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ItalianoROMEO, GIOVANNI
Dettaglio
ROMEO, GIOVANNI
DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE
G.ROMEO; Giovanni Romeo; ROMEO G
Pubblicazioni
Risultati 1 - 20 di 85 (tempo di esecuzione: 0.001 secondi).
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File | |
|---|---|---|---|---|---|---|---|
| 1 | A cellular model for cancer progression: Role of mitochondrial mutations and metabolism | G. Romeo; G. Gasparre; A.M. Porcelli; M. Rugolo | 2010 | JOURNAL OF BIOTECHNOLOGY | 4.02 Riassunto (Abstract) | - | |
| 2 | 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 | THYROID | 1.01 Articolo in rivista | - | |
| 3 | 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 | EUROPEAN JOURNAL OF HUMAN GENETICS | 1.01 Articolo in rivista | - | |
| 4 | A Yellow Fluorescent Protein variant as an intracellular iodide biosensor in thyroid cells | K. J. Rhoden; S. Cianchetta; G. Romeo | 2009 | Nova Science Publishers | 2.01 Capitolo / saggio in libro | - | |
| 5 | 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 | INTERNATIONAL JOURNAL OF CANCER | 1.01 Articolo in rivista | - | |
| 6 | 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 | NEUROGASTROENTEROLOGY AND MOTILITY | 1.01 Articolo in rivista | - | |
| 7 | 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 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | 1.01 Articolo in rivista | - | |
| 8 | 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 | BLOOD | 1.01 Articolo in rivista | - | |
| 9 | 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 | COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL | 1.01 Articolo in rivista | - | |
| 10 | 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 | EUROPEAN JOURNAL OF NEUROLOGY | 1.01 Articolo in rivista | - | |
| 11 | The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies. | E. Panza; G. Gimelli; M. Passalacqua; A. Cohen; S. Gimelli; S. Giglio; C. Ghezzi; B. Sparatore; B.... Heye; O. Zuffardi; E. Rugarli; T. Meitinger; G. Romeo; R. Ravazzolo; M. Seri. | 2007 | INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE | 1.01 Articolo in rivista | - | |
| 12 | 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 | INTERNATIONAL JOURNAL OF CANCER | 1.01 Articolo in rivista | - | |
| 13 | 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 | AMERICAN JOURNAL OF PHYSIOLOGY. CELL PHYSIOLOGY | 1.01 Articolo in rivista | - | |
| 14 | 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 | BULLETIN DU CANCER | 4.02 Riassunto (Abstract) | - | |
| 15 | 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 | HUMAN MOLECULAR GENETICS | 1.01 Articolo in rivista | - | |
| 16 | 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 | MOLECULAR CYTOGENETICS | 1.01 Articolo in rivista | ||
| 17 | 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 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | 1.01 Articolo in rivista | - | |
| 18 | Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III | BONORA E.; PORCELLI A.M.; GASPARRE G.; BIONDI A.; GHELLI A.; CARELLI V.; BARACCA A.; TALLINI G.; ...MARTINUZZI A.; LENAZ G.; RUGOLO M.; ROMEO G. | 2006 | CANCER RESEARCH | 1.01 Articolo in rivista | - | |
| 19 | Discordant patterns of mtDNA and ethno-linguistic variation in 14 Iranian Ethnic groups. | Farjadian S.; Sazzini M.; Tofanelli S.; Castrì L.; Taglioli L.; Pettener D.; Ghaderi A.; Romeo G....; Luiselli D. | 2011 | HUMAN HEREDITY | 1.01 Articolo in rivista | - | |
| 20 | Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours. | Gasparre G.; Porcelli A.M.; Bonora E.; Pennisi L.F.; Toller M.; Iommarini L.; Ghelli A.; Moretti ...M.; Betts C.M.; Martinelli G.N.; Ceroni A.R.; Curcio F.; Carelli V.; Rugolo M.; Tallini G.; Romeo G. | 2007 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | 1.01 Articolo in rivista | - |
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