ROMEO, GIOVANNI

ROMEO, GIOVANNI  

DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE  

G.ROMEO; Giovanni Romeo; ROMEO G  

Mostra records
Risultati 1 - 20 di 89 (tempo di esecuzione: 0.025 secondi).
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.pdfScienceDirect_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