gläser, F Grützner, K Taylor, et al.
Human Molecular Genetics|April 1, 1994
A gene from the Xp22.3 region shares homology with voltage-gated chloride channelsM A van Slegtenhorst, M T Bassi, G Borsani, et al.
Nature Genetics|July 1, 1993
A high resolution deletion map of human chromosome Xp22L Schaefer, G B Ferrero, A Grillo, et al.
Pageof 20