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Journal Abstract Search

352 related items for PubMed ID: 20212137

  • 1. Pain perception is altered by a nucleotide polymorphism in SCN9A.
    Reimann F, Cox JJ, Belfer I, Diatchenko L, Zaykin DV, McHale DP, Drenth JP, Dai F, Wheeler J, Sanders F, Wood L, Wu TX, Karppinen J, Nikolajsen L, Männikkö M, Max MB, Kiselycznyk C, Poddar M, Te Morsche RH, Smith S, Gibson D, Kelempisioti A, Maixner W, Gribble FM, Woods CG.
    Proc Natl Acad Sci U S A; 2010 Mar 16; 107(11):5148-53. PubMed ID: 20212137
    [Abstract] [Full Text] [Related]

  • 2. The Effect of SCN9A Variation on Basal Pain Sensitivity in the General Population: An Experimental Study in Young Women.
    Duan G, Guo S, Zhang Y, Ying Y, Huang P, Wang Q, Zhang L, Zhang X.
    J Pain; 2015 Oct 16; 16(10):971-80. PubMed ID: 26168879
    [Abstract] [Full Text] [Related]

  • 3. The non-synonymous SNP, R1150W, in SCN9A is not associated with chronic widespread pain susceptibility.
    Holliday KL, Thomson W, Neogi T, Felson DT, Wang K, Wu FC, Huhtaniemi IT, Bartfai G, Casanueva F, Forti G, Kula K, Punab M, Vanderschueren D, Macfarlane GJ, Horan MA, Ollier W, Payton A, Pendleton N, McBeth J.
    Mol Pain; 2012 Sep 24; 8():72. PubMed ID: 23006801
    [Abstract] [Full Text] [Related]

  • 4. SCN9A rs6746030 Polymorphism and Pain Perception in Combat Athletes and Non-Athletes.
    Leźnicka K, Pawlak M, Sawczuk M, Gasiorowska A, Leońska-Duniec A.
    Genes (Basel); 2023 Mar 16; 14(3):. PubMed ID: 36981004
    [Abstract] [Full Text] [Related]

  • 5. A SCN9A gene-encoded dorsal root ganglia sodium channel polymorphism associated with severe fibromyalgia.
    Vargas-Alarcon G, Alvarez-Leon E, Fragoso JM, Vargas A, Martinez A, Vallejo M, Martinez-Lavin M.
    BMC Musculoskelet Disord; 2012 Feb 20; 13():23. PubMed ID: 22348792
    [Abstract] [Full Text] [Related]

  • 6. Linkage between increased nociception and olfaction via a SCN9A haplotype.
    Heimann D, Lötsch J, Hummel T, Doehring A, Oertel BG.
    PLoS One; 2013 Feb 20; 8(7):e68654. PubMed ID: 23874707
    [Abstract] [Full Text] [Related]

  • 7. Genotypic Analysis of SCN9A for Prediction of Postoperative Pain in Female Patients Undergoing Gynecological Laparoscopic Surgery.
    Duan G, Xiang G, Guo S, Zhang Y, Ying Y, Huang P, Zheng H, Zhang M, Li N, Zhang X.
    Pain Physician; 2016 Jan 20; 19(1):E151-62. PubMed ID: 26752484
    [Abstract] [Full Text] [Related]

  • 8. Common Missense Variant of SCN9A Gene Is Associated with Pain Intensity in Patients with Chronic Pain from Disc Herniation.
    Kurzawski M, Rut M, Dziedziejko V, Safranow K, Machoy-Mokrzynska A, Drozdzik M, Bialecka M.
    Pain Med; 2018 May 01; 19(5):1010-1014. PubMed ID: 29106681
    [Abstract] [Full Text] [Related]

  • 9. [Neuropathic pain associated with Nav1.7 mutations: clinical picture and treatment].
    Doppler K, Sommer C.
    Nervenarzt; 2013 Dec 01; 84(12):1428-35. PubMed ID: 24202110
    [Abstract] [Full Text] [Related]

  • 10. Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations.
    Cox JJ, Sheynin J, Shorer Z, Reimann F, Nicholas AK, Zubovic L, Baralle M, Wraige E, Manor E, Levy J, Woods CG, Parvari R.
    Hum Mutat; 2010 Sep 01; 31(9):E1670-86. PubMed ID: 20635406
    [Abstract] [Full Text] [Related]

  • 11. Primary erythermalgia as a sodium channelopathy: screening for SCN9A mutations: exclusion of a causal role of SCN10A and SCN11A.
    Drenth JP, Te Morsche RH, Mansour S, Mortimer PS.
    Arch Dermatol; 2008 Mar 01; 144(3):320-4. PubMed ID: 18347287
    [Abstract] [Full Text] [Related]

  • 12. Two novel SCN9A gene heterozygous mutations may cause partial deletion of pain perception.
    Yuan R, Zhang X, Deng Q, Si D, Wu Y, Gao F, Zhou B.
    Pain Med; 2011 Oct 01; 12(10):1510-4. PubMed ID: 21939494
    [Abstract] [Full Text] [Related]

  • 13. Paroxysmal extreme pain disorder M1627K mutation in human Nav1.7 renders DRG neurons hyperexcitable.
    Dib-Hajj SD, Estacion M, Jarecki BW, Tyrrell L, Fischer TZ, Lawden M, Cummins TR, Waxman SG.
    Mol Pain; 2008 Sep 19; 4():37. PubMed ID: 18803825
    [Abstract] [Full Text] [Related]

  • 14. Polymorphism in the SCN9A voltage-gated sodium channel gene associated with interstitial cystitis/bladder pain syndrome.
    Reeder JE, Byler TK, Foster DC, Landas SK, Okafor H, Stearns G, Wood RW, Zhang Y, Mayer RD.
    Urology; 2013 Jan 19; 81(1):210.e1-4. PubMed ID: 23102778
    [Abstract] [Full Text] [Related]

  • 15. Novel SCN9A mutations underlying extreme pain phenotypes: unexpected electrophysiological and clinical phenotype correlations.
    Emery EC, Habib AM, Cox JJ, Nicholas AK, Gribble FM, Woods CG, Reimann F.
    J Neurosci; 2015 May 20; 35(20):7674-81. PubMed ID: 25995458
    [Abstract] [Full Text] [Related]

  • 16. No mutations in the voltage-gated NaV1.7 sodium channel alpha1 subunit gene SCN9A in familial complex regional pain syndrome.
    de Rooij AM, Gosso MF, Alsina-Sanchis E, Marinus J, van Hilten JJ, van den Maagdenberg AM.
    Eur J Neurol; 2010 Jun 01; 17(6):808-14. PubMed ID: 20074229
    [Abstract] [Full Text] [Related]

  • 17. Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders.
    Drenth JP, Waxman SG.
    J Clin Invest; 2007 Dec 01; 117(12):3603-9. PubMed ID: 18060017
    [Abstract] [Full Text] [Related]

  • 18. An SCN9A channelopathy causes congenital inability to experience pain.
    Cox JJ, Reimann F, Nicholas AK, Thornton G, Roberts E, Springell K, Karbani G, Jafri H, Mannan J, Raashid Y, Al-Gazali L, Hamamy H, Valente EM, Gorman S, Williams R, McHale DP, Wood JN, Gribble FM, Woods CG.
    Nature; 2006 Dec 14; 444(7121):894-8. PubMed ID: 17167479
    [Abstract] [Full Text] [Related]

  • 19. Two novel SCN9A mutations causing insensitivity to pain.
    Nilsen KB, Nicholas AK, Woods CG, Mellgren SI, Nebuchennykh M, Aasly J.
    Pain; 2009 May 14; 143(1-2):155-8. PubMed ID: 19304393
    [Abstract] [Full Text] [Related]

  • 20. SCN9A mutations in paroxysmal extreme pain disorder: allelic variants underlie distinct channel defects and phenotypes.
    Fertleman CR, Baker MD, Parker KA, Moffatt S, Elmslie FV, Abrahamsen B, Ostman J, Klugbauer N, Wood JN, Gardiner RM, Rees M.
    Neuron; 2006 Dec 07; 52(5):767-74. PubMed ID: 17145499
    [Abstract] [Full Text] [Related]

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