160 related articles for article (PubMed ID: 32817686)
1. Gain-of-function mutation in SCN11A causes itch and affects neurogenic inflammation and muscle function in Scn11a+/L799P mice.
Ebbinghaus M; Tuchscherr L; Segond von Banchet G; Liebmann L; Adams V; Gajda M; Hübner CA; Kurth I; Schaible HG
PLoS One; 2020; 15(8):e0237101. PubMed ID: 32817686
[TBL] [Abstract][Full Text] [Related]
2. 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.
Phatarakijnirund V; Mumm S; McAlister WH; Novack DV; Wenkert D; Clements KL; Whyte MP
Bone; 2016 Mar; 84():289-298. PubMed ID: 26746779
[TBL] [Abstract][Full Text] [Related]
3. Alcohol-aggravated episodic pain in humans with SCN11A mutation and ALDH2 polymorphism.
Yang L; Li L; Tang H; Ma T; Li Y; Zhang X; Shi X; Liu JY
Pain; 2020 Jul; 161(7):1470-1482. PubMed ID: 32132394
[TBL] [Abstract][Full Text] [Related]
4. Ciguatoxins Evoke Potent CGRP Release by Activation of Voltage-Gated Sodium Channel Subtypes Na
Touska F; Sattler S; Malsch P; Lewis RJ; Reeh PW; Zimmermann K
Mar Drugs; 2017 Aug; 15(9):. PubMed ID: 28867800
[TBL] [Abstract][Full Text] [Related]
5. Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant.
Leipold E; Hanson-Kahn A; Frick M; Gong P; Bernstein JA; Voigt M; Katona I; Oliver Goral R; Altmüller J; Nürnberg P; Weis J; Hübner CA; Heinemann SH; Kurth I
Nat Commun; 2015 Dec; 6():10049. PubMed ID: 26645915
[TBL] [Abstract][Full Text] [Related]
6. A disease mutation reveals a role for NaV1.9 in acute itch.
Salvatierra J; Diaz-Bustamante M; Meixiong J; Tierney E; Dong X; Bosmans F
J Clin Invest; 2018 Dec; 128(12):5434-5447. PubMed ID: 30395542
[TBL] [Abstract][Full Text] [Related]
7. Mechanical allodynia triggered by cold exposure in mice with the Scn11a p.R222S mutation: a novel model of drug therapy for neuropathic pain related to Na
Matsubara Y; Okuda H; Harada KH; Youssefian S; Koizumi A
Naunyn Schmiedebergs Arch Pharmacol; 2021 Feb; 394(2):299-306. PubMed ID: 32970203
[TBL] [Abstract][Full Text] [Related]
8. A de novo gain-of-function mutation in SCN11A causes loss of pain perception.
Leipold E; Liebmann L; Korenke GC; Heinrich T; Giesselmann S; Baets J; Ebbinghaus M; Goral RO; Stödberg T; Hennings JC; Bergmann M; Altmüller J; Thiele H; Wetzel A; Nürnberg P; Timmerman V; De Jonghe P; Blum R; Schaible HG; Weis J; Heinemann SH; Hübner CA; Kurth I
Nat Genet; 2013 Nov; 45(11):1399-404. PubMed ID: 24036948
[TBL] [Abstract][Full Text] [Related]
9. Painful and painless mutations of SCN9A and SCN11A voltage-gated sodium channels.
Baker MD; Nassar MA
Pflugers Arch; 2020 Jul; 472(7):865-880. PubMed ID: 32601768
[TBL] [Abstract][Full Text] [Related]
10. The Gain-of-Function R222S Variant in
Zhao C; Jin J; Hu H; Zhou X; Shi X
Front Neurol; 2022; 13():856459. PubMed ID: 35711274
[TBL] [Abstract][Full Text] [Related]
11. Gain-of-function mutations in SCN11A cause familial episodic pain.
Zhang XY; Wen J; Yang W; Wang C; Gao L; Zheng LH; Wang T; Ran K; Li Y; Li X; Xu M; Luo J; Feng S; Ma X; Ma H; Chai Z; Zhou Z; Yao J; Zhang X; Liu JY
Am J Hum Genet; 2013 Nov; 93(5):957-66. PubMed ID: 24207120
[TBL] [Abstract][Full Text] [Related]
12. Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families.
Okuda H; Noguchi A; Kobayashi H; Kondo D; Harada KH; Youssefian S; Shioi H; Kabata R; Domon Y; Kubota K; Kitano Y; Takayama Y; Hitomi T; Ohno K; Saito Y; Asano T; Tominaga M; Takahashi T; Koizumi A
PLoS One; 2016; 11(5):e0154827. PubMed ID: 27224030
[TBL] [Abstract][Full Text] [Related]
13. SCN11A gene deletion causes sensorineural hearing loss by impairing the ribbon synapses and auditory nerves.
Zu M; Guo WW; Cong T; Ji F; Zhang SL; Zhang Y; Song X; Sun W; He DZZ; Shi WG; Yang SM
BMC Neurosci; 2021 Mar; 22(1):18. PubMed ID: 33752606
[TBL] [Abstract][Full Text] [Related]
14. Specialized functions of Nav1.5 and Nav1.9 channels in electrogenesis of myenteric neurons in intact mouse ganglia.
Osorio N; Korogod S; Delmas P
J Neurosci; 2014 Apr; 34(15):5233-44. PubMed ID: 24719102
[TBL] [Abstract][Full Text] [Related]
15. [Pain and analgesia : Mutations of voltage-gated sodium channels].
Eberhardt MJ; Leffler A
Schmerz; 2017 Feb; 31(1):14-22. PubMed ID: 27402262
[TBL] [Abstract][Full Text] [Related]
16. Maladaptive activation of Nav1.9 channels by nitric oxide causes triptan-induced medication overuse headache.
Bonnet C; Hao J; Osorio N; Donnet A; Penalba V; Ruel J; Delmas P
Nat Commun; 2019 Sep; 10(1):4253. PubMed ID: 31534133
[TBL] [Abstract][Full Text] [Related]
17. Familial gain-of-function Na
Han C; Yang Y; Te Morsche RH; Drenth JP; Politei JM; Waxman SG; Dib-Hajj SD
J Neurol Neurosurg Psychiatry; 2017 Mar; 88(3):233-240. PubMed ID: 27503742
[TBL] [Abstract][Full Text] [Related]
18. The influence of Nav1.9 channels on intestinal hyperpathia and dysmotility.
Zhao C; Zhou X; Shi X
Channels (Austin); 2023 Dec; 17(1):2212350. PubMed ID: 37186898
[TBL] [Abstract][Full Text] [Related]
19. Protein arginine methyltransferase 7 modulates neuronal excitability by interacting with NaV1.9.
Ma T; Li L; Chen R; Yang L; Sun H; Du S; Xu X; Cao Z; Zhang X; Zhang L; Shi X; Liu JY
Pain; 2022 Apr; 163(4):753-764. PubMed ID: 34326297
[TBL] [Abstract][Full Text] [Related]
20. Heterologous expression of NaV1.9 chimeras in various cell systems.
Goral RO; Leipold E; Nematian-Ardestani E; Heinemann SH
Pflugers Arch; 2015 Dec; 467(12):2423-35. PubMed ID: 25916202
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]