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Publications by John Morten

A Stop Codon Mutation in SCN9A Causes Lack of Pain Sensation

Human Molecular Genetics

Molecular Biology

English

Sequence Variants in the Melatonin-Related Receptor Gene (GPR50) Associate With Circulating Triglyceride and HDL Levels

Journal of Lipid Research

English

Related publications

Cytochrome C Oxidase Deficiency Associated With the First Stop-Codon Point Mutation in Human mtDNA

American Journal of Human Genetics

English

TRPs in Pain Sensation

Frontiers in Physiology

English

Pain Sensation in Man.

English

A Start Codon Mutation of the TSPAN12 Gene in Chinese Families Causes Clinical Heterogeneous Familial Exudative Vitreoretinopathy

Molecular genetics & genomic medicine

Molecular Biology

English

Complex Management of a Patient With Refractory Primary Erythromelalgia Lacking a SCN9A Mutation

Journal of Pain Research

English

Regulation of Gene Expression by Stop Codon Recoding: Selenocysteine

English

FK506 (Tacrolimus) Causes Pain Sensation Through the Activation of Transient Receptor Potential Ankyrin 1 (TRPA1) Channels

Journal of Physiological Sciences

English

Pyrrolysine Amber Stop Codon Suppression: Development and Applications

Organic Chemistry

Molecular Medicine

Molecular Biology

English

Unusual Base Pairing During the Decoding of a Stop Codon by the Ribosome

Multidisciplinary

English