12 results for author:"Mazzola G." in Literature citations
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| The conundrum of HLA-DRB1*14:01/*14:54 and HLA-DRB3*02:01/*02:02 mismatches in unrelated hematopoietic SCT. Pasi A., Crocchiolo R., Bontempelli M., Carcassi C., Carella G., Crespiatico L., Garbarino L., Mascaretti L., Mazzi B., Mazzola G. et al. Bone Marrow Transplant. 46:916-922(2011) · Mapped (306) |
| Molecular aspects of a novel HLA-A*02 allele (A*0297): the first HLA class I allele mutated at codon 232. Garino E., Miertus J., Berrino M., Bertinetto F., Caropreso P., Gay V., Mazzola G., Tondat F., Frecer V., Miertus S. et al. Tissue Antigens 69:342-347(2007) · Mapped (449) |
| Lipoprotein(a), fibrinogen and vascular mortality in an elderly northern Italian population. D'Angelo A., Ruotolo G., Garancini P., Sampietro F., Mazzola G., Calori G. Haematologica 91:1613-1620(2006) · Mapped (7) |
| Role of non-HLA genetic polymorphisms in graft-versus-host disease after haematopoietic stem cell transplantation. Bertinetto F.E., Dall'Omo A.M., Mazzola G.A., Rendine S., Berrino M., Bertola L., Magistroni P., Caropreso P., Falda M., Locatelli F. et al. Int. J. Immunogenet. 33:375-384(2006) · Mapped (30) |
| Identification of a new allele, HLA-DRB5*0113, through three different molecular biology techniques. Garino E., Berrino M., Bertinetto F., Caropreso P., Chidichimo R., Dametto E., Fasano M.E., Frisaldi E., Mazzola G., Tondat F. et al. Tissue Antigens 67:427-429(2006) · UniProtKB (1) |
| Prognostic values of soluble CD30 and CD30 gene polymorphisms in heart transplantation. Frisaldi E., Conca R., Magistroni P., Fasano M.E., Mazzola G., Patane F., Zingarelli E., Dall'omo A.M., Brusco A., Amoroso A. Transplantation 81:1153-1156(2006) · Mapped (5) |
| Identification of a new HLA-DRB1 allele in three members of an Italian family. Garino E., Berrino M., Mazzola G., Boccadoro M., Bruno B., Bertinetto F., Bertola L., Caropreso P., Frisaldi E., Marin F. et al. Tissue Antigens 64:210-212(2004) · UniProtKB (1) |
| Interaction between gene polymorphisms of nitric oxide synthase and renin-angiotensin system in the progression of membranous glomerulonephritis. Stratta P., Bermond F., Guarrera S., Canavese C., Carturan S., Dall'Omo A., Ciccone G., Bertola L., Mazzola G., Fasano E. et al. Nephrol. Dial. Transplant. 19:587-595(2004) · Mapped (21) |
| New HLA-A*11 allele, A*1112, identified by sequence-based typing. Garino E., Belvedere M., Berrino M., Bertola L., Dall'Omo A.M., Mazzola G., Rossetto C., Carcassi C., Lai S., Gay E. et al. Tissue Antigens 60:84-87(2002) · Mapped (449) |
| AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria. Amoroso A., Pirulli D., Florian F., Puzzer D., Boniotto M., Crovella S., Zezlina S., Spano A., Mazzola G., Savoldi S. et al. J. Am. Soc. Nephrol. 12:2072-2079(2001) · Mapped (8) |
| Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene. Pirulli D., Puzzer D., Ferri L., Crovella S., Amoroso A., Ferrettini C., Marangella M., Mazzola G., Florian F. Hum. Genet. 104:523-525(1999) · UniProtKB (1) |
| Gene symbol: AGXT. Disease: primary hyperoxaluria type I. Amoroso A., Pirulli D., Puzzer D., Ferri L., Crovella S., Ferrettini C., Marangella M., Mazzola G., Florian F. Hum. Genet. 104:441-441(1999) · UniProtKB (1) |