References
- Dai YC, Xu MQ. Studies on the medicinal polypore, Phellinus baumii and its kin, P. linteus. Mycotaxon 67: 191-200 (1998)
- Heo J. Dongeuibogam (Publication on Oriental Medicine in Chosun Dynasty). Namsandang Press, Seoul, Korea. p. 719 (1993)
- Kang H-S, Choi J-H, Cho W-K, Park J-C, Choi J-S. A sphingolipid and tyrosinase inhibitors from the fruiting body of Phellinus linteus. Arch. Pharm. Res. 27: 742-750 (2004) https://doi.org/10.1007/BF02980143
- Choi J-H, Ha T-M, Kim Y-H, Rho Y-D. Studies on the main factors affecting the mycelial growth of Phellinus linteus. Korean J. Mycol. 24: 214-222 (1996)
- Han S-B, Lee C-W, Jeon Y-J, Hong N-D, Yoo I-D, Yang K-H, Kim H-M. The inhibitory effect of polysaccharides isolated from Phellinus linteus on tumor growth and metastasis. Immuopharmacology 41: 157-164 (1999) https://doi.org/10.1016/S0162-3109(98)00063-0
- Ikekawa T, Nakanishi M, Uehara N, Chihara G, Fukuoka F. Antitumor action of some basidiomycetes, especially Phellinus linteus. Gann 69: 155-157 (1968)
- Ji J-H, Kim M-N, Chung C-K, Ham S-S. Antimutagenic and cytotoxicity effects of Phellinus linteus extracts. J. Korean Soc. Food. Sci. Nutr. 29: 322-328 (2000)
- Song K-S, Cho S-M, Lee J-H. B-lymphocyte stimulating polysaccharide from mushroom Phellinus linteus. Chem. Pharm. Bull. 43: 2105-2108 (1995) https://doi.org/10.1248/cpb.43.2105
- Lee J-W, Baek S-J, Bang K-W, Kang S-W, Kang S-M, Kim B-Y, Ha I-S. Biological activity of polysaccharide extracted from the fruit body and cultured mycelia of Phellinus linteus IY001. Korean J. Food Sci. Technol. 32: 726-735 (2000)
- Kim H-M, Han S-B, Oh G-T, Kim Y-H, Hong D-H, Hong N-D, Yoo I-D. Stimulation of humoral and cell mediated immunity by polysaccharide from mushroom Phellinus linteus. Int. J. Immunopharmacol. 18: 295-303 (1996) https://doi.org/10.1016/0192-0561(96)00028-8
- Lee J-W, Bang K-W. Biological activity of Phellinus spp. Korean J. Food Ind. Nutr. 6: 25-33 (2001)
- Carmichael J, De Graff WG, Gazdar AF, Minna JD, Mitchell JB. Evaluation of tetrazolium-based semiautomated colorimetric assay assessment of chemosensitivity testing. Cancer Res. 47: 936-942 (1987)
- Bowers GN, McComb RB, Upretti A. 4-Nitrophenyl phosphate - characterization of high - purity materials for measuring alkaline phosphatase activity in human serum. Clin. Chem. 27: 135-143 (1981)
- Dempster DW, Lindsay R. Pathogenesis of osteoporosis. Lancet 34: 797-801 (1993)
- Lindsay R. Managing osteoporosis: Current trends, future possibilities. Geriatrics 42: 35-39 (1987)
- Pole HAP, Felsenberg D, Hanley DA, Stenpan J, Munoz-Torres M, Wolkins TJ, Qui-sheng G, Galich M, Vandormael K, Yates AJ. Multinational placebo-controlled, randomised trial of the effects of alendronate on bone density and fracture risk in post-menopausal women with law bone mass: Results of the FOSIT. Osteoporosis Int. 9: 461-468 (1999) https://doi.org/10.1007/PL00004171
- Ettinger B. Overview of estrogen replacement therapy: A historical perspective. P. Soc. Exp. Biol. Med. 217: 2-5 (1998)
- Schafer JM, Lee ES, O'Regan RM, Yao K, Jordan VC. Rapid development of tamoxifen-stimulated mutant p53 breast tumors (T47D) in athymic mice. Clin. Cancer Res. 6: 4373-4380 (2000)
- Kronenberg F, Fugh-Berman A. Complementary and alternative medicine for menopausal symptoms: A review of randomized, controlled trials. Ann. Intern. Med. 137: 805-813 (2002) https://doi.org/10.7326/0003-4819-137-10-200211190-00009
- Farnsworth NR, Bingel AS, Cordell GA, Crane FA, Fong HS. Potential value of plant as sources of new antifertility agents. J. Parmcol. Sci. 64: 717-754 (1975) https://doi.org/10.1002/jps.2600640504
- Hofmann WE, Everds N, Pignatello M, Solter PF. Automated and semiautomated analysis of rat alkaline phosphate isoenzyme. Toxicol. Pathol. 22: 633-638 (1994) https://doi.org/10.1177/019262339402200607
- Kress BC, Mizrahi IA, Armour KW, Marcus R, Emkey RD, Santora AC. Use of bone alkaline phosphatase to monitor alendronate therapy in individual postmenopausal osteoporotic women. Clin. Chem. 45: 1009-1017 (1999)
- Ha H-K, Ho J-N, Shin S-M, Kim H-J, Koo S-J, Kim I-H, Kim C-S. Effects of Eucommiae Cortex on osteoblast-like cell proliferation and osteoclast inhibition. Arch. Pharm. Res. 26: 929-936 (2003) https://doi.org/10.1007/BF02980202
- Delmas PD. Biochemical markers of bone turnover. J. Bone Miner. Res. 8: S549-S555 (1993) https://doi.org/10.1002/jbmr.5650081323
- Eastell R, Robins SP, Colwell T, Assiri AMA, Riggs BL, Russell RG. Evaluation of bone turnover in type I osteoporosis using biochemical markers specific for both bone formation and bone resorption. Osteoporosis Int. 3: 255-260 (1993) https://doi.org/10.1007/BF01623829
- Ducki S, Hadfield JA, Lawrence NJ, Liu CY, McGown AT, Zhang W. Isolation of E-1-(4'-hydroxyphenyl)-but-1-en-3-one from Scutellaria barbata. Planta Med. 62: 185-186 (1996)
- Tagashira M, Ohtake Y. A new antioxidative 1,3-benzodioxole from Melissa officinalis. Planta Med. 64: 555-558 (1998) https://doi.org/10.1055/s-2006-957513
- Baranovsky A, Schmitt B, Fowler DJ, Schneider B. Synthesis of new biosynthetically important diarylheptanoids and their oxa- and fluoro-analogues by three different strategies. Synthetic Commun. 33: 1019-1045 (2003) https://doi.org/10.1081/SCC-120016367
- Tsuda T, Watanabe M, Ohshima K, Yamamoto A, Kawakishi S, Osawa T. Antioxidative components isolated from the seed of tamarind (Tamarindus indica L.). J. Agr. Food Chem. 42: 2671-2674 (1994) https://doi.org/10.1021/jf00048a004
- Reddy PS, Jamil K, Madhusudhan P, Anjani G, Das B. Antibacterial activity of isolates from Piper longum and Taxus baccata. Pharm. Biol. 39: 236-238 (2001) https://doi.org/10.1076/phbi.39.3.236.5926
- Liu GT, Ahang TM, Wang BE, Wang YW. Protective action of seven natural phenolic compounds against peroxidative damage to biomembranes. Biochem. Pharmacol. 43: 147-152 (1992) https://doi.org/10.1016/0006-2952(92)90271-J
- Watanabe K, Hayashi H, Mori Y. Effect of a benzylidene derivative, a novel antirheumatic agent, on IL-1 production. Pharm. Res. 28: 57-72 (1993)
- Kikuzaki H, Kawai Y, Nakatani N. 1,1-Diphenyl-2-picrylhydrazyl radical scavenging active compounds from greater cardamom (Amomum subulatum Roxb.). J. Nutr. Sci. Vitaminol. 47: 167-171 (2001) https://doi.org/10.3177/jnsv.47.167
- Wang Y, Hasuma T, Yano Y, Morishima Y, Matsui-Yuasa I, Otani S. Induction of apoptosis in CTLL-2 cells by protocatechualdehyde. Anticancer Res. 21: 1095-1101 (2001)
- Wilairat R, Kijjoa A, Pinto M, Nascimento MSJ, Silva AMS, Eaton G, Herz W. Constituents of Schisandra verruculosa and their cytotoxic effect on human cancer cell lines. Pharm. Biol. 44: 411-415 (2006) https://doi.org/10.1080/13880200600794105
-
Gray TK, Flynn TC, Gray KM, Nabell LM.
$17{\beta}-Estradiol$ acts directly on the clonal osteoblastic cell line UMR106. P. Natl. Acad. Sci. USA 84: 6267-6271 (1987) - Yamaguchi M, Gao YH. Anabolic effect of genistein and genistin on bone metabolism in the femarol-metaphyseal tissues of elderly rats: The genistein effect is enhanced by zinc. Mol. Cell. Biochem. 178: 377-382 (1998) https://doi.org/10.1023/A:1006809031836
- Nishibe S, Hisada S, Inagaki I. Lignans of Trachelospermum liukiuense and T. foetidum. Chem. Pharm. Bull. 21: 674-675 (1973) https://doi.org/10.1248/cpb.21.674
- Sakamura S, Terayama Y, Kawakatsu S, Ichihara A, Saito H. Conjugated serotonins and phenolic constituents in safflower seed. Agr. Biol. Chem. Tokyo 44: 2951-2954 (1980) https://doi.org/10.1271/bbb1961.44.2951