SORRENTINO, VINCENZO
SORRENTINO, VINCENZO
Dipartimento di Medicina Molecolare e dello Sviluppo
2-Aminopurine unravels a role for pRB in the regulation of gene expression by transforming growth factor beta
1997-01-01 Giannini, G.; Marcotullio, L. D.; Zazzeroni, F.; Alesse, E.; Zani, M.; T'Ang, A.; Sorrentino, V.; Screpanti, I.; Frati, L.; Gulino, A.
A Click Chemistry-Based “Grafting Through” Approach to the Synthesis of a Biorelevant Polymer Brush
2011-01-01 Cappelli, A.; Paolino, M.; Grisci, G.; Giuliani, G.; Donati, A.; Mendichi, R.; Boccia, A. C.; Samperi, F.; Battiato, S.; Paccagnini, E.; Giacomello, E.; Sorrentino, V.; Licciardi, M.; Giammona, G.; Vomero, S.
A human amniotic cell line yielding high titres of human fibroblast interferon
1982-01-01 Sorrentino, V.; Francesco, P. D.; Soria, M.; Rossi, G. B.
A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates
2014-01-01 Rossi, D.; Vezzani, B.; Galli, L.; Paolini, C.; Toniolo, L.; Pierantozzi, E.; Spinozzi, S.; Barone, V.; Pegoraro, E.; Bello, L.; Cenacchi, G.; Vattemi, G.; Tomelleri, G.; Ricci, G.; Siciliano, G.; Protasi, F.; Reggiani, C.; Sorrentino, V.
A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome)
2000-01-01 Orrico, A.; Galli, L.; Falciani, M.; Bracci, M.; Cavaliere, M. L.; Rinaldi, M. M.; Musacchio, A.; Sorrentino, V.
A novel c-kit transcript, potentially encoding a truncated receptor, originates within a kit gene intron in mouse spermatids
1992-01-01 Rossi, P.; Marziali, G.; Albanesi, C.; Charlesworth, A.; Geremia, R.; Sorrentino, V.
A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy
2017-01-01 Rossi, Daniela; Palmio, Johanna; Evilã¤, Anni; Galli, Lucia; Barone, Virginia; Caldwell, Tracy A.; Policke, Rachel A.; Aldkheil, Esraa; Berndsen, Christopher E.; Wright, Nathan T.; Malfatti, Edoardo; Brochier, Guy; Pierantozzi, Enrico; Jordanova, Albena; Guergueltcheva, Velina; Romero, Norma Beatriz; Hackman, Peter; Eymard, Bruno; Udd, Bjarne; Sorrentino, Vincenzo
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia
2020-01-01 Rossi, D.; Gigli, L.; Gamberucci, A.; Bordoni, R.; Pietrelli, A.; Lorenzini, S.; Pierantozzi, E.; Peretto, G.; De Bellis, G.; Della Bella, P.; Ferrari, M.; Sorrentino, V.; Benedetti, S.; Sala, S.; Di Resta, C.
A novel type 2 diabetes risk allele increases the promoter activity of the muscle-specific small ankyrin 1 gene
2016-01-01 Yan, Rengna; Lai, Shanshan; Yang, Yang; Shi, Hongfei; Cai, Zhenming; Sorrentino, Vincenzo; Du, Hong; Chen, Huimei
A pivotal role for cADPR-mediated Ca2+ signaling: regulation of endothelin-induced contraction in peritubular smooth muscle cells
2002-01-01 Barone, F.; Genazzani, A. A.; Conti, A.; Churchill, G. C.; Palombi, F.; Ziparo, E.; Sorrentino, V.; Galione, A.; Filippini, A.
A proteolytic cleavage to separate the sarcolemma/T-tubule from the sarcoplasmic reticulum
2013-01-01 Sorrentino, V.
A quantitative assessment of circulating progenitor cells in competitive athletes and in sedentary subjects
2015-01-01 D'Ascenzi, F.; Zacà, V.; Maiorca, S.; Neri, A.; Aldinucci, C.; Sorrentino, V.; Causarano, A.; Bonifazi, M.; Mondillo, S.
A Rett syndrome MECP2 mutation that causes mental retardation in men
2002-01-01 Dotti, Maria; Orrico, A.; DE STEFANO, Nicola; Battisti, Carla; Sicurelli, F.; Severi, S.; Lam, C. W.; Galli, L.; Sorrentino, Vincenzo; Federico, Antonio
A truncation in the RYR1 gene associated with central core lesions in skeletal muscle fibres
2007-01-01 Rossi, D.; Smet, P. D.; Lyfenko, A.; Galli, L.; Lorenzini, S.; Franci, D.; Petrioli, F.; Orrico, C.; Angelini, C.; Tegazzin, V.; Dirksen, R.; Sorrentino, V.
Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene
2010-01-01 Orrico, A.; Galli, L.; Faivre, L.; Clayton-Smith, J.; Azzarello-Burri, S. M.; Hertz, J. M.; Jacquemont, S.; Taurisano, R.; Carrera, I. A.; Tarantino, E.; Devriendt, K.; Melis, D.; Thelle, T.; Meinhardt, U.; Sorrentino, V.
Action of lysosomotropic amines on spontaneous and interferon enhanced NK and CTL cytolysis
1984-01-01 Ausiello, C.; Sorrentino, V.; Ruggiero, V.; Rossi, G. B.
Adult onset multi/minicore myopathy associated with a mutation in the RYR1 gene
2004-01-01 Pietrini, V.; Marbini, A.; Galli, L.; Sorrentino, V.
Allele-specific silencing by RNAi of R92Q and R173W mutations in cardiac troponin T
2022-01-01 Migliore, L.; Galvagni, F.; Pierantozzi, E.; Sorrentino, V.; Rossi, D.
Alpha and beta isoforms of ryanodine receptor from chicken skeletal muscle are the homologues of mammalian RyR1 and RyR3
1996-01-01 Ottini, L.; Marziali, G.; Conti, A.; Charlesworth, A.; Sorrentino, V.
Alteration in calcium handling at the subcellular level in mdx myotubes
2001-01-01 Robert, V.; Massimino, M. L.; Tosello, V.; R., Marsault; Cantini, M.; Sorrentino, V.; Pozzan, T.
| Titolo | Data di pubblicazione | Autore(i) | File | Abstract |
|---|---|---|---|---|
| 2-Aminopurine unravels a role for pRB in the regulation of gene expression by transforming growth factor beta | 1-gen-1997 | Giannini, G.; Marcotullio, L. D.; Zazzeroni, F.; Alesse, E.; Zani, M.; T'Ang, A.; Sorrentino, V.; Screpanti, I.; Frati, L.; Gulino, A. | - | |
| A Click Chemistry-Based “Grafting Through” Approach to the Synthesis of a Biorelevant Polymer Brush | 1-gen-2011 | Cappelli, A.; Paolino, M.; Grisci, G.; Giuliani, G.; Donati, A.; Mendichi, R.; Boccia, A. C.; Samperi, F.; Battiato, S.; Paccagnini, E.; Giacomello, E.; Sorrentino, V.; Licciardi, M.; Giammona, G.; Vomero, S. | - | |
| A human amniotic cell line yielding high titres of human fibroblast interferon | 1-gen-1982 | Sorrentino, V.; Francesco, P. D.; Soria, M.; Rossi, G. B. | - | |
| A mutation in the CASQ1 gene causes a vacuolar myopathy with accumulation of sarcoplasmic reticulum protein aggregates | 1-gen-2014 | Rossi, D.; Vezzani, B.; Galli, L.; Paolini, C.; Toniolo, L.; Pierantozzi, E.; Spinozzi, S.; Barone, V.; Pegoraro, E.; Bello, L.; Cenacchi, G.; Vattemi, G.; Tomelleri, G.; Ricci, G.; Siciliano, G.; Protasi, F.; Reggiani, C.; Sorrentino, V. | - | |
| A mutation in the pleckstrin homology (PH) domain of the FGD1 gene in an Italian family with faciogenital dysplasia (Aarskog-Scott syndrome) | 1-gen-2000 | Orrico, A.; Galli, L.; Falciani, M.; Bracci, M.; Cavaliere, M. L.; Rinaldi, M. M.; Musacchio, A.; Sorrentino, V. | - | |
| A novel c-kit transcript, potentially encoding a truncated receptor, originates within a kit gene intron in mouse spermatids | 1-gen-1992 | Rossi, P.; Marziali, G.; Albanesi, C.; Charlesworth, A.; Geremia, R.; Sorrentino, V. | - | |
| A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy | 1-gen-2017 | Rossi, Daniela; Palmio, Johanna; Evilã¤, Anni; Galli, Lucia; Barone, Virginia; Caldwell, Tracy A.; Policke, Rachel A.; Aldkheil, Esraa; Berndsen, Christopher E.; Wright, Nathan T.; Malfatti, Edoardo; Brochier, Guy; Pierantozzi, Enrico; Jordanova, Albena; Guergueltcheva, Velina; Romero, Norma Beatriz; Hackman, Peter; Eymard, Bruno; Udd, Bjarne; Sorrentino, Vincenzo | - | |
| A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia | 1-gen-2020 | Rossi, D.; Gigli, L.; Gamberucci, A.; Bordoni, R.; Pietrelli, A.; Lorenzini, S.; Pierantozzi, E.; Peretto, G.; De Bellis, G.; Della Bella, P.; Ferrari, M.; Sorrentino, V.; Benedetti, S.; Sala, S.; Di Resta, C. | - | |
| A novel type 2 diabetes risk allele increases the promoter activity of the muscle-specific small ankyrin 1 gene | 1-gen-2016 | Yan, Rengna; Lai, Shanshan; Yang, Yang; Shi, Hongfei; Cai, Zhenming; Sorrentino, Vincenzo; Du, Hong; Chen, Huimei | - | |
| A pivotal role for cADPR-mediated Ca2+ signaling: regulation of endothelin-induced contraction in peritubular smooth muscle cells | 1-gen-2002 | Barone, F.; Genazzani, A. A.; Conti, A.; Churchill, G. C.; Palombi, F.; Ziparo, E.; Sorrentino, V.; Galione, A.; Filippini, A. | - | |
| A proteolytic cleavage to separate the sarcolemma/T-tubule from the sarcoplasmic reticulum | 1-gen-2013 | Sorrentino, V. | - | |
| A quantitative assessment of circulating progenitor cells in competitive athletes and in sedentary subjects | 1-gen-2015 | D'Ascenzi, F.; Zacà, V.; Maiorca, S.; Neri, A.; Aldinucci, C.; Sorrentino, V.; Causarano, A.; Bonifazi, M.; Mondillo, S. | - | |
| A Rett syndrome MECP2 mutation that causes mental retardation in men | 1-gen-2002 | Dotti, Maria; Orrico, A.; DE STEFANO, Nicola; Battisti, Carla; Sicurelli, F.; Severi, S.; Lam, C. W.; Galli, L.; Sorrentino, Vincenzo; Federico, Antonio | - | |
| A truncation in the RYR1 gene associated with central core lesions in skeletal muscle fibres | 1-gen-2007 | Rossi, D.; Smet, P. D.; Lyfenko, A.; Galli, L.; Lorenzini, S.; Franci, D.; Petrioli, F.; Orrico, C.; Angelini, C.; Tegazzin, V.; Dirksen, R.; Sorrentino, V. | - | |
| Aarskog-Scott syndrome: clinical update and report of nine novel mutations of the FGD1 gene | 1-gen-2010 | Orrico, A.; Galli, L.; Faivre, L.; Clayton-Smith, J.; Azzarello-Burri, S. M.; Hertz, J. M.; Jacquemont, S.; Taurisano, R.; Carrera, I. A.; Tarantino, E.; Devriendt, K.; Melis, D.; Thelle, T.; Meinhardt, U.; Sorrentino, V. | - | |
| Action of lysosomotropic amines on spontaneous and interferon enhanced NK and CTL cytolysis | 1-gen-1984 | Ausiello, C.; Sorrentino, V.; Ruggiero, V.; Rossi, G. B. | - | |
| Adult onset multi/minicore myopathy associated with a mutation in the RYR1 gene | 1-gen-2004 | Pietrini, V.; Marbini, A.; Galli, L.; Sorrentino, V. | - | |
| Allele-specific silencing by RNAi of R92Q and R173W mutations in cardiac troponin T | 1-gen-2022 | Migliore, L.; Galvagni, F.; Pierantozzi, E.; Sorrentino, V.; Rossi, D. | - | |
| Alpha and beta isoforms of ryanodine receptor from chicken skeletal muscle are the homologues of mammalian RyR1 and RyR3 | 1-gen-1996 | Ottini, L.; Marziali, G.; Conti, A.; Charlesworth, A.; Sorrentino, V. | - | |
| Alteration in calcium handling at the subcellular level in mdx myotubes | 1-gen-2001 | Robert, V.; Massimino, M. L.; Tosello, V.; R., Marsault; Cantini, M.; Sorrentino, V.; Pozzan, T. | - |