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Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient. 1-gen-2001 Gardella, Rita; Nuytinck, L; Barlati, Sergio; Van Acker, P; Tadini, G; De Paepe, A; Colombi, Marina
Analysis of the (TA) repeat polymorphism of the UGT1A1 (UDP-Glucuronosyltransferase) gene in schizophrenia 1-gen-2002 Gardella, Rita; Barlati, Sergio; BREDA KLOBUS, Andrea; Iatropoulos, Paraskevas; Bonomi, S; Mosca, A; Sacchetti, Emilio; Barlati, S.
Genotype-phenotype correlation in Italian patients with epidermolysis bullosa dystrophica 1-gen-2002 Gardella, Rita; Castiglia, D; Posteraro, P; Bernardini, S; Zoppi, Nicoletta; Paradisi, M; Tadini, G; Barlati, Sergio; Mcgrath, Ja; Zambruno, G; Colombi, Marina
Different phenotypes in recessive dystrophic epidermolysis bullosa patients sharing the same mutation in compound heterozygosity with two novel mutations in COL7A1. 1-gen-2002 Gardella, Rita; Zoppi, Nicoletta; Zambruno, G; Barlati, Sergio; Colombi, Marina
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide 1-gen-2003 Colombi, Marina; Zoppi, Nicoletta; DE PETRO, Giuseppina; Marchina, Eleonora; Gardella, Rita; Tavian, D.; Ferraboli, Sergio; Barlati, Sergio
Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13 1-gen-2003 Coucke, Pj; Wessels, Mw; Van Acker, P; Gardella, Rita; Barlati, Sergio; Willems, Pj; Colombi, Marina; De Paepe, A.
Characterization of a 13 aminoacid human fibronectin peptide induce matrix assembly and inhibiting migration and invasion in tumor cells 1-gen-2004 Colombi, Marina; Zoppi, Nicoletta; Ritelli, Marco Giuseppe; DE PETRO, Giuseppina; Marchina, Eleonora; Gardella, Rita; Ferraboli, Sergio; Barlati, Sergio
Human fibroblasts with mutations in COL5A1 and COL3A1 genes do not organize collagens and fibronectin in the extracellular matrix, down-regulate alpha2beta1 integrin and recruit alphavbeta3 instead of alpha5beta1 integrin 1-gen-2004 Zoppi, Nicoletta; Gardella, Rita; DE PAEPE, A; Barlati, Sergio; Colombi, Marina
Exclusion of candidate genes in a family with arterial tortuosity syndrome 1-gen-2004 Gardella, Rita; Zoppi, Nicoletta; Assanelli, Deodato; Muiesan, Maria Lorenza; Barlati, Sergio; Colombi, Marina
The Italian Registry of Hereditary Epidermolysis Bullosa 1-gen-2005 Tadini, G; Gualandri, L; Colombi, Marina; Paradisi, M; Angelo, C; Zambruno, G; Castiglia, G; Annicchiarico, G; El Hachem, M; Gardella, Rita; Barlati, Sergio; Naldi, L; Bonifazi, E; Garofano, L; Stella, M; Moretti, G; Cavalli, R; Cambiaghi, S; Percivalle, S; Bellinvia, M; Di Benedetto, A; Locatelli, A; Lunardon, L; Bruni, E; Patrizi, A; Lembo, G; Cainelli, T.
Dystrophic epidermolysis bullosa pruriginosa in Italy: molecular characterization and pathogenesic aspects 1-gen-2006 Drera, Bruno Angelo; Castiglia, D; Zoppi, Nicoletta; Gardella, Rita; Tadini, G; Pedicelli, C; Barlati, Sergio; Zambruno, G; Colombi, Marina
Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sample 1-gen-2006 Magri, Chiara; Gardella, Rita; Barlati, Sergio; Podavini, D; Iatropoulos, P; Bonomi, S; Valsecchi, Paolo; Sacchetti, Emilio; Barlati, S.
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome 1-gen-2006 Coucke, Pj; Willaert, A; Wessels, Mw; Callewaert, B; Zoppi, Nicoletta; De Backer, J; Fox, Je; Mancini, Gm; Kambouris, M; Gardella, Rita; Facchetti, Fabio; Willems, Pj; Forsyth, R; Dietz, Hc; Barlati, Sergio; Colombi, Marina; Loeys, B; De Paepe, A.
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization 1-gen-2006 Drera, B; Castiglia, D; Zoppi, Nicoletta; Gardella, Rita; Tadini, G; Floriddia, G; De Luca, N; Pedicelli, C; Barlati, Sergio; Zambruno, G; Colombi, Marina
Association study between schizophrenia and the AMPA genes GRIA1, GRIA2 AND GRIA4 1-gen-2006 Magri, Chiara; Gardella, Rita; Imperadori, L; Podavini, D; Iatropoulos, P; Barlati, Sergio; Valsecchi, Paolo; Bonvicini, C; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, S.
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity sindrome 1-gen-2007 Drera, B; Guala, A; Zoppi, Nicoletta; Gardella, Rita; Franceschini, P; Barlati, Sergio; Colombi, Marina
Mitochondrial DNA haplogroups and age at onset of schizophrenia 1-gen-2007 Magri, C.; Gardella, R.; Barlati, S; Valsecchi, P.; Sacchetti, E.; Barlati, S.
Gene per la neuregulina 1 e schizofrenia: ulteriori evidenze di associazione 1-gen-2008 Gardella, Rita; Podavini, Damiano; Magri, Chiara; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, Sergio
Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients 1-gen-2008 Magri, C.; Gardella, R.; Valsecchi, P.; Barlati, S; Guizzetti, Gian Luca; Imperadori, Laura; Bonvicini, C.; Tura, Giovanni Battista; Gennarelli, M.; Sacchetti, E.; Barlati, S.
Analysis of Copy Number Variations in Schizophrenia Italian Patients 1-gen-2009 Traversa, Michele; Magri, Chiara; Valsecchi, Paolo; Gardella, Rita; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, Sergio
Mostrati risultati da 21 a 40 di 58
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