Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles
about
Conserved structural features in eukaryotic and prokaryotic fucosyltransferasesA new h allele detected in Europe has a missense mutationin alpha(1,2)-fucosyltransferase motif II.Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransferase gene responsible for the P phenotype.SCER and SCAN: two novel high-prevalence antigens in the Scianna blood group system.Codon usage in vertebrates is associated with a low risk of acquiring nonsense mutations.Neofunctionalization of the Sec1 α1,2fucosyltransferase paralogue in leporids contributes to glycan polymorphism and resistance to rabbit hemorrhagic disease virusBlood group genotyping in Germany.Widespread gene conversion of alpha-2-fucosyltransferase genes in mammalsMolecular immunohaematology round table discussions at the AABB Annual Meeting, Anaheim 2015RhCE protein variants in Southwestern Germany detected by serologic routine testing.Molecular basis of Bombay phenotype in Mashhad, Iran: identification of a novel FUT1 deletion.Rh phenotype prediction by DNA typing and its application to practice.Rare gems: null phenotypes of blood groups.ABO genotyping: the quest for clinical applications.Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.Evolution of alpha 2-fucosyltransferase genes in primates: relation between an intronic Alu-Y element and red cell expression of ABH antigens.FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon.Identification of a novel FUT1 allele with two mutations in a Chinese para-Bombay individual.Sequence analysis of the human fucosyltransferase 1 and 2 genes in Tibetan blood donors: identification of three novel alleles.A novel FUT1 allele was identified in a Chinese individual with para-Bombay phenotype.Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes.An AQP1 null allele in an Indian woman with Co(a-b-) phenotype and high-titer anti-Co3 associated with mild HDN.The RHCE allele ceSL: the second example for D antigen expression without D-specific amino acids.Four Non-functional Alleles Were Identified in Seven Chinese Individuals with Para-Bombay Phenotypes
P2860
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P2860
Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles
description
1997 nî lūn-bûn
@nan
1997 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի մարտին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@ast
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@en
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@nl
type
label
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@ast
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@en
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@nl
prefLabel
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@ast
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@en
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@nl
P2860
P1433
P1476
Polymorphism of the h allele a ...... sporadic nonfunctional alleles
@en
P2093
F F Wagner
W A Flegel
P2860
P304
P356
10.1046/J.1537-2995.1997.37397240210.X
P407
P577
1997-03-01T00:00:00Z