Associated Papers
Frequency of RHD variants among blood donors in the central region of Iran, Yazd province.
Seddighi N et al.
Transfusion Medicine (oxford, England), 2025
[Serological and Molecular Biological Detection of RhD Variants].
Ren DJ et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2025
Blood type identification and pedigree analysis of D variant with RHD*01W.100/RHD*15.
Yuan X et al.
Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2024
[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
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
Investigation of the intronic variant RHD:c.1154-31C>T designated as RHD*01EL.37.
Rui X et al.
Vox Sanguinis, 2023
Molecular and serological analysis of the D variant in the Chinese population and identification of seven novel RHD alleles.
Wen J et al.
Transfusion, 2023
Single-exon approach to non-invasive fetal RHD screening in early pregnancy: An update after 10 years' experience.
Uzunel M et al.
Vox Sanguinis, 2022
Rh Blood Group D Antigen Genotyping Using a Portable Nanopore-based Sequencing Device: Proof of Principle.
Tounsi WA et al.
Clinical Chemistry, 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
Molecular characterization of RhD variant phenotypes among blood donors: A study from the coastal region of India.
Polavarapu I et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 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
The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.
Ying Y et al.
Frontiers in Immunology, 2021
RHD genotyping of serological weak D phenotypes in the Iranian blood donors and patients.
Oodi A et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis, 2020
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
Dysregulation of neuron differentiation in an autistic savant with exceptional memory.
Song J et al.
Molecular Brain, 2019
Production of RBC autoantibody mimicking anti-D specificity following transfusion in a patient with weak D Type 15.
Takeuchi-Baba C et al.
Transfusion, 2019
[Polymorphism of RHD gene among RhD negative and D variant blood donors from Qingdao region].
Hu B et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2017
Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles.
Isa K et al.
Vox Sanguinis, 2016
Weak D alleles in Japanese: a c.960G>A silent mutation in exon 7 of the RHD gene that affects D expression.
Ogasawara K et al.
Vox Sanguinis, 2016
[Molecular mechanism of 101A>G and 845G>A mutations of RHD gene responsible for a weak RhD].
Zhang X et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2015
Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals.
He J et al.
Transfusion, 2015
A comprehensive investigation of RHD polymorphisms in the Chinese Han population in Xi'an.
Ye SH et al.
Blood Transfusion = Trasfusione Del Sangue, 2014
RHD variants in Polish blood donors routinely typed as D-.
Orzińska A et al.
Transfusion, 2013
Molecular basis of weak D and DEL in Han population in Anhui Province, China.
Chen Q et al.
Chinese Medical Journal, 2012
Partial D phenotypes and genotypes in the Chinese population.
Ye L et al.
Transfusion, 2012
Weak D and DEL alleles detected by routine SNaPshot genotyping: identification of four novel RHD alleles.
Silvy M et al.
Transfusion, 2011
Molecular basis of D variants between Uigur and Han blood donors in Xinjiang.
Li Q et al.
Transfusion Medicine (oxford, England), 2008
[Molecular background of weak D type 15 as the predominant weak D type found in Chinese population].
Sun GD et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2006
Novel weak D types 31 and 32: adsorption-elution-supported D antigen analysis and comparison to prevalent weak D types.
Körmöczi GF et al.
Transfusion, 2005
Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese.
Shao CP et al.
Vox Sanguinis, 2002
RHD sequencing: a new tool for decision making on transfusion therapy and provision of Rh prophylaxis.
Legler TJ et al.
Transfusion Medicine (oxford, England), 2001