Molecular basis for the p phenotype. Identification of distinct and multiple mutations in the alpha 1,4-galactosyltransferase gene in Swedish and Japanese individuals.
about
Two previously proposed P1/P2-differentiating and nine novel polymorphisms at the A4GALT (Pk) locus do not correlate with the presence of the P1 blood group antigen.Immunohistochemical demonstration of alpha1,4-N-acetylglucosaminyltransferase that forms GlcNAcalpha1,4Galbeta residues in human gastrointestinal mucosaThe Drosophila melanogaster homologue of the human histo-blood group Pk gene encodes a glycolipid-modifying alpha1,4-N-acetylgalactosaminyltransferaseThe blood group P1 synthase gene is identical to the Gb3/CD77 synthase gene. A clue to the solution of the P1/P2/p puzzle.International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Berlin report.Transfusion in the age of molecular diagnostics.Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransferase gene responsible for the P phenotype.Molecular basis of the globoside-deficient P(k) blood group phenotype. Identification of four inactivating mutations in the UDP-N-acetylgalactosamine: globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase gene.Molecular Bases and Genotyping for Rare Blood Types.Genetic heterogeneity at the glycosyltransferase loci underlying the GLOB blood group system and collection.A single point mutation in the gene encoding Gb3/CD77 synthase causes a rare inherited polyagglutination syndrome.Applications of DNA-based assays in blood group antigen and antibody identification.Overview of molecular methods in immunohematology.Glycosphingolipids--nature, function, and pharmacological modulation.Human genetic disorders of sphingolipid biosynthesis.Applications and Experience with PCR-Based Assays to Predict Blood Group Antigens.A novel, promoter-based, target-specific assay identifies 2-deoxy-D-glucose as an inhibitor of globotriaosylceramide biosynthesis.Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman.P1/P2 genotyping of known and novel null alleles in the P1PK and GLOB histo-blood group systems.Molecular basis for the p and P(k) phenotypes in three Chinese individuals.Expression of a novel missense mutation found in the A4GALT gene of Amish individuals with the p phenotype.Functional characterisation of a complex mutation in the α(1,4)galactosyltransferase gene in Taiwanese individuals with p phenotype.Sequence variation in the 5' untranslated region of the human A4GALT gene is associated with, but does not define, the P1 blood-group polymorphism.Molecular basis for p blood group phenotype in China.Additional molecular bases of the clinically important p blood group phenotype.
P2860
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P2860
Molecular basis for the p phenotype. Identification of distinct and multiple mutations in the alpha 1,4-galactosyltransferase gene in Swedish and Japanese individuals.
description
2000 nî lūn-bûn
@nan
2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Molecular basis for the p phen ...... dish and Japanese individuals.
@ast
Molecular basis for the p phen ...... dish and Japanese individuals.
@en
type
label
Molecular basis for the p phen ...... dish and Japanese individuals.
@ast
Molecular basis for the p phen ...... dish and Japanese individuals.
@en
prefLabel
Molecular basis for the p phen ...... dish and Japanese individuals.
@ast
Molecular basis for the p phen ...... dish and Japanese individuals.
@en
P2093
P2860
P356
P1476
Molecular basis for the p phen ...... dish and Japanese individuals.
@en
P2093
Furukawa K
Uchikawa M
P2860
P304
37752-37756
P356
10.1074/JBC.C000625200
P407
P577
2000-12-01T00:00:00Z