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

The Journal of biological chemistry·2000

Direct antimicrobial susceptibility testing in bacteriuria.

APMIS : acta pathologica, microbiologica, et immunologica Scandinavica·1999

Histo-blood group p: biosynthesis of globoseries glycolipids in EBV-transformed B cell lines.

Glycoconjugate journal·1996

A point mutation in the GYPC gene results in the expression of the blood group Ana antigen on glycophorin D but not on glycophorin C: further evidence that glycophorin D is a product of the GYPC gene.

Blood·1993

Glycosphingolipid expression in spontaneously aborted fetuses and placenta from blood group p women. Evidence for placenta being the primary target for anti-Tja-antibodies.

Glycoconjugate journal·1992

Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk.

Human heredity·2026

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Human heredity·2026

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Human heredity·2026

Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population.

Human heredity·2025

Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI.

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Generalized Stable Population and Agent-Based Models of Phenotypic Transmission in Human Populations, with an Application to Body Size.

Human heredity·2025

Chronic Hypertension and Conversion from Intermediate Age-Related Macular Degeneration (iAMD) to the Advanced Phenotypes.

Ophthalmic epidemiology·2026

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Journal of human immunity·2026

Correction: Clinical and immunological characterization of NFKB1 haploinsufficiency in Japan.

Frontiers in immunology·2026

Gut-kidney axis in IgA nephropathy: mechanisms linking microbiota dysbiosis to immune dysregulation, Gd-IgA1 generation, and renal injury.

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Collagenofibrotic Glomerulopathy With Concurrent Ostium Secundum Atrial Septal Defect and Anti-Ku Antibody Positivity: A Rare Case.

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Studies of the C3 polymorphism. Relationship between C3 phenotypes and antibody titres

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Universal newborn screening: A roadmap for action.

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

Direct antimicrobial susceptibility testing in bacteriuria.

Histo-blood group p: biosynthesis of globoseries glycolipids in EBV-transformed B cell lines.

A point mutation in the GYPC gene results in the expression of the blood group Ana antigen on glycophorin D but not on glycophorin C: further evidence that glycophorin D is a product of the GYPC gene.

Glycosphingolipid expression in spontaneously aborted fetuses and placenta from blood group p women. Evidence for placenta being the primary target for anti-Tja-antibodies.

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Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang.

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Studies of the C3 polymorphism. Relationship between C3 phenotypes and antibody titres

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