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A genome-wide association study identifies protein quantitative trait loci (pQTLs)ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferaseABO genotype and risk of thrombotic events and hemorrhagic stroke.BOOGIE: Predicting Blood Groups from High Throughput Sequencing Data.Analysis of exome sequencing data sets reveals structural variation in the coding region of ABO in individuals of African ancestry.High-throughput interpretation of gene structure changes in human and nonhuman resequencing data, using ACE.Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 womenHisto-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severityFine scale analysis of crossover and non-crossover and detection of recombination sequence motifs in the honeybee (Apis mellifera)Genetic and mechanistic evaluation for the mixed-field agglutination in B3 blood type with IVS3+5G>A ABO gene mutationAssociation between the ABO locus and hematological traits in Korean.A General Model of Negative Frequency Dependent Selection Explains Global Patterns of Human ABO Polymorphism.A Novel Variant B Allele of the ABO Blood Group Gene Associated with Lack of B Antigen Expression.Extraordinary sequence divergence at Tsga8, an X-linked gene involved in mouse spermiogenesis.Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin.Influence of single nucleotide polymorphisms in factor VIII and von Willebrand factor genes on plasma factor VIII activity: the ARIC Study.The human genome: genes, pseudogenes, and variation on chromosome 7.Genetic polymorphisms of Rh, Kell, Duffy and Kidd systems in a population from the State of Paraná, southern Brazil.Risk of advanced gastric precancerous lesions in Helicobacter pylori infected subjects is influenced by ABO blood group and cagA status.Common variation in the ABO glycosyltransferase is associated with susceptibility to severe Plasmodium falciparum malaria.Molecular genotyping of ABO blood groups in some population groups from India.Common genetic factors for hematological traits in humans.Interaction of genetic markers associated with serum alkaline phosphatase levels in the Japanese population.Genetic and mechanistic evaluation for the weak A phenotype in Ael blood type with IVS6 + 5G>A ABO gene mutation.Blood Group ABO Genotyping in Paternity Testing.Frequencies of polymorphisms of the Rh, Kell, Kidd, Duffy and Diego systems of Santa Catarina, Southern Brazil.A Novel ABO Gene Variant Leads to Discrepant Results in Forward/Reverse and Molecular Blood Grouping.NextGen sequencing reveals short double crossovers contribute disproportionately to genetic diversity in Toxoplasma gondii.Brief communication: Evolution of a specific O allele (O1vG542A) supports unique ancestry of Native Americans.H1 and H9 human embryonic stem cell lines are heterozygous for the ABO locus.The cis-AB01 allele originated from the A105 allele, and not from the A102 allele.Association between ABO blood group and severity of coronary artery disease in unstable angina.Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study.The Abantu phenotype in the ABO blood group system is due to a splice-site mutation in a hybrid between a new O1-like allelic lineage and the A2 allele.Evolution of the O alleles of the human ABO blood group gene.Identification of a novel A2 allele derived from the A transferase gene through a nucleotide substitution G539C.Molecular polymorphism of ABO blood group gene in Austronesian and non-Austronesian populations in Oceania.A weak blood group A phenotype caused by a translation-initiator mutation in the ABO gene.Polymorphisms and allele frequencies of the ABO blood group gene among the Jomon, Epi-Jomon and Okhotsk people in Hokkaido, northern Japan, revealed by ancient DNA analysis.Identification of a novel A1v-O1v hybrid allele with G829A mutation in a chimeric individual of AelBel phenotype.
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Sequence variation at the human ABO locus.
@ast
Sequence variation at the human ABO locus.
@en
Sequence variation at the human ABO locus.
@nl
type
label
Sequence variation at the human ABO locus.
@ast
Sequence variation at the human ABO locus.
@en
Sequence variation at the human ABO locus.
@nl
prefLabel
Sequence variation at the human ABO locus.
@ast
Sequence variation at the human ABO locus.
@en
Sequence variation at the human ABO locus.
@nl
P1476
Sequence variation at the human ABO locus
@en
P2093
P356
10.1017/S0003480001008995
P407
P577
2002-01-01T00:00:00Z