Associated Papers
Advancements in Blood Group Genotyping Technology and Clinical Applications.
Liu X et al.
Clinical Chemistry, 2026
Serological weak D phenotype caused by a novel RHD variant allele with a nucleotide change (c.283G>T).
Hou J et al.
Transfusion, 2026
Allelic Cataloging of RHD-RHCE Reference Sequences Using Targeted Long-Read Sequencing.
Song J et al.
Clinical Chemistry, 2025
The novel c.1227+2T>C variant in RHD results in the serological D-negative phenotype.
Lee JK et al.
Transfusion, 2025
Combining computational approaches and functional analysis for characterizing the deleterious effect of RHD gene variants on splicing in the Chinese population.
Jia S et al.
Transfusion, 2025
The need for routine detection of the Asian-type DEL allele in individuals with weak or partial D phenotypes from East and Southeast Asian populations.
Wen J et al.
Vox Sanguinis, 2025
Weak D phenotype in transfusion medicine and obstetrics: Challenges and opportunities.
Sainath PB et al.
World Journal of Experimental Medicine, 2025
Transitioning a multiethnic donor pool from serologic D-negative to molecularly RHD-negative at a hospital-based blood donor service.
Flegel WA et al.
Journal of Translational Medicine, 2025
The RhCcEe phenotype incompatibility in Chinese and presence of DEL in serologically D-, C/E+ individuals.
Xiong Y et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2025
Single-Tube Multiplex PCR-SSP for the Detection of RHD Variant Alleles Commonly Found in Serologically D- Phenotype Individuals in a Thai Population.
Pittayabumrung O et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2025
[Serological and Molecular Biological Detection of RhD Variants].
Ren DJ et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2025
A Case of Bidirectional ABO- and RhD-Incompatible Liver Transplantation in a Mongolian Patient With Asian-Type DEL.
Kang T et al.
Annals of Laboratory Medicine, 2025
Prediction of immunogenicity of Rh antigens using in silico analysis of binding to human leukocyte antigen peptide, Basic/Translational Research.
Youk HJ et al.
Plos One, 2025
A Chinese individual with DEL phenotype caused by a novel RHD allele.
Wu F et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2024
[RHD Genotyping Characteristics of RhD-Negative Blood Donors in Wuhu Area].
Li MN et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2024
Single-exon fetal RHD genotyping: a 31-month follow up in the obstetric population of Western Sweden.
Pardi C et al.
Blood Transfusion = Trasfusione Del Sangue, 2024
Evaluation of the LightCycler® PRO Instrument as a Platform for Rhesus D Typing.
Polin H et al.
Biomedicines, 2024
A Bioinformatically Initiated Approach to Evaluate GATA1 Regulatory Regions in Samples with Weak D, Del, or D- Phenotypes Despite Normal RHD Exons.
McGowan EC et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2024
40 years of researching the Del phenotype results in a change of transfusion practice.
Flegel WA et al.
Transfusion, 2024
Identification of a novel DEL allele with c.411G>C on the RHD*01EL.01 allele background.
Shao LN et al.
Transfusion, 2024
Two Cases of Anti-D Alloimmunization in D-Negative Thai Patients as a Result of the Asian-Type DEL on Transfused Red Cells.
Suksard K et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2024
Anti-D alloimmunization by Asia type DEL red blood cell units in a D-negative Thai patient.
Thongbut J et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2023
Frequency of the 'Asia type' DEL with weak D phenotype in chinese.
Hou J et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2023
Noninvasive screening of fetal RHD genotype in Chinese pregnant women with serologic RhD-negative phenotype.
Duan H et al.
Transfusion, 2023
DEL variants: review of molecular mechanisms, clinical consequences and molecular testing strategy.
Yin Q
Functional & Integrative Genomics, 2023
Asian-type DEL (RHD*DEL1) with an allo-anti-D: A paradoxical observation in a healthy multiparous woman.
Ohto H et al.
Transfusion, 2023
[Molecular Mechanism of a Rhesus D Variant Individual with RHD*845A/1227A].
Xie XH et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2023
Serologically D-negative blood donors in Thailand: molecular variants and diagnostic strategy.
Nuchnoi P et al.
Blood Transfusion = Trasfusione Del Sangue, 2023
Transfusion management of Africans with RHD variants in China.
Yin Q et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2023
Patients with Asian-type DEL can safely be transfused with RhD-positive blood.
Ji Y et al.
Blood, 2023
RHD 1227 A and hybrid Rhesus box analysis in Thai RhD+ and RhD- blood donors: Prevalence, RHD zygosity, and molecular screening.
Simtong P et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2022
A novel RHD allele, RHD c.56C>G (p.Thr19Arg), with Del phenotype identified in a Chinese family.
Jiang Z et al.
Transfusion, 2022
RHD alleles contributing to serologically weak D phenotypes in China: A single-centre study over 10 years.
Ye L et al.
Vox Sanguinis, 2022
A novel RHD allele, RHD*1166delA, with D-negative phenotype identified in a Chinese family.
Zhang X et al.
Transfusion, 2022
The efficacy of ethnic specific blood groups genotyping for routine donor investigation and rare donor identification in Taiwan.
Yang MH et al.
Vox Sanguinis, 2022
A practical and effective strategy in East Asia to prevent anti-D alloimmunization in patients by C/c phenotyping of serologic RhD-negative blood donors.
Ito S et al.
Ejhaem, 2021
DEL in China: the D antigen among serologic RhD-negative individuals.
Yin Q et al.
Journal of Translational Medicine, 2021
Molecular basis of serological weak D phenotypes and RhD typing discrepancies identified in the Korean population.
Chung YN et al.
Blood Transfusion = Trasfusione Del Sangue, 2021
[Molecular genetic analysis of two individuals with weak D variant of the Rh blood type].
He Y et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2021
Nation-wide investigation of RHD variants in Thai blood donors: Impact for molecular diagnostics.
Thongbut J et al.
Transfusion, 2021
The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.
Ying Y et al.
Frontiers in Immunology, 2021
RHD Genotypes in a Chinese Cohort of Pregnant Women.
Zhang J et al.
Frontiers in Genetics, 2021
RHD genotyping is recommended for all patients with serological weak-D phenotypes in Asian populations - Cases with coexistence of weak-D and Asia type DEL alleles results in complete expression of D-antigen.
Chun S et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2020
Comprehensive Molecular Analysis of Serologically D-Negative and Weak/Partial D Phenotype in Thai Blood Donors.
Thongbut J et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2020
Molecular and computational analysis of 45 samples with a serologic weak D phenotype detected among 132,479 blood donors in northeast China.
Zhang X et al.
Journal of Translational Medicine, 2019
Characterization of RHD alleles present in serologically RHD-negative donors determined by a sensitive microplate technique.
de Paula Vendrame TA et al.
Vox Sanguinis, 2019
Amplicon Sequencing-Based Noninvasive Fetal Genotyping for RHD-Positive D Antigen-Negative Alleles.
Takahashi K et al.
Clinical Chemistry, 2019