Cho HJ - Search Results

1

A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domain.

Cho HJ, Park HJ, Trexler M, Venselaar H, Lee KY, Robertson NG, Baek JI, Kang BS, Morton CC, Vriend G, Patthy L, Kim UK. Cho HJ, et al. J Mol Med (Berl). 2012 Nov;90(11):1321-1331. doi: 10.1007/s00109-012-0911-2. Epub 2012 May 19. J Mol Med (Berl). 2012. PMID: 22610276 Free PMC article.

2

Identification of pathogenic mechanisms of COCH mutations, abolished cochlin secretion, and intracellular aggregate formation: genotype-phenotype correlations in DFNA9 deafness and vestibular disorder.

Bae SH, Robertson NG, Cho HJ, Morton CC, Jung DJ, Baek JI, Choi SY, Lee J, Lee KY, Kim UK. Bae SH, et al. Among authors: cho hj. Hum Mutat. 2014 Dec;35(12):1506-1513. doi: 10.1002/humu.22701. Hum Mutat. 2014. PMID: 25230692 Free PMC article.

3

Evidence for a founder mutation causing DFNA5 hearing loss in East Asians.

Park HJ, Cho HJ, Baek JI, Ben-Yosef T, Kwon TJ, Griffith AJ, Kim UK. Park HJ, et al. Among authors: cho hj. J Hum Genet. 2010 Jan;55(1):59-62. doi: 10.1038/jhg.2009.114. Epub 2009 Nov 13. J Hum Genet. 2010. PMID: 19911014 Free PMC article.

4

Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss.

Kim MA, Kim YR, Sagong B, Cho HJ, Bae JW, Kim J, Lee J, Park HJ, Choi JY, Lee KY, Kim UK. Kim MA, et al. Among authors: cho hj. PLoS One. 2014 Apr 21;9(4):e95646. doi: 10.1371/journal.pone.0095646. eCollection 2014. PLoS One. 2014. PMID: 24752540 Free PMC article.

5

Genetic analysis of the CHD7 gene in Korean patients with CHARGE syndrome.

Cho HJ, Song MH, Choi SY, Kim J, Lee J, Kim UK, Bok J, Choi JY. Cho HJ, et al. Gene. 2013 Apr 1;517(2):164-8. doi: 10.1016/j.gene.2013.01.010. Epub 2013 Jan 17. Gene. 2013. PMID: 23333604

6

Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.

Kwon TJ, Cho HJ, Kim UK, Lee E, Oh SK, Bok J, Bae YC, Yi JK, Lee JW, Ryoo ZY, Lee SH, Lee KY, Kim HY. Kwon TJ, et al. Among authors: cho hj. Hum Mol Genet. 2014 Mar 15;23(6):1591-601. doi: 10.1093/hmg/ddt549. Epub 2013 Nov 3. Hum Mol Genet. 2014. PMID: 24191262

7

Methionine Sulfoxide Reductase B3-Targeted In Utero Gene Therapy Rescues Hearing Function in a Mouse Model of Congenital Sensorineural Hearing Loss.

Kim MA, Cho HJ, Bae SH, Lee B, Oh SK, Kwon TJ, Ryoo ZY, Kim HY, Cho JH, Kim UK, Lee KY. Kim MA, et al. Among authors: cho hj, cho jh. Antioxid Redox Signal. 2016 Apr 10;24(11):590-602. doi: 10.1089/ars.2015.6442. Epub 2016 Jan 21. Antioxid Redox Signal. 2016. PMID: 26649646 Free PMC article.

8

CHD7 mutational analysis and clinical considerations for auditory rehabilitation in deaf patients with CHARGE syndrome.

Song MH, Cho HJ, Lee HK, Kwon TJ, Lee WS, Oh S, Bok J, Choi JY, Kim UK. Song MH, et al. Among authors: cho hj. PLoS One. 2011;6(9):e24511. doi: 10.1371/journal.pone.0024511. Epub 2011 Sep 13. PLoS One. 2011. PMID: 21931733 Free PMC article.

9

Galangin prevents aminoglycoside-induced ototoxicity by decreasing mitochondrial production of reactive oxygen species in mouse cochlear cultures.

Kim YR, Kim MA, Cho HJ, Oh SK, Lee IK, Kim UK, Lee KY. Kim YR, et al. Among authors: cho hj. Toxicol Lett. 2016 Mar 14;245:78-85. doi: 10.1016/j.toxlet.2016.01.005. Epub 2016 Jan 14. Toxicol Lett. 2016. PMID: 26778349

10

Molecular cloning, characterization, and expression of pannexin genes in chicken.

Kwon TJ, Kim DB, Bae JW, Sagong B, Choi SY, Cho HJ, Kim UK, Lee KY. Kwon TJ, et al. Among authors: cho hj. Poult Sci. 2014 Sep;93(9):2253-61. doi: 10.3382/ps.2013-03867. Epub 2014 Jul 7. Poult Sci. 2014. PMID: 25002553 Free article.

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