MOTTES, Monica
MOTTES, Monica
DIPARTIMENTO DI NEUROSCIENZE, BIOMEDICINA E MOVIMENTO
A 931 +2T-C transition in one COL1A2 allele causes exon 16 skipping in pro alpha 2(I) mRNA and produces moderately severe OI
1995-01-01 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
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 new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments
1984-01-01 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
2001-01-01 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
1999-01-01 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
1997-01-01 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)
2020-01-01 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
2020-01-01 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
2000-01-01 Mottes, M.; Mirandola, S.; Rigatelli, F.; Zolezzi, F.; Lisi, V.; Gordon, D.; Pignatti, P. F.
An integrated approach identifies new oncotargets in melanoma
2018-01-01 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
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
1990-01-01 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
1987-01-01 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
2000-01-01 Braga, V; Mottes, Monica; Mirandola, S; Lisi, Veronica; Malerba, Giovanni; Sartori, L; Bianchi, G; Gatti, Davide; Rossini, Maurizio; Bianchini, D; Adami, Silvano
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.
BEL β‐Trefoil Reduces the Migration Ability of RUNX2 Expressing Melanoma Cells in Xenotransplanted Zebrafish
2020-01-01 Valenti, Mt; Marchetto, G; Perduca, M; Tiso, N; Mottes, M; Dalle Carbonare, L
Bone histomorphometry in acromegaly patients with fragility vertebral fractures
2018-01-01 Dalle Carbonare, L.; Micheletti, V.; Cosaro, E.; Valenti, M. T.; Mottes, M.; Francia, G.; Davì, M. V.
Can half-marathon affect overall health? The yin-yang of sport
2018-01-01 DALLE CARBONARE, Luca Giuseppe; Manfredi, Marcello; Caviglia, Giuseppe; Conte, Eleonora; Robotti, Elisa; Marengo, Emilio; Cheri, Samuele; Zamboni, Francesco; Gabbiani, Daniele; Deiana, Michela; Cecconi, Daniela; Schena, Federico; Mottes, Monica; Valenti, Maria Teresa
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| 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 | |
| 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. | |
| BEL β‐Trefoil Reduces the Migration Ability of RUNX2 Expressing Melanoma Cells in Xenotransplanted Zebrafish | 1-gen-2020 | Valenti, Mt; Marchetto, G; Perduca, M; Tiso, N; Mottes, M; Dalle Carbonare, L | |
| Bone histomorphometry in acromegaly patients with fragility vertebral fractures | 1-gen-2018 | Dalle Carbonare, L.; Micheletti, V.; Cosaro, E.; Valenti, M. T.; Mottes, M.; Francia, G.; Davì, M. V. | |
| Can half-marathon affect overall health? The yin-yang of sport | 1-gen-2018 | DALLE CARBONARE, Luca Giuseppe; Manfredi, Marcello; Caviglia, Giuseppe; Conte, Eleonora; Robotti, Elisa; Marengo, Emilio; Cheri, Samuele; Zamboni, Francesco; Gabbiani, Daniele; Deiana, Michela; Cecconi, Daniela; Schena, Federico; Mottes, Monica; Valenti, Maria Teresa |