Sfoglia per Autore
The human Y chromosome shows a low level of DNA polymorphism
1990-01-01 Malaspina, P; Persichetti, F; Novelletto, A; Iodice, C; Terrenato, L; Wolfe, J; Ferraro, M; Prantera, G
An additional HindIII polymorphism at the coagulation factor XIIIA locus
1990-01-01 Iodice, C; Novelletto, A; Malaspina, P; Persichetti, F
Epidemiological and linkage studies on Huntington's disease in Italy
1990-01-01 Frontali, M; Malaspina, P; Rossi, C; Jacopini, A; Vivona, G; Pergola, M; Palena, A; Novelletto, A
Protection against malaria morbidity - near-fixation of the alpha-thalassemia gene in a Nepalese population
1991-01-01 Modiano, G; Morpurgo, G; Terrenato, L; Novelletto, A; Di Rienzo, A; Colombo, B; Purpura, M; Mariani, M; Santachiara Benerecetti, S; Brega, A; Dixit, K; Shrestha, S; Lania, A; Wanachiwanawin, W; Luzzatto, L
SPINOCEREBELLAR ATAXIA (SCA1) IN 2 LARGE ITALIAN KINDREDS - EVIDENCE IN FAVOR OF A LOCUS POSITION DISTAL TO GLO1 AND THE HLA CLUSTER
1991-01-01 Frontali, M; Iodice, C; Lulli, P; Spadaro, M; Cappellacci, S; Giunti, P; Malaspina, P; Morellini, M; Morocutti, C; Novelletto, A; Persichetti, F; Trabace, S; Anastasi, R; Terrenato, L
Linkage analysis and linkage disequilibrium studies between SCA1 and TG microsatellite VNTRs on 6p.
1991-01-01 Iodice, C; Persichetti, F; Frontali, M; Lulli, P; Spadaro, M; Cappellacci, S; Giunti, P; Malaspina, P; Morellini, M; Morocutti, C; Novelletto, A; Trabace, S; Terrenato, L
Disequilibrium of multiple DNA markers on the human Y chromosome
1992-01-01 Persichetti, F; Blasi, P; Hammer, M; Malaspina, P; Iodice, C; Terrenato, L; Novelletto, A
The Huntington's disease candidate region exhibits many different haplotypes
1992-01-01 Macdonald, Me; Novelletto, A; Lin, C; Tagle, D; Barnes, G; Bates, G; Taylor, S; Allitto, B; Altherr, M; Myers, R; Lehrach, H; Collins, Fs; Wasmuth, Jj; Frontali, M; Gusella, Jf
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
1993-01-01 Kwiatkowski, T; Orr, T; Banfi, S; Mccall, A; Iodice, C; Persichetti, F; Novelletto, A; Le Borgne De Marquois, F; Duvick, L; Frontali, M; Subramony, S; Beaudet, A; Terrenato, L; Zoghbi, H; Ranum, L
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci
1993-01-01 Iodice, C; Frontali, M; Persichetti, F; 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
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I
1994-01-01 Iodice, C; Malaspina, P; Persichetti, F; Novelletto, A; Spadaro, M; Giunti, P; Morocutti, C; Terrenato, L; Harding, A; Frontali, M
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
1994-01-01 Giunti, P; Sweeney, M; Spadaro, M; Iodice, C; Novelletto, A; Malaspina, P; Frontali, M; Harding, A
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
1994-01-01 Giunti, P; Sweeney, M; Spadaro, M; Iodice, C; Novelletto, A; Malaspina, P; Frontali, M; Harding, A
Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulations
1995-01-01 Ciminelli, Bm; Pompei, F; Malaspina, P; Hammer, M; Persichetti, F; Pignatti, P; Palena, A; Anagnou, N; Guanti, G; Iodice, C; Terrenato, L; Novelletto, A
Genetic fitness in Huntington’s Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions.
1996-01-01 Frontali, M; Sabbadini, G; Novelletto, A; Iodice, C; Naso, F; Spadaro, M; Giunti, P; Jacopini, A; Veneziano, L; Mantuano, E; Malaspina, P; Ulizzi, L; Brice, A; Durr, A; Terrenato, L
Ordering of 44 genetic markers in the 6p22 cytogenetic band
1996-01-01 Trettel, F; Malaspina, P; Blasi, P; Iodice, C; Novelletto, A; Sabbadini, G; Veneziano, L; Frontali, M; Terrenato, L
Construction of a YAC contig covering human chromosome 6p22
1996-01-01 Malaspina, P; Roetto, A; Trettel, F; Iodice, C; Blasi, P; Frontali, M; Carella, M; Franco, B; Camaschella, C; Novelletto, A
Genetic fitness in Huntington's disease and spinocerebellar ataxia 1: A population genetics model for CAG repeat expansions
1996-01-01 Frontali, M; Sabbadini, G; Novelletto, A; Jodice, C; Naso, F; Spadaro, M; Giunti, P; Jacopini, A; Veneziano, L; Mantuano, E; Malaspina, P; Ulizzi, L; Brice, A; Durr, A; Terrenato, L
Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats
1996-01-01 Rubinsztein, D; Leggo, J; Coles, R; Almqvist, E; Biancalana, V; Cassiman, J; Chotai, K; Connarty, M; Craufurd, D; Curtis, A; Curtis, D; Davidson, M; Differ, A; Dode, C; Dodge, A; Frontali, M; Ranen, N; Stine, O; Sherr, M; Abbott, M; Franz, M; Graham, C; Harper, P; Hedreen, J; Jackson, A; Kaplan, J; Losekoot, M; Macmillan, J; Morrison, P; Trottier, Y; Novelletto, A; Simpson, S; Theilmann, J; Whittaker, J; Folstein, S; Ross, C; Hayden, M
Differential structuring of human populations for homologous X and Y microsatellite loci
1997-01-01 Scozzari, R; Cruciani, F; Malaspina, P; Santolamazza, P; Ciminelli, Bm; Torroni, A; Modiano, D; Wallace, D; Kidd, K; Olckers, A; Moral, P; Terrenato, L; Akar, N; Qamar, R; Mansoor, A; Mehdi, S; Meloni, G; Vona, G; Cole, D; Cai, W; Novelletto, A
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-gen-1990 | The human Y chromosome shows a low level of DNA polymorphism | Malaspina, P; Persichetti, F; Novelletto, A; Iodice, C; Terrenato, L; Wolfe, J; Ferraro, M; Prantera, G | Articolo su rivista | |
1-gen-1990 | An additional HindIII polymorphism at the coagulation factor XIIIA locus | Iodice, C; Novelletto, A; Malaspina, P; Persichetti, F | Articolo su rivista | |
1-gen-1990 | Epidemiological and linkage studies on Huntington's disease in Italy | Frontali, M; Malaspina, P; Rossi, C; Jacopini, A; Vivona, G; Pergola, M; Palena, A; Novelletto, A | Articolo su rivista | |
1-gen-1991 | Protection against malaria morbidity - near-fixation of the alpha-thalassemia gene in a Nepalese population | Modiano, G; Morpurgo, G; Terrenato, L; Novelletto, A; Di Rienzo, A; Colombo, B; Purpura, M; Mariani, M; Santachiara Benerecetti, S; Brega, A; Dixit, K; Shrestha, S; Lania, A; Wanachiwanawin, W; Luzzatto, L | Articolo su rivista | |
1-gen-1991 | SPINOCEREBELLAR ATAXIA (SCA1) IN 2 LARGE ITALIAN KINDREDS - EVIDENCE IN FAVOR OF A LOCUS POSITION DISTAL TO GLO1 AND THE HLA CLUSTER | Frontali, M; Iodice, C; Lulli, P; Spadaro, M; Cappellacci, S; Giunti, P; Malaspina, P; Morellini, M; Morocutti, C; Novelletto, A; Persichetti, F; Trabace, S; Anastasi, R; Terrenato, L | Articolo su rivista | |
1-gen-1991 | Linkage analysis and linkage disequilibrium studies between SCA1 and TG microsatellite VNTRs on 6p. | Iodice, C; Persichetti, F; Frontali, M; Lulli, P; Spadaro, M; Cappellacci, S; Giunti, P; Malaspina, P; Morellini, M; Morocutti, C; Novelletto, A; Trabace, S; Terrenato, L | Intervento a convegno | |
1-gen-1992 | Disequilibrium of multiple DNA markers on the human Y chromosome | Persichetti, F; Blasi, P; Hammer, M; Malaspina, P; Iodice, C; Terrenato, L; Novelletto, A | Articolo su rivista | |
1-gen-1992 | The Huntington's disease candidate region exhibits many different haplotypes | Macdonald, Me; Novelletto, A; Lin, C; Tagle, D; Barnes, G; Bates, G; Taylor, S; Allitto, B; Altherr, M; Myers, R; Lehrach, H; Collins, Fs; Wasmuth, Jj; Frontali, M; Gusella, Jf | Articolo su rivista | |
1-gen-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 locus | Kwiatkowski, T; Orr, T; Banfi, S; Mccall, A; Iodice, C; Persichetti, F; Novelletto, A; Le Borgne De Marquois, F; Duvick, L; Frontali, M; Subramony, S; Beaudet, A; Terrenato, L; Zoghbi, H; Ranum, L | Articolo su rivista | |
1-gen-1993 | The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci | Iodice, C; Frontali, M; Persichetti, F; 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 | Articolo su rivista | |
1-gen-1994 | Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I | Iodice, C; Malaspina, P; Persichetti, F; Novelletto, A; Spadaro, M; Giunti, P; Morocutti, C; Terrenato, L; Harding, A; Frontali, M | Articolo su rivista | |
1-gen-1994 | The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias | Giunti, P; Sweeney, M; Spadaro, M; Iodice, C; Novelletto, A; Malaspina, P; Frontali, M; Harding, A | Articolo su rivista | |
1-gen-1994 | The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias | Giunti, P; Sweeney, M; Spadaro, M; Iodice, C; Novelletto, A; Malaspina, P; Frontali, M; Harding, A | Articolo su rivista | |
1-gen-1995 | Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulations | Ciminelli, Bm; Pompei, F; Malaspina, P; Hammer, M; Persichetti, F; Pignatti, P; Palena, A; Anagnou, N; Guanti, G; Iodice, C; Terrenato, L; Novelletto, A | Articolo su rivista | |
1-gen-1996 | Genetic fitness in Huntington’s Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions. | Frontali, M; Sabbadini, G; Novelletto, A; Iodice, C; Naso, F; Spadaro, M; Giunti, P; Jacopini, A; Veneziano, L; Mantuano, E; Malaspina, P; Ulizzi, L; Brice, A; Durr, A; Terrenato, L | Articolo su rivista | |
1-gen-1996 | Ordering of 44 genetic markers in the 6p22 cytogenetic band | Trettel, F; Malaspina, P; Blasi, P; Iodice, C; Novelletto, A; Sabbadini, G; Veneziano, L; Frontali, M; Terrenato, L | Articolo su rivista | |
1-gen-1996 | Construction of a YAC contig covering human chromosome 6p22 | Malaspina, P; Roetto, A; Trettel, F; Iodice, C; Blasi, P; Frontali, M; Carella, M; Franco, B; Camaschella, C; Novelletto, A | Articolo su rivista | |
1-gen-1996 | Genetic fitness in Huntington's disease and spinocerebellar ataxia 1: A population genetics model for CAG repeat expansions | Frontali, M; Sabbadini, G; Novelletto, A; Jodice, C; Naso, F; Spadaro, M; Giunti, P; Jacopini, A; Veneziano, L; Mantuano, E; Malaspina, P; Ulizzi, L; Brice, A; Durr, A; Terrenato, L | Articolo su rivista | |
1-gen-1996 | Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats | Rubinsztein, D; Leggo, J; Coles, R; Almqvist, E; Biancalana, V; Cassiman, J; Chotai, K; Connarty, M; Craufurd, D; Curtis, A; Curtis, D; Davidson, M; Differ, A; Dode, C; Dodge, A; Frontali, M; Ranen, N; Stine, O; Sherr, M; Abbott, M; Franz, M; Graham, C; Harper, P; Hedreen, J; Jackson, A; Kaplan, J; Losekoot, M; Macmillan, J; Morrison, P; Trottier, Y; Novelletto, A; Simpson, S; Theilmann, J; Whittaker, J; Folstein, S; Ross, C; Hayden, M | Articolo su rivista | |
1-gen-1997 | Differential structuring of human populations for homologous X and Y microsatellite loci | Scozzari, R; Cruciani, F; Malaspina, P; Santolamazza, P; Ciminelli, Bm; Torroni, A; Modiano, D; Wallace, D; Kidd, K; Olckers, A; Moral, P; Terrenato, L; Akar, N; Qamar, R; Mansoor, A; Mehdi, S; Meloni, G; Vona, G; Cole, D; Cai, W; Novelletto, A | Articolo su rivista |
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