SANGALLI, Antonella

SANGALLI, Antonella  

DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO  

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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 Malerba, Giovanni; Petrelli, Elena; 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 Petrelli, E.; Malerba, Giovanni; 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