Sfoglia per Autore

Mostrati risultati da 1 a 20 di 183
Titolo Data di pubblicazione Autore(i) File
Friedreich's disease. A linkage study in southern and central Italia 1-gen-1992 Cavalcanti, F; Cocozza, S; Filla, A; De Michele, G; Pianese, L; Porcellini, A; Monticelli, A; Pandolfo, M; Banfi, Sandro; Varrone S., And
An easy and rapid method for the detection of chimeric yeast artificial chromosome clones 1-gen-1992 Banfi, Sandro; Ledbetter, Sa; Chinault, Ac; Zoghbi, H. Y.
Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb 1-gen-1993 Banfi, Sandro; Chung, My; Kwiatkowski, Tj; J., R.; Ranum, Lp; Mccall, Ae; Chinault, Ac; Orr, Ht; Zoghbi, Hy
Epidemiological survey of hereditary ataxias and spastic paraplegias in Molise, Italia 1-gen-1993 Filla, A; De Michele, G; Santorelli, F; Banfi, Sandro; Campanella, G; Marconi, R; Rossi, B; Cavalcanti, F.
A double-blind cross-over trial of amantadine hydrochloride in Friedreich's ataxia 1-gen-1993 Filla, A; De Michele, G; Orefice, G; Santorelli, F; Trombetta, L; Banfi, Sandro; Squitieri, F; Napolitano, G; Puma, D; Campanella, G.
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1 1-gen-1993 Orr, Ht; Chung, My; Banfi, Sandro; Kwiatkowski, Tj; J., R.; Servadio, A; Beaudet, Al; Mccall, Ae; Duvick, La; Ranum, Lp; Zoghbi, Hy
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 locus 1-gen-1993 Kwiatkowski, Tj; J., R.; Orr, Ht; Banfi, Sandro; Mccall, Ae; Jodice, C; Persichetti, F; Novelletto, A; LeBorgne DeMarquoy, F; Duvick, La; Frontali M., And
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset 1-gen-1994 Ranum, Lp; Chung, My; Banfi, Sandro; Bryer, A; Schut, Lj; Ramesar, R; Duvick, La; Mccall, A; Subramony, Sh; Goldfarb L., And
Identification and characterization of the gene causing type 1 spinocerebellar ataxia 1-gen-1994 Banfi, Sandro; Servadio, A; Chung, My; Kwiatkowski, Tj; J., R.; Mccall, Ae; Duvick, La; Shen, Y; Roth, Ej; Orr, Ht; Zoghbi, Hy
Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family 1-gen-1995 Filla, A; De Michele, G; Banfi, Sandro; Santoro, L; Perretti, A; Cavalcanti, F; Pianese, L; Castaldo, I; Barbieri, F; Campanella G., And
Cloning and developmental expression analysis of the murine homolog of the spinocerebellar ataxia type 1 gene (Sca1) 1-gen-1996 Banfi, Sandro; Servadio, A; Chung, M; Capozzoli, F; Duvick, La; Elde, R; Zoghbi, Hy; Orr, Ht
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching 1-gen-1996 Banfi, Sandro; Borsani, G; Rossi, E; Bernard, L; Guffanti, A; Rubboli, F; Marchitiello, A; Giglio, S; Coluccia, E; Zollo, M; Zuffardi, O; Ballabio, A.
A novel zinc finger-containing RNA-binding protein conserved from fruitflies to humans 1-gen-1997 Jackson, Fr; Banfi, Sandro; Guffanti, A; Rossi, E.
Drosophila-related expressed sequences 1-gen-1997 Banfi, Sandro; Borsani, G; Bulfone, A; Ballabio, A.
A mammalian homologue of the Drosophila retinal degeneration B gene: implications for the evolution of phototransduction mechanisms 1-gen-1997 Rubboli, F; Bulfone, A; Bogni, S; Marchitiello, A; Zollo, M; Borsani, G; Ballabio, A; Banfi, Sandro
DRES search engine: of flies, men and ESTs 1-gen-1997 Guffanti, A; Banfi, Sandro; Simon, G; Ballabio, A; Borsani, G.
Sequencing analysis of forty-eight human IMAGE cDNA clones similar to Drosophila mutant protein 1-gen-1998 Volorio, S; Simon, G; Repetto, M; Cucciardi, M; Banfi, Sandro; Borsani, G; Ballabio, A; Zollo, M.
A practical guide to orient yourself in the labyrinth of genome databases 1-gen-1998 Borsani, G; Ballabio, A; Banfi, Sandro
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 sterility 1-gen-1998 Bione, S; Sala, C; Manzini, C; Arrigo, G; Zuffardi, O; Banfi, Sandro; Borsani, G; Jonveaux, P; Philippe, C; Zuccotti, M; Ballabio, A; Toniolo, D.
Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domains 1-gen-1998 de Conciliis, L; Marchitiello, A; Wapenaar, Mc; Borsani, G; Giglio, S; Mariani, M; Consalez, Gg; Zuffardi, O; Franco, B; Ballabio, A; Banfi, Sandro
Mostrati risultati da 1 a 20 di 183
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