Han MY - Search Results

1

Cinnamaldehydes inhibit cyclin dependent kinase 4/cyclin D1.

Jeong HW, Kim MR, Son KH, Han MY, Ha JH, Garnier M, Meijer L, Kwon BM. Jeong HW, et al. Among authors: han my. Bioorg Med Chem Lett. 2000 Aug 21;10(16):1819-22. doi: 10.1016/s0960-894x(00)00357-7. Bioorg Med Chem Lett. 2000. PMID: 10969976

2

Biological effects of G1 phase arrest compound, sesquicillin, in human breast cancer cell lines.

Jeong HW, Lee HJ, Kho YH, Son KH, Han MY, Lim JS, Lee MY, Han DC, Ha JH, Kwon BM. Jeong HW, et al. Among authors: han my, han dc. Bioorg Med Chem. 2002 Oct;10(10):3129-34. doi: 10.1016/s0968-0896(02)00225-0. Bioorg Med Chem. 2002. PMID: 12150857

3

Actinomycin D, C2 and VII, inhibitors of Grb2-SHC interaction produced by Streptomyces.

Nam JY, Kim HK, Son KH, Kim SU, Kwon BM, Han MY, Chung YJ, Bok SH. Nam JY, et al. Among authors: han my. Bioorg Med Chem Lett. 1998 Aug 4;8(15):2001-2. doi: 10.1016/s0960-894x(98)00345-x. Bioorg Med Chem Lett. 1998. PMID: 9873474

4

Natural and synthetic analogues of actinomycin D as Grb2-SH2 domain blockers.

Kim HK, Nam JY, Han MY, Son KH, Choi JD, Kwon BM, Takusagawa HL, Huang Y, Takusagawa F. Kim HK, et al. Among authors: han my. Bioorg Med Chem Lett. 2000 Jul 3;10(13):1455-7. doi: 10.1016/s0960-894x(00)00258-4. Bioorg Med Chem Lett. 2000. PMID: 10888331

5

Antitumor effect of the cinnamaldehyde derivative CB403 through the arrest of cell cycle progression in the G2/M phase.

Jeong HW, Han DC, Son KH, Han MY, Lim JS, Ha JH, Lee CW, Kim HM, Kim HC, Kwon BM. Jeong HW, et al. Among authors: han my, han dc. Biochem Pharmacol. 2003 Apr 15;65(8):1343-50. doi: 10.1016/s0006-2952(03)00038-8. Biochem Pharmacol. 2003. PMID: 12694875

6

Cinnamaldehyde inhibits lymphocyte proliferation and modulates T-cell differentiation.

Koh WS, Yoon SY, Kwon BM, Jeong TC, Nam KS, Han MY. Koh WS, et al. Among authors: han my. Int J Immunopharmacol. 1998 Nov;20(11):643-60. doi: 10.1016/s0192-0561(98)00064-2. Int J Immunopharmacol. 1998. PMID: 9848396

7

8-O-Methylsclerotiorinamine, antagonist of the Grb2-SH2 domain, isolated from Penicillium multicolor.

Nam JY, Kim HK, Kwon JY, Han MY, Son KH, Lee UC, Choi JD, Kwon BM. Nam JY, et al. Among authors: han my. J Nat Prod. 2000 Sep;63(9):1303-5. doi: 10.1021/np0001169. J Nat Prod. 2000. PMID: 11000046

8

Actinomycin D as a novel SH2 domain ligand inhibits Shc/Grb2 interaction in B104-1-1 (neu*-transformed NIH3T3) and SAA (hEGFR-overexpressed NIH3T3) cells.

Kim HK, Nam JY, Han MY, Lee EK, Choi JD, Bok SH, Kwon BM. Kim HK, et al. Among authors: han my. FEBS Lett. 1999 Jun 18;453(1-2):174-8. doi: 10.1016/s0014-5793(99)00710-3. FEBS Lett. 1999. PMID: 10403397 Free article.

9

A screening method of SH2 domain ligands and blockers using a solid phase binding.

Koh WS, Yoon SY, Lee EK, Lee EK, Kwon BM, Kim JW, Han MY. Koh WS, et al. Among authors: han my. Cancer Lett. 1997 Nov 25;120(1):1-7. doi: 10.1016/s0304-3835(97)00284-x. Cancer Lett. 1997. PMID: 9570379

10

Activation of dynamin I gene expression by Sp1 and Sp3 is required for neuronal differentiation of N1E-115 cells.

Yoo J, Jeong MJ, Kwon BM, Hur MW, Park YM, Han MY. Yoo J, et al. Among authors: han my. J Biol Chem. 2002 Apr 5;277(14):11904-9. doi: 10.1074/jbc.M111788200. Epub 2002 Jan 23. J Biol Chem. 2002. PMID: 11809758 Free article.

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