Sfoglia per Autore
Polymorphisms of the TSH Receptor gene in children with resistance to TSH and in helthy young controls
2004-01-01 Teofoli, Francesca; Camilot, Marta; Gandini, Alberto; Franceschi, Roberto; F., Pellegrini; Monti, Elena; Perlini, Silvia; A., Rapa; A., Corrias; G., Bona; L., Tatò
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
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
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
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
How to cope with a severe skeletal dysplasia
2010-01-01 Monti, Elena; Grazzina, Nicoletta; Corradi, Massimiliano; Gandini, Alberto; Venturi, Giacomo; Doro, Francesco; Morandi, G.; Maines, Evelina; Pietrobelli, Angelo; Antoniazzi, Franco; Padovani, Ezio Maria
A Novel Splicing Mutation in FKBP10 in a patient with a moderate Osteogenesis Imperfecta histologically classificable as type VI
2011-01-01 Venturi, Giacomo; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Gandini, A.; Valenti, Maria Teresa; Morandi, Grazia; Doro, F.; Maines, E.; Boner, Attilio; Antoniazzi, Franco
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I
2011-01-01 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
Novel Splicing Mutation in FKBP10 gene in a patient with moderate-severe form of Osteogenesis imperfecta
2011-01-01 Corradi, Massimiliano; Venturi, Giacomo; Monti, Elena; Gandini, Alberto; DALLE CARBONARE, Luca Giuseppe; Valenti, Maria Teresa; Morandi, G; Doro, Francesco; Maines, Evelina; Boner, Attilio; Antoniazzi, Franco
Hypercalciuria and renal function in children affected by Osteogenesis Imperfecta
2011-01-01 Doro, F.; Monti, Elena; Morandi, Grazia; Maines, E.; Brugnara, Milena; Gandini, A.; Corradi, Massimiliano; Venturi, Giacomo; Antoniazzi, Franco
No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta.
2011-01-01 Maines, Evelina; Monti, Elena; Doro, Francesco; Morandi, G; Venturi, Giacomo; Corradi, Massimiliano; Gandini, Alberto; Mottes, Monica; Antoniazzi, Franco
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
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
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
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
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
CRISPR/Cas9 mediated knock-out of RUNX2 in melanoma cells
2017-01-01 Valenti, Maria Teresa; Zipeto, Donato; Deiana, Michela; Serena, Michela; Parolini, Francesca; Cheri, Samuele; Gandini, Alberto; Mina, Maria Mihaela; Mutascio, Simona; Viser, A; DALLE CARBONARE, Luca Giuseppe
CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain
2017-01-01 Cheri, Samuele; Zipeto, Donato; Deiana, Michela; Serena, Michela; Parolini, Francesca; Gandini, Alberto; Mina, Maria Mihaela; Mutascio, Simona; Visser, Arianna; Mottes, M; DALLE CARBONARE, Luca Giuseppe; Valenti, Maria Teresa
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.
The Runt domain of RUNX2 induces the migration of melanoma cells to bone
2018-01-01 Valenti, Maria Teresa; Deiana, Michela; Serena, Michela; Cheri, Samuele; Parolini, Francesca; Marchetto, Giulia; Mina, Maria Mihaela; Mori, Antonio; Gandini, Alberto; Antoniazzi, Franco; Tiso, Natascia; Malerba, Giovanni; Gennari, Luigi; Mottes, Monica; Zipeto, Donato; DALLE CARBONARE, Luca Giuseppe
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Polymorphisms of the TSH Receptor gene in children with resistance to TSH and in helthy young controls | 1-gen-2004 | Teofoli, Francesca; Camilot, Marta; Gandini, Alberto; Franceschi, Roberto; F., Pellegrini; Monti, Elena; Perlini, Silvia; A., Rapa; A., Corrias; G., Bona; L., Tatò | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| How to cope with a severe skeletal dysplasia | 1-gen-2010 | Monti, Elena; Grazzina, Nicoletta; Corradi, Massimiliano; Gandini, Alberto; Venturi, Giacomo; Doro, Francesco; Morandi, G.; Maines, Evelina; Pietrobelli, Angelo; Antoniazzi, Franco; Padovani, Ezio Maria | |
| A Novel Splicing Mutation in FKBP10 in a patient with a moderate Osteogenesis Imperfecta histologically classificable as type VI | 1-gen-2011 | Venturi, Giacomo; Monti, Elena; DALLE CARBONARE, Luca Giuseppe; Corradi, Massimiliano; Gandini, A.; Valenti, Maria Teresa; Morandi, Grazia; Doro, F.; Maines, E.; Boner, Attilio; Antoniazzi, Franco | |
| Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I | 1-gen-2011 | 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 | |
| Novel Splicing Mutation in FKBP10 gene in a patient with moderate-severe form of Osteogenesis imperfecta | 1-gen-2011 | Corradi, Massimiliano; Venturi, Giacomo; Monti, Elena; Gandini, Alberto; DALLE CARBONARE, Luca Giuseppe; Valenti, Maria Teresa; Morandi, G; Doro, Francesco; Maines, Evelina; Boner, Attilio; Antoniazzi, Franco | |
| Hypercalciuria and renal function in children affected by Osteogenesis Imperfecta | 1-gen-2011 | Doro, F.; Monti, Elena; Morandi, Grazia; Maines, E.; Brugnara, Milena; Gandini, A.; Corradi, Massimiliano; Venturi, Giacomo; Antoniazzi, Franco | |
| No osteonecrosis of the jaw in children and adolescents treated with Neridronate for osteogenesis imperfecta. | 1-gen-2011 | Maines, Evelina; Monti, Elena; Doro, Francesco; Morandi, G; Venturi, Giacomo; Corradi, Massimiliano; Gandini, Alberto; Mottes, Monica; Antoniazzi, Franco | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| 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 | |
| CRISPR/Cas9 mediated knock-out of RUNX2 in melanoma cells | 1-gen-2017 | Valenti, Maria Teresa; Zipeto, Donato; Deiana, Michela; Serena, Michela; Parolini, Francesca; Cheri, Samuele; Gandini, Alberto; Mina, Maria Mihaela; Mutascio, Simona; Viser, A; DALLE CARBONARE, Luca Giuseppe | |
| CRISPR/Cas9 genome editing in melanoma cells: new insight of RUNT domain | 1-gen-2017 | Cheri, Samuele; Zipeto, Donato; Deiana, Michela; Serena, Michela; Parolini, Francesca; Gandini, Alberto; Mina, Maria Mihaela; Mutascio, Simona; Visser, Arianna; Mottes, M; DALLE CARBONARE, Luca Giuseppe; Valenti, Maria Teresa | |
| 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. | |
| The Runt domain of RUNX2 induces the migration of melanoma cells to bone | 1-gen-2018 | Valenti, Maria Teresa; Deiana, Michela; Serena, Michela; Cheri, Samuele; Parolini, Francesca; Marchetto, Giulia; Mina, Maria Mihaela; Mori, Antonio; Gandini, Alberto; Antoniazzi, Franco; Tiso, Natascia; Malerba, Giovanni; Gennari, Luigi; Mottes, Monica; Zipeto, Donato; DALLE CARBONARE, Luca Giuseppe |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile