CATALOGO DEI PRODOTTI DELLA RICERCA

MOTTES, Monica

MOTTES, Monica  

DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO  

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A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI 1-gen-1995 Zolezzi, F.; Forlino, A.; Mottes, M.; Valli, M.; Sensi, A.; Calzolari, E.; Pignatti, P. F.; Cetta, G.
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 new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments 1-gen-1984 Mottes, Monica; S. A., Tsai Lai; J., Montoya; G., Attardi
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 1-gen-2001 Gomez-Lira, M.; Mottes, M.; Perusi, C.; Pignatti, P. F.; Rizzuto, N.; Gatti, R.; Salviati, A.
A novel intragenic polymorphism within the COL1A1 locus which can be detected by Taq I restriction of amplified genomic DNA 1-gen-1999 S., Mirandola; Pignatti, Pierfranco; Mottes, Monica
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 1-gen-1997 C., Perusi; Gomez, Maria Macarena; Mottes, Monica; Pignatti, Pierfranco; Rizzuto, Nicolo'; Salviati, Alessandro
A potential role for astaxanthin in the treatment of bone diseases (Review) 1-gen-2020 Valenti, Maria Teresa; Perduca, Massimiliano; Romanelli, Maria Grazia; Mottes, Monica; Dalle Carbonare, Luca
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 1-gen-2020 Deiana, Michela; Dalle Carbonare, Luca; Serena, Michela; Cheri, Samuele; Mutascio, Simona; Gandini, Alberto; Innamorati, Giulio; Lorenzi, Pamela; Cumerlato, Michela; Bertacco, Jessica; Antoniazzi, Franco; Romanelli, Maria Grazia; Mottes, Monica; Zipeto, Donato; Valenti, Maria Teresa
Allelic frequencies of FBN1 gene polymorphisms and genetic analysis of Italian families with Marfan syndrome 1-gen-2000 Mottes, M.; Mirandola, S.; Rigatelli, F.; Zolezzi, F.; Lisi, V.; Gordon, D.; Pignatti, P. F.
An integrated approach identifies new oncotargets in melanoma 1-gen-2018 Cecconi, Daniela; Dalle Carbonare, Luca; Mori, Antonio; Cheri, Samuele; Deiana, Michela; Brandi, Jessica; Degaetano, Vincenzo; Masiero, Valentina; Innamorati, Giulio; Mottes, Monica; Malerba, Giovanni; Valenti, Maria Teresa
Analisi di linkage di geni candidati per densità minerale 1-gen-2002 Sangalli, Antonella; Malerba, Giovanni; Xumerle, Luciano; Braga, V.; Adami, Silvano; Mottes, Monica
Anomalous cysteine in type I collagen. Localisation by chemical cleavage of the protein using 2-nitro-5-thiocyanobenzoic acid and by mismatch analysis of cDNA heteroduplexes 1-gen-1990 R., Tenni; A., Rossi; M., Valli; Mottes, Monica; Pignatti, Pierfranco; G., Cetta
Association of BK virus with human brain tumors and tumors of pancreatic islets 1-gen-1987 A., Corallini; M., Pagnani; P., Viadana; E., Silini; Mottes, Monica; G., Milanesi; G., Gerna; R., Vettor; G., Trapella; V., Silvani
Association of CTR and COLIA1 alleles with BMD values in peri and postmenopausal women 1-gen-2000 Braga, V; Mottes, Monica; Mirandola, S; Lisi, Veronica; Malerba, Giovanni; Sartori, L; Bianchi, G; Gatti, Davide; Rossini, Maurizio; Bianchini, D; Adami, Silvano
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.