Effect of prostaglandins on cyclic AMP concentrations in toad bladder and rat kidney

Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutation.

Journal of inherited metabolic disease·2001

Five cases of isolated glycerol kinase deficiency, including two families: failure to find genotype:phenotype correlation.

Journal of medical genetics·2000

Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease.

Journal of lipid research·2000

Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.

Human mutation·1999

Generalised uridine diphosphate galactose-4-epimerase deficiency.

Archives of disease in childhood·1999

Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene.

Nature genetics·1997

Phosphoproteomics identifies PAK2-associated developmental modules in mouse embryos.

FEBS letters·2026

From junk to function - How weak selection in eukaryotes builds new parts and drives genomic complexity.

FEBS letters·2026

Stress-induced trained immunity-A key mechanism linking psychosocial stress, atherosclerosis, and cardiovascular disease.

FEBS letters·2026

Translophagy-A potential link between autophagy impairment and translational errors.

FEBS letters·2026

Engineering peptides into antibodies-opportunities and strategies for therapeutic innovation.

FEBS letters·2026

Emerging experimental and computational methods for studying redox-regulated structural transitions.

FEBS letters·2026

DOF Transcription Factors: Regulatory Hubs Coordinating Plant Growth, Development and Stress Tolerance.

Journal of experimental botany·2026

Determination of Spontaneous Mutation Rate by Fluctuation Analysis Using 5-Fluoroorotic Acid (5-FOA).

Methods in molecular biology (Clifton, N.J.)·2026

Cognitive abilities show distinct developmental trajectories in wild meerkats.

Proceedings. Biological sciences·2026

Dynamic DNA methylation remodeling in the brain during flatfish metamorphosis.

Biochimica et biophysica acta. Gene regulatory mechanisms·2026

Stemness as a Systems-Level State: From Ancestral Plasticity to Systemic Control in Regeneration, Aging, and Cancer.

Annual review of genetics·2026

A novel homeotic mutation in morphology using skeletal specimens in four breeds of Japanese indigenous chickens.

Poultry science·2026

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Effect of prostaglandins on cyclic AMP concentrations in toad bladder and rat kidney

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Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutation.

Five cases of isolated glycerol kinase deficiency, including two families: failure to find genotype:phenotype correlation.

Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease.

Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.

Generalised uridine diphosphate galactose-4-epimerase deficiency.

Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene.

Phosphoproteomics identifies PAK2-associated developmental modules in mouse embryos.

From junk to function - How weak selection in eukaryotes builds new parts and drives genomic complexity.

Stress-induced trained immunity-A key mechanism linking psychosocial stress, atherosclerosis, and cardiovascular disease.

Translophagy-A potential link between autophagy impairment and translational errors.

Engineering peptides into antibodies-opportunities and strategies for therapeutic innovation.

Emerging experimental and computational methods for studying redox-regulated structural transitions.

DOF Transcription Factors: Regulatory Hubs Coordinating Plant Growth, Development and Stress Tolerance.

Determination of Spontaneous Mutation Rate by Fluctuation Analysis Using 5-Fluoroorotic Acid (5-FOA).

Cognitive abilities show distinct developmental trajectories in wild meerkats.

Dynamic DNA methylation remodeling in the brain during flatfish metamorphosis.

Stemness as a Systems-Level State: From Ancestral Plasticity to Systemic Control in Regeneration, Aging, and Cancer.

A novel homeotic mutation in morphology using skeletal specimens in four breeds of Japanese indigenous chickens.

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Effect of prostaglandins on cyclic AMP concentrations in toad bladder and rat kidney

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