Oh SK - Search Results

1

Genetic analysis of auditory neuropathy spectrum disorder in the Korean population.

Bae SH, Baek JI, Lee JD, Song MH, Kwon TJ, Oh SK, Jeong JY, Choi JY, Lee KY, Kim UK. Bae SH, et al. Among authors: oh sk. Gene. 2013 Jun 10;522(1):65-9. doi: 10.1016/j.gene.2013.02.057. Epub 2013 Apr 4. Gene. 2013. PMID: 23562982

2

Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families.

Baek JI, Oh SK, Kim DB, Choi SY, Kim UK, Lee KY, Lee SH. Baek JI, et al. Among authors: oh sk. Orphanet J Rare Dis. 2012 Sep 3;7:60. doi: 10.1186/1750-1172-7-60. Orphanet J Rare Dis. 2012. PMID: 22938506 Free PMC article.

3

A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean population.

Sagong B, Baek JI, Oh SK, Na KJ, Bae JW, Choi SY, Jeong JY, Choi JY, Lee SH, Lee KY, Kim UK. Sagong B, et al. Among authors: oh sk. PLoS One. 2013;8(3):e57237. doi: 10.1371/journal.pone.0057237. Epub 2013 Mar 1. PLoS One. 2013. PMID: 23469187 Free PMC article.

4

Genetic association of MYH genes with hereditary hearing loss in Korea.

Kim SJ, Lee S, Park HJ, Kang TH, Sagong B, Baek JI, Oh SK, Choi JY, Lee KY, Kim UK. Kim SJ, et al. Among authors: oh sk. Gene. 2016 Oct 10;591(1):177-182. doi: 10.1016/j.gene.2016.07.011. Epub 2016 Jul 5. Gene. 2016. PMID: 27393652

5

Application of allele-specific primer extension-based microarray for simultaneous multi-gene mutation screening in patients with non-syndromic hearing loss.

Choi SY, Lee KY, Kim YE, Bae JW, Oh SK, Kim SY, Hwang SJ, Kim UK, Lee SH. Choi SY, et al. Among authors: oh sk. Int J Mol Med. 2010 Mar;25(3):315-20. doi: 10.3892/ijmm_00000347. Int J Mol Med. 2010. PMID: 20127034

6

Evaluation of the pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss.

Oh SK, Choi SY, Yu SH, Lee KY, Hong JH, Hur SW, Kim SJ, Jeon CJ, Kim UK. Oh SK, et al. Biochim Biophys Acta. 2013 Jan;1832(1):285-91. doi: 10.1016/j.bbadis.2012.05.009. Epub 2012 May 19. Biochim Biophys Acta. 2013. PMID: 22617145 Free article.

7

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: oh sk. 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

8

The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss.

Kwon TJ, Oh SK, Park HJ, Sato O, Venselaar H, Choi SY, Kim S, Lee KY, Bok J, Lee SH, Vriend G, Ikebe M, Kim UK, Choi JY. Kwon TJ, et al. Among authors: oh sk. Open Biol. 2014 Jul;4(7):140107. doi: 10.1098/rsob.140107. Open Biol. 2014. PMID: 25080041 Free PMC article.

9

A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.

Oh SK, Baek JI, Weigand KM, Venselaar H, Swarts HG, Park SH, Hashim Raza M, Jung DJ, Choi SY, Lee SH, Friedrich T, Vriend G, Koenderink JB, Kim UK, Lee KY. Oh SK, et al. Eur J Hum Genet. 2015 May;23(5):639-45. doi: 10.1038/ejhg.2014.154. Epub 2014 Aug 20. Eur J Hum Genet. 2015. PMID: 25138102 Free PMC article.

10

Methionine sulfoxide reductase A, B1 and B2 are likely to be involved in the protection against oxidative stress in the inner ear.

Kwon TJ, Oh SK, Kim YR, Kim MA, Lee B, Choi KS, Lee J, Kim UK, Lee KY. Kwon TJ, et al. Among authors: oh sk. Cells Tissues Organs. 2014;199(4):294-300. doi: 10.1159/000368893. Epub 2014 Dec 13. Cells Tissues Organs. 2014. PMID: 25531578

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