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Recipient mHag-HA1 disparity and aGVHD in thalassemic-transplanted patients

Autor: Nesci S, Marco Andreani, Guido Lucarelli, A. Iliescu, O Buffi

Publikováno v: Bone Marrow Transplantation. 31:575-578

In order to determine the influence of HA-1 minor histocompatibility antigen mismatch on BMT outcome, we analyzed a pool of 94 thalassemic transplanted patients all selected for the presence of HLA-A(*)0201 allele. The HA-1 typing was performed using

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1bea0f788b5a0b17ccd8483ca939062
https://doi.org/10.1038/sj.bmt.1703880

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A new HLA-DRB1*11 allele, DRB1*1144, identified by cloning and sequencing

Autor: Marco Andreani, Michele Maria Luchetti, G. Visani, M. Amadei, A. Iliescu, M.R. Battarra, S. Nesci, O. Buffi

Publikováno v: Tissue antigens. 63(3)

We report here the identification of a novel DRB1*11 allele, DRB1*1144, identified during sequence-based HLA-DRB1 typing. Molecular cloning and direct sequencing confirmed that the new allele is identical to DRB1*110401 at exon 2, except for a single

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c33fa8b6c21c7073a9a79b0788970b5
https://pubmed.ncbi.nlm.nih.gov/14989721

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Identification of a new HLA-B*08 allele in a family of Iraqi origin

Autor: M. Valentini, S. Nesci, A. Iliescu, M. Amadei, O. Buffi

Publikováno v: Tissue Antigens. 78:153-154

The novel allele HLA-B*08:62 differs from HLA-B* 08:01:01 by a nonsynonymous nucleotide substitution at position 24 of exon 2 (codon 9 changes from GAC to CAC).

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf7e6714a222d19a2f89292e44d2a1b3
https://doi.org/10.1111/j.1399-0039.2011.01679.x

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A novel HLA-A*02 allele, A*02202, identified by nucleotide sequencing

Autor: S, Nesci, A, Iliescu, O, Buffi, M, Andreani, G, Lucarelli

Publikováno v: Tissue antigens. 57(4)

In this paper we report the identification of a new HLA-A*02 allele in two members of an Afghan family. This novel allele, designed as A*02202, differs from A*02201 by a silent substitution at codon 66 (AAC--AAT) in the alpha1 domain. A*02202 appears

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cb55689c975a954ee003398f35abd963
https://pubmed.ncbi.nlm.nih.gov/11380949

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Identification of a novel HLA-C*08 variant allele, C*08:31. Sequence analysis from exons 1 through 8

Autor: Andrea Bontadini, O. Buffi, S. Nesci, A. Iliescu, Silvia Manfroi

Publikováno v: Tissue Antigens. 77:84-85

A novel allele, HLA- C*08:31 has been identified by sequence based typing in an Italian hematological patient undergoing bone marrow transplantation.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6c193e7ca4d332cebf83638ef9dee89
https://doi.org/10.1111/j.1399-0039.2010.01564.x

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The importance of erythroid expansion in determining the extent of apoptosis in erythroid precursors in patients with beta-thalassemia major

Autor: F, Centis, L, Tabellini, G, Lucarelli, O, Buffi, P, Tonucci, B, Persini, M, Annibali, R, Emiliani, A, Iliescu, S, Rapa, R, Rossi, L, Ma, E, Angelucci, S L, Schrier

Publikováno v: Blood. 96(10)

Beta-thalassemia major is characterized by ineffective erythropoiesis leading to severe anemia and extensive erythroid expansion. The ineffective erythropoiesis is in part due to accelerated apoptosis of the thalassemic erythroid precursors; however,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d7684a49f0fc720c26d535c08cc8d796
https://pubmed.ncbi.nlm.nih.gov/11071663

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Characterization of the novel allele HLA-Cw*0331 by sequence-based typing

Autor: A. Iliescu, G. Carella, O. Buffi, S. Nesci, A. Malagoli

Publikováno v: Tissue Antigens. 69:203-204

A novel allele HLA-C allele, Cw*0331, has been identified by sequence based typing in a German individual selected as a potential bone marrow unrelated donor.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b33e64d3ec70b0755b4b7f9b5b57332a
https://doi.org/10.1111/j.1399-0039.2006.00737.x

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