Jeong SY - Search Results

1

TAGLN expression is upregulated in NF1-associated malignant peripheral nerve sheath tumors by hypomethylation in its promoter and subpromoter regions.

Park GH, Lee SJ, Yim H, Han JH, Kim HJ, Sohn YB, Ko JM, Jeong SY. Park GH, et al. Among authors: jeong sy. Oncol Rep. 2014 Oct;32(4):1347-54. doi: 10.3892/or.2014.3379. Epub 2014 Aug 4. Oncol Rep. 2014. PMID: 25109740 Free PMC article.

2

The spectrum of NF1 mutations in Korean patients with neurofibromatosis type 1.

Jeong SY, Park SJ, Kim HJ. Jeong SY, et al. J Korean Med Sci. 2006 Feb;21(1):107-12. doi: 10.3346/jkms.2006.21.1.107. J Korean Med Sci. 2006. PMID: 16479075 Free PMC article.

3

Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array.

Park SJ, Jeong SY, Kim HJ. Park SJ, et al. Among authors: jeong sy. Cancer Genet Cytogenet. 2006 Apr 1;166(1):56-64. doi: 10.1016/j.cancergencyto.2005.08.022. Cancer Genet Cytogenet. 2006. PMID: 16616112

4

A case of Birt-Hogg-Dubé syndrome.

Kim EH, Jeong SY, Kim HJ, Kim YC. Kim EH, et al. Among authors: jeong sy. J Korean Med Sci. 2008 Apr;23(2):332-5. doi: 10.3346/jkms.2008.23.2.332. J Korean Med Sci. 2008. PMID: 18437022 Free PMC article.

5

Loss of Y chromosome in the malignant peripheral nerve sheet tumor of a patient with Neurofibromatosis type 1.

Jeong SY, Park SJ, Lee SJ, Park HJ, Kim HJ. Jeong SY, et al. J Korean Med Sci. 2010 May;25(5):804-8. doi: 10.3346/jkms.2010.25.5.804. Epub 2010 Apr 16. J Korean Med Sci. 2010. PMID: 20436723 Free PMC article.

6

A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome.

Jeong SY, Kim BY, Kim HJ, Yang JA, Kim OH. Jeong SY, et al. J Hum Genet. 2010 Nov;55(11):764-6. doi: 10.1038/jhg.2010.102. Epub 2010 Aug 19. J Hum Genet. 2010. PMID: 20720557

7

Clinical and genetic characteristics of Korean patients with Gaucher disease.

Jeong SY, Park SJ, Kim HJ. Jeong SY, et al. Blood Cells Mol Dis. 2011 Jan 15;46(1):11-4. doi: 10.1016/j.bcmd.2010.07.010. Epub 2010 Aug 21. Blood Cells Mol Dis. 2011. PMID: 20729108

8

Hereditary palmoplantar keratoderma and deafness resulting from genetic mutation of Connexin 26.

Lee JY, In SI, Kim HJ, Jeong SY, Choung YH, Kim YC. Lee JY, et al. Among authors: jeong sy. J Korean Med Sci. 2010 Oct;25(10):1539-42. doi: 10.3346/jkms.2010.25.10.1539. Epub 2010 Sep 17. J Korean Med Sci. 2010. PMID: 20890442 Free PMC article.

9

Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach.

Jeong SY, Kim SJ, Yang JA, Hong JH, Lee SJ, Kim HJ. Jeong SY, et al. J Hum Genet. 2011 Jun;56(6):469-71. doi: 10.1038/jhg.2011.37. Epub 2011 Apr 14. J Hum Genet. 2011. PMID: 21490608

10

Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism.

Ko JM, Yang JA, Jeong SY, Kim HJ. Ko JM, et al. Among authors: jeong sy. Mol Med Rep. 2012 Apr;5(4):943-8. doi: 10.3892/mmr.2012.764. Epub 2012 Jan 25. Mol Med Rep. 2012. PMID: 22294196 Free PMC article.

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