Latest papers

Vitamin K-dependent carboxylation.

The vitamin K cycle.

Leaf succulence determines the interplay between carboxylase systems and light use during Crassulacean acid metabolism in Kalanchöe species.

Determinants of vitamin K status in humans.

Reaction mechanism of the vitamin K-dependent glutamate carboxylase: a computational study.

Potential misdiagnosis of 3-methylcrotonyl-coenzyme A carboxylase deficiency associated with absent or trace urinary 3-methylcrotonylglycine.

Vitamin K2 induces phosphorylation of protein kinase A and expression of novel target genes in osteoblastic cells.

Nutritional effects of gamma-glutamyl carboxylase gene polymorphism on the correlation between the vitamin K status and gamma-carboxylation of osteocalcin in young males.

[Gas-6 and protein S: vitamin K-dependent factors and ligands for the TAM tyrosine kinase receptors family]

A quantum chemical study of the mechanism of action of Vitamin K carboxylase (VKC)

Quantum chemical study of the mechanism of action of vitamin K carboxylase (VKC). IV. Intermediates and transition states.

Building individualized medicine: prevention of adverse reactions to warfarin therapy.

Fatal hemorrhage in mice lacking gamma-glutamyl carboxylase.

Expression, purification, characterization of human 3-methylcrotonyl-CoA carboxylase (MCCC).

Susceptibility to heat stress and aberrant gene expression patterns in holocarboxylase synthetase-deficient Drosophila melanogaster are caused by decreased biotinylation of histones, not of carboxylases.

Two-dimensional crystallization of human vitamin K-dependent gamma-glutamyl carboxylase.

3-methylcrotonyl-CoA carboxylase deficiency and severe multiple sclerosis.

A functional single nucleotide polymorphism in the vitamin-K-dependent gamma-glutamyl carboxylase gene (Arg325Gln) is associated with bone mineral density in elderly Japanese women

AccD6, a member of the Fas II locus, is a functional carboxyltransferase subunit of the acyl-coenzyme A carboxylase in Mycobacterium tuberculosis.

High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population.