about
Rh Immunoprophylaxis for Women With a Serologic Weak D PhenotypeStructural and functional impacts of amino acid substitutions that create blood group antigens: implications for immunogenicity.BOOGIE: Predicting Blood Groups from High Throughput Sequencing Data.Evolutionary genetics of the human Rh blood group system.RHD variants in Polish blood donors routinely typed as D-Distribution of Rhesus blood group antigens and weak D alleles in the population of AlbaniaFactors Influencing RBC Alloimmunization: Lessons Learned from Murine Models.Variant RH alleles and Rh immunisation in patients with sickle cell disease.It's time to phase in RHD genotyping for patients with a serologic weak D phenotype. College of American Pathologists Transfusion Medicine Resource Committee Work Group.High-throughput Kell, Kidd, and Duffy matrix-assisted laser desorption/ionization, time-of-flight mass spectrometry-based blood group genotyping of 4000 donors shows close to full concordance with serotyping and detects new alleles.Rh D blood group conversion using transcription activator-like effector nucleases.Worse Health Status and Higher Incidence of Health Disorders in Rhesus Negative Subjects.Heterozygote Advantage Probably Maintains Rhesus Factor Blood Group Polymorphism: Ecological Regression Study.Impact of a confirmatory RhD test on the correct serologic typing of blood donors.Inhibition of phagocytic recognition of anti-D opsonized Rh D+ RBC by polymer-mediated immunocamouflage.Evaluation of red blood cell and platelet antigen genotyping platforms (ID CORE XT/ID HPA XT) in routine clinical practice.RHD*weak D type 38: a family study.Enigmatic Weak D antigen: An Experience in a Tertiary Care Hospital of East Delhi.Survey on the prevention and incidence of haemolytic disease of the newborn in ItalyVariants of RhD--current testing and clinical consequences.Red blood cell alloimmunization in sickle cell disease and in thalassaemia: current status, future perspectives and potential role of molecular typing.Combining serology and molecular typing of weak D role in improving D typing strategy in Egypt.RH diversity in Mali: characterization of a new haplotype RHD*DIVa/RHCE*ceTI(D2).Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype.Low incidence of D alloimmunization among patients with a serologic weak D phenotype after D+ transfusion.Extensive functional analyses of RHD splice site variants: Insights into the potential role of splicing in the physiology of Rh.The DAU cluster: a comparative analysis of 18 RHD alleles, some forming partial D antigens.Prevalence of RhD variants among blood donors at Gulu Regional Blood Bank, Gulu, Northern Uganda.Weak D and partial D: our experience in daily activity.Performance of a microarray-based genotyping system for red cell and platelet antigens in China.Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare alleles.Molecular structures identified in serologically D- samples of an admixed population.RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification.Weak D caused by a founder deletion in the RHD gene.Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia.Application of Multiplex Ligation-Dependent Probe Amplification Assay for Genotyping Major Blood Group Systems Including DEL Variants in the D-Negative Korean Population.Two large deletions extending beyond either end of the RHD gene and their red cell phenotypes.A case of high-titer anti-D hemolytic disease of the newborn in which late onset and mild course is associated with the D variant, RHD-CE(9)-D.Weak D type 1, 2 and 3 subtype alleles are rare in the Western French population.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Molecular genetics and clinical applications for RH.
@ast
Molecular genetics and clinical applications for RH.
@en
Molecular genetics and clinical applications for RH.
@nl
type
label
Molecular genetics and clinical applications for RH.
@ast
Molecular genetics and clinical applications for RH.
@en
Molecular genetics and clinical applications for RH.
@nl
prefLabel
Molecular genetics and clinical applications for RH.
@ast
Molecular genetics and clinical applications for RH.
@en
Molecular genetics and clinical applications for RH.
@nl
P2860
P1476
Molecular genetics and clinical applications for RH.
@en
P2093
Willy A Flegel
P2860
P356
10.1016/J.TRANSCI.2010.12.013
P577
2011-01-28T00:00:00Z