A Stop Codon Mutation in SCN9A Causes Lack of Pain Sensation

Human Molecular Genetics - United Kingdom
doi 10.1093/hmg/ddm160
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Oxford University Press (OUP)

Related search

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

American Journal of Human Genetics
Genetics
1998English

TRPs in Pain Sensation

Frontiers in Physiology
Physiology
2017English

Pain Sensation in Man.

BMJ
1977English

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

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

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

Journal of Pain Research
AnesthesiologyPain Medicine
2017English

Regulation of Gene Expression by Stop Codon Recoding: Selenocysteine

Gene
MedicineGenetics
2003English

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

Journal of Physiological Sciences
Physiology
2018English

Pyrrolysine Amber Stop Codon Suppression: Development and Applications

ChemBioChem
Organic ChemistryBiochemistryMolecular MedicineMolecular Biology
2017English

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

Nature
Multidisciplinary
2013English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy