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A bio-anthropological study on the Central African Mbugu, Sango and Yakpa: some genetic erythrocyte and serum polymorphisms
1982-01-01 Spedini, G; Walter, H; Capucci, E; Fuciarelli, Mf; Rickards, O
A bio-anthropological study on the Central African Mbugu, Sango, and Yakpa. I. Some genetic erythrocyte and serum polymorphisms
1982-01-01 Spedini, G; Walter, H; Capucci, E; Fuciarelli, Mf; Rickards, O
A biogeographic view of Apodemus in Asia and Europe inferred from nuclear and mitochondrial gene sequences
2008-01-01 Suzuki, H; Filippucci, Mg; Chelomina, G; Sato, J; Serizawa, K; Nevo, E
A common African polymorphism abolishes tyrosine sulfation of human anionic trypsinogen (PRSS2)
2009-01-01 Ronai, Z; Witt, H; Rickards, O; Destro Bisol, G; Bradbury, A; Sahin Toth, M
A comparison between short-term evolution of micronuclei induced by X-rays and colchicine in root tips of Vicia faba. 24. Gustavino B, Vitagliano E, Sottili A, Rizzoni M. A comparison between short-term evolution of micronuclei induced by X-rays and colchicine in root tips of Vicia faba.
1987-01-01 Gustavino, B; Vitagliano, E; Sottili, A; Rizzoni, M
A competitive polymerase chain reaction-based approach for the identification and semiquantification of mitochondrial DNA in differently heat-treated bovine meat and bone meal
2003-01-01 Frezza, D; Favaro, M; Vaccari, G; Von Holst, C; Giambra, V; Anklam, E; Dove, D; Battaglia, Pa; Agrimi, U; Brambilla, G; Ajmone_marsan, P; Tartaglia, M
A correction of the estimates of the least common cystic fibrosis (CF) mutations published by "The Cystic Fibrosis Genetic Analysis Consortium" in 1994.
1997-01-01 Giorgi, S; Tandoi, C; Ciminelli, Bm; Modiano, G
A cosmid library specific for human chromosome regions 6p23.1 and 6q27.
1993-01-01 Shortle, V; Malaspina, P; Fox, M; Dooley, J; Volz, A; Ziegler, A; Trowsdale, J; Morrison, K; Edwards, Y
A crystal milestone: the structure of regulated Src
1997-06-01 Superti Furga, G; Gonfloni, S
A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis
2006-01-01 Witt, H; Sahin Toth, M; Landt, O; Chen, J; Kahne, T; Drenth, J; Kukor, Z; Szepessy, E; Halangk, W; Dahm, S; Rohde, K; Schulz, H; Le Marechal, C; Akar, N; Ammann, R; Truninger, K; Bargetzi, M; Bhatia, E; Castellani, C; Cavestro, G; Cerny, M; Destro Bisol, G; Spedini, G; Eiberg, H; Jansen, J; Koudova, M; Rausova, E; Macek, M; Malats, N; Real, F; Menzel, H; Moral, P; Galavotti, R; Pignatti, P; Rickards, O; Spicak, J; Zarnescu, N; Bock, W; Gress, T; Friess, H; Ockenga, J; Schmidt, H; Pfutzer, R; Lohr, M; Simon, P; Weiss, F; Lerch, M; Teich, N; Keim, V; Berg, T; Wiedenmann, B; Luck, W; Groneberg, D; Becker, M; Keil, T; Kage, A; Bernardova, J; Braun, M; Guldner, C; Halangk, J; Rosendahl, J; Witt, U; Treiber, M; Nickel, R; Ferec, C
A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosome
2000-01-01 Trettel, F; Mantuano, E; Calabresi, V; Veneziano, L; Olsen, A; Georgescu, A; Gordon, L; Sabbadini, G; Frontali, M; Iodice, C
A functional role for some Fugu introns larger than the typical short ones: the example of the gene coding for ribosomal protein S7 and snoRNA U17
1996-01-01 Cecconi, F; Crosio, C; Mariottini, P; Cesareni, G; Giorgi, M; Brenner, S; Amaldi, F
A further polymorphism of the Gd locus for glucose-6-phosphate dehydrogenase present among blacks (Nigerians) and apparently absent among caucasoids: The quantitative isoelectrophoretic variation of the Gd+ allele
1991-01-01 Modiano, G; Ciminelli, Bm; Malaspina, P; Santolamazza, P; Sedran, L; Meloni, T; Forteleoni, G; Mela, G
A gene conversion hotspot in the human growth hormone (GH1) gene promoter
2009-01-01 Wolf, A; Millar, D; Caliebe, A; Horan, M; Newsway, V; Kumpf, D; Steinmann, K; Chee, I; Lee, Y; Mutirangura, A; Pepe, G; Rickards, O; Schmidtke, J; Schempp, W; Chuzhanova, N; Kehrer Sawatzki, H; Krawczak, M; Cooper, D
A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevus
2000-01-01 Terrinoni, A; Candi, E; Oddi, S; Gobello, T; Camaione, Db; Mazzanti, C; Zambruno, G; Knight, R; Melino, G
A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region
1998-01-01 Mari, A; Amati, F; Conti, E; Bengala, M; Novelli, G; Dallapiccola, B
A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome
2005-12-01 Cassidy, A; van Steensel, M; Steijlen, P; van Geel, M; van der Velden, J; Morley, S; Terrinoni, A; Melino, G; Candi, E; Mclean, W
A human derived SSADH coding variant is replacing the ancestral allele shared with primates.
2006-01-01 Leone, O; Blasi, P; Palmerio, F; Kozlov, A; Malaspina, P; Novelletto, A
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene
2005-01-01 Modiano, G; Bombieri, C; Ciminelli, Bm; Belpinati, F; Giorgi, S; De_georges, M; Scotet, V; Pompei, F; Ciccacci, C; Guittard, C; Audrezet, Mp; Begnini, A; Toepfer, ; M., Mmjr; Ferec, C; Claustres, M; Pignatti, Pf
A meta-analysis approach to gene regulatory network inference identifies key regulators of cardiovascular diseases
2024-04-11 Pepe, G; Appierdo, R; Ausiello, G; Helmer-Citterich, M; Gherardini, Pf
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-gen-1982 | A bio-anthropological study on the Central African Mbugu, Sango and Yakpa: some genetic erythrocyte and serum polymorphisms | Spedini, G; Walter, H; Capucci, E; Fuciarelli, Mf; Rickards, O | Contributo in libro | |
1-gen-1982 | A bio-anthropological study on the Central African Mbugu, Sango, and Yakpa. I. Some genetic erythrocyte and serum polymorphisms | Spedini, G; Walter, H; Capucci, E; Fuciarelli, Mf; Rickards, O | Intervento a convegno | |
1-gen-2008 | A biogeographic view of Apodemus in Asia and Europe inferred from nuclear and mitochondrial gene sequences | Suzuki, H; Filippucci, Mg; Chelomina, G; Sato, J; Serizawa, K; Nevo, E | Articolo su rivista | |
1-gen-2009 | A common African polymorphism abolishes tyrosine sulfation of human anionic trypsinogen (PRSS2) | Ronai, Z; Witt, H; Rickards, O; Destro Bisol, G; Bradbury, A; Sahin Toth, M | Articolo su rivista | |
1-gen-1987 | A comparison between short-term evolution of micronuclei induced by X-rays and colchicine in root tips of Vicia faba. 24. Gustavino B, Vitagliano E, Sottili A, Rizzoni M. A comparison between short-term evolution of micronuclei induced by X-rays and colchicine in root tips of Vicia faba. | Gustavino, B; Vitagliano, E; Sottili, A; Rizzoni, M | Articolo su rivista | |
1-gen-2003 | A competitive polymerase chain reaction-based approach for the identification and semiquantification of mitochondrial DNA in differently heat-treated bovine meat and bone meal | Frezza, D; Favaro, M; Vaccari, G; Von Holst, C; Giambra, V; Anklam, E; Dove, D; Battaglia, Pa; Agrimi, U; Brambilla, G; Ajmone_marsan, P; Tartaglia, M | Articolo su rivista | |
1-gen-1997 | A correction of the estimates of the least common cystic fibrosis (CF) mutations published by "The Cystic Fibrosis Genetic Analysis Consortium" in 1994. | Giorgi, S; Tandoi, C; Ciminelli, Bm; Modiano, G | Articolo su rivista | |
1-gen-1993 | A cosmid library specific for human chromosome regions 6p23.1 and 6q27. | Shortle, V; Malaspina, P; Fox, M; Dooley, J; Volz, A; Ziegler, A; Trowsdale, J; Morrison, K; Edwards, Y | Articolo su rivista | |
1-giu-1997 | A crystal milestone: the structure of regulated Src | Superti Furga, G; Gonfloni, S | Articolo su rivista | |
1-gen-2006 | A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis | Witt, H; Sahin Toth, M; Landt, O; Chen, J; Kahne, T; Drenth, J; Kukor, Z; Szepessy, E; Halangk, W; Dahm, S; Rohde, K; Schulz, H; Le Marechal, C; Akar, N; Ammann, R; Truninger, K; Bargetzi, M; Bhatia, E; Castellani, C; Cavestro, G; Cerny, M; Destro Bisol, G; Spedini, G; Eiberg, H; Jansen, J; Koudova, M; Rausova, E; Macek, M; Malats, N; Real, F; Menzel, H; Moral, P; Galavotti, R; Pignatti, P; Rickards, O; Spicak, J; Zarnescu, N; Bock, W; Gress, T; Friess, H; Ockenga, J; Schmidt, H; Pfutzer, R; Lohr, M; Simon, P; Weiss, F; Lerch, M; Teich, N; Keim, V; Berg, T; Wiedenmann, B; Luck, W; Groneberg, D; Becker, M; Keil, T; Kage, A; Bernardova, J; Braun, M; Guldner, C; Halangk, J; Rosendahl, J; Witt, U; Treiber, M; Nickel, R; Ferec, C | Articolo su rivista | |
1-gen-2000 | A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosome | Trettel, F; Mantuano, E; Calabresi, V; Veneziano, L; Olsen, A; Georgescu, A; Gordon, L; Sabbadini, G; Frontali, M; Iodice, C | Articolo su rivista | |
1-gen-1996 | A functional role for some Fugu introns larger than the typical short ones: the example of the gene coding for ribosomal protein S7 and snoRNA U17 | Cecconi, F; Crosio, C; Mariottini, P; Cesareni, G; Giorgi, M; Brenner, S; Amaldi, F | Articolo su rivista | |
1-gen-1991 | A further polymorphism of the Gd locus for glucose-6-phosphate dehydrogenase present among blacks (Nigerians) and apparently absent among caucasoids: The quantitative isoelectrophoretic variation of the Gd+ allele | Modiano, G; Ciminelli, Bm; Malaspina, P; Santolamazza, P; Sedran, L; Meloni, T; Forteleoni, G; Mela, G | Articolo su rivista | |
1-gen-2009 | A gene conversion hotspot in the human growth hormone (GH1) gene promoter | Wolf, A; Millar, D; Caliebe, A; Horan, M; Newsway, V; Kumpf, D; Steinmann, K; Chee, I; Lee, Y; Mutirangura, A; Pepe, G; Rickards, O; Schmidtke, J; Schempp, W; Chuzhanova, N; Kehrer Sawatzki, H; Krawczak, M; Cooper, D | Articolo su rivista | |
1-gen-2000 | A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevus | Terrinoni, A; Candi, E; Oddi, S; Gobello, T; Camaione, Db; Mazzanti, C; Zambruno, G; Knight, R; Melino, G | Articolo su rivista | |
1-gen-1998 | A highly polymorphic CA/GT repeat (LIMK1GT) within the Williams syndrome critical region | Mari, A; Amati, F; Conti, E; Bengala, M; Novelli, G; Dallapiccola, B | Articolo su rivista | |
1-dic-2005 | A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome | Cassidy, A; van Steensel, M; Steijlen, P; van Geel, M; van der Velden, J; Morley, S; Terrinoni, A; Melino, G; Candi, E; Mclean, W | Articolo su rivista | |
1-gen-2006 | A human derived SSADH coding variant is replacing the ancestral allele shared with primates. | Leone, O; Blasi, P; Palmerio, F; Kozlov, A; Malaspina, P; Novelletto, A | Articolo su rivista | |
1-gen-2005 | A large-scale study of the random variability of a coding sequence: a study on the CFTR gene | Modiano, G; Bombieri, C; Ciminelli, Bm; Belpinati, F; Giorgi, S; De_georges, M; Scotet, V; Pompei, F; Ciccacci, C; Guittard, C; Audrezet, Mp; Begnini, A; Toepfer, ; M., Mmjr; Ferec, C; Claustres, M; Pignatti, Pf | Articolo su rivista | |
11-apr-2024 | A meta-analysis approach to gene regulatory network inference identifies key regulators of cardiovascular diseases | Pepe, G; Appierdo, R; Ausiello, G; Helmer-Citterich, M; Gherardini, Pf | Articolo su rivista |
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