Koo SK - Search Results

1

Transient retinoic acid signaling confers anterior-posterior polarity to the inner ear.

Bok J, Raft S, Kong KA, Koo SK, Dräger UC, Wu DK. Bok J, et al. Among authors: koo sk. Proc Natl Acad Sci U S A. 2011 Jan 4;108(1):161-6. doi: 10.1073/pnas.1010547108. Epub 2010 Dec 20. Proc Natl Acad Sci U S A. 2011. PMID: 21173260 Free PMC article.

2

Conditional deletion of pten leads to defects in nerve innervation and neuronal survival in inner ear development.

Kim HJ, Woo HM, Ryu J, Bok J, Kim JW, Choi SB, Park MH, Park HY, Koo SK. Kim HJ, et al. Among authors: koo sk. PLoS One. 2013;8(2):e55609. doi: 10.1371/journal.pone.0055609. Epub 2013 Feb 5. PLoS One. 2013. PMID: 23393595 Free PMC article.

3

Lmx1a maintains proper neurogenic, sensory, and non-sensory domains in the mammalian inner ear.

Koo SK, Hill JK, Hwang CH, Lin ZS, Millen KJ, Wu DK. Koo SK, et al. Dev Biol. 2009 Sep 1;333(1):14-25. doi: 10.1016/j.ydbio.2009.06.016. Epub 2009 Jun 18. Dev Biol. 2009. PMID: 19540218 Free PMC article.

4

Patterns of gene expression associated with Pten deficiency in the developing inner ear.

Kim HJ, Ryu J, Woo HM, Cho SS, Sung MK, Kim SC, Park MH, Park T, Koo SK. Kim HJ, et al. Among authors: koo sk. PLoS One. 2014 Jun 3;9(6):e97544. doi: 10.1371/journal.pone.0097544. eCollection 2014. PLoS One. 2014. PMID: 24893171 Free PMC article.

5

Reversal of gene expression profile in the phenylketonuria mouse model after adeno-associated virus vector-mediated gene therapy.

Oh HJ, Lee H, Park JW, Rhee H, Koo SK, Kang S, Jo I, Jung SC. Oh HJ, et al. Among authors: koo sk. Mol Genet Metab. 2005 Dec;86 Suppl 1:S124-32. doi: 10.1016/j.ymgme.2005.06.015. Epub 2005 Sep 16. Mol Genet Metab. 2005. PMID: 16150627

6

Heterogeneity in the processing defect of SLC26A4 mutants.

Yoon JS, Park HJ, Yoo SY, Namkung W, Jo MJ, Koo SK, Park HY, Lee WS, Kim KH, Lee MG. Yoon JS, et al. Among authors: koo sk. J Med Genet. 2008 Jul;45(7):411-9. doi: 10.1136/jmg.2007.054635. Epub 2008 Feb 29. J Med Genet. 2008. PMID: 18310264

7

In vivo differentiation of mouse embryonic stem cells into hepatocytes.

Choi D, Oh HJ, Chang UJ, Koo SK, Jiang JX, Hwang SY, Lee JD, Yeoh GC, Shin HS, Lee JS, Oh B. Choi D, et al. Among authors: koo sk. Cell Transplant. 2002;11(4):359-68. Cell Transplant. 2002. PMID: 12162376

8

Identification and functional analysis of cystathionine beta-synthase gene mutations in patients with homocystinuria.

Lee SJ, Lee DH, Yoo HW, Koo SK, Park ES, Park JW, Lim HG, Jung SC. Lee SJ, et al. Among authors: koo sk. J Hum Genet. 2005;50(12):648-54. doi: 10.1007/s10038-005-0312-2. Epub 2005 Oct 5. J Hum Genet. 2005. PMID: 16205833

9

Rapid detection of duplication/deletion of the PMP22 gene in patients with Charcot-Marie-Tooth disease Type 1A and hereditary neuropathy with liability to pressure palsy by real-time quantitative PCR using SYBR Green I dye.

Kim SW, Lee KS, Jin HS, Lee TM, Koo SK, Lee YJ, Jung SC. Kim SW, et al. Among authors: koo sk. J Korean Med Sci. 2003 Oct;18(5):727-32. doi: 10.3346/jkms.2003.18.5.727. J Korean Med Sci. 2003. PMID: 14555828 Free PMC article.

10

Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta.

Lee KS, Song HR, Cho TJ, Kim HJ, Lee TM, Jin HS, Park HY, Kang S, Jung SC, Koo SK. Lee KS, et al. Among authors: koo sk. Hum Mutat. 2006 Jun;27(6):599. doi: 10.1002/humu.9423. Hum Mutat. 2006. PMID: 16705691

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