Liu Q - Search Results

1

SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans.

Guan J, Wang D, Cao W, Zhao Y, Du R, Yuan H, Liu Q, Lan L, Zong L, Yang J, Yin Z, Han B, Zhang F, Wang Q. Guan J, et al. Among authors: liu q. J Hum Genet. 2016 Nov;61(11):917-922. doi: 10.1038/jhg.2016.86. Epub 2016 Jul 7. J Hum Genet. 2016. PMID: 27383657 Free PMC article.

2

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

Wang Q, Li R, Zhao H, Peters JL, Liu Q, Yang L, Han D, Greinwald JH Jr, Young WY, Guan MX. Wang Q, et al. Among authors: liu q. Am J Med Genet A. 2005 Feb 15;133A(1):27-30. doi: 10.1002/ajmg.a.30424. Am J Med Genet A. 2005. PMID: 15637703 Free PMC article.

3

[Correlation between phonetically balanced maximum and pure tone auditory threshold among 106 auditory neuropathy patients].

Lan L, Han DY, Shi W, Han MK, Liu Q, Ding HN, Chen ZH, Wang DY, Li SH, Guo ML, Rao SQ, Wang QJ. Lan L, et al. Among authors: liu q. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008 May;43(5):341-6. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2008. PMID: 18717308 Chinese.

4

Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy.

Wang DY, Wang YC, Weil D, Zhao YL, Rao SQ, Zong L, Ji YB, Liu Q, Li JQ, Yang HM, Shen Y, Benedict-Alderfer C, Zheng QY, Petit C, Wang QJ. Wang DY, et al. Among authors: liu q. BMC Med Genet. 2010 May 26;11:79. doi: 10.1186/1471-2350-11-79. BMC Med Genet. 2010. PMID: 20504331 Free PMC article.

5

[Analyzing GRIA3 gene mutations located in AUNX1 locus in a Chinese pedigree with auditory neuropathy].

Liu Q, Han DY, Ji YB, Li JQ, Lan L, Zhao C, Wang QJ. Liu Q, et al. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2010 Apr;26(4):376-8. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2010. PMID: 20564826 Chinese.

6

Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.

Ji YB, Han DY, Lan L, Wang DY, Zong L, Zhao FF, Liu Q, Benedict-Alderfer C, Zheng QY, Wang QJ. Ji YB, et al. Among authors: liu q. Acta Otolaryngol. 2011 Feb;131(2):124-9. doi: 10.3109/00016489.2010.483479. Epub 2010 Dec 16. Acta Otolaryngol. 2011. PMID: 21162657 Free PMC article.

7

Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss.

Wang H, Zhao Y, Yi Y, Gao Y, Liu Q, Wang D, Li Q, Lan L, Li N, Guan J, Yin Z, Han B, Zhao F, Zong L, Xiong W, Yu L, Song L, Yi X, Yang L, Petit C, Wang Q. Wang H, et al. Among authors: liu q. PLoS One. 2014 Aug 12;9(8):e103133. doi: 10.1371/journal.pone.0103133. eCollection 2014. PLoS One. 2014. PMID: 25116015 Free PMC article.

8

Identification of Two Disease-causing Genes TJP2 and GJB2 in a Chinese Family with Unconditional Autosomal Dominant Nonsyndromic Hereditary Hearing Impairment.

Wang HY, Zhao YL, Liu Q, Yuan H, Gao Y, Lan L, Yu L, Wang DY, Guan J, Wang QJ. Wang HY, et al. Among authors: liu q. Chin Med J (Engl). 2015 Dec 20;128(24):3345-51. doi: 10.4103/0366-6999.171440. Chin Med J (Engl). 2015. PMID: 26668150 Free PMC article.

9

Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype-phenotype review for DFNA11.

Li L, Yuan H, Wang H, Guan J, Lan L, Wang D, Zong L, Liu Q, Han B, Huang D, Wang Q. Li L, et al. Among authors: liu q. Acta Otolaryngol. 2018 May;138(5):463-470. doi: 10.1080/00016489.2017.1397743. Epub 2018 Feb 5. Acta Otolaryngol. 2018. PMID: 29400105

10

ACP-5862 suppresses esophageal squamous cell carcinoma growth through inducing apoptosis via activation of endoplasmic reticulum stress and ROS production.

Liu Q, He J, Zhou X, Han M, Li J, Liu C, Yuan H. Liu Q, et al. Among authors: liu c. Biochem Biophys Res Commun. 2021 Jan 1;534:995-1002. doi: 10.1016/j.bbrc.2020.10.052. Epub 2020 Nov 6. Biochem Biophys Res Commun. 2021. PMID: 33168189

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