Kim CM - Search Results

1

[Natural YMDD motif mutations of HBV polymerase in the chronic hepatitis B virus infected patients].

Shin YM, Heo J, Kim GH, Kang DH, Song GA, Cho M, Yang US, Kim CM, Park HK, Jang HJ. Shin YM, et al. Among authors: kim gh, kim cm. Taehan Kan Hakhoe Chi. 2003 Mar;9(1):1-9. Taehan Kan Hakhoe Chi. 2003. PMID: 12657823 Korean.

2

Detection of YMDD motif mutants by oligonucleotide chips in lamivudine-untreated patients with chronic hepatitis B virus infection.

Heo J, Cho M, Kim HH, Shin YM, Jang HJ, Park HK, Kim CM, Kim GH, Kang DH, Song GA, Yang US. Heo J, et al. Among authors: kim hh, kim gh, kim cm. J Korean Med Sci. 2004 Aug;19(4):541-6. doi: 10.3346/jkms.2004.19.4.541. J Korean Med Sci. 2004. PMID: 15308845 Free PMC article.

3

Oligonucleotide chip for detection of Lamivudine-resistant hepatitis B virus.

Jang H, Cho M, Heo J, Kim H, Jun H, Shin W, Cho B, Park H, Kim C. Jang H, et al. J Clin Microbiol. 2004 Sep;42(9):4181-8. doi: 10.1128/JCM.42.9.4181-4188.2004. J Clin Microbiol. 2004. PMID: 15365009 Free PMC article.

4

Quality control probes for spot-uniformity and quantitative analysis of oligonucleotide array.

Jang H, Cho M, Kim H, Kim C, Park H. Jang H, et al. J Microbiol Biotechnol. 2009 Jul;19(7):658-65. doi: 10.4014/jmb.0804.255. J Microbiol Biotechnol. 2009. PMID: 19652512 Free article.

5

Development and evaluation of oligonucleotide chip based on the 16S-23S rRNA gene spacer region for detection of pathogenic microorganisms associated with sepsis.

Kim CM, Song ES, Jang HJ, Kim HJ, Lee S, Shin JH, Kim SJ, Jeong SH, Jeong J, Koh K, Choi GE, Lee EY, Chang CL. Kim CM, et al. Among authors: kim hj, kim sj. J Clin Microbiol. 2010 May;48(5):1578-83. doi: 10.1128/JCM.01130-09. Epub 2010 Mar 17. J Clin Microbiol. 2010. PMID: 20237100 Free PMC article.

6

Histochemical and molecular genetic study of MELAS and MERRF in Korean patients.

Kim DS, Jung DS, Park KH, Kim IJ, Kim CM, Lee WH, Rho SK. Kim DS, et al. Among authors: kim ij, kim cm. J Korean Med Sci. 2002 Feb;17(1):103-12. doi: 10.3346/jkms.2002.17.1.103. J Korean Med Sci. 2002. PMID: 11850598 Free PMC article.

7

Diagnostic mutational analysis of MECP2 in Korean patients with Rett syndrome.

Kim IJ, Kim YJ, Son BH, Nam SO, Kang HC, Kim HD, Yoo MA, Choi OH, Kim CM. Kim IJ, et al. Among authors: kim yj, kim cm, kim hd. Exp Mol Med. 2006 Apr 30;38(2):119-25. doi: 10.1038/emm.2006.15. Exp Mol Med. 2006. PMID: 16672765 Free article.

8

[A case of R122H mutation of cationic trypsinogen gene in a pediatric patient with hereditary pancreatitis complicated by pseudocyst and hemosuccus pancreaticus].

Kim JY, Choi SH, Ihm JS, Kim SJ, Kim IJ, Kim CM. Kim JY, et al. Among authors: kim ij, kim sj, kim cm. Korean J Gastroenterol. 2005 Feb;45(2):130-6. Korean J Gastroenterol. 2005. PMID: 15725718 Korean.

9

Mutations of CAPN3 in Korean patients with limb-girdle muscular dystrophy.

Shin JH, Kim HS, Lee CH, Kim CM, Park KH, Kim DS. Shin JH, et al. Among authors: kim ds, kim cm, kim hs. J Korean Med Sci. 2007 Jun;22(3):463-9. doi: 10.3346/jkms.2007.22.3.463. J Korean Med Sci. 2007. PMID: 17596655 Free PMC article.

10

A Korean family with Arg1448Cys mutation of SCN4A channel causing paramyotonia congenita: electrophysiologic, histopathologic, and molecular genetic studies.

Kim DS, Kim EJ, Jung DS, Park KH, Kim IJ, Kwak KY, Kim CM, Ko HY. Kim DS, et al. Among authors: kim ij, kim ej, kim cm. J Korean Med Sci. 2002 Dec;17(6):856-60. doi: 10.3346/jkms.2002.17.6.856. J Korean Med Sci. 2002. PMID: 12483017 Free PMC article.

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