ROMEO, GIOVANNI
ROMEO, GIOVANNI
DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE
G.ROMEO; Giovanni Romeo; ROMEO G
A cellular model for cancer progression: Role of mitochondrial mutations and metabolism
2010 G. Romeo; G. Gasparre; A.M. Porcelli; M. Rugolo
A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation
2007 Graziano C.; D'Elia AV.; Mazzanti L.; Moscano F.; Guidelli Guidi S.; Scarano E.; Turchetti D.; Franzoni E.; Romeo G.; Damante G.; Seri M.
A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci
2005 Tsilchorozidou T; Vafiadou E; Yovos JG; Romeo G; McKay J; Lesueur F; Bonora E
A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function
2011 Gasparre G; Kurelac I; Capristo M; Iommarini L; Ghelli A; Ceccarelli C; Nicoletti G; Nanni P; De Giovanni C; Scotlandi K; Betts CM; Carelli V; Lollini PL; Romeo G; Rugolo M; Porcelli AM
A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24.
2007 Deglincerti A; De Giorgio R; Cefle K; Devoto M; Pippucci T; Castegnaro G; Panza E; Barbara G; Cogliandro RF; Mungan Z; Palanduz S; Corinaldesi R; Romeo G; Seri M; Stanghellini V.
A Yellow Fluorescent Protein variant as an intracellular iodide biosensor in thyroid cells
2009 K. J. Rhoden; S. Cianchetta; G. Romeo
Allelic loss on chromosomes 2q21 and 19p13.2 in Hürthle thyroid tumors.
2004 STANKOV K.; PASTORE A.; TOSCHI L.; KRAIMPS J.L.; BONNEAU D.; GIBELIN H.; LEVILLAIN P.; VOLANTE M.; PAPOTTI M.; ROMEO G.
An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene.
2009 Sazzini M; Zuntini R; Farjadian S; Quinti I; Ricci G; Romeo G; Ferrari S; Calafell F; Luiselli D.
An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells.
2009 G.Gasparre; L. Iommarini; A.M. Porcelli; M. Lang; G.G. Ferri; I.Kurelac; E. Mariani; L.F. Pennisi; E. Pasquini; G. Pasquinelli; A. Ghelli; E. Bonora; C. Ceccarelli; M. Rugolo; N. Salfi; G. Romeo; V. Carelli.
An interdisciplinary approach to investigate the English spotting locus and its association with megacolon in the domestic rabbit: a new putative model of enteric neuronal dysfunction
2009 Fontanesi L.; Mazzoni M.; Faussone-Pellegrini M.S.; Clavenzani P.; Vargiolu M.; Scotti E.; Chiocchetti R.; Gori A.; Romeo G.; Russo V.; Stanghellini V.; Barbara G.; De Giorgio R.
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways
2012 C. Evangelisti;F. Bianco;L. M. Pradella;A. Puliti;A. Goldoni;I. Sbrana;M. Rossi;M. Vargiolu;M. Seri;G. Romeo;V. Stanghellini;R. de Giorgio;E. Bonora
Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer.
2009 Raitila A; Georgitsi M; Bonora E; Vargiolu M; Tuppurainen K; Mäkinen MJ; Vierimaa O; Salmela PI; Launonen V; Vahteristo P; Aaltonen LA; Romeo G; Karhu A.
Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation.
2009 Graziano C; Carone S; Panza E; Marino F; Magini P; Romeo G; Pession A; Seri M.
AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics
2020 Magi A.; Giangregorio T.; Semeraro R.; Carangelo G.; Palombo F.; Romeo G.; Seri M.; Pippucci T.
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity.
2009 Pippucci T.; Panza E.; Pompilii E.; Donadio V.; Borreca A.; Babalini C.; Patrono C.; Zuntini R.; Kawarai T.; Bernardi G.; Liguori R.; Romeo G.; Montagna P.; Orlacchio A.; Seri M.
C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes.
2007 Yin L.; Puliti A.; Bonora E.; Evangelisti C.; Conti V.; Tong WM.; Medard JJ.; Lavoué MF.; Forey N.; Wang LC.; Manié S.; Morel G.; Raccurt M.; Wang ZQ.; Romeo G.
Cell-based imaging of sodium iodide symporter activity with the yellow fluorescent protein variant YFP-H148Q/I152L.
2007 Rhoden KJ.; Cianchetta S.; Stivani V.; Portulano C.; Galietta L.; Romeo G.
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in renal oncocytoma
2008 E. De Laplanche; G. Gasparre; E. Hervouet; F. Mege-Lechevallier; C. Godinot; G. Romeo; H. Simonnet
Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma
2008 Gasparre G.; Hervouet E.; de Laplanche E.; Demont J.; Pennisi L.F.; Colombel M.; Mège-Lechevallier F.; Scoazec J.Y.; Bonora E.; Smeets R.; Smeitink J.; Lazar V.; Lespinasse J.; Giraud S.; Godinot C.; Romeo G.; Simonnet H.
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration
2015 Magini, Pamela; Poscente, Monica; Ferrari, Simona; Vargiolu, Manuela; Bacchelli, Elena; Graziano, Claudio; Wischmeijer, Anita; Turchetti, Daniela; Malaspina, Elisabetta; Marchiani, Valentina; Cordelli, Duccio Maria; Franzoni, Emilio; Romeo, Giovanni; Seri, Marco
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| A cellular model for cancer progression: Role of mitochondrial mutations and metabolism | G. Romeo; G. Gasparre; A.M. Porcelli; M. Rugolo | 2010-01-01 | JOURNAL OF BIOTECHNOLOGY | - | 4.02 Riassunto (Abstract) | - |
| A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation | Graziano C.; D'Elia AV.; Mazzanti L.; Moscano F.; Guidelli Guidi S.; Scarano E.; Turchetti D.; Fr...anzoni E.; Romeo G.; Damante G.; Seri M. | 2007-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
| A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci | Tsilchorozidou T; Vafiadou E; Yovos JG; Romeo G; McKay J; Lesueur F; Bonora E | 2005-01-01 | THYROID | - | 1.01 Articolo in rivista | - |
| A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function | Gasparre G; Kurelac I; Capristo M; Iommarini L; Ghelli A; Ceccarelli C; Nicoletti G; Nanni P; De ...Giovanni C; Scotlandi K; Betts CM; Carelli V; Lollini PL; Romeo G; Rugolo M; Porcelli AM | 2011-01-01 | CANCER RESEARCH | - | 1.01 Articolo in rivista | - |
| A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24. | Deglincerti A; De Giorgio R; Cefle K; Devoto M; Pippucci T; Castegnaro G; Panza E; Barbara G; Cog...liandro RF; Mungan Z; Palanduz S; Corinaldesi R; Romeo G; Seri M; Stanghellini V. | 2007-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| A Yellow Fluorescent Protein variant as an intracellular iodide biosensor in thyroid cells | K. J. Rhoden; S. Cianchetta; G. Romeo | 2009-01-01 | - | Nova Science Publishers | 2.01 Capitolo / saggio in libro | - |
| Allelic loss on chromosomes 2q21 and 19p13.2 in Hürthle thyroid tumors. | STANKOV K.; PASTORE A.; TOSCHI L.; KRAIMPS J.L.; BONNEAU D.; GIBELIN H.; LEVILLAIN P.; VOLANTE M....; PAPOTTI M.; ROMEO G. | 2004-01-01 | INTERNATIONAL JOURNAL OF CANCER | - | 1.01 Articolo in rivista | - |
| An evolutionary approach to the medical implications of the tumor necrosis factor receptor superfamily member 13B (TNFRSF13B) gene. | Sazzini M; Zuntini R; Farjadian S; Quinti I; Ricci G; Romeo G; Ferrari S; Calafell F; Luiselli D. | 2009-01-01 | GENES AND IMMUNITY | - | 1.01 Articolo in rivista | - |
| An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells. | G.Gasparre; L. Iommarini; A.M. Porcelli; M. Lang; G.G. Ferri; I.Kurelac; E. Mariani; L.F. Pennisi...; E. Pasquini; G. Pasquinelli; A. Ghelli; E. Bonora; C. Ceccarelli; M. Rugolo; N. Salfi; G. Romeo; V. Carelli. | 2009-01-01 | HUMAN MUTATION | - | 1.01 Articolo in rivista | - |
| An interdisciplinary approach to investigate the English spotting locus and its association with megacolon in the domestic rabbit: a new putative model of enteric neuronal dysfunction | Fontanesi L.; Mazzoni M.; Faussone-Pellegrini M.S.; Clavenzani P.; Vargiolu M.; Scotti E.; Chiocc...hetti R.; Gori A.; Romeo G.; Russo V.; Stanghellini V.; Barbara G.; De Giorgio R. | 2009-01-01 | ITALIAN JOURNAL OF ANIMAL SCIENCE | - | 4.02 Riassunto (Abstract) | 18 aspa Fontanesi.pdf |
| Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways | C. Evangelisti;F. Bianco;L. M. Pradella;A. Puliti;A. Goldoni;I. Sbrana;M. Rossi;M. Vargiolu;M. Se...ri;G. Romeo;V. Stanghellini;R. de Giorgio;E. Bonora | 2012-01-01 | NEUROGASTROENTEROLOGY AND MOTILITY | - | 1.01 Articolo in rivista | - |
| Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer. | Raitila A; Georgitsi M; Bonora E; Vargiolu M; Tuppurainen K; Mäkinen MJ; Vierimaa O; Salmela PI; ...Launonen V; Vahteristo P; Aaltonen LA; Romeo G; Karhu A. | 2009-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
| Association of hereditary thrombocythemia and distal limb defects with a thrombopoietin gene mutation. | Graziano C; Carone S; Panza E; Marino F; Magini P; Romeo G; Pession A; Seri M. | 2009-01-01 | BLOOD | - | 1.01 Articolo in rivista | - |
| AUDACITY: A comprehensive approach for the detection and classification of Runs of Homozygosity in medical and population genomics | Magi A.; Giangregorio T.; Semeraro R.; Carangelo G.; Palombo F.; Romeo G.; Seri M.; Pippucci T. | 2020-01-01 | COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL | - | 1.01 Articolo in rivista | 1-s2.0-S2001037020303354-main.pdf; ScienceDirect_files_24Jan2023_11-11-38.150.zip |
| Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. | Pippucci T.; Panza E.; Pompilii E.; Donadio V.; Borreca A.; Babalini C.; Patrono C.; Zuntini R.; ...Kawarai T.; Bernardi G.; Liguori R.; Romeo G.; Montagna P.; Orlacchio A.; Seri M. | 2009-01-01 | EUROPEAN JOURNAL OF NEUROLOGY | - | 1.01 Articolo in rivista | - |
| C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes. | Yin L.; Puliti A.; Bonora E.; Evangelisti C.; Conti V.; Tong WM.; Medard JJ.; Lavoué MF.; Forey N....; Wang LC.; Manié S.; Morel G.; Raccurt M.; Wang ZQ.; Romeo G. | 2007-01-01 | INTERNATIONAL JOURNAL OF CANCER | - | 1.01 Articolo in rivista | - |
| Cell-based imaging of sodium iodide symporter activity with the yellow fluorescent protein variant YFP-H148Q/I152L. | Rhoden KJ.; Cianchetta S.; Stivani V.; Portulano C.; Galietta L.; Romeo G. | 2007-01-01 | AMERICAN JOURNAL OF PHYSIOLOGY. CELL PHYSIOLOGY | - | 1.01 Articolo in rivista | - |
| Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in renal oncocytoma | E. De Laplanche; G. Gasparre; E. Hervouet; F. Mege-Lechevallier; C. Godinot; G. Romeo; H. Simonnet | 2008-01-01 | BULLETIN DU CANCER | - | 4.02 Riassunto (Abstract) | - |
| Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma | Gasparre G.; Hervouet E.; de Laplanche E.; Demont J.; Pennisi L.F.; Colombel M.; Mège-Lechevallie...r F.; Scoazec J.Y.; Bonora E.; Smeets R.; Smeitink J.; Lazar V.; Lespinasse J.; Giraud S.; Godinot C.; Romeo G.; Simonnet H. | 2008-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
| Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration | Magini, Pamela; Poscente, Monica; Ferrari, Simona; Vargiolu, Manuela; Bacchelli, Elena; Graziano,... Claudio; Wischmeijer, Anita; Turchetti, Daniela; Malaspina, Elisabetta; Marchiani, Valentina; Cordelli, Duccio Maria; Franzoni, Emilio; Romeo, Giovanni; Seri, Marco | 2015-01-01 | MOLECULAR CYTOGENETICS | - | 1.01 Articolo in rivista | Magini P et al Recombinant X Chromosome.pdf |