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S Banfi

Showing results (61-70 of 75) with videos related to

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Nature Genetics|June 1, 1996
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searchingS Banfi, G Borsani, E Rossi, et al.
The British Journal of Ophthalmology|August 21, 2003
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian familiesF Simonelli, G Cennamo, C Ziviello, et al.
American Journal of Human Genetics|April 29, 1998
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterilityS Bione, C Sala, C Manzini, et al.
American Journal of Human Genetics|August 1, 1994
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onsetL P Ranum, M Y Chung, S Banfi, et al.
American Journal of Human Genetics|August 1, 1993
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusT J Kwiatkowski, H T Orr, S Banfi, et al.
Genomics|September 21, 2000
Cloning of PC3B, a novel member of the PC3/BTG/TOB family of growth inhibitory genes, highly expressed in the olfactory epitheliumP Buanne, G Corrente, L Micheli, et al.
Genomics|September 2, 1998
Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domainsL de Conciliis, A Marchitiello, M C Wapenaar, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1999
A homeobox gene, vax2, controls the patterning of the eye dorsoventral axisA M Barbieri, G Lupo, A Bulfone, et al.
Nature Genetics|August 1, 1994
Identification and characterization of the gene causing type 1 spinocerebellar ataxiaS Banfi, A Servadio, M Y Chung, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 3, 1998
Mice lacking ataxin-1 display learning deficits and decreased hippocampal paired-pulse facilitationA Matilla, E D Roberson, S Banfi, et al.
Pageof 8

Showing results (61-70 of 75) with videos related to

Sort By:
Pageof 8
Nature Genetics|June 1, 1996
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searchingS Banfi, G Borsani, E Rossi, et al.
The British Journal of Ophthalmology|August 21, 2003
Clinical features of X linked juvenile retinoschisis associated with new mutations in the XLRS1 gene in Italian familiesF Simonelli, G Cennamo, C Ziviello, et al.
American Journal of Human Genetics|April 29, 1998
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterilityS Bione, C Sala, C Manzini, et al.
American Journal of Human Genetics|August 1, 1994
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onsetL P Ranum, M Y Chung, S Banfi, et al.
American Journal of Human Genetics|August 1, 1993
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusT J Kwiatkowski, H T Orr, S Banfi, et al.
Genomics|September 21, 2000
Cloning of PC3B, a novel member of the PC3/BTG/TOB family of growth inhibitory genes, highly expressed in the olfactory epitheliumP Buanne, G Corrente, L Micheli, et al.
Genomics|September 2, 1998
Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domainsL de Conciliis, A Marchitiello, M C Wapenaar, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1999
A homeobox gene, vax2, controls the patterning of the eye dorsoventral axisA M Barbieri, G Lupo, A Bulfone, et al.
Nature Genetics|August 1, 1994
Identification and characterization of the gene causing type 1 spinocerebellar ataxiaS Banfi, A Servadio, M Y Chung, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 3, 1998
Mice lacking ataxin-1 display learning deficits and decreased hippocampal paired-pulse facilitationA Matilla, E D Roberson, S Banfi, et al.
Pageof 8