Detalhe da pesquisa
1.
Compound heterozygosity induces a rare Gerbich-negative phenotype in an immunized blood donor.
Transfusion
; 64(2): 406-411, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38235836
2.
Platelet CD36 deficiency is present in 2.6% of Arabian individuals and can cause NAIT and platelet refractoriness.
Transfusion
; 61(6): 1932-1942, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33822386
3.
Multicenter Study on Differential Human Neutrophil Antigen 2 Expression and Underlying Molecular Mechanisms.
Transfus Med Hemother
; 47(5): 385-395, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-33173457
4.
HNA-1d: a new human neutrophil antigen located on Fcγ receptor IIIb associated with neonatal immune neutropenia.
Transfusion
; 53(10): 2145-51, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23347194
5.
Expression of the CTL2 transcript variants in human peripheral blood cells and human tissues.
Transfusion
; 53(12): 3217-23, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23480595
6.
Genetic variation of the HNA-3a encoding gene.
Transfusion
; 51(11): 2391-7, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21564101
7.
Update on the nomenclature of human neutrophil antigens and alleles.
Transfusion
; 56(6): 1477-9, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27039828
8.
Characterization of the novel HLA-DPB1*1219:01 allele by next-generation sequencing.
HLA
; 98(3): 256-257, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34255436
9.
A serologic weakly reactive RhD is caused by a RHD 374T>A (Ile125Asn).
Transfusion
; 55(6 Pt 2): 1586-7, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25646655
10.
Paired crossover study of two plateletpheresis systems concerning platelet product quality and donor comfort.
Transfusion
; 50(4): 894-901, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19951314
11.
Amino Acid Polymorphisms in Hla Class II Differentiate Between Thyroid and Polyglandular Autoimmunity.
J Clin Endocrinol Metab
; 105(6)2020 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31675055
12.
Sex Alters the MHC Class I HLA-A Association With Polyglandular Autoimmunity.
J Clin Endocrinol Metab
; 104(5): 1680-1686, 2019 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30520966
13.
Variant FCGR3 genes: transcription and possible origins.
Asian Pac J Allergy Immunol
; 26(4): 223-8, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19317341
14.
The AQP1 mutation c.601delG causes the Co-negative phenotype in four patients belonging to the Romani (Gypsy) ethnic group.
Blood Transfus
; 12(1): 73-7, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24333057
15.
The AQP1 del601G mutation in different European Romani (Gypsy) populations.
Blood Transfus
; 14(6): 580-581, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27177406
16.
Transfusion-related acute lung injury caused by human leucocyte antigen class II antibody.
Br J Haematol
; 116(3): 673-6, 2002 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-11849232
17.
FCGR3 variants and expression of human neutrophil antigen-1a, -1b, and -1c in the populations of northern Germany and Uganda.
Transfusion
; 42(4): 469-75, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-12076295
18.
FCGR3B gene frequencies and FCGR3 variants in a Chinese population from Zhejiang Province.
Ann Hematol
; 82(9): 574-8, 2003 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-12898191