Sfoglia per Autore
"Thermodynamic characterization of chromatin stuctural alterations related to cell cycle progression"
1987-01-01 Vergani, Laura; Diaspro, ALBERTO GIOVANNI; G., Cittadini; DI MARIA, Emilio; Nicolini, Claudio
"The true native chromatin- DNA stucture and cell cycle"
1988-01-01 Vergani, Laura; Diaspro, ALBERTO GIOVANNI; DI MARIA, Emilio; I., Grasso; A., Pastorino; Nicolini, Claudio
Native chromatin-DNA structure and cell-cycle: differential scanning calorimetry and gel electrophoresis
1989-01-01 Nicolini, Claudio; Vergani, Laura; Diaspro, ALBERTO GIOVANNI; DI MARIA, Emilio
Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's disease.
1996-01-01 Mandich, Paola; DI MARIA, Emilio; Bellone, Emilia; Ajmar, Franco; Abbruzzese, Giovanni
mRNA distribution in adult human brain of GRIN2B, a N-methyl-D-aspartate (NMDA) receptor subunit.
1997-01-01 Schito, Am; Pizzuti, A; DI MARIA, Emilio; Schenone, Angelo; Ratti, A; Defferrari, R; Bellone, Emilia; Mancardi, GIOVANNI LUIGI; Ajmar, F; Mandich, Paola
Opinion about genetic information, prenatal diagnosis and pregnancy termination; Analysis in a sample of Italian women
1997-01-01 Origone, P.; Di Maria, E.; Carabbio, C.; Celesti, R.; Ajmar, F.; Coviello, D. A.
Predictive testing for Huntington's disease: ten years' experience in two Italian centres
1998-01-01 Mandich, P; Jacopini, G; DI MARIA, Emilio; Sabbadini, G; Abbruzzese, G; Chimirri, F; Bellone, Emilia; Novelletto, A; Ajmar, F; AND FRONTALI, M.
A novel mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease.
1999-01-01 Bellone, Emilia; DI MARIA, Emilio; Soriani, S; Varese, A; Doria, Ll; Ajmar, Franco; Mandich, Paola
Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II
1999-01-01 Mandich, Paola; Bellone, Emilia; DI MARIA, Emilio; Pigullo, S.; Pizzuti, A.; Schenone, Angelo; Soriani, S.; Varese, A.; Windebank, A. J.; Ajmar, Franco
Mental function in males and females
1999-01-01 Ajmar, F; DI MARIA, Emilio; Padovani, L.
Congenital hypomyelination (CH) due to myelin protein zero (P0) Q215X mutation
1999-01-01 Mandich, Paola; Mancardi, GIOVANNI LUIGI; Varese, A.; Soriani, S.; DI MARIA, Emilio; Bellone, Emilia; Bado, M.; Gross, L.; Windebank, A. J.; Ajmar, Franco; Schenone, Angelo
Family and molecular data for a fine analysis of age at onset in Huntington disease
2000-01-01 Squitieri, F.; Sabbadini, G.; Mandich, Paola; Gellera, C.; DI MARIA, Emilio; Bellone, Emilia; Castellotti, B.; Nargi, E.; DE GRAZIA, U.; Frontali, M.; Novelletto, A.
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy
2000-01-01 DI MARIA, Emilio; Tabaton, Massimo; Vigo, T.; Abbruzzese, Giovanni; Bellone, Emilia; Donati, C.; Frasson, E.; Marchese, R.; Montagna, P.; Munoz, D. G.; Pramstaller, P. P.; Zanusso, G.; Ajmar, Franco; Mandich, Paola
The D355V mutation decreases EGR2 binding to an element within the Cx32 promoter.
2001-01-01 M., Musso; P., Balestra; Bellone, Emilia; D., Cassandrini; E. D., Maria; L. L., Doria; Grandis, Marina; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; G., Levi; F., Ajmar; Mandich, Paola
No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patient
2001-01-01 Pigullo, S.; DI MARIA, Emilio; Marchese, R.; Assini, A.; Bellone, Emilia; Scaglione, C.; Vitale, C.; Bonuccelli, U.; Barone, P.; Ajmar, Franco; Martinelli, P.; Abbruzzese, G.; Mandich, Paola
Clinical and genetic study of essential tremor in the Italian population.
2001-01-01 Abbruzzese, Giovanni; S., Pigullo; DI MARIA, Emilio; P., Martinelli; P., Barone; R., Marchese; C., Scaglione; A., Assini; C., Lucetti; A., Berardelli; S., Calzetti; Bellone, Emilia; Ajmar, Franco; Mandich, Paola
Glutamate hypothesis of schizophrenia: No evidence that the N-Methyl-D-Aspartate receptor 2B gene (GRIN2B) is associated with susceptibility to schizophrenia
2001-01-01 Di Maria, E.; Gulli, R.; Pioli, R.; De Luca, A.; Novelli, G.; Gennarelli, M.; Mandich, P.
Genetic testing of Huntington disease
2001-01-01 Mandich, P; DI MARIA, Emilio; Ajmar, F.
A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci.
2002-01-01 Bellone, Emilia; Rodolico, C.; Toscano, A.; DI MARIA, Emilio; Cassandrini, D.; Pizzuti, A.; Pigullo, S.; Mazzeo, A.; Macaione, V.; Girlanda, P.; Vita, G.; Ajmar, Franco; Mandich, Paola
Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathies
2002-01-01 Venken, K.; DI MARIA, Emilio; Bellone, Emilia; Balestra, P.; Cassandrini, D.; Mandich, Paola; DE JONGHE, P.; Timmerman, V.; Svaren, J.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
"Thermodynamic characterization of chromatin stuctural alterations related to cell cycle progression" | 1-gen-1987 | Vergani, Laura; Diaspro, ALBERTO GIOVANNI; G., Cittadini; DI MARIA, Emilio; Nicolini, Claudio | |
"The true native chromatin- DNA stucture and cell cycle" | 1-gen-1988 | Vergani, Laura; Diaspro, ALBERTO GIOVANNI; DI MARIA, Emilio; I., Grasso; A., Pastorino; Nicolini, Claudio | |
Native chromatin-DNA structure and cell-cycle: differential scanning calorimetry and gel electrophoresis | 1-gen-1989 | Nicolini, Claudio; Vergani, Laura; Diaspro, ALBERTO GIOVANNI; DI MARIA, Emilio | |
Molecular analysis of the IT15 gene in patients with apparently 'sporadic' Huntington's disease. | 1-gen-1996 | Mandich, Paola; DI MARIA, Emilio; Bellone, Emilia; Ajmar, Franco; Abbruzzese, Giovanni | |
mRNA distribution in adult human brain of GRIN2B, a N-methyl-D-aspartate (NMDA) receptor subunit. | 1-gen-1997 | Schito, Am; Pizzuti, A; DI MARIA, Emilio; Schenone, Angelo; Ratti, A; Defferrari, R; Bellone, Emilia; Mancardi, GIOVANNI LUIGI; Ajmar, F; Mandich, Paola | |
Opinion about genetic information, prenatal diagnosis and pregnancy termination; Analysis in a sample of Italian women | 1-gen-1997 | Origone, P.; Di Maria, E.; Carabbio, C.; Celesti, R.; Ajmar, F.; Coviello, D. A. | |
Predictive testing for Huntington's disease: ten years' experience in two Italian centres | 1-gen-1998 | Mandich, P; Jacopini, G; DI MARIA, Emilio; Sabbadini, G; Abbruzzese, G; Chimirri, F; Bellone, Emilia; Novelletto, A; Ajmar, F; AND FRONTALI, M. | |
A novel mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 disease. | 1-gen-1999 | Bellone, Emilia; DI MARIA, Emilio; Soriani, S; Varese, A; Doria, Ll; Ajmar, Franco; Mandich, Paola | |
Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type II | 1-gen-1999 | Mandich, Paola; Bellone, Emilia; DI MARIA, Emilio; Pigullo, S.; Pizzuti, A.; Schenone, Angelo; Soriani, S.; Varese, A.; Windebank, A. J.; Ajmar, Franco | |
Mental function in males and females | 1-gen-1999 | Ajmar, F; DI MARIA, Emilio; Padovani, L. | |
Congenital hypomyelination (CH) due to myelin protein zero (P0) Q215X mutation | 1-gen-1999 | Mandich, Paola; Mancardi, GIOVANNI LUIGI; Varese, A.; Soriani, S.; DI MARIA, Emilio; Bellone, Emilia; Bado, M.; Gross, L.; Windebank, A. J.; Ajmar, Franco; Schenone, Angelo | |
Family and molecular data for a fine analysis of age at onset in Huntington disease | 1-gen-2000 | Squitieri, F.; Sabbadini, G.; Mandich, Paola; Gellera, C.; DI MARIA, Emilio; Bellone, Emilia; Castellotti, B.; Nargi, E.; DE GRAZIA, U.; Frontali, M.; Novelletto, A. | |
Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy | 1-gen-2000 | DI MARIA, Emilio; Tabaton, Massimo; Vigo, T.; Abbruzzese, Giovanni; Bellone, Emilia; Donati, C.; Frasson, E.; Marchese, R.; Montagna, P.; Munoz, D. G.; Pramstaller, P. P.; Zanusso, G.; Ajmar, Franco; Mandich, Paola | |
The D355V mutation decreases EGR2 binding to an element within the Cx32 promoter. | 1-gen-2001 | M., Musso; P., Balestra; Bellone, Emilia; D., Cassandrini; E. D., Maria; L. L., Doria; Grandis, Marina; Mancardi, GIOVANNI LUIGI; Schenone, Angelo; G., Levi; F., Ajmar; Mandich, Paola | |
No evidence of association between CAG expansions and essential tremor in a large cohort of Italian patient | 1-gen-2001 | Pigullo, S.; DI MARIA, Emilio; Marchese, R.; Assini, A.; Bellone, Emilia; Scaglione, C.; Vitale, C.; Bonuccelli, U.; Barone, P.; Ajmar, Franco; Martinelli, P.; Abbruzzese, G.; Mandich, Paola | |
Clinical and genetic study of essential tremor in the Italian population. | 1-gen-2001 | Abbruzzese, Giovanni; S., Pigullo; DI MARIA, Emilio; P., Martinelli; P., Barone; R., Marchese; C., Scaglione; A., Assini; C., Lucetti; A., Berardelli; S., Calzetti; Bellone, Emilia; Ajmar, Franco; Mandich, Paola | |
Glutamate hypothesis of schizophrenia: No evidence that the N-Methyl-D-Aspartate receptor 2B gene (GRIN2B) is associated with susceptibility to schizophrenia | 1-gen-2001 | Di Maria, E.; Gulli, R.; Pioli, R.; De Luca, A.; Novelli, G.; Gennarelli, M.; Mandich, P. | |
Genetic testing of Huntington disease | 1-gen-2001 | Mandich, P; DI MARIA, Emilio; Ajmar, F. | |
A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci. | 1-gen-2002 | Bellone, Emilia; Rodolico, C.; Toscano, A.; DI MARIA, Emilio; Cassandrini, D.; Pizzuti, A.; Pigullo, S.; Mazzeo, A.; Macaione, V.; Girlanda, P.; Vita, G.; Ajmar, Franco; Mandich, Paola | |
Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathies | 1-gen-2002 | Venken, K.; DI MARIA, Emilio; Bellone, Emilia; Balestra, P.; Cassandrini, D.; Mandich, Paola; DE JONGHE, P.; Timmerman, V.; Svaren, J. |
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