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Identification of the Syrian hamster cardiomyopathy gene 1-gen-1997 Nigro, Vincenzo; Okazaki, Y; Belsito, Angela; Piluso, Giulio; Matsuda, Y; Politano, Luisa; Nigro, G; Ventura, C; Abbondanza, Ciro; Molinari, Anna Maria; Acampora, D; Nishimura, M; Hayashizaki, Y; Puca, Ga
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample 1-gen-1997 Mora, M; Cartegni, L; DI BLASI, C; Barresi, R; Bione, S; RAFFAELE DI BARLETTA, M; Morandi, L; Merlini, L; Nigro, Vincenzo; Politano, Luisa; Donati, Ma; Cornelio, F; Cobianchi, F; Toniolo, D.
Exon-intron organization of the human dystrophin gene 1-gen-1997 Nobile, C; Marchi, J; Nigro, Vincenzo; Roberts, Rg; Danieli, Ga
The fourth component of the sarcoglycan complex 1-gen-1997 Yoshida, M; Noguchi, S; Wakabayashi, E; Piluso, Giulio; Belsito, Angela; Nigro, Vincenzo; Ozawa, E.
Regolazione dell’espressione di p53 p21(WAF-1/CIP1) e di Bcl-2 da parte dell’estradiolo, dell’acido all-trans retinico e dell’ICI 182,780 in cellule di carcinoma mammario 1-gen-1998 Bontempo, Paola; Tortora, V; Armetta, I; Abbondanza, Ciro; Nigro, Vincenzo; Medici, N; Nola, E; Schiavone, Em; Puca, Ga; Molinari, A. M.
Gene redundancies in the dystrophin-associated protein complex 1-gen-1998 Nigro, Vincenzo; Piluso, Giulio; Belsito, Angela; Puca, Aa; Politano, Luisa
Serum anti-p53 antibodies and progression of hepatic diseases HCV related. 1-gen-1998 Gazzerro, P; Cioffi, Michele; Vietri, Maria Teresa; Abbondanza, Ciro; Nigro, Vincenzo; Raimondi, Sa; Catalano, T; Puca, Ga; Molinari, Am
A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies 1-gen-1998 Moreira, Es; Vainzof, M; Marie, Sk; Nigro, Vincenzo; Zatz, M; PASSOS BUENO, Mr
Clinical and genetic findings in sarcoglycanopathies 1-gen-1998 Politano, Luisa; Nigro, Vincenzo; Passamano, L; Petretta, V; Esposito, Mg; Papparella, S; Ricci, E; Nigro, G.
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy families 1-gen-1998 Speer, Mc; Vance, Jm; LENNON GRAHAM, F; Stajich, Jm; Viles, Kd; Gilchrist, Jm; Nigro, Vincenzo; Mcmichael, R; Chutkow, Jg; Bartoloni, L; Horrigan, Sk; Westbrook, Ca; PERICAK VANCE, Ma
Identification and characterization of a novel member of the dystrobrevin gene family 1-gen-1998 Puca, Aa; Nigro, Vincenzo; Piluso, Giulio; Belsito, Angela; Sampaolo, Simone; Quaderi, N; Rossi, E; DI IORIO, Giuseppe; Ballabio, A; Franco, B.
Interaction of vault particles with estrogen receptor in the MCF-7 breast cancer cell 1-gen-1998 Abbondanza, Ciro; Rossi, V; Roscigno, A; Gallo, L; Belsito, Angela; Piluso, Giulio; Medici, Nicola; Nigro, Vincenzo; Molinari, Anna Maria; Moncharmont, B; Puca, Ga
An improved polymerase chain reaction (PCR) protocol for unambigous detection of growth hormone gene deletions 1-gen-1998 Mone, Cm; Nigro, Vincenzo; Rotondi, M; DEL BUONO, A; Mazziotti, G; Riondino, M; Sinisi, Am; Ghizzoni, L; PHILLIPS JA, 3rd; Bellastella, A; Carella, C.
Dystrophin gene scanning by DHPLC of DMD carriers without deletions or duplications 1-gen-1999 Belsito, Angela; Politano, Luisa; Piluso, Giulio; Comi, Li; Nigro, Vincenzo
Diagnostic aspects in sarcoglycanopathies 1-gen-1999 Ricci, E; Galluzzi, G; Mela, J; Nigro, Vincenzo; Merico, B; Damiani, A; Giglio, V; Tonali, P.
Clinical and genetic aspects of sarcoglycanopathies 1-gen-1999 Nigro, Vincenzo; Comi, Li; Politano, Luisa
Hereditary spherocytosis due to a novel frameshift mutation in AE1 cytoplasmic COOH terminal tail: band 3 Vesuvio 1-gen-1999 Perrotta, Silverio; Polito, F; Cone, Ml; Nobili, Bruno; Cutillo, S; Nigro, Vincenzo; Iolascon, A; Amendola, G; MIRAGLIA DEL GIUDICE, Emanuele
Dystrophin and utrophin complexed with different associated proteins in cardiac Purkinje fibres 1-gen-1999 Rivier, F; Robert, A; Hugon, G; BONET KERRACHE, A; Nigro, Vincenzo; Fehrentz, Ja; Martinez, J; Mornet, D.
Successful combined prenatal diagnosis for Duchenne and facio-scapulo- humeral dystrophies 1-gen-1999 Politano, Luisa; Galluzzi, G; Felicetti, L; Tedeschi, S; Fortuna, R; Passamano, L; Esposito, Mg; Nigro, Vincenzo
Familial dilated cardiomyopathy associated with the typical dystrophin BMD mutation. Report on two additional cases 1-gen-1999 Politano, Luisa; Passamano, L; Petretta, V; Nigro, Vincenzo; Papparella, S; Nigro, Ge; Santangelo, Lucio; Esposito, Mg; Comi, Li; Nigro, Gerardo
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