Foto del docente

Elena Bonora

Professoressa associata

Dipartimento di Scienze Mediche e Chirurgiche

Settore scientifico disciplinare: MEDS-01/A Genetica medica

Direttrice Scuola di Spec.in Genetica Medica ad accesso non medico

Pubblicazioni

Fusco D; Vargiolu M; Vidone M; Mariani E; Pennisi LF; Bonora E; Capellari S; Dirnberger D; Baumeister R; Martinelli P; Romeo G., The RET51/FKBP52 complex and its involvement in Parkinson disease., «HUMAN MOLECULAR GENETICS», 2010, 19(14), pp. 2804 - 2816 [articolo]

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 inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells., «HUMAN MUTATION», 2009, 30 (3), pp. 391 - 396 [articolo]

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., Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer., «JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION», 2009, 32, pp. 426 - 429 [articolo]

Fontanesi L.; Fronza R.; Scotti E.; Colombo M.; Speroni C.; Tognazzi L.; Galimberti G.; Calò DG; Bonora E.; Vargiolu M.; Romeo G.; Casadio R.; Russo V., The FAGenomicH project: Towards a whole candidate gene approach to identify markers associated with fatness and production traits in pigs and investigate the pig as a model for human obesity, «ITALIAN JOURNAL OF ANIMAL SCIENCE», 2009, 8, pp. 87 - 89 [articolo]Open Access

Vargiolu M; Fusco D; Kurelac I; Dirnberger D; Baumeister R; Morra I; Melcarne A; Rimondini R; Romeo G; Bonora E, The tyrosine kinase receptor RET interacts in vivo with aryl hydrocarbon receptor-interacting protein to alter survivin availability., «THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM», 2009, 94, pp. 2571 - 2578 [articolo]

Vargiolu M.; Silvestri T.; Bonora E.; Dolzani P.; Pulsatelli L.; Punzi L.; Fioravanti A.; Facchini A.; Romeo G.; Meliconi R., Association of the interleukin-4/interleukin-4 receptor genetic variants with hand osteoathrtitis., in: , «OSTEOARTHRITIS AND CARTILAGE», 2008, 16, pp. S156 - S156 (atti di: 2008 World Congress on Osteoarthritis, Roma, 18-21 settembre 2008) [atti di convegno-abstract]

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., Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma, «HUMAN MOLECULAR GENETICS», 2008, 17, pp. 986 - 995 [articolo]

Masotti D.; Nardini C.; Rossi S.; Bonora E.; Romeo G.; Volinia S.; Benini L., TOM: enhancement and extension of a tool suite for in silico approaches to multigenic complex disorders., «BIOINFORMATICS», 2008, 24 (3), pp. 428 - 429 [articolo]

Fontanesi L.; Fronza R.; Scotti E.; Galimberti G.; Calò D.G.; Bonora E.; Vargiolu M.; Colombo M.; Casadio R.; Romeo G.; Russo V., The FAGenomicH project: a whole candidate gene approach to identify markers associated with fatness traits in pigs and investigate the pig as a model for human obesity, in: Proceedings of the Second European Conference on Pig Genomics, Pig Genome II, LJUBLJANA, University of Ljubljana, Biotechnical Faculty, 2008, pp. 35 - 36 (atti di: Second European Conference on Pig Genomics, Pig Genome II, Ljubljana, Slovenia, 4-5 June 2008) [atti di convegno-abstract]

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., C620R mutation of the murine ret proto-oncogene: loss of function effect in homozygotes and possible gain of function effect in heterozygotes., «INTERNATIONAL JOURNAL OF CANCER», 2007, 121, pp. 292 - 300 [articolo]

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., Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumours., «PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA», 2007, 104, pp. 9001 - 9006 [articolo]

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., Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III, «CANCER RESEARCH», 2006, 66, pp. 6087 - 6096 [articolo]

Stankov K; Landi S; Gioia-Patricola L; Bonora E; Volante M; Papotti M; Romeo G, GSTT1 and M1 polymorphisms in Hurthle thyroid cancer patients, «CANCER LETTERS», 2006, 240, pp. 76 - 82 [articolo]

S. Rossi; D. Masotti; C. Nardini; E. Bonora; E. Macii; S. Volinia; L. Benini, Integrated web-based approach to multigenic diseases, in: Consortium for Post Genome Science Conference, 2006, MANCHESTER, s.n, 2006(atti di: Consortium for Post Genome Science Conference, 2006, Manchster, United Kingdom, Feb. 22-24, 2006) [atti di convegno-abstract]

Bonora E.; Evangelisti C.; Bonichon F.; Tallini G.; Romeo G., Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas., «BRITISH JOURNAL OF CANCER», 2006, 95, pp. 1529 - 1536 [articolo]

Ultimi avvisi

Al momento non sono presenti avvisi.