GARDELLA, Rita
GARDELLA, Rita
Dipartimento di Medicina Molecolare e Traslazionale
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
2000-01-01 Gardella, Rita; Barlati, Sergio; Zoppi, Nicoletta; Tadini, G; Colombi, Marina
A common MspI RFLP of the human fibronectin gene (FN1)
1988-01-01 Gardella, Rita; Colombi, Marina; Barlati, Sergio
A frequent HaeIII RFLP of the human fibronectin gene
1987-01-01 Colombi, Marina; Gardella, Rita; Barlati, Sergio; Vaheri, A.
A frequent Hind RFLP of the human fibronectin) gene (FN1)
1988-01-01 Colombi, Marina; Gardella, Rita; Barlati, Sergio
A new Taq RFLP of the human fibronecin gene (FN1)
1989-01-01 Gardella, Rita; Colombi, Marina; Barlati, Sergio
A Taq RFLP for the human fibronectin (FN1) gene
1988-01-01 Gardella, Rita; Colombi, Marina; Barlati, Sergio
Analysis of Copy Number Variations in Schizophrenia Italian Patients
2009-01-01 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
2002-01-01 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
1996-01-01 Barlati, Sergio; Belletti, L; Gardella, Rita; Ferraboli, Sergio
Angiocheratomas and arterovenous fistulas with dominant trasmission in the absence of metabolic disorders.
1995-01-01 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.
1995-01-01 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
2009-01-01 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
2006-01-01 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
1991-01-01 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
2004-01-01 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.
2001-01-01 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
2017-01-01 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.
2012-01-01 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
2012-01-01 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.
2002-01-01 Gardella, Rita; Zoppi, Nicoletta; Zambruno, G; Barlati, Sergio; Colombi, Marina
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 |