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 transferase

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 transferase

Item
http://www.wikidata.org/entity/Q24802111
Imbalance in A₂ and A₂B phenotype frequency of ABO group in South IndiaStructural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferaseVariant ABO blood group alleles, secretor status, and risk of pancreatic cancer: results from the pancreatic cancer cohort consortium.Molecular testing in transfusion medicine.Expression of the histo-blood group B gene predominates in AB-genotype cells.Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual.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.Thorough analysis of unorthodox ABO deletions called by the 1000 Genomes project.A weak blood group A phenotype caused by a translation-initiator mutation in the ABO gene.Deletion of the RUNX1 binding site in the erythroid cell-specific regulatory element of the ABO gene in two individuals with the Am phenotype.Identification of a novel A1v-O1v hybrid allele with G829A mutation in a chimeric individual of AelBel phenotype.New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes.Evolution of technology for molecular genotyping in blood group systems.Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes.Association of ABO gene mutations resulting in a rare B subgroup.Patterns of human genetic variation inferred from comparative analysis of allelic mutations in blood group antigen genes.Blood group B gene is barely expressed in in vitro erythroid culture of Bm-derived CD34+ cells without an erythroid cell-specific regulatory element.
P2860

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 transferase

Item
http://www.wikidata.org/entity/Q24802111
description
2003 nî lūn-bûn
@nan
2003 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
ABO exon and intron analysis i ...... mutations in the A transferase
@ast
ABO exon and intron analysis i ...... mutations in the A transferase
@en
ABO exon and intron analysis i ...... mutations in the A transferase
@nl
type
label
ABO exon and intron analysis i ...... mutations in the A transferase
@ast
ABO exon and intron analysis i ...... mutations in the A transferase
@en
ABO exon and intron analysis i ...... mutations in the A transferase
@nl
prefLabel
ABO exon and intron analysis i ...... mutations in the A transferase
@ast
ABO exon and intron analysis i ...... mutations in the A transferase
@en
ABO exon and intron analysis i ...... mutations in the A transferase
@nl
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P407
P433
P478
P577
P5875
P6179
P698
P932
P356
P1433
P1476
ABO exon and intron analysis i ...... mutations in the A transferase
@en
P2093
P2860
P2888
P304
P31
P356
P407
P433
P478
P577
P5875
P6179
P698
P932