The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.
about
Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant.Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9.Integrated Computational Analysis of Genes Associated with Human Hereditary Insensitivity to Pain. A Drug Repurposing Perspective.Protective alleles and modifier variants in human health and disease.Sodium channel NaV1.9 mutations associated with insensitivity to pain dampen neuronal excitability.Electrophysiological and Pharmacological Analyses of Nav1.9 Voltage-Gated Sodium Channel by Establishing a Heterologous Expression System.NaV channel variants in patients with painful and nonpainful peripheral neuropathy.A novel human pain insensitivity disorder caused by a point mutation in ZFHX2.Sodium channels in pain disorders: pathophysiology and prospects for treatment.Voltage-gated sodium channels: (NaV )igating the field to determine their contribution to visceral nociception.NaV1.9 Potentiates Oxidized Phospholipid-Induced TRP Responses Only under Inflammatory Conditions.[Sensory and autonomic neuropathies and pain-related channelopathies].Genetic studies of human neuropathic pain conditions: a review.The Na1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons
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P2860
The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.
@en
type
label
The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.
@en
prefLabel
The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.
@en
P2093
P2860
P356
P1476
The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.
@en
P2093
Christopher Geoffrey Woods
Iain Horrocks
John Tolmie
Mohamed Osman Eltahir Babiker
P2860
P2888
P304
P356
10.1038/EJHG.2014.166
P50
P577
2014-08-13T00:00:00Z
P5875
P6179
1039030994