Functional characterisation of a complex mutation in the α(1,4)galactosyltransferase gene in Taiwanese individuals with p phenotype.

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Human genetic disorders of sphingolipid biosynthesis.Molecular basis for the p and P(k) phenotypes in three Chinese individuals.ECG imaging of ventricular tachycardia: evaluation against simultaneous non-contact mapping and CMR-derived grey zone.

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P2860

Functional characterisation of a complex mutation in the α(1,4)galactosyltransferase gene in Taiwanese individuals with p phenotype.

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2010 nî lūn-bûn

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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2010年學術文章

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Functional characterisation of ...... individuals with p phenotype.

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Functional characterisation of ...... individuals with p phenotype.

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Functional characterisation of ...... individuals with p phenotype.

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Functional characterisation of ...... individuals with p phenotype.

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Functional characterisation of ...... individuals with p phenotype.

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Functional characterisation of ...... individuals with p phenotype.

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Functional characterisation of ...... e individuals with p phenotype

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C-M Hung

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H-C Lin

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K-S Lin

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K-T Lin

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T-M Lin

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Y-C Wang

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P2860

Cloning and expression of the histo-blood group Pk UDP-galactose: Ga1beta-4G1cbeta1-cer alpha1, 4-galactosyltransferase. Molecular genetic basis of the p phenotype

Molecular cloning of globotriaosylceramide/CD77 synthase, a glycosyltransferase that initiates the synthesis of globo series glycosphingolipids

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.

Evolution in health and medicine Sackler colloquium: Consanguinity, human evolution, and complex diseases

Cloning of Gb3 synthase, the key enzyme in globo-series glycosphingolipid synthesis, predicts a family of alpha 1, 4-glycosyltransferases conserved in plants, insects, and mammals

Expression cloning of human globoside synthase cDNAs. Identification of beta 3Gal-T3 as UDP-N-acetylgalactosamine:globotriaosylceramide beta 1,3-N-acetylgalactosaminyltransferase.

Globotriaosyl ceramide receptor function - where membrane structure and pathology intersect.

Molecular basis for the p phenotype. Identification of distinct and multiple mutations in the alpha 1,4-galactosyltransferase gene in Swedish and Japanese individuals.

Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransferase gene responsible for the P phenotype.

The ABO blood group gene: a locus of considerable genetic diversity.

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84-89

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10.1111/J.1365-3148.2010.01055.X

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49623278

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21092013

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Functional characterisation of a complex mutation in the α(1,4)galactosyltransferase gene in Taiwanese individuals with p phenotype.

about

P2860

P2860

Functional characterisation of a complex mutation in the α(1,4)galactosyltransferase gene in Taiwanese individuals with p phenotype.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

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P433

P478

P50

P577

P5875

P698

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P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698