SANGALLI, Antonella
SANGALLI, Antonella
DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO
A base substitution at IVS-19 3' splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta
1994-01-01 Mottes, Monica; Sangalli, Antonella; Valli, M.; Forlino, A.; Gomez, Maria Macarena; Antoniazzi, Franco; CONSTANTINOU DELTAS, C. D.; Cetta, G.; Pignatti, Pierfranco
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta
1994-01-01 Mottes, M.; Sangalli, A.; Valli, M.; Forlino, A.; Gomez-Lira, M.; Antoniazzi, F.; Constantinou-Deltas, C. D.; Cetta, G.; Pignatti, P. F.
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients.
1995-01-01 Gomez, Maria Macarena; Sangalli, Antonella; Mottes, Monica; Perusi, C; Pignatti, Pierfranco; Rizzuto, Nicolo'; Salviati, Alessandro
A de novo G to T transversion in a pro-alpha 1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain
1991-01-01 Valli, M.; Mottes, Monica; Tenni, R.; Sangalli, Antonella; Gomez, Maria Macarena; Rossi, A.; Antoniazzi, Franco; Cetta, G.; Pignatti, Pierfranco
A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophy
2017-01-01 Margoni, M.; Soli, F.; Sangalli, Antonella; Bellizzi, M.; Cecchini, E.; Buganza, M.
Analisi di linkage di geni candidati per densità minerale
2002-01-01 Sangalli, Antonella; Malerba, Giovanni; Xumerle, Luciano; Braga, V.; Adami, Silvano; Mottes, Monica
Association of promoter polymorphism -765G>C in the PTGS2 gene with malignant melanoma in Italian patients and its correlation to gene expression in dermal fibroblasts.
2014-01-01 Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; Santinami, M; Maurichi, A; Sangalli, Antonella; Turco, Alberto; Perego, P; Rodolfo, M.
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts.
2014-01-01 Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; M., Santinami; A., Maurichi; Sangalli, Antonella; Turco, Alberto; P., Perego; M., Rodolfo
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females
2005-01-01 Petrelli, E.; Malerba, Giovanni; Sangalli, Antonella; Xumerle, Luciano; Braga, V.; Pignatti, Pierfranco; Mottes, Monica
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females
2005-01-01 Malerba, Giovanni; Petrelli, Elena; Sangalli, Antonella; Xumerle, Luciano; Braga, V.; Pignatti, Pierfranco; Mottes, Monica
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24
2000-01-01 Floreani, A.; Molaro, M.; Mottes, M.; Sangalli, A.; Baragiotta, A.; Roda, A.; Naccarato, R.; Clementi, M.
Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5' flanking region.
2009-01-01 Romanelli, Maria; Lorenzi, Pamela; Sangalli, Antonella; Diani, Erica; Mottes, Monica
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale
2005-01-01 Ramponi, V; Sangalli, Antonella; Mottes, Monica
Determination of a new collagen type I alpha 2 gene point mutation which causes a Gly640 Cys substitution in osteogenesis imperfecta and prenatal diagnosis by DNA hybridisation
1994-01-01 Gomez-Lira, M.; Sangalli, A.; Pignatti, P. F.; Digilio, M. C.; Giannotti, A.; Carnevale, E.; Mottes, M.
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk
2020-01-01 Belpinati, F.; Malerba, G.; Dal Toè, M.; Ceccuzzi, L.; Rodolfo, M.; Poli, A.; Turco, A.; Vergani, E.; Sangalli, A.; Gomez-Lira, M.
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families.
1993-01-01 Mottes, Monica; Sangalli, Antonella; Pignatti, Pierfranco
HLA-C stability and AIDS progression
2021-01-01 Stefani, Chiara.; Sangalli, A.; Locatelli, E.; Argañaraz, Er.; Argañaraz, Ga.; Bosco da Silva, Cm.; da Silva Duarte, Aj.; Casseb, J.; Romanelli, Mg.; Zipeto, D.
Identification of a novelABCD1 mutation in a family with Adrenoleukodistrophy
2016-01-01 Margoni, M; Buganza, M; Soli, Fiorenza; Sangalli, Antonella; Bellizzi, M; Cecchini, E; Tranquillini, E.
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS).
2006-01-01 Romanelli, Maria; Lorenzi, P; Sangalli, Antonella; Mottes, Monica
Increased prevalence of unstable HLA-C variants in HIV-1 rapid-progressor patients
2022-01-01 Stefani, Chiara; Sangalli, Antonella; Locatelli, Elena; Federico, Tania; Malerba, Giovanni; Romanelli, Maria Grazia; Argañaraz, Gustavo Adolfo; Da Silva, Bosco Christiano Maciel; Da Silva, Alberto Jose Duarte; Casseb, Jorge; Argañaraz, Enrique Roberto; Ruggiero, Alessandra; Zipeto, Donato
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A base substitution at IVS-19 3' splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta | 1-gen-1994 | Mottes, Monica; Sangalli, Antonella; Valli, M.; Forlino, A.; Gomez, Maria Macarena; Antoniazzi, Franco; CONSTANTINOU DELTAS, C. D.; Cetta, G.; Pignatti, Pierfranco | |
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta | 1-gen-1994 | Mottes, M.; Sangalli, A.; Valli, M.; Forlino, A.; Gomez-Lira, M.; Antoniazzi, F.; Constantinou-Deltas, C. D.; Cetta, G.; Pignatti, P. F. | |
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. | 1-gen-1995 | Gomez, Maria Macarena; Sangalli, Antonella; Mottes, Monica; Perusi, C; Pignatti, Pierfranco; Rizzuto, Nicolo'; Salviati, Alessandro | |
A de novo G to T transversion in a pro-alpha 1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain | 1-gen-1991 | Valli, M.; Mottes, Monica; Tenni, R.; Sangalli, Antonella; Gomez, Maria Macarena; Rossi, A.; Antoniazzi, Franco; Cetta, G.; Pignatti, Pierfranco | |
A novel mutation in ABCD1 unveils different clinical phenotypes in a family with adrenoleukodystrophy | 1-gen-2017 | Margoni, M.; Soli, F.; Sangalli, Antonella; Bellizzi, M.; Cecchini, E.; Buganza, M. | |
Analisi di linkage di geni candidati per densità minerale | 1-gen-2002 | Sangalli, Antonella; Malerba, Giovanni; Xumerle, Luciano; Braga, V.; Adami, Silvano; Mottes, Monica | |
Association of promoter polymorphism -765G>C in the PTGS2 gene with malignant melanoma in Italian patients and its correlation to gene expression in dermal fibroblasts. | 1-gen-2014 | Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; Santinami, M; Maurichi, A; Sangalli, Antonella; Turco, Alberto; Perego, P; Rodolfo, M. | |
Association of variant -765G>C in the PTGS2 gene promoter with melanoma in Italian patients and its relation to gene expression in dermal fibroblasts. | 1-gen-2014 | Gomez, Maria Macarena; Ferronato, Silvia; Malerba, Giovanni; M., Santinami; A., Maurichi; Sangalli, Antonella; Turco, Alberto; P., Perego; M., Rodolfo | |
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females | 1-gen-2005 | Petrelli, E.; Malerba, Giovanni; Sangalli, Antonella; Xumerle, Luciano; Braga, V.; Pignatti, Pierfranco; Mottes, Monica | |
Association study of Estrogen receptor-alpha gene with mineral bone density in a group of unrelated Italian females | 1-gen-2005 | Malerba, Giovanni; Petrelli, Elena; Sangalli, Antonella; Xumerle, Luciano; Braga, V.; Pignatti, Pierfranco; Mottes, Monica | |
Autosomal dominant benign recurrent intrahepatic cholestasis (BRIC) unlinked to 18q21 and 2q24 | 1-gen-2000 | Floreani, A.; Molaro, M.; Mottes, M.; Sangalli, A.; Baragiotta, A.; Roda, A.; Naccarato, R.; Clementi, M. | |
Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5' flanking region. | 1-gen-2009 | Romanelli, Maria; Lorenzi, Pamela; Sangalli, Antonella; Diani, Erica; Mottes, Monica | |
Densità dei siti variabili in sequenze codificanti del gene COL1A1 con diversa rilevanza funzionale | 1-gen-2005 | Ramponi, V; Sangalli, Antonella; Mottes, Monica | |
Determination of a new collagen type I alpha 2 gene point mutation which causes a Gly640 Cys substitution in osteogenesis imperfecta and prenatal diagnosis by DNA hybridisation | 1-gen-1994 | Gomez-Lira, M.; Sangalli, A.; Pignatti, P. F.; Digilio, M. C.; Giannotti, A.; Carnevale, E.; Mottes, M. | |
Enhancer of zeste 2 polycomb repressive complex 2 subunit polymorphisms in melanoma skin cancer risk | 1-gen-2020 | Belpinati, F.; Malerba, G.; Dal Toè, M.; Ceccuzzi, L.; Rodolfo, M.; Poli, A.; Turco, A.; Vergani, E.; Sangalli, A.; Gomez-Lira, M. | |
Haplotype analysis of collagen type I genes in the general population and in osteogenesis imperfecta families. | 1-gen-1993 | Mottes, Monica; Sangalli, Antonella; Pignatti, Pierfranco | |
HLA-C stability and AIDS progression | 1-gen-2021 | Stefani, Chiara.; Sangalli, A.; Locatelli, E.; Argañaraz, Er.; Argañaraz, Ga.; Bosco da Silva, Cm.; da Silva Duarte, Aj.; Casseb, J.; Romanelli, Mg.; Zipeto, D. | |
Identification of a novelABCD1 mutation in a family with Adrenoleukodistrophy | 1-gen-2016 | Margoni, M; Buganza, M; Soli, Fiorenza; Sangalli, Antonella; Bellizzi, M; Cecchini, E; Tranquillini, E. | |
Identificazione ed analisi della regione 5' del gene umano per l'enzima farnesil difosfato sintetasi (FDPS). | 1-gen-2006 | Romanelli, Maria; Lorenzi, P; Sangalli, Antonella; Mottes, Monica | |
Increased prevalence of unstable HLA-C variants in HIV-1 rapid-progressor patients | 1-gen-2022 | Stefani, Chiara; Sangalli, Antonella; Locatelli, Elena; Federico, Tania; Malerba, Giovanni; Romanelli, Maria Grazia; Argañaraz, Gustavo Adolfo; Da Silva, Bosco Christiano Maciel; Da Silva, Alberto Jose Duarte; Casseb, Jorge; Argañaraz, Enrique Roberto; Ruggiero, Alessandra; Zipeto, Donato |