筛选条件 共查询到13条结果
排序方式
Analysis of the molecular mechanism and pedigree investigation of para-Bombay phenotype caused by combined mutations at position h(649) and h(768) of FUT1 gene

期刊: BLOOD TRANSFUSION, 2022; 20 (5)

Background - The para-Bombay phenotype is a rare red blood cell phenotype characterised by the lack of ABH antigens on red blood cells, but ABH substa......

JIF:2.591

Expanding restrictive transfusion evidence in surgical practice: a multicentre, prospective cohort study

期刊: BLOOD TRANSFUSION, 2022; 20 (5)

Background - Findings of observational studies investigating the impact of transfusions are at odds with those of randomised controlled trials, raisin......

JIF:2.591

ABO incompatibility does not affect transfusion requirements or clinical outcomes of unrelated cord blood transplantation after myeloablative conditioning for haematological malignancies

期刊: BLOOD TRANSFUSION, 2022; 20 (2)

Background - The effects of ABO incompatibility on cord blood transplantation (CBT) have not been confirmed. We retrospectively investigated the effec......

JIF:2.591

Successful prenatal management of two foetuses affected by antibodies against GP.Mur with prenatal genotyping analysis and a literature review

期刊: BLOOD TRANSFUSION, 2021; 19 (2)

Background - GP.Mur belongs to the GP(B-A-B) hybrid glycophorin family, which is the most common hybrid glycophorin in Southeast Asia. Antibodies agai......

Two novel mutations p. L319V and p. L91P in ABO glycosyltransferases lead to A(el) and B-el phenotypes

期刊: BLOOD TRANSFUSION, 2020; 18 (6)

Background - Mutations of the ABO gene may cause the dysfunction of ABO glycosyltransferase (GT) that can result in weak ABO phenotypes. Here, we iden......

Screening and identification of RhD antigen mimic epitopes from a phage display random peptide library for the serodiagnosis of haemolytic disease of the foetus and newborn

期刊: BLOOD TRANSFUSION, 2019; 17 (1)

Background. Identification of RhD antigen epitopes is a key component in understanding the pathogenesis of haemolytic disease of the foetus and newbor......

JIF:3.35

Molecular genetic analysis of weak ABO subgroups in the Chinese population reveals ten novel ABO subgroup alleles

期刊: BLOOD TRANSFUSION, 2019; 17 (3)

Background. A weak ABO subgroup is one of the most important causes of an ABO blood grouping discrepancy. Here, we investigated the distribution of we......

JIF:3.35

Single-stranded DNA aptamer targeting and neutralization of anti-D alloantibody: a potential therapeutic strategy for haemolytic diseases caused by Rhesus alloantibody

期刊: BLOOD TRANSFUSION, 2018; 16 (2)

Background. Rhesus (Rh) D antigen is the most important antigen in the Rh blood group system because of its strong immunogenicity. When RhD-negative i......

JIF:3.35

Characterisation and follow-up study of occult hepatitis B virus infection in anti-HBc-positive qualified blood donors in southern China

期刊: BLOOD TRANSFUSION, 2017; 15 (1)

Background: Most major Chinese blood centres look for hepatitis B surface antigen (HBsAg) and perform nucleic acid testing to screen blood for hepatit......

JIF:2.14

共13条页码: 1/1页15条/页