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2008 1
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Page 1
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. Among authors: liu x. 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.
4,4'-Bipyridinium 1,4-phenyl-ene-diacetate.
Jia M, Liu X, Miao J, Xiong W, Chen Z. Jia M, et al. Among authors: liu x. Acta Crystallogr Sect E Struct Rep Online. 2009 Sep 19;65(Pt 10):o2490. doi: 10.1107/S1600536809036836. Acta Crystallogr Sect E Struct Rep Online. 2009. PMID: 21577940 Free PMC article.
N-(1H-1,2,4-Triazol-5-yl)pyridine-2-carboxamide.
Miao J, Jia M, Liu X, Xiong W, Chen Z. Miao J, et al. Among authors: liu x. Acta Crystallogr Sect E Struct Rep Online. 2009 Oct 17;65(Pt 11):o2738. doi: 10.1107/S1600536809041269. Acta Crystallogr Sect E Struct Rep Online. 2009. PMID: 21578333 Free PMC article.
Gene regulation analysis of patient-derived iPSCs and its CRISPR-corrected control provides a new tool for studying perturbations of ELMOD3 c.512A>G mutation during the development of inherited hearing loss.
Liu X, Wen J, Liu X, Chen A, Li S, Liu J, Sun J, Gong W, Kang X, Feng Z, He C, Mei L, Ling J, Feng Y. Liu X, et al. PLoS One. 2023 Sep 14;18(9):e0288640. doi: 10.1371/journal.pone.0288640. eCollection 2023. PLoS One. 2023. PMID: 37708136 Free PMC article.
25 results