Научная электронная библиотека
Монографии, изданные в издательстве Российской Академии Естествознания
Николаева Т. В., Сетко Н. П., Полякова В. С., Воронина Л. Г.,
СПИСОК ЛИТЕРАТУРЫ
1. Бурак Ж.М., Сукало А.В., Терехова Т.Н. Воздействие свинцовой интоксикации на человека и животных, влияние на развитие и функции зубо-челюстной системы (обзор литературы) // Медицинский журнал. – 2005. – № 4. – С. 10-13.
2. Дерматология Фицпатрика в клинической практике: В 3 т. / Л.А. Голдсмит, С.И. Кац, Б.А. Джилкрест, Э.С. Паллер, Д.Д. Леффель,
К. Вольф; пер. с англ.; общ. ред. Н.Н. Потекаева, А.Н. Львова. – Изд. 2-е, исп., перер., доп. – М.: Издательство Панфилова, 2015. – Т. 1. – 2015.
3. Новые методы иммуногистохимической диагностики опухолевого роста: Учебное пособие / Бабиченко И.И., Ковязин В.А. – М.: РУДН, 2008. – 109 с.
4. Руководство по иммуногистохимической диагностике опухолей человека / под ред. С.В. Петрова, Н.Т. Райхлина. – 3-е изд. доп. и перераб. – Казань: Титул, 2004. – 456 с.
5. Теплая Г.А. Тяжелые металлы как фактор загрязнения окружающей среды (обзор литературы) // Астраханский вестник экологического образования. – 2013. – Т. 1. – № 23. – С. 182-192.
6. Ярилин, А.А. Апоптоз. Природа феномена и его роль в целостном организме // Патологическая физиология и экспериментальная терапия. –1998. – № 2. – С. 38-48.
7. Яровая Г.А., Нешкова Е.А., Мартынова Е.А., Блохина Т.Б. Роль протеолитических ферментов в контроле различных стадий апоптоза // Лабораторная медицина. – 2011. – № 11. – С. 39-53.
8. Alcaraz-Contreras Y., Mendoza-Lozano R.P., Martínez-Alcaraz E.R., Martínez-Alfaro M., Gallegos-Corona M.A., Ramírez-Morales M.A., Vázquez-Guevara M.A. Silymarin and dimercaptosuccinic acid ameliorate lead-induced nephrotoxicity and genotoxicity in rats // Hum. Exp. Toxicol. – 2016. – Vol. 35. – № 4. – P. 398-403.
9. Anderson S.E., Meade B.J. Potential health effects associated with dermal exposure to occupational chemicals // Environ. Health Insights. – 2014. – Vol. 17. – № 8. – P. 51-62.
10. Araya M., Pizarro F., Olivares M., Arredondo M., González M., Méndez M. Understanding copper homeostasis in humans and copper effects on health // Biol. Res. – 2006. – Vol. 39. – № 1. – P. 183-187.
11. Azman M.S., Wan Saudi W.S., Ilhami M., Mutalib M.S., Rahman M.T. Zinc intake during pregnancy increases the proliferation at ventricular zone of the newborn brain // Nutr. Neurosci. – 2009. – Vol. 12. – № 1. – P. 9-12.
12. Beaver L.M., Stemmy E.J., Schwartz A.M., Damsker J.M., Constant S.L., Ceryak S.M., et al. Lung inflammation, injury, and proliferative response after repetitive particulate hexavalent chromium exposure // Environ. Health Perspect. – 2009. – Vol. 117. № 12. – P. 1896-1902.
13. Bridges C.C., Zalups R.K. Molecular and ionic mimicry and the transport of toxic metals // Toxicol. Appl. Pharmacol. – 2005. – Vol. 204. – № 3. – P. 274–308.
14. Bustos R.I., Jensen E.L., Ruiz L.M., Rivera S., Ruiz S., Simon F., et al. Copper deficiency alters cell bioenergetics and induces mitochondrial fusion through up-regulation of MFN2 and OPA1 in erythropoietic cells // Biochem. Biophys. Res. Commun. – 2013. – Vol. 437. – № 3. – P. 426-432.
15. Chai F., Truong-Tran A.Q., Evdokiou A., Young G.P., Zalewski P.D. Intracellular zinc depletion induces caspase activation and p21 Waf1/Cip1 cleavage in human epithelial cell lines // J. Infect. Dis. – 2000. – Vol. 182. – № 1. – P. S85-S92.
16. Colvin R.A., Fontaine C.P., Laskowski M., Thomas D. Zn2+ transporters and Zn2+ homeostasis in neurons // Eur. J. Pharmacol. – 2003. – Vol. 479. – № 1-3). – P. 171-185.
17. Cullen J.M., Ward J.M., Thompson C.M. Reevaluation and Classification of Duodenal Lesions in B6C3F1 Mice and F344 Rats from 4 Studies of Hexavalent Chromium in Drinking Water // Toxicol. Pathol. – 2016. – Vol. 44. – № 2. – P. 279-289.
18. Ding M., Shi X. Molecular mechanisms of Cr(VI)-induced carcinogenesis // Mol. Cell. Biochem. – 2002. – Vol. 234-235. – № 1-2. –
P. 293-300.
19. Donadelli M., Dalla Pozza E., Costanzo C., Scupoli M.T., Scarpa A., Palmieri M. Zinc depletion efficiently inhibits pancreatic cancer cell growth by increasing the ratio of antiproliferative/proliferative genes // J. Cell. Biochem. – 2008. – Vol. 104. – № 1. – P. 202-212.
20. Engstrom A., Wang H., Xia Z. Lead decreases cell survival, proliferation, and neuronal differentiation of primary cultured adult neural precursor cells through activation of the JNK and p38 MAP kinases // Toxicol. In Vitro. – 2015. – Vol. 29. – № 5. – P. 1146-1155.
21. Flora S.J.S., Mittal M., Mehta A. Heavy metal induced oxidative stress & its possible reversal by chelation therapy // Indian. J. Med. Res. – 2008. – Vol. 128. – № 4. – P. 501-523.
22. Fukuyama S., Matsunaga Y., Zhanghui W., Noda N., Asai Y., Moriwaki A., et al. A zinc chelator TPEN attenuates airway hyperresponsiveness and airway inflammation in mice in vivo // Allergol. Int. – 2011. – Vol. 60. – № 3. – P. 259-266.
23. Hashemi M., Ghavami S., Eshraghi M., Booy E.P., Los M. Cytotoxic effects of intra and extracellular zinc chelation on human breast cancer cells // Eur. J. Pharmacol. – 2007. – Vol. 557. – № 1. – P. 9-19.
24. Itoh S., Kim H.W., Nakagawa O., Ozumi K., Lessner S.M., Aoki H., Akram K., McKinney R.D., Ushio-Fukai M., Fukai T. Novel role of antioxidant-1 (Atox1) as a copper-dependent transcription factor involved in cell proliferation // J. Biol. Chem. – 2008. – Vol. 283. – № 14. – P. 9157-9167.
25. Jan A.T., Azam M., Siddiqui K., Ali A., Choi I., Haq Q.M. Heavy Metals and Human Health: Mechanistic Insight into Toxicity and Counter Defense System of Antioxidants // Int. J. Mol. Sci. – 2015. – Vol. 16. – № 12. – P. 29592-29630.
26. Jenerowicz D., Silny W., Dańczak-Pazdrowska A., Polańska A., Osmola-Mańkowska A., Olek-Hrab K. Environmental factors and allergic diseases // Ann. Agric. Environ. Med. – 2012. – Vol. 19. – № 3. – P. 475-481.
27. Jimenez-Cervantes C., Martinez-Esparza M., Perez C., Daum N., Solano F., Garcia-Borron J. C. Inhibition of melanogenesis in response to oxidative stress: transient downregulation of melanocyte differentiation markers and possible involvement of microphthalmia transcription factor // J. Cell. Sci. – 2001. – Vol. 114. – № 12. – P. 2335-2344.
28. Kang M., Zhao L., Ren M., Deng M., Li C. Reduced metallothionein expression induced by Zinc deficiency results in apoptosis in hepatic stellate cell line LX-2 // Int. J. Clin. Exp. Med. – 2015. – Vol. 8. – № 11. – P. 20603-20609.
29. Kang X., Song Z., McClain C.J., Kang Y.J., Zhou Z. Zinc supplementation enhances hepatic regeneration by preserving hepatocyte nuclear factor-4alpha in mice subjected to long-term ethanol administration // Am. J. Pathol. – 2008. – Vol. 172. – № 4. – P. 916-925.
30. Lansdown A.B. Metal ions affecting the skin and eyes // Met. Ions Life Sci. 2011. – Vol. 8. – P. 187-246.
31. Leventhal J.S., Ross M.J. LAPping up dead cells to prevent lupus nephritis: a novel role for noncanonical autophagy in autoimmunity // Kidney Int. – 2016. – Vol. 90. – № 2. – P. 238-239.
32. Macfie A., Hagan E., Zhitkovich A. Mechanism of DNA-protein cross-linking by chromium // Chem. Res. Toxicol. – 2010. – Vol. 15. – № 23. – P. 341-347.
33. Madejczyk M.S., Baer C.E., Dennis W.E., Minarchick V.C., Leonard S.S., Jackson D.A., Stallings J.D., Lewis J.A. Temporal changes in rat liver gene expression after acute cadmium and chromium exposure // PLoS One. – 2015. – Vol. 10. – № 5. – P. e0127327.
34. Mastrofrancesco A., Alfè M., Rosato E., Gargiulo V., Beatrice C., Di Blasio G., Zhang B., Su D. S., Picardo M., Fiorito S. Proinflammatory Effects of Diesel Exhaust Nanoparticles on Scleroderma Skin Cells [Electronic resource] // J. Immunol. Res. – 2014. – Vol. 2014. – Article ID 138751. – P. 9. Available at: http://dx.doi.org/10.1155/2014/138751 (Accessed 15.10.2014).
35. Maurer M., Handjiski B., Paus R. Hair growth modulation by toal immunophilin ligands: induction of anagen, inhibition of massive catagen development, and relative protection from chemotherapy-induced alopecia // Am. J. Pathol. – 1997. – Vol. 150. – № 4. – P. 1433-1441.
36. Muller P.A., Klomp L.W. ATOX1: a novel copper-responsive transcription factor in mammals? // Int. J. Biochem. Cell. Biol. – 2009. –
Vol. 41. – № 6. – P. 1233-1236.
37. Müller-Röver S., Handjiski B., van der Veen C., Eichmüller S., Foitzik K., McKay I.A., et al. A comprehensive guide for the accurate classification of murine hair follicles in distinct hair cycle stages // J. Invest. Dermatol. – 2001. – Vol. 117. – № 1. – P. 3-15.
38. Nydegger I. Explorations of hippocampal zinc using zinc-selective fluorescent dyes: PhD (Doctor of Philosophy) thesis [Electronic resource]. University of Iowa, 2009. Available at: http://ir.uiowa.edu/cgi/viewcontent.cgi?article = 1599 &context = etd (Accessed 20.10.2014).
39. Oliveira da Costa Mattos R de C., Xavier E.C. Jr., Domingos Mainenti H.R., Mitri Nogueira S., Ribeiro de Carvalho M.A., Ramos
Moreira M. de F., Vargas de Carvalho L.B., Tabalipa M., Borges R., Malizia Alves Mde F. Evaluation of calcium excretion in Brazilian infantile and young population environmentally exposed to lead // Hum. Exp. Toxicol. – 2009. – Vol. 28. – № 9. – P. 567-575.
40. Osredkar J., Sustar N. Copper and Zinc, Biological Role and Significance of Copper/Zinc Imbalance [Electronic resource] // J. Clin. Toxicol. – 2011. – P. S3. Available at: http://dx.doi.org/10.4172/2161-0495.S3–001 (Accessed 21.10.2014).
41. Ostrakhovitch, E. A., Lordnejad, M. D., Schliess, F., Sies, H. & Klotz, L. O. Copper ions strongly activate the phosphoinositide-3-kinase/Akt pathway independent of the generation of reactive oxygen species // Arch. Biochem. Biophys. – 2002. – Vol. 397. – № 2. – P. 232-239.
42. Paus R., Handjiski B., Eichmüller S., Czarnetzki B.M. Chemotherapy-induced alopecia in mice. Induction by cyclophosphamide, inhibition by cyclosporine A, and modulation by dexamethasone // Am. J. Pathol. – 1994. – Vol. 144. – № 4. – 719-734.
43. Peled T., Landau E., Prus E., Treves A.J., Nagler A., Fibach E. Cellular copper content modulates differentiation and self-renewal in cultures of cord blood-derived CD34 + cells // Br. J. Haematol. – 2002. – Vol. 116. – № 3. – P. 655-661.
44. Peng Y., Martin D.A., Kenkel J., Zhang K., Ogden C.A., Elkon K.B. Innate and adaptive immune response to apoptotic cells // J. Autoimmun. – 2007. – Vol. 29. – P. 303-309.
45. Plonka P.M., Handjiski B., Popik M., Michalczyk D., Paus R. Zinc as an ambivalent but potent modulator of murine hair growth in vivo- preliminary observations // Exp. Dermatol. – 2005. – Vol. 14. – № 11. – P. 844-853.
46. Plonka P.M., Handjiski B., Michalczyk D., Popik M., Paus R. Oral zinc sulphate causes murine hair hypopigmentation and is a potent inhibitor of eumelanogenesis in vivo // Br. J. Dermatol. – 2006. – Vol. 155. – № 1. – P. 39-49.
47. Quan F.S., Yu X.F., Gao Y., Ren W.Z. Protective effects of folic acid against central nervous system neurotoxicity induced by lead exposure in rat pups // Genet. Mol. Res. – 2015. – Vol. 14. – № 4. – P. 12466-12471.
48. Ramírez-Sandoval R., Luévano-Rodríguez N., Rodríguez-Rodríguez M., Pérez-Pérez M.E., Saldívar-Elias S., Gurrola-Carlos R., Avalos-Díaz E., Bollain-y-Goytia J.J., Herrera-Esparza R. An Animal Model Using Metallic Ions to Produce Autoimmune Nephritis [Electronic resource] // J. Immunol. Res. – 2015. – Vol. 2015. – Article ID 269610. – P. 11. Available at: http://dx.doi.org/ 10.1155/2015/269610 (Accessed 15.09.2014).
49. Shen H., Qin H., Guo J. Cooperation of metallothionein and zinc transporters for regulating zinc homeostasis in human intestinal Caco-2 cells // Nutr. Res. –2008. – Vol. 28. – № 6. – P. 406-413.
50. Sidhom E., Pilmane M., Kisis J. Local antimicrobial, protease and cytokine defense systems in psoriatic skin // Indian J. Dermatol. Venereol. Leprol. – 2016. – Vol. 82. – № 3. – P. 284-291.
51. Slominski A., Paus R., Costantino R. Differential expression and activity of melanogenesis-related proteins during induced hair growth in mice // J. Invest. Dermatol. – 1991. – Vol. 96. – № 2. – P. 172-179.
52. Su L., Deng Y., Zhang Y., Li C., Zhang R., Sun Y., et al. Protective effects of grape seed procyanidin extract against nickel sulfate-induced apoptosis and oxidative stress in rat testes // Toxicol. Mech. Methods. – 2011. – Vol. 21. – № 6. – P. 487-494.
53. Tang K., Guo H., Deng J., Cui H., Peng X., Fang J., et al. Inhibitive effects of nickel chloride (NiCl2) on thymocytes // Biol. Trace Elem. Res. – 2015. – Vol. 164. – № 2. – P. 242-252.
54. Tinkov A.A., Polyakova V.S., Nikonorov A.A.Chronic administration of iron and copper potentiates adipogenic effect of high fat diet in Wistar rats // Biometals. – 2013. – Vol. 26. – № 3. – P. 447-463.
55. Tobin D.J. Aging of the hair follicle pigmentation system // Int J Trichology. –2009. – Vol. 1. – № 2. – P. 83-93.
56. Wei H., Frei B., Beckman J.S., Zhang W.J. Copper chelation by tetrathiomolybdate inhibits lipopolysaccharide-induced inflammatory responses in vivo // Am. J. Physiol. Heart Circ. Physiol. – 2011. – Vol. 301. – № 3. – P. H712- H720.
57. Yu C., Chang C., Zhang J. Immunologic and genetic considerations of cutaneous lupus erythematosus: a comprehensive review // J. Autoimmun. – 2013. – Vol. 4. – P. 34 – 45.
58. Zhang Y., Zhang Y., Xie Y., Gao Y., Ma J., Yuan J., et al. Multitargeted inhibition of hepatic fibrosis in chronic iron-overloaded mice by Salvia miltiorrhiza // J. Ethnopharmacol. – 2013. – Vol. 148. – № 2. – P. 671-681.