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Page 1
Genetic pain loss disorders.
Lischka A, Lassuthova P, Çakar A, Record CJ, Van Lent J, Baets J, Dohrn MF, Senderek J, Lampert A, Bennett DL, Wood JN, Timmerman V, Hornemann T, Auer-Grumbach M, Parman Y, Hübner CA, Elbracht M, Eggermann K, Geoffrey Woods C, Cox JJ, Reilly MM, Kurth I. Lischka A, et al. Among authors: wood jn. Nat Rev Dis Primers. 2022 Jun 16;8(1):41. doi: 10.1038/s41572-022-00365-7. Nat Rev Dis Primers. 2022. PMID: 35710757 Review.
Potent analgesic effects of GDNF in neuropathic pain states.
Boucher TJ, Okuse K, Bennett DL, Munson JB, Wood JN, McMahon SB. Boucher TJ, et al. Among authors: wood jn. Science. 2000 Oct 6;290(5489):124-7. doi: 10.1126/science.290.5489.124. Science. 2000. PMID: 11021795
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. Cox JJ, et al. Among authors: wood jn. Nature. 2006 Dec 14;444(7121):894-8. doi: 10.1038/nature05413. Nature. 2006. PMID: 17167479 Free PMC article.
Pain channelopathies.
Cregg R, Momin A, Rugiero F, Wood JN, Zhao J. Cregg R, et al. Among authors: wood jn. J Physiol. 2010 Jun 1;588(Pt 11):1897-904. doi: 10.1113/jphysiol.2010.187807. Epub 2010 Feb 8. J Physiol. 2010. PMID: 20142270 Free PMC article. Review.
A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome.
Kremeyer B, Lopera F, Cox JJ, Momin A, Rugiero F, Marsh S, Woods CG, Jones NG, Paterson KJ, Fricker FR, Villegas A, Acosta N, Pineda-Trujillo NG, Ramírez JD, Zea J, Burley MW, Bedoya G, Bennett DL, Wood JN, Ruiz-Linares A. Kremeyer B, et al. Among authors: wood jn. Neuron. 2010 Jun 10;66(5):671-80. doi: 10.1016/j.neuron.2010.04.030. Neuron. 2010. PMID: 20547126 Free PMC article.
Pain as a channelopathy.
Raouf R, Quick K, Wood JN. Raouf R, et al. Among authors: wood jn. J Clin Invest. 2010 Nov;120(11):3745-52. doi: 10.1172/JCI43158. Epub 2010 Nov 1. J Clin Invest. 2010. PMID: 21041956 Free PMC article. Review.
Novel mutations mapping to the fourth sodium channel domain of Nav1.7 result in variable clinical manifestations of primary erythromelalgia.
Cregg R, Laguda B, Werdehausen R, Cox JJ, Linley JE, Ramirez JD, Bodi I, Markiewicz M, Howell KJ, Chen YC, Agnew K, Houlden H, Lunn MP, Bennett DL, Wood JN, Kinali M. Cregg R, et al. Among authors: wood jn. Neuromolecular Med. 2013 Jun;15(2):265-78. doi: 10.1007/s12017-012-8216-8. Epub 2013 Jan 6. Neuromolecular Med. 2013. PMID: 23292638 Free PMC article.
A role for Piezo2 in EPAC1-dependent mechanical allodynia.
Eijkelkamp N, Linley JE, Torres JM, Bee L, Dickenson AH, Gringhuis M, Minett MS, Hong GS, Lee E, Oh U, Ishikawa Y, Zwartkuis FJ, Cox JJ, Wood JN. Eijkelkamp N, et al. Among authors: wood jn. Nat Commun. 2013;4:1682. doi: 10.1038/ncomms2673. Nat Commun. 2013. PMID: 23575686 Free PMC article.
No pain, more gain.
Cox JJ, Wood JN. Cox JJ, et al. Among authors: wood jn. Nat Genet. 2013 Nov;45(11):1271-2. doi: 10.1038/ng.2810. Nat Genet. 2013. PMID: 24165728
397 results