Kim UK - Search Results

1

Pou3f4 deficiency causes defects in otic fibrocytes and stria vascularis by different mechanisms.

Song MH, Choi SY, Wu L, Oh SK, Lee HK, Lee DJ, Shim DB, Choi JY, Kim UK, Bok J. Song MH, et al. Among authors: kim uk. Biochem Biophys Res Commun. 2011 Jan 7;404(1):528-33. doi: 10.1016/j.bbrc.2010.12.019. Epub 2010 Dec 7. Biochem Biophys Res Commun. 2011. PMID: 21144821

2

Different functional consequences of two missense mutations in the GJB2 gene associated with non-syndromic hearing loss.

Choi SY, Park HJ, Lee KY, Dinh EH, Chang Q, Ahmad S, Lee SH, Bok J, Lin X, Kim UK. Choi SY, et al. Among authors: kim uk. Hum Mutat. 2009 Jul;30(7):E716-27. doi: 10.1002/humu.21036. Hum Mutat. 2009. PMID: 19384972

3

Construction of a DNA chip for screening of genetic hearing loss.

Choi SY, Kim YE, Ahn DB, Kim TH, Choi JH, Lee HR, Hwang SJ, Kim UK, Lee SH. Choi SY, et al. Among authors: kim th, kim uk, kim ye. Clin Exp Otorhinolaryngol. 2009 Mar;2(1):44-7. doi: 10.3342/ceo.2009.2.1.44. Epub 2009 Mar 26. Clin Exp Otorhinolaryngol. 2009. PMID: 19434291 Free PMC article.

4

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.

5

A novel frameshift mutation in the EYA1 gene in a Korean family with branchio-oto-renal syndrome.

Lee JD, Kim SC, Koh YW, Lee HJ, Choi SY, Kim UK. Lee JD, et al. Among authors: kim sc, kim uk. Ann Clin Lab Sci. 2009 Summer;39(3):303-6. Ann Clin Lab Sci. 2009. PMID: 19667416

6

Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein.

Lee HK, Song MH, Kang M, Lee JT, Kong KA, Choi SJ, Lee KY, Venselaar H, Vriend G, Lee WS, Park HJ, Kwon TK, Bok J, Kim UK. Lee HK, et al. Among authors: kim uk. Physiol Genomics. 2009 Nov 6;39(3):195-201. doi: 10.1152/physiolgenomics.00100.2009. Epub 2009 Aug 11. Physiol Genomics. 2009. PMID: 19671658

7

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: kim sy, kim uk, kim ye. Int J Mol Med. 2010 Mar;25(3):315-20. doi: 10.3892/ijmm_00000347. Int J Mol Med. 2010. PMID: 20127034

8

A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss.

Lee HK, Park HJ, Lee KY, Park R, Kim UK. Lee HK, et al. Among authors: kim uk. Biochem Biophys Res Commun. 2010 Jun 4;396(3):626-30. doi: 10.1016/j.bbrc.2010.04.132. Epub 2010 Apr 29. Biochem Biophys Res Commun. 2010. PMID: 20434433

9

Functional evaluation of GJB2 variants in nonsyndromic hearing loss.

Choi SY, Lee KY, Kim HJ, Kim HK, Chang Q, Park HJ, Jeon CJ, Lin X, Bok J, Kim UK. Choi SY, et al. Among authors: kim hj, kim hk, kim uk. Mol Med. 2011 May-Jun;17(5-6):550-6. doi: 10.2119/molmed.2010.00183. Epub 2011 Jan 8. Mol Med. 2011. PMID: 21298213 Free PMC article.

10

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: kim uk. PLoS One. 2011;6(9):e24511. doi: 10.1371/journal.pone.0024511. Epub 2011 Sep 13. PLoS One. 2011. PMID: 21931733 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

218 results

Search Page

Filters