8. Egeberg A1, Skov L, Gislason GH, Thyssen JP, Mallbris L. Incidence and Prevalence of Psoriasis in Denmark // Acta Derm Venereol. – 2017. – 97/ -7. – pp. 808-812.

9. Haworth R.A., Hunter D.R. The Ca 2+ -induced membrane transition in mitochondria. II. Nature of the Ca 2+ trigger site // Archives of biochemistry and biophysics. – 1979. – V.195(2). – P. 460-467.

10. He L., Lemasters J.J. Heat shock suppresses the permeability transition in rat liver mitochondria // J. Biol. Chem. 2003. V. 278. N. 19. P. 16755-16760.

11. Jin H., Wang L., Xu C., et al. Effects of Psoraleae fructus and its major component psoralen on Th2 response in allergic asthma // American Journal of Chinese Medicine. – 2014. – 42, -3. – pp. 665–678.

12. K. Schneider, L. Wronka-Edwards, M. Leggett-Embrey, E. Walker, P.Sun, B. Ondov, T. H. Wyman, MJ Rosovitz, Sherry S. Bohn, J. Burans, T. Kochel. Psoralen Inactivation of Viruses: A Process for the Safe Manipulation of Viral Antigen and Nucleic Acid // Viruses. – 2015. – 7, - 11. – pp. 5875–5888.

13. Kavita Bisherwal, Archana Singal, Deepika Pandhi, and Sonal Sharma1 Hypopigmented Mycosis Fungoides: Clinical, Histological, and Immunohistochemical Remission Induced by Narrow-band Ultraviolet B. // Indian J Dermatol. – 2017. – 62, -2. - 203–206.

14. Khafagy N. H., Salem S. A. M., Ghaly E. G. Comparative study of systemic psoralen and ultraviolet A and narrowband ultraviolet B in treatment of chronic urticaria. // Photodermatology Photoimmunology and Photomedicine. -2013. -29, -1. – pp.12–17.

15. Lu H., Zhang L., Liu D., Tang P., Song F. Isolation and purification of psoralen and isopsoralen and their efficacy and safety in the treatment of osteosarcoma in nude rats. // African Health Sciences. – 2014. – 14, - 3. – рр. 641–647.

16. Peterson G.L. A simplification of the protein assay method of Lowry et al. which is more generally applicable // Analyt. biochem. 1977. V. 83. N. 2. P. 346-356.

17. Salvi M., Fiore C., Battaglia V., Palermo M., Armanini D., Toninello A. Carbenoxolone induces oxidative stress in liver mitochondria, which is responsible for transition pore opening. // Endocrinology. – 2005. – V.146.-iss.5. – P.2306-2312.

18. Schneider W.C., Hageboom G.H., Pallade G.E. Cytochemical studies of mammalian tissues; isolation of intact mitochondria from rat liver; some biochemical properties of mitochondria and submicroscopic particulate material // J. Biol. Chem. – 1948. – V. 172 (2). – P. 619-635.

19. Silva FS, Oliveira H, Moreiras A, Fernandes JC, Bronze-da-Rocha E, Figueiredo A, Custódio JB, RochaPereira P, Santos-Silva A.Cytotoxic and genotoxic effects of acitretin, alone or in combination with psoralenultraviolet A or narrow-band ultraviolet B-therapy in psoriatic patients. // Mutat Res. - 2013. -753, -1. - рр. 42-47.

20. Szewczyk A., Wojtczak L. Mitochondria as a pharmacological target // Pharmacol Rev. – 2002. – 54(1). – P. 101-127.

21. Tang D.-Z., Yang F., Yang Z., et al. Psoralen stimulates osteoblast differentiation through activation of BMP signaling. // Biochemical and Biophysical Research Communications. – 2011. – 405, - 2. - 256–261.

22. Tzung T, Wu K, Wu J, Tseng H. Primary cutaneous plasmacytosis successfully treated with topical photodynamic therapy. // Acta Dermato-Venereologica. – 2005. – 85, - 6. – рр. 542–543.

23. Victor V.M., Rocha M., Bañuls C., Bellod L., Hernandez-Mijares A. Mitochondrial dysfunction and targeted drugs: a focus on diabetes // Curr Pharm Des. – 2011. – V. 17(20). – P. 1986-2001.

24. Yang L., Sun X., Geng X. Effects of psoralen on chondrocyte degeneration in lumbar intervertebral disc of rats. // Pakistan journal of pharmaceutical sciences. – 2015. – 28, -2. – рр. 667–670.

25. Yang Z., Huang J.-H., Liu S.-F., et al. The osteoprotective effect of psoralen in ovariectomyinduced osteoporotic rats via stimulating the osteoblastic differentiation from bone mesenchymal stem cells. // Menopause. – 2012. -19, -10. – рр. 1156–1164.

26. Абидова А.Д., Цеомашко Н.Е., Ботыралиева Г.К., Хегай Л.Н. Изучение фармако-токсикологических свойств фурокумаринов, выделенных из растения ficus caracal // Конф. “Фармация: фан, таълим, инновация ва ишлаб чиқариш” Республика илмийғамалий анжумани (халқаро иштирокда) материаллари /Т-2017. –с.397-399.

1. Allen K., Frederic J., Renee V., Vladimir V. A novel mechanism of regulation of cardiac contractility by mitochondrial functional state. // The FASEB Journal. – 2004. – V.18. – P.1219-1227.

2. An J, Yang H, Zhang Q, Liu C, Zhao J, Zhang L, Chen B. Natural products for treatment of osteoporosis: The effects and mechanisms on promoting osteoblast-mediated bone formation // Life Sci. – 2016. – 15, -147. – pp. 46-58.

3. Bansal S., Sahoo B., Garg V. Psoralen-narrowband UVB phototherapy for the treatment of vitiligo in comparison to narrowband UVB alone // Photodermatology, Photoimmunology & Photomedicine. – 2013. – 29, -6. – pp. 311–317.

4. Caffieri S 1 , Di Lisa F, Bolesani F, Facco M, Semenzato G, Dall'Acqua F, Canton M. The mitochondrial effects of novel apoptogenic molecules generated by psoralen photolysis as a crucial mechanism in PUVA therapy. Blood. 2007; 1;109(11):4988-94.

5. Cantona M., Caffieri S., Dall’Acqua F., Di Lisa F. PUVA-induced apoptosis involves mitochondrial dysfunction caused by the opening of the permeability transition pore.//FEBS Letters. - 2002. - V.522. - P. 168-172.

6. Chopra B., Dhingra A. K., Dhar K. L. Psoralea corylifolia L. (Buguchi)—folklore to modern evidence: review // Fitoterapia. - 2013. - 90. – pp. 44–56.

7. Duchen, M.R. Roles of mitochondria in health and disease (invited review). Diabetes. – 2004. – 53 Suppl 1. – P. 96-102.