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Comparison of Midazolam versus Midazolam/Meperidine during Colonoscopy in a Prospective, Randomized, Double-Blind Study

Jung HK, Bae KS, Yoon SJ, Lee JS, Kwon JM, Yoo MA

  • KMID: 772612
  • Korean J Gastroenterol.
  • 2004 Feb;43(2):96-103.
BACKGROUND/AIMS: Colonoscopy is a painful procedure. Therefore conscious sedation is often used. However, the value of adding analgesics to sedatives has not been well evaluated. METHODS: The double blind,...
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Relationship of CDX1 mRNA and CDX2 mRNA expression and clinicopathologic features in colorectal cancers

Kim GH, Lee DH, Kim HW, Cheong JY, Seo SB, Heo J, Kang DH, Song GA, Cho M, Yang US, Park DY, Yoo MA

  • KMID: 2306008
  • Korean J Med.
  • 2004 Oct;67(4):349-357.
BACKGROUND: CDX1 and CDX2, members of the caudal-type homeobox gene family, control proliferation and differentiation of intestinal mucosal cells. Their expression is reduced commonly in colorectal cancers, but reports about...
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Role of Ras/ERK-dependent pathway in the erythroid differentiation of K562 cells

Kang CD, Do IR, Kim KW, Ahn BK, Kim SH, Chung BS, Jhun BH, Yoo MA

  • KMID: 1029935
  • Exp Mol Med.
  • 1999 Jun;31(2):76-82.
The chronic myelogenous leukemic K562 cell line carrying Bcr-Abl tyrosine kinase is considered as pluripotent hematopoietic progenitor cells expressing markers for erythroid, granulocytic, monocytic, and megakaryocytic lineages. Here we investigated the signaling modulations...
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Relationships Between the Expressions of CDX1 and CDX2 mRNA and Clinicopathologic Features in Colorectal Cancers

Kim GH, Lee DH, Kim HW, Cheong JY, Seo SB, Heo J, Kang DH, Song GA, Cho M, Yang US, Park DY, Yoo MA

BACKGROUND: CDX1 and CDX2 are members of the caudal-type homeobox gene family and control the proliferation and differentiation of intestinal mucosal cells. Their expressions are commonly reduced in colorectal cancer,...
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Functional Profiling of Human MeCP2 by Automated Data Comparison Analysis and Computerized Expression Pathway Modeling

Kim I, Lee SH, Jeong J, Park JH, Yoo MA, Kim CM

OBJECTIVES: Methyl-CpG binding protein 2 (MeCP2) is a ubiquitous epigenetic factor that represses gene expression by modifying chromatin. Mutations in the MeCP2 gene cause Rett syndrome, a progressive neurodevelopmental disorder....
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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

  • KMID: 1111404
  • Exp Mol Med.
  • 2006 Apr;38(2):119-125.
Rett syndrome (RTT) is an X-linked dominant neurodevelopmental disorder affecting 1 per 10,000- 15,000 female births worldwide. The disease-causing gene has been identified as MECP2 (methyl- CpG-binding protein 2). In...
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