Zhao HB - Search Results

1

The effects and outcomes of electrolyte disturbances and asphyxia on newborns hearing.

Liang C, Hong Q, Jiang TT, Gao Y, Yao XF, Luo XX, Zhuo XH, Shinn JB, Jones RO, Zhao HB, Lu GJ. Liang C, et al. Among authors: zhao hb. Int J Pediatr Otorhinolaryngol. 2013 Jul;77(7):1072-6. doi: 10.1016/j.ijporl.2013.03.031. Epub 2013 May 4. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23648318 Free PMC article.

2

Paradoxical enhancement of active cochlear mechanics in long-term administration of salicylate.

Huang ZW, Luo Y, Wu Z, Tao Z, Jones RO, Zhao HB. Huang ZW, et al. Among authors: zhao hb. J Neurophysiol. 2005 Apr;93(4):2053-61. doi: 10.1152/jn.00959.2004. Epub 2004 Dec 8. J Neurophysiol. 2005. PMID: 15590729 Free article.

3

Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss.

Liang C, Zhu Y, Zong L, Lu GJ, Zhao HB. Liang C, et al. Among authors: zhao hb. Neurosci Lett. 2012 Oct 18;528(1):36-41. doi: 10.1016/j.neulet.2012.08.085. Epub 2012 Sep 11. Neurosci Lett. 2012. PMID: 22975134 Free PMC article.

4

Active cochlear amplification is dependent on supporting cell gap junctions.

Zhu Y, Liang C, Chen J, Zong L, Chen GD, Zhao HB. Zhu Y, et al. Among authors: zhao hb. Nat Commun. 2013;4:1786. doi: 10.1038/ncomms2806. Nat Commun. 2013. PMID: 23653198 Free PMC article.

5

Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders.

Chen J, Chen J, Zhu Y, Liang C, Zhao HB. Chen J, et al. Among authors: zhao hb. Biochem Biophys Res Commun. 2014 May 23;448(1):28-32. doi: 10.1016/j.bbrc.2014.04.016. Epub 2014 Apr 13. Biochem Biophys Res Commun. 2014. PMID: 24732355 Free PMC article.

6

Pannexin 1 deficiency can induce hearing loss.

Zhao HB, Zhu Y, Liang C, Chen J. Zhao HB, et al. Biochem Biophys Res Commun. 2015 Jul 17-24;463(1-2):143-7. doi: 10.1016/j.bbrc.2015.05.049. Epub 2015 May 20. Biochem Biophys Res Commun. 2015. PMID: 26002464 Free PMC article.

7

A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall.

Mei L, Chen J, Zong L, Zhu Y, Liang C, Jones RO, Zhao HB. Mei L, et al. Among authors: zhao hb. Neurobiol Dis. 2017 Dec;108:195-203. doi: 10.1016/j.nbd.2017.08.002. Epub 2017 Aug 17. Neurobiol Dis. 2017. PMID: 28823936 Free PMC article.

8

Knockout of Pannexin-1 Induces Hearing Loss.

Chen J, Liang C, Zong L, Zhu Y, Zhao HB. Chen J, et al. Among authors: zhao hb. Int J Mol Sci. 2018 Apr 30;19(5):1332. doi: 10.3390/ijms19051332. Int J Mol Sci. 2018. PMID: 29710868 Free PMC article.

9

Cx26 heterozygous mutations cause hyperacusis-like hearing oversensitivity and increase susceptibility to noise.

Liu LM, Liang C, Chen J, Fang S, Zhao HB. Liu LM, et al. Among authors: zhao hb. Sci Adv. 2023 Feb 10;9(6):eadf4144. doi: 10.1126/sciadv.adf4144. Epub 2023 Feb 8. Sci Adv. 2023. PMID: 36753545 Free PMC article.

10

Pannexin1 channels dominate ATP release in the cochlea ensuring endocochlear potential and auditory receptor potential generation and hearing.

Chen J, Zhu Y, Liang C, Chen J, Zhao HB. Chen J, et al. Among authors: zhao hb. Sci Rep. 2015 Jun 2;5:10762. doi: 10.1038/srep10762. Sci Rep. 2015. PMID: 26035172 Free PMC article.

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