GENUARDI, MAURIZIO

GENUARDI, MAURIZIO  

Scienze Biomediche, Sperimentali e Cliniche 'Mario Serio'  

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Risultati 1 - 20 di 148 (tempo di esecuzione: 0.029 secondi).
Titolo Data di pubblicazione Autore(i) File
[Williams syndrome without cardiovascular abnormalities]. 1998 P. Cincinnati;M. Genuardi;C. Rutiloni
A founder MLH1 mutation in hereditary non polyposis colorectal cancer families from the districts of Modena and Reggio-Emilia in Northern Italy associated with protein elongation and instability 2004 CALUSERIU O.; DI GREGORIO C.; LUCCICORDISCO E.; SANTAROSA M.; TROJAN J.; BRIEGER A.; COLIBAZZI T.; BENATTI P.; PEDRONI M.; BELLACOSA A.; NERI G.; PONZ DE LEON M.; VIEL A.; M. GENUARDI
A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability 2006 MARRONI F.; PASTRELLO C.; BENATTI P.; TORRINI M.; BARANA D.; LUCCI-CORDISCO E.; VIEL A.; MARENI C.; OLIANI C.; M. GENUARDI; BAILEY-WILSON J.E.; PONZ DE LEON M.; PRESCIUTTINI S
A girl with G syndrome and agenesis of the corpus callosum. 1987 G. Neri;M. Genuardi;G. Natoli;P. Costa;G. Maggioni
A kindred with MYH-associated polyposis and pilomatricomas. 2005 Silvana Baglioni; German Melean; Francesca Gensini; Marco Santucci; Marco Scatizzi; Laura Papi; Maurizio Genuardi
A mononucleotide markers panel to identify hMLH1/hMSH2 germline mutations. 2007 M. PEDRONI; B. RONCARI; S. MAFFEI; L. LOSI; A. SCARSELLI; C. DI GREGORIO; M. MARINO; L. RONCUCCI; P. BENATTI; G. PONTI; G. ROSSI; M. MENIGATTI; A. VIEL; M. GENUARDI; M. PONZ DE LEON
A new case of interstitial deletion of chromosome 3q, del(3q)(q13.12q21.3), with agenesis of the corpus callosum. 1994 M. Genuardi;F. Calvieri;C. Tozzi;R. Coslovi;G. Neri
A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease. 1993 M. Pocchiari;M. Salvatore;F. Cutruzzolá;M. Genuardi;C. T. Allocatelli;C. Masullo;G. Macchi;G. Alemá;S. Galgani;Y. G. Xi
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancer. 2005 E. Lucci-Cordisco; M. Zollino; S. Baglioni; I. Mancuso; R. Lecce; F. Gurrieri; A. Crucitti; L. Papi; G. Neri; M. Genuardi
A proteomics approach to identify changes in protein profiles in serum of Familial Adenomatous Polyposis patients 2008 Quaresima B; Crugliano T; Gaspari M; Faniello MC; Cosimo P; Valanzano R; Genuardi M; Cannataro M; Veltri P; Baudi F; Doldo P; Cuda G; Venuta S; Costanzo F.
A rare combination consisting of aldosterone-producing adenoma and adrenal myelolipoma in a patient with heterozygosity for retinoblastoma (RB) gene. 2004 C. Caliumi;G. D. Toma;A. Bossini;R. Cianci;C. Bosman;M. Genuardi;S. Cerci;C. Letizia
A single mutation in the FGA locus responsible for false homozygosities and discrepancies between commercial kits in an unusual paternity test case 2007 Ricci U; Melean G; Robino C; Genuardi M.
A split hand-split foot (SHFM3) gene is located at 10q24-->25. 1996 F. Gurrieri; P. Prinos; D. Tackels; M. W. Kilpatrick; J. Allanson; M. Genuardi; A. Vuckov; L. Nanni; E. Sangiorgi; G. Garofalo; M. E. Nunes; G. Neri; C. Schwartz; P. Tsipouras
Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors. 2006 S. Martinelli;C. Carta;E. Flex;F. Binni;E. L. Cordisco;S. Moretti;E. Puxeddu;M. Tonacchera;A. Pinchera;H. P. McDowell;C. Dominici;A. Rosolen;C. D. Rocco;R. Riccardi;P. Celli;M. Picardo;M. Genuardi;P. Grammatico;M. Sorcini;M. Tartaglia
Aetiology of colorectal cancer and relevance of monogenic inheritance 2004 PONZ DE LEON M.; BENATTI P.; BORGHI F.; PEDRONI M.; SCARSELLI A.; DI GREGORIO C.; LOSI L.; VIEL A.; M. GENUARDI; ABBATI G.; ROSSI G.; MENIGATTI M.; LAMBERTI I.; PONTI G.; RONCUCCI L
Alterazioni somatiche del gene kras in pazienti con mutazioni mono e bialleliche di MUTYH. 2009 Tricarico R.; Mareni C.; Ciambotti B.; Nardone V.; Gentile A.; Lucci Cordisco E.; Pedroni M.; Piepoli A.; Ponz de Leon M.; Varesco L.; Viel A.; Genuardi M.
Analysis of 138 consecutive ovarian cancer patients: incidence and characteristics of familial cases. 1990 S. Greggi;M. Genuardi;P. Benedetti-Panici;R. Cento;G. Scambia;G. Neri;S. Mancuso
Anti-miR21 oligonucleotide enhances chemosensitivity of T98G cell line to doxorubicin by inducing apoptosis. 2014 Giunti, L; da Ros, M; Vinci, S; Gelmini, S; Iorio, Al; Buccoliero, Am; Cardellicchio, S; Castiglione, F; Genitori, L; de Martino, M; Giglio, S; Genuardi, M; Sardi, I.
Assessment of pathogenicity criteria for constitutional missense mutations of the hereditary nonpolyposis colorectal cancer genes MLH1 and MSH2 1999 M. GENUARDI; CARRARA S.; ANTI M.; PONZ DE LEN M.; VIEL A
Association between cyclin D1 (CCND1) gene amplification and human papillomavirus infection in human laryngeal squamous cell carcinoma. 1998 P. Cattani;S. Hohaus;A. Bellacosa;M. Genuardi;S. Cavallo;V. Rovella;G. Almadori;G. Cadoni;J. Galli;M. Maurizi;G. Fadda;G. Neri