PubMed for id: 6336

Year	Number of Results
1993	1
1998	1
1999	1
2003	1
2005	3
2006	2
2008	1
2009	7
2010	11
2011	3
2012	5
2013	10
2014	11
2015	6
2016	8
2017	4
2018	10
2019	8
2020	3
2021	4
2022	4
2023	2
2024	1

1

Heterologous expression of the human wild-type and variant Na_V 1.8 (A1073V) in rat sensory neurons.

Kapur MM, Soliman M, Blanke EN, Herold PB, Janicki PK, Vrana KE, Coates MD, Ruiz-Velasco V. Kapur MM, et al. Neurogastroenterol Motil. 2024 Mar;36(3):e14748. doi: 10.1111/nmo.14748. Epub 2024 Jan 23. Neurogastroenterol Motil. 2024. PMID: 38263802

2

Biallelic Loss of Function Mutation in Sodium Channel Gene SCN10A in an Autism Spectrum Disorder Trio from Pakistan.

Rabia A, Harripaul R, Mikhailov A, Mahmood S, Maqbool S, Vincent JB, Ayub M. Rabia A, et al. Genes (Basel). 2022 Sep 11;13(9):1633. doi: 10.3390/genes13091633. Genes (Basel). 2022. PMID: 36140801 Free PMC article.

3

Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population.

Paludan-Müller C, Larsen S, Ahlberg G, Andreasen L, Monfort LM, Svendsen JH, Jespersen T, Bundgaard H, Kanters JK, Olesen MS. Paludan-Müller C, et al. Circ Genom Precis Med. 2022 Feb;15(1):e003574. doi: 10.1161/CIRCGEN.121.003574. Epub 2022 Feb 1. Circ Genom Precis Med. 2022. PMID: 35103494 No abstract available.

4

Common variants in SCN10A gene associated with Brugada syndrome.

Huang Y, Chen XM, Barajas-Martinez H, Jiang H, Antzelevitch C, Hu D. Huang Y, et al. Hum Mol Genet. 2021 Dec 27;31(2):157-165. doi: 10.1093/hmg/ddab217. Hum Mol Genet. 2021. PMID: 34312669 Free PMC article.

5

Absence of Functional Na_v1.8 Channels in Non-diseased Atrial and Ventricular Cardiomyocytes.

Casini S, Marchal GA, Kawasaki M, Nariswari FA, Portero V, van den Berg NWE, Guan K, Driessen AHG, Veldkamp MW, Mengarelli I, de Groot JR, Verkerk AO, Remme CA. Casini S, et al. Cardiovasc Drugs Ther. 2019 Dec;33(6):649-660. doi: 10.1007/s10557-019-06925-6. Cardiovasc Drugs Ther. 2019. PMID: 31916131 Free PMC article.

6

Impact of the Na_V1.8 variant, A1073V, on post-sigmoidectomy pain and electrophysiological function in rat sympathetic neurons.

Coates MD, Kim JS, Carkaci-Salli N, Vrana KE, Koltun WA, Puhl HL, Adhikary SD, Janicki PK, Ruiz-Velasco V. Coates MD, et al. J Neurophysiol. 2019 Dec 1;122(6):2591-2600. doi: 10.1152/jn.00542.2019. Epub 2019 Oct 23. J Neurophysiol. 2019. PMID: 31642403 Free PMC article.

7

Polymorphisms of the SCN10A Gene in Patients With Sick Sinus Syndrome.

Nikulina SY, Marilovceva OV, Chernova AA, Tret'Jakova SS, Nikulin DA, Maksimov VN. Nikulina SY, et al. Kardiologiia. 2018 Nov 18;58(4):53-59. doi: 10.18087/cardio.2018.4.10096. Kardiologiia. 2018. PMID: 30704383

8

The functional consequences of sodium channel Na_V 1.8 in human left ventricular hypertrophy.

Ahmad S, Tirilomis P, Pabel S, Dybkova N, Hartmann N, Molina CE, Tirilomis T, Kutschka I, Frey N, Maier LS, Hasenfuss G, Streckfuss-Bömeke K, Sossalla S. Ahmad S, et al. ESC Heart Fail. 2019 Feb;6(1):154-163. doi: 10.1002/ehf2.12378. Epub 2018 Oct 30. ESC Heart Fail. 2019. PMID: 30378291 Free PMC article.

9

Loss-of-function of Nav1.8/D1639N linked to human pain can be rescued by lidocaine.

Kaluza L, Meents JE, Hampl M, Rösseler C, Hautvast PAI, Detro-Dassen S, Hausmann R, Schmalzing G, Lampert A. Kaluza L, et al. Pflugers Arch. 2018 Dec;470(12):1787-1801. doi: 10.1007/s00424-018-2189-x. Epub 2018 Aug 11. Pflugers Arch. 2018. PMID: 30099632

10

Loss-of-function mutations of SCN10A encoding Na_V1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease.

Nettuwakul C, Praditsap O, Sawasdee N, Rungroj N, Ruamyod K, Watanapa WB, Junking M, Sangnual S, Sritippayawan S, Cheunsuchon B, Chuawattana D, Rojsatapong S, Chaowagul W, Dib-Hajj SD, Waxman SG, Yenchitsomanus PT. Nettuwakul C, et al. Sci Rep. 2018 Jul 11;8(1):10453. doi: 10.1038/s41598-018-28623-3. Sci Rep. 2018. PMID: 29992996 Free PMC article.

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