1 - 25 of 37 results for author:"Cama A." in Literature citations
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| FZD6 is a novel gene for human neural tube defects. De Marco P., Merello E., Rossi A., Piatelli G., Cama A., Kibar Z., Capra V. |
| Increased variance in germline allele-specific expression of APC associates with colorectal cancer. Curia M.C., De Iure S., De Lellis L., Veschi S., Mammarella S., White M.J., Bartlett J., Di Iorio A., Amatetti C., Lombardo M. et al. Gastroenterology 142:71-77.e1(2012) · Mapped (10) |
| High levels of PROM1 (CD133) transcript are a potential predictor of poor prognosis in medulloblastoma. Raso A., Mascelli S., Biassoni R., Nozza P., Kool M., Pistorio A., Ugolotti E., Milanaccio C., Pignatelli S., Ferraro M. et al. Neuro-oncology 13:500-508(2011) · Mapped (4) |
| Prognostic relevance of MLH1 and MSH2 mutations in hereditary non-polyposis colorectal cancer patients. Russo A., Sala P., Alberici P., Gazzoli I., Radice P., Montefusco C., Torrini M., Mareni C., Fornasarig M., Santarosa M. et al. Tumori 95:731-738(2009) · Mapped (42) |
| Telomere shortening is associated to TRF1 and PARP1 overexpression in Duchenne muscular dystrophy. Aguennouz M., Vita G.L., Messina S., Cama A., Lanzano N., Ciranni A., Rodolico C., Di Giorgio R.M., Vita G. Neurobiol. Aging 32:2190-2197(2011) · Mapped (9) |
| Transitions at CpG dinucleotides, geographic clustering of TP53 mutations and food availability patterns in colorectal cancer. Verginelli F., Bishehsari F., Napolitano F., Mahdavinia M., Cama A., Malekzadeh R., Miele G., Raiconi G., Tagliaferri R., Mariani-Costantini R. PLoS ONE 4:e6824-e6824(2009) · Mapped (33) |
| IRS1 G972R polymorphism and type 2 diabetes: a paradigm for the difficult ascertainment of the contribution to disease susceptibility of 'low-frequency-low-risk' variants. Morini E., Prudente S., Succurro E., Chandalia M., Zhang Y.Y., Mammarella S., Pellegrini F., Powers C., Proto V., Dallapiccola B. et al. Diabetologia 52:1852-1857(2009) · Mapped (1) |
| VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5. Szumska D., Pieles G., Essalmani R., Bilski M., Mesnard D., Kaur K., Franklyn A., El Omari K., Jefferis J., Bentham J. et al. Genes Dev. 22:1465-1477(2008) · Mapped (23) |
| No major role for the EMX2 gene in schizencephaly. Merello E., Swanson E., De Marco P., Akhter M., Striano P., Rossi A., Cama A., Leventer R.J., Guerrini R., Capra V. et al. Am. J. Med. Genet. A 146A:1142-1150(2008) · Mapped (1) |
| P53 mutations in colorectal cancer from northern Iran: Relationships with site of tumor origin, microsatellite instability and K-ras mutations. Mahdavinia M., Bishehsari F., Verginelli F., Cumashi A., Lattanzio R., Sotoudeh M., Ansari R., Semeraro D., Hormazdi M., Fakheri H. et al. J. Cell. Physiol. 216:543-550(2008) · Mapped (41) |
| Sporadic childhood hepatoblastomas show activation of beta-catenin, mismatch repair defects and p53 mutations. Curia M.C., Zuckermann M., De Lellis L., Catalano T., Lattanzio R., Aceto G., Veschi S., Cama A., Otte J.B., Piantelli M. et al. Mod. Pathol. 21:7-14(2008) · Mapped (39) |
| High prevalence of BRCA1 deletions in BRCAPRO-positive patients with high carrier probability. Veschi S., Aceto G., Scioletti A.P., Gatta V., Palka G., Cama A., Mariani-Costantini R., Battista P., Calo V., Barbera F. et al. Ann. Oncol. 18 Suppl 6:vi86-92(2007) · Mapped (18) |
| BRCA1 and BRCA2 status in a Central Sudanese series of breast cancer patients: interactions with genetic, ethnic and reproductive factors. Awadelkarim K.D., Aceto G., Veschi S., Elhaj A., Morgano A., Mohamedani A.A., Eltayeb E.A., Abuidris D., Di Gioacchino M., Battista P. et al. Breast Cancer Res. Treat. 102:189-199(2007) · Mapped (18) |
| Patterns of K-ras mutation in colorectal carcinomas from Iran and Italy (a Gruppo Oncologico dell'Italia Meridionale study): influence of microsatellite instability status and country of origin. Bishehsari F., Mahdavinia M., Malekzadeh R., Verginelli F., Catalano T., Sotoudeh M., Bazan V., Agnese V., Esposito D.L., De Lellis L. et al. Ann. Oncol. 17 Suppl 7:vii91-6(2006) · Mapped (8) |
| HLXB9 homeobox gene and caudal regression syndrome. Merello E., De Marco P., Mascelli S., Raso A., Calevo M.G., Torre M., Cama A., Lerone M., Martucciello G., Capra V. Birth Defects Res. Part A Clin. Mol. Teratol. 76:205-209(2006) · Mapped (3) |
| Mutational screening of the CYP26A1 gene in patients with caudal regression syndrome. De Marco P., Merello E., Mascelli S., Raso A., Santamaria A., Ottaviano C., Calevo M.G., Cama A., Capra V. Birth Defects Res. Part A Clin. Mol. Teratol. 76:86-95(2006) · Mapped (1) |
| Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk. De Marco P., Merello E., Calevo M.G., Mascelli S., Raso A., Cama A., Capra V. J. Hum. Genet. 51:98-103(2006) · Mapped (6) |
| Variation of the insulin receptor substrate gene (IRS-1) in African Pygmies and Bantus. Battaggia C., Verginelli F., Palmirotta R., Mariani-Costantini R., Cama A., Destro-Bisol G. Diabetes Res. Clin. Pract. 72:108-109(2006) · Mapped (1) |
| Mutations in the p53 and Ki-ras genes, microsatellite instability and site of tumor origin in colorectal cancer. Catalano T., Curia M.C., Aceto G., Verginelli F., Cascinu S., Cama A., Mariani-Costantini R., Teti D., Battista P. Oncol. Rep. 14:625-631(2005) · Mapped (41) |
| Subtype-specific expression and genetic alterations of the chemokinereceptor gene CXCR4 in medulloblastomas. Schuller U., Koch A., Hartmann W., Garre M.L., Goodyer C.G., Cama A., Sorensen N., Wiestler O.D., Pietsch T. Int. J. Cancer 117:82-89(2005) · Mapped (2) |
| Molecular genetic analysis of human homologs of Caenorhabditis elegans mab-21-like 1 gene in patients with neural tube defects. Merello E., De Marco P., Moroni A., Raso A., Calevo M.G., Consalez G.G., Cama A., Capra V. Birth Defects Res. A Clin. Mol. Teratol. 70:885-888(2004) · UniProtKB (1) |
| A novel T608R missense mutation in insulin receptor substrate-1 identified in a subject with type 2 diabetes impairs metabolic insulin signaling. Esposito D.L., Li Y., Vanni C., Mammarella S., Veschi S., Della Loggia F., Mariani-Costantini R., Battista P., Quon M.J., Cama A. J. Clin. Endocrinol. Metab. 88:1468-1475(2003) · UniProtKB (1) · Mapped (4) |
| Reduced folate carrier polymorphism (80A-->G) and neural tube defects. De Marco P., Calevo M.G., Moroni A., Merello E., Raso A., Finnell R.H., Zhu H., Andreussi L., Cama A., Capra V. Eur. J. Hum. Genet. 11:245-252(2003) · Mapped (13) |
| BRCA1 and BRCA2 mutation status and tumor characteristics in male breast cancer: a population-based study in Italy. Ottini L., Masala G., D'Amico C., Mancini B., Saieva C., Aceto G., Gestri D., Vezzosi V., Falchetti M., De Marco M. et al. Cancer Res. 63:342-347(2003) · Mapped (18) |
| Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population. De Marco P., Calevo M.G., Moroni A., Arata L., Merello E., Finnell R.H., Zhu H., Andreussi L., Cama A., Capra V. J. Hum. Genet. 47:319-324(2002) · Mapped (12) |