GARDELLA, Rita

GARDELLA, Rita  

Dipartimento di Medicina Molecolare e Traslazionale  

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A -96C-T mutation in the promoter of the collagen type VII gene (COL7A1) abolishing transcription in a patient affected by recessive dystrophic epidermolys bullosa 1-gen-2000 Gardella, Rita; Barlati, Sergio; Zoppi, Nicoletta; Tadini, G; Colombi, Marina
A common MspI RFLP of the human fibronectin gene (FN1) 1-gen-1988 Gardella, Rita; Colombi, Marina; Barlati, Sergio
A frequent HaeIII RFLP of the human fibronectin gene 1-gen-1987 Colombi, Marina; Gardella, Rita; Barlati, Sergio; Vaheri, A.
A frequent Hind RFLP of the human fibronectin) gene (FN1) 1-gen-1988 Colombi, Marina; Gardella, Rita; Barlati, Sergio
A new Taq RFLP of the human fibronecin gene (FN1) 1-gen-1989 Gardella, Rita; Colombi, Marina; Barlati, Sergio
A Taq RFLP for the human fibronectin (FN1) gene 1-gen-1988 Gardella, Rita; Colombi, Marina; Barlati, Sergio
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
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.
Analysis of triplet repeats of the FRAXA locus using a novel sequencing procedure 1-gen-1996 Barlati, Sergio; Belletti, L; Gardella, Rita; Ferraboli, Sergio
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders. 1-gen-1995 CALZAVARA PINTON, Piergiacomo; Colombi, Marina; Carlino, A; Gardella, Rita; Clemente, M; Moro, L; Zoppi, Nicoletta; Caimi, L; Barlati, Sergio; DE PANFILIS, G.
Angiokeratoma Corporis Diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders. 1-gen-1995 CALZAVARA PINTON, Piergiacomo; Colombi, Marina; Carlino, A.; Zane, C.; Gardella, Rita; Clemente, M.; Facchetti, Fabio; Moro, L.; Zoppi, Nicoletta; Caimi, Luigi; Barlati, S.; DE PANFILIS, G.
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophrenia 1-gen-2009 Iatropoulos, P; Gardella, Rita; Valsecchi, Paolo; Magri, Chiara; Ratti, C; Podavini, D; Rossi, G; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, Sergio
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.
Cerebellar ataxia in a family with recurrent epidermolysis bullosa dystrophica 1-gen-1991 Colombi, Marina; Gardella, Rita; Barlati, Sergio; Cappa, Sf; Marini, Dario Camillo Cesare; Gasparotti, Roberto
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
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
Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia 1-gen-2017 Gardella, Rita; Sacchetti, Emilio; Legati, Andrea; Magri, Chiara; Traversa, Michele; Gennarelli, Massimo
Compound heterozygosity for a large CNV deletion and a rare missense mutation in the FSTL5 gene of a patient affected by schizophrenia. 1-gen-2012 Gardella, Rita; Legati, Andrea; Magri, Chiara; Traversa, Michele; Gennarelli, Massimo; Sacchetti, Emilio; Barlati, Sergio
Detection of high level of autozygosity in a group of Italian schizophrenia patients 1-gen-2012 Traversa, Michele; Magri, Chiara; Gardella, Rita; Valsecchi, Paolo; Sacchetti, Emilio; Gennarelli, Massimo; Barlati, Sergio
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