GANDINI, Alberto
GANDINI, Alberto
DIPARTIMENTO DI SCIENZE CHIRURGICHE, ODONTOSTOMATOLOGICHE E MATERNO-INFANTILI
A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect
2012-01-01 Venturi, Giacomo; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Gandini, Alberto; Valenti, Maria Teresa; Boner, Attilio; Antoniazzi, Franco
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
A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis
2008-01-01 Camilot, Marta; Teofoli, Francesca; S., Longobardi; Gandini, Alberto; C., Lievore; S., Lauriola; Tato', Luciano
Analysis of the d3-growth hormone receptor polymorphism in large cohorts of small, appropriate and large for gestational age newborns.
2016-01-01 Vincenzi, Monica; ION POPA, Florina; Corradi, Massimiliano; Gandini, Alberto; Teofoli, Francesca; Camilot, Marta; Boner, Attilio; Cavarzere, Paolo; Gaudino, Rossella; Antoniazzi, Franco
Apparent Mineralocorticoid Excess by a Novel Mutation and Epigenetic Modulation by HSD11B2 Promoter Methylation
2015-01-01 Pizzolo, Francesca; Friso, Simonetta; Morandini, Francesca; Antoniazzi, Franco; Zaltron, Chiara; Udali, Silvia; Gandini, Alberto; Cavarzere, Paolo; Salvagno, GIAN LUCA; Giorgetti, Alejandro; Speziali, Giulia; Choi, Sang Woon; Olivieri, Oliviero
Exploring the Interplay of RUNX2 and CXCR4 in Melanoma Progression
2024-01-01 Dalle Carbonare, Luca; Minoia, Arianna; Vareschi, Anna; Piritore, Francesca Cristiana; Zouari, Sharazed; Gandini, Alberto; Meneghel, Mirko; Elia, Rossella; Lorenzi, Pamela; Antoniazzi, Franco; Pessoa, João; Zipeto, Donato; Romanelli, Maria Grazia; Guardavaccaro, Daniele; Valenti, Maria Teresa
Expression of FBXW11 in normal and disease-associated osteogenic cells
2023-01-01 Dalle Carbonare, Luca; Gomez Lira, Macarena; Minoia, Arianna; Bertacco, Jessica; Orsi, Silvia; Lauriola, Angela; Li Vigni, Veronica; Gandini, Alberto; Antoniazzi, Franco; Zipeto, Donato; Mottes, Monica; Bhandary, Lekhana; Guardavaccaro, Daniele; Valenti, Maria Teresa
Fisetin: an integrated approach to identify a strategy promoting osteogenesis
2022-01-01 Dalle Carbonare, Luca; Bertacco, Jessica; Gaglio, Salvatore Calogero; Minoia, Arianna; Cominacini, Mattia; Cheri, Samuele; Deiana, Michela; Marchetto, Giulia; Bisognin, Anna; Gandini, Alberto; Antoniazzi, Franco; Perduca, Massimiliano; Mottes, Monica; Valenti, Maria Teresa
Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern italian neonatal screening
2005-01-01 Zaffanello, Marco; Zamboni, Giorgio; Maselli, M; Gandini, Alberto; Camilot, Marta; Maffeis, Claudio; Burlina, Ab; Tato', Luciano
Hypophosphatasia in adults: A new manifestation, a new mutation. A case report
2018-01-01 Adami, G.; Viapiana, O.; Rossini, M.; Risoli, M.; Gandini, A.; Bertoldo, F.; Fassio, A.; Idolazzi, L.; Antoniazzi, F.; Gatti, D.
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen
2012-01-01 Venturi, Giacomo; Gandini, Alberto; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Vincenzi, Monica; Valenti, Maria Teresa; Valli, M.; Pelilli, E.; Boner, Attilio; Mottes, Monica; Antoniazzi, Franco
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration
2018-01-01 Deiana, Michela; Dalle Carbonare, Luca; Serena, Michela; Cheri, Samuele; Parolini, Francesca; Gandini, Alberto; Marchetto, Giulia; Innamorati, Giulio; Manfredi, Marcello; Marengo, Emilio; Brandi, Jessica; Cecconi, Daniela; Mori, Antonio; Mina, Maria Mihaela; Antoniazzi, Franco; Mottes, Monica; Tiso, Natascia; Malerba, Giovanni; Zipeto, Donato; Valenti, Maria Teresa
Prostaglandin D2 synthase and its post-translational modifications in neurological disorders
2005-01-01 Lescuyer, Pierre; Gandini, Alberto; Burkhard, Pierre R.; Hochstrasser, Denis F.; Sanchez, Jean-Charles
Role of genetic investigation in the diagnosis of short stature in a cohort of Italian children
2024-01-01 Cavarzere, P; Pietrobelli, A; Gandini, A; Munari, S; Baffico, A M; Maffei, M; Gaudino, R; Guzzo, A; Arrigoni, M; Coviello, D; Piacentini, G; Antoniazzi, F
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma
2019-01-01 Cecconi, Daniela; Brandi, Jessica; Manfredi, Marcello; Serena, Michela; Carbonare, Luca Dalle; Deiana, Michela; Cheri, Samuele; Parolini, Francesca; Gandini, Alberto; Marchetto, Giulia; Innamorati, Giulio; Avanzi, Francesco; Antoniazzi, Franco; Marengo, Emilio; Tiso, Natascia; Mottes, Monica; Zipeto, Donato; Valenti, Maria Teresa
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene
2014-01-01 Corradi, Massimiliano; Monti, E.; Venturi, Giacomo; Gandini, Alberto; Mottes, Monica; Antoniazzi, Franco
Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes.
2005-01-01 Camilot, Marta; Teofoli, Francesca; Gandini, Alberto; Franceschi, R; Rapa, A; Corrias, A; Bona, G; Radetti, G; Tato', Luciano
Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression
2021-01-01 DALLE CARBONARE, Luca Giuseppe; Antoniazzi, Franco; Gandini, Alberto; Orsi, Silvia; Bertacco, Jessica; LI VIGNI, Veronica; Minoia, Arianna; Griggio, Francesca; Perduca, Massimiliano; Mottes, Monica; Valenti, Maria Teresa
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism
2022-01-01 Antoniazzi, F; Pietrobelli, A; Gandini, A.; Cavarzere, P.; Ramaroli, D. A.; Mottes, M.; Guzzo, A.; Gironcoli, De; Genesini, S.; Zaffanello, M.; Gaudino, R.; Dalle Carbonare, L; Valenti, Mt; Gatti, D; Fassio, A; Bertoldo, F; Tardivo, S; Piacentini, G.
West Nile Virus Encephalitis in Haematological Setting: Report of Two Cases and a Brief Review of the Literature
2019-01-01 Ferrarini, Isacco; Rigo, Antonella; Gandini, Alberto; Vinante, Fabrizio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect | 1-gen-2012 | Venturi, Giacomo; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Gandini, Alberto; Valenti, Maria Teresa; Boner, Attilio; Antoniazzi, Franco | |
| 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 | |
| A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis | 1-gen-2008 | Camilot, Marta; Teofoli, Francesca; S., Longobardi; Gandini, Alberto; C., Lievore; S., Lauriola; Tato', Luciano | |
| Analysis of the d3-growth hormone receptor polymorphism in large cohorts of small, appropriate and large for gestational age newborns. | 1-gen-2016 | Vincenzi, Monica; ION POPA, Florina; Corradi, Massimiliano; Gandini, Alberto; Teofoli, Francesca; Camilot, Marta; Boner, Attilio; Cavarzere, Paolo; Gaudino, Rossella; Antoniazzi, Franco | |
| Apparent Mineralocorticoid Excess by a Novel Mutation and Epigenetic Modulation by HSD11B2 Promoter Methylation | 1-gen-2015 | Pizzolo, Francesca; Friso, Simonetta; Morandini, Francesca; Antoniazzi, Franco; Zaltron, Chiara; Udali, Silvia; Gandini, Alberto; Cavarzere, Paolo; Salvagno, GIAN LUCA; Giorgetti, Alejandro; Speziali, Giulia; Choi, Sang Woon; Olivieri, Oliviero | |
| Exploring the Interplay of RUNX2 and CXCR4 in Melanoma Progression | 1-gen-2024 | Dalle Carbonare, Luca; Minoia, Arianna; Vareschi, Anna; Piritore, Francesca Cristiana; Zouari, Sharazed; Gandini, Alberto; Meneghel, Mirko; Elia, Rossella; Lorenzi, Pamela; Antoniazzi, Franco; Pessoa, João; Zipeto, Donato; Romanelli, Maria Grazia; Guardavaccaro, Daniele; Valenti, Maria Teresa | |
| Expression of FBXW11 in normal and disease-associated osteogenic cells | 1-gen-2023 | Dalle Carbonare, Luca; Gomez Lira, Macarena; Minoia, Arianna; Bertacco, Jessica; Orsi, Silvia; Lauriola, Angela; Li Vigni, Veronica; Gandini, Alberto; Antoniazzi, Franco; Zipeto, Donato; Mottes, Monica; Bhandary, Lekhana; Guardavaccaro, Daniele; Valenti, Maria Teresa | |
| Fisetin: an integrated approach to identify a strategy promoting osteogenesis | 1-gen-2022 | Dalle Carbonare, Luca; Bertacco, Jessica; Gaglio, Salvatore Calogero; Minoia, Arianna; Cominacini, Mattia; Cheri, Samuele; Deiana, Michela; Marchetto, Giulia; Bisognin, Anna; Gandini, Alberto; Antoniazzi, Franco; Perduca, Massimiliano; Mottes, Monica; Valenti, Maria Teresa | |
| Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern italian neonatal screening | 1-gen-2005 | Zaffanello, Marco; Zamboni, Giorgio; Maselli, M; Gandini, Alberto; Camilot, Marta; Maffeis, Claudio; Burlina, Ab; Tato', Luciano | |
| Hypophosphatasia in adults: A new manifestation, a new mutation. A case report | 1-gen-2018 | Adami, G.; Viapiana, O.; Rossini, M.; Risoli, M.; Gandini, A.; Bertoldo, F.; Fassio, A.; Idolazzi, L.; Antoniazzi, F.; Gatti, D. | |
| Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen | 1-gen-2012 | Venturi, Giacomo; Gandini, Alberto; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Vincenzi, Monica; Valenti, Maria Teresa; Valli, M.; Pelilli, E.; Boner, Attilio; Mottes, Monica; Antoniazzi, Franco | |
| New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration | 1-gen-2018 | Deiana, Michela; Dalle Carbonare, Luca; Serena, Michela; Cheri, Samuele; Parolini, Francesca; Gandini, Alberto; Marchetto, Giulia; Innamorati, Giulio; Manfredi, Marcello; Marengo, Emilio; Brandi, Jessica; Cecconi, Daniela; Mori, Antonio; Mina, Maria Mihaela; Antoniazzi, Franco; Mottes, Monica; Tiso, Natascia; Malerba, Giovanni; Zipeto, Donato; Valenti, Maria Teresa | |
| Prostaglandin D2 synthase and its post-translational modifications in neurological disorders | 1-gen-2005 | Lescuyer, Pierre; Gandini, Alberto; Burkhard, Pierre R.; Hochstrasser, Denis F.; Sanchez, Jean-Charles | |
| Role of genetic investigation in the diagnosis of short stature in a cohort of Italian children | 1-gen-2024 | Cavarzere, P; Pietrobelli, A; Gandini, A; Munari, S; Baffico, A M; Maffei, M; Gaudino, R; Guzzo, A; Arrigoni, M; Coviello, D; Piacentini, G; Antoniazzi, F | |
| Runx2 stimulates neoangiogenesis through the Runt domain in melanoma | 1-gen-2019 | Cecconi, Daniela; Brandi, Jessica; Manfredi, Marcello; Serena, Michela; Carbonare, Luca Dalle; Deiana, Michela; Cheri, Samuele; Parolini, Francesca; Gandini, Alberto; Marchetto, Giulia; Innamorati, Giulio; Avanzi, Francesco; Antoniazzi, Franco; Marengo, Emilio; Tiso, Natascia; Mottes, Monica; Zipeto, Donato; Valenti, Maria Teresa | |
| The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene | 1-gen-2014 | Corradi, Massimiliano; Monti, E.; Venturi, Giacomo; Gandini, Alberto; Mottes, Monica; Antoniazzi, Franco | |
| Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes. | 1-gen-2005 | Camilot, Marta; Teofoli, Francesca; Gandini, Alberto; Franceschi, R; Rapa, A; Corrias, A; Bona, G; Radetti, G; Tato', Luciano | |
| Two novel C-terminus RUNX2 mutations in two cleidocranial dysplasia (CCD) patients impairing p53 expression | 1-gen-2021 | DALLE CARBONARE, Luca Giuseppe; Antoniazzi, Franco; Gandini, Alberto; Orsi, Silvia; Bertacco, Jessica; LI VIGNI, Veronica; Minoia, Arianna; Griggio, Francesca; Perduca, Massimiliano; Mottes, Monica; Valenti, Maria Teresa | |
| Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism | 1-gen-2022 | Antoniazzi, F; Pietrobelli, A; Gandini, A.; Cavarzere, P.; Ramaroli, D. A.; Mottes, M.; Guzzo, A.; Gironcoli, De; Genesini, S.; Zaffanello, M.; Gaudino, R.; Dalle Carbonare, L; Valenti, Mt; Gatti, D; Fassio, A; Bertoldo, F; Tardivo, S; Piacentini, G. | |
| West Nile Virus Encephalitis in Haematological Setting: Report of Two Cases and a Brief Review of the Literature | 1-gen-2019 | Ferrarini, Isacco; Rigo, Antonella; Gandini, Alberto; Vinante, Fabrizio |