Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
Pt 8
pubmed:dateCreated
2005-7-20
pubmed:abstractText
Erythromelalgia is an autosomal dominant disorder characterized by burning pain in response to warm stimuli or moderate exercise. We describe a novel mutation in a family with erythromelalgia in SCN9A, the gene that encodes the Na(v)1.7 sodium channel. Na(v)1.7 produces threshold currents and is selectively expressed within sensory neurons including nociceptors. We demonstrate that this mutation, which produces a hyperpolarizing shift in activation and a depolarizing shift in steady-state inactivation, lowers thresholds for single action potentials and high frequency firing in dorsal root ganglion neurons. Erythromelalgia is the first inherited pain disorder in which it is possible to link a mutation with an abnormality in ion channel function and with altered firing of pain signalling neurons.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1460-2156
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
128
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1847-54
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15958509-Action Potentials, pubmed-meshheading:15958509-Adolescent, pubmed-meshheading:15958509-Adult, pubmed-meshheading:15958509-Aged, pubmed-meshheading:15958509-Base Sequence, pubmed-meshheading:15958509-Child, pubmed-meshheading:15958509-Child, Preschool, pubmed-meshheading:15958509-DNA, pubmed-meshheading:15958509-Erythromelalgia, pubmed-meshheading:15958509-Family Health, pubmed-meshheading:15958509-Female, pubmed-meshheading:15958509-Ganglia, Spinal, pubmed-meshheading:15958509-Humans, pubmed-meshheading:15958509-Male, pubmed-meshheading:15958509-Middle Aged, pubmed-meshheading:15958509-Mutation, pubmed-meshheading:15958509-Neurons, Afferent, pubmed-meshheading:15958509-Nociceptors, pubmed-meshheading:15958509-Patch-Clamp Techniques, pubmed-meshheading:15958509-Pedigree, pubmed-meshheading:15958509-Sodium Channels
pubmed:year
2005
pubmed:articleTitle
Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons.
pubmed:affiliation
Department of Neurology, Center for Neuroscience and Regeneration Research, Yale University School of Medicine, New Haven, CT 06510, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't