Zobrazeno 1 - 10
of 40
pro vyhledávání: '"R. Azzarone"'
Autor:
Carla Cervelli, Antonella Dal Mas, Giovanna Maisto, Mario Toriello, Olaida Valdez, Maria Scimitarra, Donato Madalese, Franco Papola, Maria Assunta Scarnecchia, Caterina Fusco, Angelica Canossi, C. Battistoni, Daniela Fracassi, R. Azzarone, Laura Auriemma, Roberta Penta de Vera d'Aragona
Publikováno v:
HLAREFERENCES. 95(5)
The identification of null or questionably expressed HLA allelic variants is a major issue in HLA diagnostics, because the mistyping of the aberrant expression of such alleles can have a major impact on the outcome of both hematopoietic stem cell tra
Autor:
A. Canossi, R. Azzarone, R. Penta, M. Toriello, C. Fusco, M. Pagano, F. Papola, V. Poggi, L. Auriemma, B. Di Iulio
Publikováno v:
International journal of immunogenetics (Online) 42 (2015): 294–296. doi:10.1111/iji.12208
info:cnr-pdr/source/autori:Fusco C.; Azzarone R.; Penta R.; Canossi A.; Di Iulio B.; Toriello M.; Auriemma L.; Pagano M.; Poggi V.; Papola F./titolo:HLA-B*38:55Q: A new alternatively expressed allele identified in a three-generation Italian family/doi:10.1111%2Fiji.12208/rivista:International journal of immunogenetics (Online)/anno:2015/pagina_da:294/pagina_a:296/intervallo_pagine:294–296/volume:42
info:cnr-pdr/source/autori:Fusco C.; Azzarone R.; Penta R.; Canossi A.; Di Iulio B.; Toriello M.; Auriemma L.; Pagano M.; Poggi V.; Papola F./titolo:HLA-B*38:55Q: A new alternatively expressed allele identified in a three-generation Italian family/doi:10.1111%2Fiji.12208/rivista:International journal of immunogenetics (Online)/anno:2015/pagina_da:294/pagina_a:296/intervallo_pagine:294–296/volume:42
The new allelic variant HLA-B*38:55Q differs from the closest related B*38:01:01 by one nucleotide substitution at position 373 in exon 3 (TGC>CGC). This results in a difference of one amino acid at residue 101 of the HLA-B heavy chain, from a neutra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5b14f609faa1371c78126fe49d8105
http://www.cnr.it/prodotto/i/330988
http://www.cnr.it/prodotto/i/330988
Autor:
Annalisa Blasetti, D. Merante, Emma Altobelli, Fioroni Ma, Sergio Tiberti, R Petrocelli, R. Azzarone, F. Papola, G. Poccia, C. Battistoni, R. Iannarelli, Alberto Verrotti, Stefano Tumini
Publikováno v:
Clinical and Experimental Medicine. 5:72-79
The objective was to evaluate HLA DR/DQ alleles and their risk factor for type 1 diabetes in the Abruzzo region (central Italy). Sixty incident cases from the Abruzzo region were studied together with 120 unrelated control subjects living in the same
Publikováno v:
Tissue Antigens. 81:466-468
The HLA-B*50:18 allele differs from the closest related B*50:01:01 by one nucleotide substitution at position 454 in exon 3.
Publikováno v:
Tissue antigens. 81(6)
The HLA-B*50:18 allele differs from the closest related B*50:01:01 by one nucleotide substitution at position 454 in exon 3.
Publikováno v:
Tissue antigens 77(2) (2011): 152–153.
info:cnr-pdr/source/autori:Cervelli C, Canossi A, Azzarone R, Scimitarra M, Papola F/titolo:Sequence-based typing identification of the novel HLA-A*24:135 variant in a Maldivian family with a bone marrow patient./doi:/rivista:Tissue antigens/anno:2011/pagina_da:152/pagina_a:153/intervallo_pagine:152–153/volume:77(2)
info:cnr-pdr/source/autori:Cervelli C, Canossi A, Azzarone R, Scimitarra M, Papola F/titolo:Sequence-based typing identification of the novel HLA-A*24:135 variant in a Maldivian family with a bone marrow patient./doi:/rivista:Tissue antigens/anno:2011/pagina_da:152/pagina_a:153/intervallo_pagine:152–153/volume:77(2)
We describe the identification of the novel HLA-A*24:135 allele [nucleotide 397 (TC) in exon 3, PheLeu at codon 109 in ±2 domain, compared with A*24:02:01] by sequence-based typing (SBT).
Autor:
C. Cervelli, A. Canossi, R. Azzarone, M. Scimitarra, D. Fracassi, C. Battistoni, B. Di Iulio, M. A. Scarnecchia, F. Papola
Publikováno v:
24th European Immunogenetics and Histocompatibility Conference 17th Annual Meeting of the Italian Society for Immunogenetics and Transplantation Biology May 1518, pp. 152–153, Florence, Italy, 2011
info:cnr-pdr/source/autori:C. Cervelli, A. Canossi, R. Azzarone, M. Scimitarra, D. Fracassi, C. Battistoni, B. Di Iulio, M. A. Scarnecchia, F. Papola/congresso_nome:24th European Immunogenetics and Histocompatibility Conference 17th Annual Meeting of the Italian Society for Immunogenetics and Transplantation Biology May 1518/congresso_luogo:Florence, Italy,/congresso_data:2011/anno:2011/pagina_da:152/pagina_a:153/intervallo_pagine:152–153
info:cnr-pdr/source/autori:C. Cervelli, A. Canossi, R. Azzarone, M. Scimitarra, D. Fracassi, C. Battistoni, B. Di Iulio, M. A. Scarnecchia, F. Papola/congresso_nome:24th European Immunogenetics and Histocompatibility Conference 17th Annual Meeting of the Italian Society for Immunogenetics and Transplantation Biology May 1518/congresso_luogo:Florence, Italy,/congresso_data:2011/anno:2011/pagina_da:152/pagina_a:153/intervallo_pagine:152–153
We describe the identification of the novel HLA-A*24:135 allele [nucleotide 397 (T->C) in exon 3, Phe->Leu at codon 109 in ?2 domain, compared with A*24:02:01] by sequence-based typing (SBT).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::5fd4cae846d7d193762a4272109cb3ff
https://publications.cnr.it/doc/99183
https://publications.cnr.it/doc/99183
Autor:
R. Azzarone, I. Parzanese, F. Papola, K. Clemente, G. Liberatore, D. Maccarone, F. Pisani, D. Piancatelli, A. Famulari
Publikováno v:
Transplantation proceedings 41 (2009): 1187–1188.
info:cnr-pdr/source/autori:Piancatelli D; Maccarone D; Liberatore G; Parzanese I; Clemente K; Azzarone R; Pisani F; Famulari A; Papola F/titolo:HLA-G 14-BP INSERTION%2FDELETION POLYMORPHISM IN KIDNEY TRANSPLANT PATIENTS WITH METABOLIC COMPLICATIONS/doi:/rivista:Transplantation proceedings/anno:2009/pagina_da:1187/pagina_a:1188/intervallo_pagine:1187–1188/volume:41
info:cnr-pdr/source/autori:Piancatelli D; Maccarone D; Liberatore G; Parzanese I; Clemente K; Azzarone R; Pisani F; Famulari A; Papola F/titolo:HLA-G 14-BP INSERTION%2FDELETION POLYMORPHISM IN KIDNEY TRANSPLANT PATIENTS WITH METABOLIC COMPLICATIONS/doi:/rivista:Transplantation proceedings/anno:2009/pagina_da:1187/pagina_a:1188/intervallo_pagine:1187–1188/volume:41
HLA-G, a nonclassical HLA molecule with limited polymorphism has immunomodulating/tolerogenic properties. The most common polymorphism of HLA-G is a deletion/insertion of 14 bp, located at the 3'UTR region of the gene (exon 8). This polymorphism is a
Autor:
C. Cervelli, A. Famulari, G Fontecchio, F. Papola, D. Fracassi, M. Scimitarra, C. Battistoni, R. Azzarone, F. Pisani, B. Di Iulio, M.A. Scarnecchia
Despite new immunosuppressive approaches, acute rejection episodes (ARE) are still a major cause of early kidney dysfunction with a negative impact on long-term allograft survival. Noninvasive markers able to identify renal ARE earlier than creatinin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7cf032d69abaa44bd2e725e25f73030
http://hdl.handle.net/11697/2382
http://hdl.handle.net/11697/2382
Autor:
C Mercurio, Luca Ventura, Fioroni Ma, C. Battistoni, F. Papola, C. Cervelli, R. Azzarone, Gino Fornaciari, G Fontecchio
Publikováno v:
Europe PubMed Central
Rheumatoid arthritis (RA) is currently believed to have originated in America, and after the discovery of this continent in 1492, to have been exported to the Old World. We evaluated the genetic predisposition to RA in the “Braids Lady” from Arez