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Titolo Data di pubblicazione Autore(i) File
Inactivation of the mouse Huntington’s disease gene homolog (Hdh) 1-gen-1995 Duyao, Mp; Auerbach, Ab; Ryan, A; Persichetti, Francesca; Barnes, Gt; Mcneil, Sm; Ge, P; Vonsattel, Jp; Gusella, Jf; Joyner, Al; Macdonald, Me
CEPH consortium map of chromosome 14 1-gen-1995 Cox, Dw; Billingsley, Gd; Bale, Ae; COOPERATIVE HUMAN LINKAGE, Center; DONIS KELLER, H; Edwards, Jh; Litt, M; Mcbride, W; Persichetti, Francesca; Spurr, Nk; Weber, Jl; Weissenbach, J; White, Rl
Recurrent simple tandem repeat mutations during human Y chromosome radiation in Caucasian subpopulation 1-gen-1995 Ciminelli, Bm; Pompei, F; Malaspina, P; Hammer, M; Persichetti, Francesca; Pignatti, Pf; Palena, A; Anagnou, N; Guanti, G; Iodice, C; Terrenato, L; Novelletto, A.
Normal and expanded Huntington’s disease gene alleles produce distinguishable proteins due to translation across the CAG repeat 1-gen-1995 Persichetti, Francesca; Ambrose, Cm; Ge, P; Mcneil, Sm; Srinidhi, J; Anderson, Ma; Jenkins, B; Barnes, Gt; Duyao, Mp; Kanaley, L; Wexler, Ns; Myers, Rh; Bird, Ed; Vonsattel, Jp; Macdonald, Me; Gusella, Jf
Huntington’s disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains 1-gen-1994 Persichetti, Francesca; Srinidhi, J; Kanaley, L; Ge, P; Myers, Rh; Darrigo, K; Barnes, Gt; Macdonald, Me; Vonsattel, Jp; Gusella, Jf; Bird, Ed
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia 1 1-gen-1994 Iodice, C; Malaspina, P; Persichetti, Francesca; Novelletto, A; Spadaro, M; Giunti, P; Morocutti, C; Terrenato, L; Harding, Ae; Frontali, M.
The mouse Huntington’s disease gene homologue (Hdh) 1-gen-1994 Barnes, Gt; Duyao, Mp; Ambrose, Cm; MC NEIL, S; Persichetti, Francesca; Srinidhi, J; Gusella, Jf; Macdonald, Me
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease 1-gen-1994 Novelletto, A; Persichetti, Francesca; Sabbadini, G; Mandich, P; Bellone, E; Ajmar, F; Squitieri, F; Campanella, G; Bozza, A; Macdonald, Me; Gusella, Jf; Frontali, M.
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington’s disease 1-gen-1994 Novelletto, A; Persichetti, Francesca; Sabbadini, G; Mandich, P; Bellone, E; Ajmar, F; Pergola, M; DEL SENNO, L; Macdonald, Me; Gusella, Jf; Frontali, M.
Trinucleotide repeat length: instability and age of onset in Huntington’s disease 1-gen-1993 Duyao, Mp; Ambrose, Cm; Myers, Rh; Novelletto, A; Persichetti, Francesca; Frontali, M; Folstein, Se; Ross, C; Fran, Ml; Abbott, M; Gray, J; Conneally, Pm; Young, A; Penney, J; Hollingsworth, Z; Shoulson, I; Lazzarini, Am; Falek, A; Koroshetz, W; Bird, E; Vonsattel, Jp; Bonilla, E; Alvir, J; BICKAM CONDE, J; Cha, Jh; Dure, L; Gome, F; Ramos, M; SANCHEZ RAMOS, J; Snodgrass, Sr; DE YOUNG, M; Wexler, N; Barnes, G; Srinidhi, J; MAC DONALD, Me; Gusella, Jf
The gene for autosomal dominant spinocerebellar ataxia (SCA 1) 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; Orr, Ht; Banfi, S; Mccall, Ae; Iodice, C; Persichetti, Francesca; Novelletto, A; LE BORNIE DE MARQUOY, F; Duvick, La; Frontali, M; Subramony, Sh; Beaudet, Al; Terrenato, L; Zoghby, Hy; Ranum, Lpv
The gene for spinal cerebellar ataxia 1 (SCA 1) is flanked by two closely linked highly polymorphic microsatellite loci 1-gen-1993 Iodice, V; Frontali, M; Persichetti, Francesca; Novelletto, A; Pandolfo, M; Spadaro, M; Giunti, P; Schinaia, G; Lulli, P; Malaspina, P; Plasmati, R; Tola, R; Antonelli, A; DI DONATO, S; Morocutti, C; Weissenbach, J; Cann, Hm; Terrenato, L.
Disequilibrium of multiple DNA markers on the human Y chromosome 1-gen-1992 Persichetti, Francesca; Blasi, P; Hammer, M; Malaspina, P; Iodice, C; Terrenato, L; Novelletto, A.
Autosomal dominant pure cerebellar ataxia 1-gen-1992 Frontali, M; Spadaro, M; Giunti, P; Bianco, F; Iodice, C; Persichetti, Francesca; Colazza, Gb; Lulli, P; Terrenato, L; Morocutti, C.
HLA linked spinocerebellar ataxia: a clinical, neuropathologic and genetic study of large Italian kindreds 1-gen-1992 Spadaro, M; Giunti, P; Lulli, P; Frontali, M; Iodice, C; Cappellacci, S; Morellini, M; Persichetti, Francesca; Trabace, S; Anastasi, R; Morocutti, C.
Spinocerebellar ataxia (SCA 1) in two large Italian kindreds: evidence in favor of a locus position distal to GLO 1 and HLA cluster 1-gen-1991 Frontali, M; Iodice, C; Lulli, P; Spadaro, M; Cappellacci, S; Giunti, P; Malaspina, P; Morellini, M; Morocutti, C; Novelletto, A; Persichetti, Francesca; Trabace, S; Anastasi, R; Terrenato, L.
The human Y chromosome shows a reduced level of DNA polymorphism 1-gen-1990 Malaspina, P; Persichetti, Francesca; Novelletto, A; Iodice, C; Terrenato, L; Wolfe, J; Ferraro, M; Prantera, G.
An additional HindIII polymorphism at the coagulation factor XIII A locus 1-gen-1990 Iodice, C; Novelletto, A; Malaspina, P; Persichetti, Francesca
Entrapment into liposomes of fusicoccin binding sites 1-gen-1986 Patrizia, Aducci; Alessandro, Ballio; Maria Rosaria, Fullone; Persichetti, Francesca
Mostrati risultati da 41 a 59 di 59
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