Detalles de la búsqueda
1.
[Study of the molecular characteristics of a Bweak phenotype due to a novel c.398T>C variant of the ABO gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(1): 110-113, 2023 Jan 10.
Artículo
en Zh
| MEDLINE | ID: mdl-36585013
2.
Six splice site variations, three of them novel, in the ABO gene occurring in nine individuals with ABO subtypes.
J Transl Med
; 19(1): 470, 2021 11 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-34809663
3.
Mechanism evaluation for an amino acid substitution p.Y246C of B-glycosyltransferase enzyme with Bweak phenotype.
Vox Sang
; 116(4): 464-470, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33326610
4.
[Identification of a glycosyltransferase allele associated with Bw subtype and analysis of the protein structure].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(3): 278-281, 2021 Mar 10.
Artículo
en Zh
| MEDLINE | ID: mdl-33751542
5.
[Molecular characterization of a recombination allele of ABO blood group].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 38(1): 15-19, 2021 Jan 10.
Artículo
en Zh
| MEDLINE | ID: mdl-33423250
6.
Molecular Basis of ABO Variants Including Identification of 16 Novel ABO Subgroup Alleles in Chinese Han Population.
Transfus Med Hemother
; 47(2): 160-166, 2020 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-32355476
7.
ABO antigen levels on platelets of normal and variant ABO blood group individuals.
Platelets
; 30(7): 854-860, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30475664
8.
Identification of a novel A allele with initiator codon variant (c.2T > A) in the ABO gene associated with weak A phenotype.
Transfusion
; 63(4): E23-E24, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36825445
9.
Identification of a novel A allele with a c.102C > A variation on the ABO*A1.02 allele.
Transfusion
; 63(4): E15-E16, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36718785
10.
Identification of a novel B allele with a c.256G>A mutation on the ABO*B.01 allele.
Transfusion
; 62(2): E10-E11, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34913491
11.
Identification of a novel A allele with a c.977A>C variation on the ABO*A1.02 allele.
Transfusion
; 62(9): E45-E46, 2022 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35950301
12.
[Application of recombinant GPâ ¢a combined Luminex beads for the detection of HPA-1a antibody].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(1): 40-44, 2017 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-28186591
13.
[Study of the molecular basis for an individual with Bel variant due to deletion of B glycosyltransferase gene].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 34(3): 423-426, 2017 Jun 10.
Artículo
en Zh
| MEDLINE | ID: mdl-28604970
14.
Identification of a novel B allele with c.10-14dupGTGTT and c.17G>A variants in a Chinese individual with a weak B phenotype.
Transfusion
; 61(9): E67-E68, 2021 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34343341
15.
Two novel A alleles with c.322C>T or c.410C>T mutations on the ABO*A1.02 allele were identified in the Chinese individuals.
Transfusion
; 60(10): E38-E39, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32851653
16.
Identification of a novel A allele with a c.731T>C mutation on the ABO*A1.02 allele.
Transfusion
; 60(8): E30-E31, 2020 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-32619045
17.
Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals.
Transfusion
; 55(1): 137-43, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25070883
18.
[Molecular basis for an individual with rare p phenotype in P1Pk blood group system].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 32(2): 250-3, 2015 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-25863098
19.
Identification of a novel B allele with a nucleotide deletion (c.3_4 del G) in the ABO gene associated with a Bx phenotype individual.
Transfusion
; 59(2): 793-794, 2019 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-30549285
20.
[Analysis of erythroid-specific blood group genes using un-mobilized peripheral stem cells cultured in vitro].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 31(4): 487-90, 2014 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-25119917