Ascorbate action on normal and mutant human lysyl hydroxylases from cultured dermal fibroblasts

Characterization and regulation of insulin binding by embryonic chick heart cells.

Developmental biology·2010

Molecular and biochemical characterization of human galactokinase and its small molecule inhibitors.

Chemico-biological interactions·2010

RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions.

Journal of medical genetics·2005

Cystathionine beta-synthase deficiency in Georgia (USA): correlation of clinical and biochemical phenotype with genotype.

Human mutation·2003

GALT deficiency causes UDP-hexose deficit in human galactosemic cells.

Glycobiology·2003

Decreased half-life of insulin-like growth factor I in Rabson-Mendenhall syndrome.

Journal of inherited metabolic disease·2002

Part I. Quantitative provocation and assessment of cutaneous pain in experimental systems: Methods, techniques, and applications.

The Journal of investigative dermatology·2026

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The Journal of investigative dermatology·2026

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The Journal of investigative dermatology·2026

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The Journal of investigative dermatology·2026

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Cold atmospheric plasma affects metabolic processes in malignant melanoma.

Cancer cell international·2026

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Nature cell biology·2026

Cyclic Thiosulfinates: Synthesis and Applications in Chemical Biology and Materials Science.

Chembiochem : a European journal of chemical biology·2026

Rh/C-catalyzed room-temperature electrocatalytic hydrogenation of aromatic compounds in aqueous electrolyte.

Organic & biomolecular chemistry·2026

Ligand-dependent hydrogen evolution rates for (PNNP)Co catalysts.

Dalton transactions (Cambridge, England : 2003)·2026

An Unusual Presentation of Frontal Pneumosinus Dilatans as Flight-Related Headache With Favorable Response to Carbamazepine.

Cureus·2026

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Ascorbate action on normal and mutant human lysyl hydroxylases from cultured dermal fibroblasts

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Characterization and regulation of insulin binding by embryonic chick heart cells.

Molecular and biochemical characterization of human galactokinase and its small molecule inhibitors.

RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions.

Cystathionine beta-synthase deficiency in Georgia (USA): correlation of clinical and biochemical phenotype with genotype.

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