PubMed (OMIM) for id: 22953

Year	Number of Results
1994	1
1995	1
1999	2
2000	1
2002	1
2005	2
2008	1
2013	3
2014	1
2021	1
2024	0

1

Generation and characterization of a P2rx2 V60L mouse model for DFNA41.

Chen X, Abad C, Chen ZY, Young JI, Gurumurthy CB, Walz K, Liu XZ. Chen X, et al. Hum Mol Genet. 2021 May 31;30(11):985-995. doi: 10.1093/hmg/ddab077. Hum Mol Genet. 2021. PMID: 33791800 Free PMC article.

2

A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss.

Faletra F, Girotto G, D'Adamo AP, Vozzi D, Morgan A, Gasparini P. Faletra F, et al. Gene. 2014 Jan 25;534(2):236-9. doi: 10.1016/j.gene.2013.10.052. Epub 2013 Nov 6. Gene. 2014. PMID: 24211385

3

ATP-gated ion channels mediate adaptation to elevated sound levels.

Housley GD, Morton-Jones R, Vlajkovic SM, Telang RS, Paramananthasivam V, Tadros SF, Wong AC, Froud KE, Cederholm JM, Sivakumaran Y, Snguanwongchai P, Khakh BS, Cockayne DA, Thorne PR, Ryan AF. Housley GD, et al. Proc Natl Acad Sci U S A. 2013 Apr 30;110(18):7494-9. doi: 10.1073/pnas.1222295110. Epub 2013 Apr 16. Proc Natl Acad Sci U S A. 2013. PMID: 23592720 Free PMC article.

4

Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noise.

Yan D, Zhu Y, Walsh T, Xie D, Yuan H, Sirmaci A, Fujikawa T, Wong AC, Loh TL, Du L, Grati M, Vlajkovic SM, Blanton S, Ryan AF, Chen ZY, Thorne PR, Kachar B, Tekin M, Zhao HB, Housley GD, King MC, Liu XZ. Yan D, et al. Proc Natl Acad Sci U S A. 2013 Feb 5;110(6):2228-33. doi: 10.1073/pnas.1222285110. Epub 2013 Jan 23. Proc Natl Acad Sci U S A. 2013. PMID: 23345450 Free PMC article.

5

ATP activates P2x receptors and requires extracellular Ca(++) participation to modify outer hair cell nonlinear capacitance.

Yu N, Zhao HB. Yu N, et al. Pflugers Arch. 2008 Nov;457(2):453-61. doi: 10.1007/s00424-008-0522-5. Epub 2008 May 20. Pflugers Arch. 2008. PMID: 18491132 Free PMC article.

6

ATP signaling is crucial for communication from taste buds to gustatory nerves.

Finger TE, Danilova V, Barrows J, Bartel DL, Vigers AJ, Stone L, Hellekant G, Kinnamon SC. Finger TE, et al. Science. 2005 Dec 2;310(5753):1495-9. doi: 10.1126/science.1118435. Science. 2005. PMID: 16322458

7

Refinement of the DFNA41 locus and candidate genes analysis.

Yan D, Ouyang XM, Zhu X, Du LL, Chen ZY, Liu XZ. Yan D, et al. J Hum Genet. 2005;50(10):516-522. doi: 10.1007/s10038-005-0286-0. Epub 2005 Sep 30. J Hum Genet. 2005. PMID: 16195816

8

A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter.

Blanton SH, Liang CY, Cai MW, Pandya A, Du LL, Landa B, Mummalanni S, Li KS, Chen ZY, Qin XN, Liu YF, Balkany T, Nance WE, Liu XZ. Blanton SH, et al. J Med Genet. 2002 Aug;39(8):567-70. doi: 10.1136/jmg.39.8.567. J Med Genet. 2002. PMID: 12161595 Free PMC article.

9

State-dependent cross-inhibition between transmitter-gated cation channels.

Khakh BS, Zhou X, Sydes J, Galligan JJ, Lester HA. Khakh BS, et al. Nature. 2000 Jul 27;406(6794):405-10. doi: 10.1038/35019066. Nature. 2000. PMID: 10935636 Free article.

10

Molecular and functional characterization of human P2X(2) receptors.

Lynch KJ, Touma E, Niforatos W, Kage KL, Burgard EC, van Biesen T, Kowaluk EA, Jarvis MF. Lynch KJ, et al. Mol Pharmacol. 1999 Dec;56(6):1171-81. doi: 10.1124/mol.56.6.1171. Mol Pharmacol. 1999. PMID: 10570044

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