Kim UK - Search Results

1

Multiplex minisequencing screening for PTC genotype associated with bitter taste perception.

Sagong B, Bae JW, Rhyu MR, Kim UK, Ye MK. Sagong B, et al. Among authors: kim uk. Mol Biol Rep. 2014 Mar;41(3):1563-7. doi: 10.1007/s11033-013-3002-8. Epub 2014 Jan 12. Mol Biol Rep. 2014. PMID: 24413990

2

Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss.

Bae JW, Lee KY, Choi SY, Lee SH, Park HJ, Kim UK. Bae JW, et al. Among authors: kim uk. Int J Mol Med. 2008 Aug;22(2):175-80. Int J Mol Med. 2008. PMID: 18636170

3

A Family of H723R Mutation for SLC26A4 Associated with Enlarged Vestibular Aqueduct Syndrome.

Kim S, Song DG, Bae JW, Choi SY, Kim UK, Choi YJ, Lee KY, Lee SH, Lee JR. Kim S, et al. Among authors: kim uk. Clin Exp Otorhinolaryngol. 2009 Jun;2(2):100-2. doi: 10.3342/ceo.2009.2.2.100. Epub 2009 Jun 29. Clin Exp Otorhinolaryngol. 2009. PMID: 19565036 Free PMC article.

4

Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss.

Sagong B, Park R, Kim YH, Lee KY, Baek JI, Cho HJ, Cho IJ, Kim UK, Lee SH. Sagong B, et al. Among authors: kim yh, kim uk. Ann Clin Lab Sci. 2010 Fall;40(4):380-5. Ann Clin Lab Sci. 2010. PMID: 20947814

5

Identification and functional characterization of novel compound heterozygotic mutations in the TECTA gene.

Sagong B, Park HJ, Lee KY, Kim UK. Sagong B, et al. Among authors: kim uk. Gene. 2012 Jan 15;492(1):239-43. doi: 10.1016/j.gene.2011.10.022. Epub 2011 Oct 20. Gene. 2012. PMID: 22037481

6

Associations between matrilin-1 gene polymorphisms and adolescent idiopathic scoliosis curve patterns in a Korean population.

Bae JW, Cho CH, Min WK, Kim UK. Bae JW, et al. Among authors: kim uk. Mol Biol Rep. 2012 May;39(5):5561-7. doi: 10.1007/s11033-011-1360-7. Epub 2011 Dec 23. Mol Biol Rep. 2012. PMID: 22193623

7

Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation.

Bae JW, Kim DB, Choi JY, Park HJ, Lee JD, Hur DG, Bae SH, Jung DJ, Lee SH, Kim UK, Lee KY. Bae JW, et al. Among authors: kim uk, kim db. PLoS One. 2012;7(8):e42463. doi: 10.1371/journal.pone.0042463. Epub 2012 Aug 6. PLoS One. 2012. PMID: 22879993 Free PMC article.

8

A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome.

Sagong B, Seok JH, Kwon TJ, Kim UK, Lee SH, Lee KY. Sagong B, et al. Among authors: kim uk. Gene. 2012 Oct 15;508(1):135-9. doi: 10.1016/j.gene.2012.07.033. Epub 2012 Aug 4. Gene. 2012. PMID: 22884721

9

A systematic survey of carbonic anhydrase mRNA expression during mammalian inner ear development.

Wu L, Sagong B, Choi JY, Kim UK, Bok J. Wu L, et al. Among authors: kim uk. Dev Dyn. 2013 Mar;242(3):269-80. doi: 10.1002/dvdy.23917. Epub 2013 Jan 28. Dev Dyn. 2013. PMID: 23233153 Free article.

10

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: kim uk. PLoS One. 2013;8(3):e57237. doi: 10.1371/journal.pone.0057237. Epub 2013 Mar 1. PLoS One. 2013. PMID: 23469187 Free PMC article.

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