Detalhe da pesquisa
1.
Two new JK silencing alleles identified by single molecule sequencing with 20-Kb long-reads.
Transfusion;
63(8): 1441-1446, 2023 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37165957
2.
DSLK and Kg: Antithetical antigens in the RHAG blood group system, and characterization of anti-DSLK antibody.
Vox Sang;
118(5): 392-397, 2023 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36908196
3.
Frequencies of glycophorin variants and alloantibodies against Hil and MINY antigens in Japanese.
Vox Sang;
117(1): 94-98, 2022 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34227688
4.
GP.MOT: A novel glycophorin variant identified in a Japanese blood donor.
Transfusion;
61(10): 2825-2829, 2021 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34369596
5.
The Kg-antigen, RhAG with a Lys164Gln mutation, gives rise to haemolytic disease of the newborn.
Br J Haematol;
191(5): 920-926, 2020 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32705675
6.
A new antigen SUMI carried on glycophorin A encoded by the GYPA*M with c.91A>C (p.Thr31Pro) belongs to the MNS blood group system.
Transfusion;
60(6): 1287-1293, 2020 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32358867
7.
An unusual variant glycophorin expressing protease-resistant M antigen encoded by the GYPB-E(2-4)-B hybrid gene.
Vox Sang;
115(7): 579-585, 2020 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32314425
8.
Novel hybrid genes and a splice site mutation encoding the Sta antigen among Japanese blood donors.
Vox Sang;
115(8): 756-766, 2020 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32394466
9.
Integrative genome analysis identified the KANNO blood group antigen as prion protein.
Transfusion;
59(7): 2429-2435, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31020675
10.
A novel c.166A>T (p.Thr56Ser) mutation in GYPB*S accounting for unusual S antigen expression.
Vox Sang;
114(2): 171-173, 2019 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30523644
11.
Application of immortalized human erythroid progenitor cell line in serologic tests to detect red blood cell alloantibodies.
Transfusion;
58(11): 2675-2682, 2018 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30180269
12.
A new ABCG2 null allele with a 27-kb deletion including the promoter region causing the Jr(a-) phenotype.
Transfusion;
55(6 Pt 2): 1467-71, 2015 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25522810
13.
Expression of ABO blood-group genes is dependent upon an erythroid cell-specific regulatory element that is deleted in persons with the B(m) phenotype.
Blood;
119(22): 5301-10, 2012 May 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22408256
14.
Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual.
Transfusion;
53(11 Suppl 2): 2917-27, 2013 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23560502
15.
Anemic Disease of the Newborn With Little Increase in Hemolysis and Erythropoiesis Due to Maternal Anti-Jra: A Case Study and Review of the Literature.
Transfus Med Rev;
33(3): 183-188, 2019 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31227265
16.
ABO chimerism with a minor allele detected by the peptide nucleic acid-mediated polymerase chain reaction clamping method.
Blood Transfus;
12(3): 431-4, 2014 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24887221
17.
Anaphylactic transfusion reactions in haptoglobin-deficient patients with IgE and IgG haptoglobin antibodies.
Transfusion;
42(6): 766-73, 2002 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12147031