Zhao L - Search Results

1

Further evidence for "gain-of-function" mechanism of DFNA5 related hearing loss.

Wang H, Guan J, Guan L, Yang J, Wu K, Lin Q, Xiong W, Lan L, Zhao C, Xie L, Yu L, Dan Bing, Zhao L, Wang D, Wang Q. Wang H, et al. Among authors: zhao c, zhao l. Sci Rep. 2018 May 30;8(1):8424. doi: 10.1038/s41598-018-26554-7. Sci Rep. 2018. PMID: 29849037 Free PMC article.

2

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.

Zhao L, Young WY, Li R, Wang Q, Qian Y, Guan MX. Zhao L, et al. Biochem Biophys Res Commun. 2004 Dec 24;325(4):1503-8. doi: 10.1016/j.bbrc.2004.10.199. Biochem Biophys Res Commun. 2004. PMID: 15555598

3

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.

Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH Jr, Guan MX. Young WY, et al. Among authors: zhao l. Biochem Biophys Res Commun. 2005 Mar 25;328(4):1244-51. doi: 10.1016/j.bbrc.2005.01.085. Biochem Biophys Res Commun. 2005. PMID: 15708009

4

Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.

Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX. Zhao L, et al. Biochem Biophys Res Commun. 2005 Oct 28;336(3):967-73. doi: 10.1016/j.bbrc.2005.08.199. Biochem Biophys Res Commun. 2005. PMID: 16168391

5

Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation.

Wang Q, Li QZ, Han D, Zhao Y, Zhao L, Qian Y, Yuan H, Li R, Zhai S, Young WY, Guan MX. Wang Q, et al. Among authors: zhao y, zhao l. Biochem Biophys Res Commun. 2006 Feb 10;340(2):583-8. doi: 10.1016/j.bbrc.2005.12.045. Epub 2005 Dec 19. Biochem Biophys Res Commun. 2006. PMID: 16380089

6

Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss.

Young WY, Zhao L, Qian Y, Li R, Chen J, Yuan H, Dai P, Zhai S, Han D, Guan MX. Young WY, et al. Among authors: zhao l. Am J Med Genet A. 2006 Oct 15;140(20):2188-97. doi: 10.1002/ajmg.a.31434. Am J Med Genet A. 2006. PMID: 16955413

7

A de novo silencer causes elimination of MITF-M expression and profound hearing loss in pigs.

Chen L, Guo W, Ren L, Yang M, Zhao Y, Guo Z, Yi H, Li M, Hu Y, Long X, Sun B, Li J, Zhai S, Zhang T, Tian S, Meng Q, Yu N, Zhu D, Tang G, Tang Q, Ren L, Liu K, Zhang S, Che T, Yu Z, Wu N, Jing L, Zhang R, Cong T, Chen S, Zhao Y, Zhang Y, Bai X, Guo Y, Zhao L, Zhang F, Zhao H, Zhang L, Hou Z, Zhao J, Li J, Zhang L, Sun W, Zou X, Wang T, Ge L, Liu Z, Hu X, Wang J, Yang S, Li N. Chen L, et al. Among authors: zhao j, zhao h, zhao y, zhao l. BMC Biol. 2016 Jun 27;14:52. doi: 10.1186/s12915-016-0273-2. BMC Biol. 2016. PMID: 27349893 Free PMC article.

8

Novel recessive PDZD7 biallelic mutations in two Chinese families with non-syndromic hearing loss.

Guan J, Wang H, Lan L, Wang L, Yang J, Xie L, Yin Z, Xiong W, Zhao L, Wang D, Wang Q. Guan J, et al. Among authors: zhao l. Am J Med Genet A. 2018 Jan;176(1):99-106. doi: 10.1002/ajmg.a.38477. Epub 2017 Oct 19. Am J Med Genet A. 2018. PMID: 29048736 Free PMC article.

9

Comparison between Bilateral and Unilateral Sudden Sensorineural Hearing Loss.

Bing D, Wang DY, Lan L, Zhao LD, Yin ZF, Yu L, Chen GH, Guan J, Wang QJ. Bing D, et al. Among authors: zhao ld. Chin Med J (Engl). 2018 Feb 5;131(3):307-315. doi: 10.4103/0366-6999.223843. Chin Med J (Engl). 2018. PMID: 29363646 Free PMC article.

10

Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China.

Wang Q, Xiang J, Sun J, Yang Y, Guan J, Wang D, Song C, Guo L, Wang H, Chen Y, Leng J, Wang X, Zhang J, Han B, Zou J, Yan C, Zhao L, Luo H, Han Y, Yuan W, Zhang H, Wang W, Wang J, Yang H, Xu X, Yin Y, Morton CC, Zhao L, Zhu S, Shen J, Peng Z. Wang Q, et al. Among authors: zhao l. Genet Med. 2019 Oct;21(10):2231-2238. doi: 10.1038/s41436-019-0481-6. Epub 2019 Mar 20. Genet Med. 2019. PMID: 30890784 Free article.

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