References
- 내과학 이문호
- Int. Rev. Cytol. v.68 Cell death: significance of apoptosis. Cell death: significance of apoptosis. Wyllie, A. H.;Kerr, F. R.;Currie, A. R. https://doi.org/10.1016/S0074-7696(08)62312-8
- FEBS Lett. v.307 Apoptosis. Biochemical events and relevance to cancer chemotherapy. Sen, S.;Incalci, M. D. https://doi.org/10.1016/0014-5793(92)80914-3
- J. Steroid Biochem. v.18 Glucocorticoid effects on thymidine incorporation into the DNA og S49 lymphoma cells. Bradshaw, H. D. J.;Vedeckis, W. V. https://doi.org/10.1016/0022-4731(83)90247-9
- J. Biol. Chem. v.243 Metabolic site and the course of cortisol action on glucose uptake, lactic acid output, and glucose 6-phosphate levels of rat thymus cells in vitro. Munck, A.
- Anal. Sci. Technol. v.11 no.5 Separation of 20(R&S) prosapogenin isomers of ginsenoside-Rg2 and Rg3 from ginseng saponins by reversed-phase high performance liquid chromatography. Jeong, S. I.;Kim, C. S.;Lee, Y. G.;Lee, H. S.;Kim, I.K.
- Biochem. Mol. Biol. Inter. v.40 no.4 Ginsenoside-Rh1 and Rh2 inhibit the induction of nitric oxide synthesis in murine peritoneal macrophages. Park, Y. C.;Lee, C. H.;Kang, H. S.;Kim, K. W.
- J. Nat. Prod. v.63 Isolation of the pharmacologically active saponin ginsenoside Rb1 from ginseng by immunoaffinity column chromatography. Fukuda, N.;Tanaka, H.;Shoyama, Y https://doi.org/10.1021/np990356s
- Planta Medica. v.63 Role of human intestinal prevotella oris in hydrolyzing ginseng saponins. Hasegawa, H.;Sung, J. H.;Benno, Y. https://doi.org/10.1055/s-2006-957729
- Planta medica. v.63 Modulation of protein kinase C activity in NIH3T3 cells by plant glycosides from panax ginseng. Byun, B. H.;Shin, I. C.;Yoon, Y. S.;Kim, S. I.;Joe. C. O. https://doi.org/10.1055/s-2006-957719
- Arch. pharm. Res. v.6 Isolation of ginsenosides Rb1, Rb2, Rc, Rd, Re, Rf and Rg1 from ginseng root by high performance liquid chromatography. Paik, N.H.;Choi, M.G.;Cho, K.G.
- Life Sci. v.65 no.15 Effects of Ginseng components on c-DNA-expressed cytochrome P450 enzyme catalytic activity. Henderson, G. L.;Harkey, M. R.;Gershwin, M. E.;Hackman, R. M.; Stern, J. S.;Stresser, D. M. https://doi.org/10.1016/S0024-3205(99)00407-5
- J. Ethnopharmacol. v.16 no.(2-3) Effect of ginsenosides Rg1, Rc And Rb2 on hormone-induced lipoysis and lipogenesis in rat epididymal fat cells. Ng, T. B.;Wong, C. M.;Yeung, H. W.
- Exp. Cell Res. v.15 Nigrosin as a dye for differentiating live and dead ascites cells. Kaltenbach, J. P.;Kaltenbach, M. H.;Lyons, W. P. https://doi.org/10.1016/0014-4827(58)90067-3
- Cell death in biology and Pathology Munck, A.;Crabtree, G. R.
- Cancer Res. v.53 Detection of DNA strand breaks in individual apoptotic cells by the in situ terminal deoxynucleotidyl transferase and nick tranlation assays. Gorczyca, W.;Gong, J.;Darzynkiewicz, Z.
- J. Cell Biol. v.119 Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. Gavrieli, Y.;Sherman, Y.;Ben-Sasson, S. A. https://doi.org/10.1083/jcb.119.3.493
- Exp. Neurol. v.133 End labeling (TUNEL) in Huntington's disease and other neuropathological conditions. Thomas, L. B.;Gates, D. J.;Richfield, E. K.;O' Brien, T. F.;Schweitzer, J. B.;Steindler, D. A. https://doi.org/10.1006/exnr.1995.1029
- Science v.245 Monoclonal antibody-mediated tumor regressin by induction of apoptosis. Trauth, B. C.;Klas, C.;Peters, A. M.;Matzku, S.;Moller, P.;Debatin, K. M.;Krammer, P. M. https://doi.org/10.1126/science.2787530
- J. Exp. Med. v.169 A cell-killing monoclonal antibody (anti-Fas) to a cell surface antigen co-downregulated with the receptor of tumor necrosis factor. Yonehara, S.;Ishii, A.;Yonehara, M. https://doi.org/10.1084/jem.169.5.1747