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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 2 |
2011 | 2 |
2013 | 1 |
2021 | 2 |
2024 | 0 |
PubMed (cited) for id: 612048
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Page 1
A Deafness Associated Protein TMEM43 Interacts with KCNK3 (TASK-1) Two-pore Domain K+ (K2P) Channel in the Cochlea.
Exp Neurobiol. 2021 Oct 31;30(5):319-328. doi: 10.5607/en21028.
Exp Neurobiol. 2021.
PMID: 34737237
Free PMC article.
A nonsense TMEM43 variant leads to disruption of connexin-linked function and autosomal dominant auditory neuropathy spectrum disorder.
Jang MW, Oh DY, Yi E, Liu X, Ling J, Kim N, Sharma K, Kim TY, Lee S, Kim AR, Kim MY, Kim MA, Lee M, Han JH, Han JJ, Park HR, Kim BJ, Lee SY, Woo DH, Oh J, Oh SJ, Du T, Koo JW, Oh SH, Shin HW, Seong MW, Lee KY, Kim UK, Shin JB, Sang S, Cai X, Mei L, He C, Blanton SH, Chen ZY, Chen H, Liu X, Nourbakhsh A, Huang Z, Kang KW, Park WY, Feng Y, Lee CJ, Choi BY.
Jang MW, et al.
Proc Natl Acad Sci U S A. 2021 Jun 1;118(22):e2019681118. doi: 10.1073/pnas.2019681118.
Proc Natl Acad Sci U S A. 2021.
PMID: 34050020
Free PMC article.
Item in Clipboard
TMEM43 mutations associated with arrhythmogenic right ventricular cardiomyopathy in non-Newfoundland populations.
Baskin B, Skinner JR, Sanatani S, Terespolsky D, Krahn AD, Ray PN, Scherer SW, Hamilton RM.
Baskin B, et al.
Hum Genet. 2013 Nov;132(11):1245-52. doi: 10.1007/s00439-013-1323-2. Epub 2013 Jun 29.
Hum Genet. 2013.
PMID: 23812740
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TMEM43 mutations in Emery-Dreifuss muscular dystrophy-related myopathy.
Liang WC, Mitsuhashi H, Keduka E, Nonaka I, Noguchi S, Nishino I, Hayashi YK.
Liang WC, et al.
Ann Neurol. 2011 Jun;69(6):1005-13. doi: 10.1002/ana.22338. Epub 2011 Mar 9.
Ann Neurol. 2011.
PMID: 21391237
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Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy.
Christensen AH, Andersen CB, Tybjaerg-Hansen A, Haunso S, Svendsen JH.
Christensen AH, et al.
Clin Genet. 2011 Sep;80(3):256-64. doi: 10.1111/j.1399-0004.2011.01623.x. Epub 2011 Jan 24.
Clin Genet. 2011.
PMID: 21214875
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Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene.
Merner ND, Hodgkinson KA, Haywood AF, Connors S, French VM, Drenckhahn JD, Kupprion C, Ramadanova K, Thierfelder L, McKenna W, Gallagher B, Morris-Larkin L, Bassett AS, Parfrey PS, Young TL.
Merner ND, et al.
Am J Hum Genet. 2008 Apr;82(4):809-21. doi: 10.1016/j.ajhg.2008.01.010. Epub 2008 Feb 28.
Am J Hum Genet. 2008.
PMID: 18313022
Free PMC article.
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LUMA interacts with emerin and influences its distribution at the inner nuclear membrane.
Bengtsson L, Otto H.
Bengtsson L, et al.
J Cell Sci. 2008 Feb 15;121(Pt 4):536-48. doi: 10.1242/jcs.019281. Epub 2008 Jan 29.
J Cell Sci. 2008.
PMID: 18230648
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