Диссертация (1140068), страница 23
Текст из файла (страница 23)
238, № 5. – Р. 539–548.127. Changes in macrophage colony-stimulating factor concentration inserum and follicular fluid in in-vitro fertilization and embryo transfer cycles /K. Nishimura, N. Tanaka, T. Kawano [et al.] // Fertility and Sterility. – 1998. –Vol. 69. – P. 53–57.128. Chitu V. Regulation of Embryonic and Postnatal Development by theCSF-1 Receptor [Электрон. ресурс] / V.
Chitu, E. R. Stanley // Current Topics inDevelopmental Biology. – 2017. – Vol. 123. – Р. 229–275. Режим доступа :https://doi.org/10.1016/bs.ctdb.2016.10.004.155129. Chromatin-associated CSF-1R binds to the promoter of proliferationrelated genes in breast cancer cells / V. Barbetti, A. Morandi, I. Tusa [et al.] //Oncogene. 2014.
Vol. 33(34). P. 4359–4364.130. Circulating level of macrophage colony-stimulating factor can bepredictive for human in vitro fertilization outcome / A. Salmassi, L. Mettler, W.Jonat [et al.] // Fertility and Sterility. – 2010. – Vol. 93, № 1. – Р. 116–123.131. Clinical use of colony-stimulating factor-1 in ovulation induction forpoor responders / A. Takasaki, T. Ohba, Y.
Okamura [et al.] // Fertil. Steril. – 2008.– Vol. 90, № 6. – Р. 2287–2290.132. Cloning and chromosome mapping of the human interleukin-1receptor antagonist gene / A. Lennard, P. Gorman, M. Carrier [et al.] // Cytokine. –1992. – Vol. 4 (2). – P. 83–89.133. Cloning and expression of porcine Colony Stimulating Factor-1 (CSF1) and Colony Stimulating Factor-1 Receptor (CSF-1R) and analysis of the speciesspecificity of stimulation by CSF-1 and Interleukin 34 / D. J. Gow, V. Garceau, R.Kapetanovic [et al.] // Cytokine. – 2012. Vol.
60(3). – P. 793-805.134. Cohen P. E. Absence of colony stimulating factor-1 in osteopetrotic(csfmop/csfmop) mice disrupts estrous cycles and ovulation / P. E. Cohen, L. Zhu,J. W. Pollard // Biology of Reproduction. – 1997. – Vol. 56. – Р. 110–118.135. Cohen P. E. Colony-stimulating factor-1 plays a major role in thedevelopment of reproductive function in male mice / P.
E. Cohen, M. P. Hardy,J. W. Pollard // Mol. Endocrinol. – 1997. – Vol. 11. – Р. 1636–1650.136. Colony-stimulating factor-1 and c-fms expression in human endometrialtissues and placenta during the menstrual cycle and early pregnancy / S. W. Kauma, S.L. Aukerman, D. Eirman, T.
Turner // Journal of Clinical Endocrinology andMetabolism. – 1991. – Vol. 73. – P. 746–751.137. Colony-stimulating factor-1 (CSF-1) directly inhibits receptoractivator of nuclear factor-{kappa}B ligand (RANKL) expression by osteoblasts. /Y. Wittrant, Y. Gorin, S. Mohan [et al.].// Endocrinology. – 2009. Vol. 150(11). –P. 4977-4988.156138. Colony stimulating factor-1 concentrations in blood and follicular fluidduring the human menstrual cycle and ovarian stimulation: possible role in theovulatory process / B.
Shinetugs, E. Runesson, N. P. Bonello [et al.] // Hum.Reprod. –1999. – Vol. 14. – Р. 1302–1306.139. Colony stimulating factor-1 exerts direct effects on the proliferationand invasiveness of endometrial epithelial cells [Электрон. ресурс] / S. Aligeti,N. B. Kirma, P. A. Binkely [et al.] // Fertility and Sterility. – 2011. – Vol. 95(8).– Р. 2464–2466.
– Режим доступа : http://doi.org/10.1016/j. fertnstert.2011.03.026.140. Comparison of two polymorphisms of IL-1 gene family: IL-1receptor antagonist polymorphism contributes to susceptibility to severe sepsis/ X. Fang, C. Schroder, A. Hoeft, F. Stuber // Crit.
Care Med. – 1999. – Vol. 27.– P. 1330–1334.141. Corbacioğlu A. Effects of endometrial thickness and echogenic patternon assisted reproductive treatment outcome / A. Corbacioğlu, B. Baysal // Clin.Exp. Obstet. Gynecol. – 2009. – Vol. 36, № 3. – P. 145–147.142. CSF-1-a mononuclear phagocyte lineage-specific hemopoietic growthfactor / E. R. Stanley, L. J.
Guilbert, R. J. Tushinski, S. H. Bartelmez // J. Cell.Biochem. – 1983. – Vol. 21. – P. 151–159.143. CSF-1-induced Src signaling can instruct monocytic lineage choice /M. Endele, D. Loeffler, K. D. Kokkaliaris [et al.] // Blood. – 2017. – Vol. 129(12).– P. 1691-1701.144. Cui W. Mother or nothing: the agony of infertility / W.
Cui // Bull.World. Health. Organ. – 2010. – Vol. 88. – P. 881–882.145. Cytokine production by maternal limphocytes during normal humanpregnancy and in recurrent abortion / R. Raghupathy, M. Makhseed, F. Azizieh //Hum. Reprod. – 2000. – Vol. 15. – P. 713–718.146. Cytokine production by normal human monocytes: inter-subjectvariation and relationship to IL-1 receptor gene polymorphism / V.
Danis, M.157Millington, V. Hyland, D. Grennan // Clin. Exp. Immunol. – 1995. – Vol. 99. –P. 303–310.147. Cytokines, chemokines and growth factors in endometrium related toimplantation [Электрон. ресурс] / E. Dimitriadis, C. A. White, R. L. Jones,L. A. Salamonsen // Human Reproduction Update. – 2005. – Vol. 11, Iss.
6, 1 Nov.– P. 613–630. – Режим доступа : https://doi.org/10.1093/humupd/ dmi023.148. Cytokines in ovarian folliculogenesis, oocyte maturation andluteinisation / S. L. Field, T. Dasgupta, M. Cummings, N. M. Orsi // Mol. Reprod.Dev. –2014. – Vol. 81(4). – Р. 284–314.149. Day 4 estradiol levels predict pregnancy success in womenundergoing controlled ovarian hyperstimulation for IVF / J. Y.
Phelps, A. S.Levine, T. N. Hickman [et al.] // Fertility and Sterility. – 1998. – Vol. 69, № 6.– P. 1015–1019.150. Decidual natural killer cytotoxicity decreased in normal pregnancy butnot in anembryonic pregnancy and recurrent spontaneous abortion / K. H. Chao,Y. S. Yang, H. N. Ho [et al.] // Am. J. Reprod. Immunol. – 1995. – Vol. 34. – P.274–280.151. Detection of IL-1β in culture media supernatants of pre-implantationhuman embryos; its relation with embryo grades and development / E. A.
Taşkın,V. Baltacı, G. Cağıran [et al.] // Gynecol. Endocrinol. 2012. Vol. 28, № 4. 296-298.152. Detection ofimplantation-relatedcytokinesin cervicovaginalsecretions and peripheral blood of fertile women during ovulatory menstrual cycles/ A. R. Gargiulo, R. N. Fichorova, J. A. Politch [et al.] // Fertility and Sterility. –2004. – Vol. 82, Suppl. 3. – P. 1226–1234.153. Detection of two polymorphic sites in the human c-fms gene: AllelefrequenciesinseveralRussianpopulations/A.G.Romashchenko,T. N.
Kuznetsova, Ya. S. Ruzankina [et al.] // Genetika. – 2002. – Vol. 38, № 1.– P. 33–40.158154. Developmental and functional significance of the CSF-1 proteoglycanchondroitin sulfate chain. / S. Nandi, M. P. Akhter, M. F. Seifert [et al.] // Blood. –2006. – Vol.
107(2). – P. 786-795.155. Dinarello C. A. Interleukin-1 / C. A. Dinarello // Cytokine Growth.Factor. Rev. – 1997. – Vol. 8. – P. 253–265.156. Dinarello C. A. The interleukin-1 family: 10 years of discovery /C. A. Dinarello // FASEB J. –1994. – Vol. 8. – P. 1314–1325.157. Distinct in vivo roles of colony-stimulating factor-1 isoforms in renalinflammation. / M. H. Jang, D. M. Herber, X. Jiang [et al.] // J Immunol. – 2006. –Vol. 177(6). – P. 4055-4063.158. Dunne A. The interleukin-1 receptor / Toll-like receptor superfamily:signal transduction during inflammation and host defense [Электрон. ресурс] /A. Dunne, L. A. O’Neill // Sci. STKE.
– 2003. – Vol. 2003, Iss. 171. – P. re3. – Режимдоступа : http://stke.sciencemag.org/content/2003/171/re3.159. Effect of all-trans-retinoic acid on c-fms proto-oncogene [colonystimulating factor 1 (M-CSF) receptor] expression and M-CSF-induced invasionand anchorage-independent growth of human breast carcinoma cells. / E. Sapi, M.Flick, K. Tartar [et al] // Cancer Res. – 1999. – Vol.
59(21). – P. 5578-5585.160. Effects of colony stimulating factor-1 on human extravilloustrophoblast growth and invasion / G. S. Hamilton, J. J. Lysiak, A. J. Watson, P.K. Lala // J. Endocrinol. – 1998. – Vol. 159 (1). – P. 69–77.161. Effects of interleukin-1 receptor antagonist (IL-1Ra) gene 86 bp VNTRpolymorphism on recurrent pregnancy loss: a case-control study / Y. S.
Hajizadeh, E.Emam, M. Nottagh [et al.] // Hormone Molecular Biology and ClinicalInvestigation. – 2017. – Vol. 30(3). – 3 Apr. 2018. from doi:10.1515/hmbci-20170010.162. Effects of macrophage colony-stimulating factor on folliculogenesis ingonadotrophin-primed immature rats / K. Nishimura, N. Tanaka, A. Ohshige [etal.] // Journal of Reproduction and Fertility.
– 1995. – Vol. 104. – P. 325–330.159163. Effect of macrophages on proliferation of granulosa cells in the ovaryin rats / Y. Fukumatsu, H. Katabuchi, M. Naito [et al.] // J. Reprod. Fertil. –1992. –Vol. 96. – Р. 241–249.164. Effects of tumour necrosisfactor-alpha,interleukin-1 alpha,macrophage colony stimulating factor and transforming growth factor beta ontrophoblasticmatrix metalloproteinases/ A.Meisser,D.Chardonnens,A. Campana [et al.] // Mol. Hum. Reprod. 1999.
Vol. 5. P. 252-260.165. Elevated progesterone in GnRH agonist down regulated in vitrofertilisation (IVFICSI) cycles reduces live birth rates but not embryo quality /R. Lahoud, M. Kwik, J. Ryan [et al.] // Arch. Gynecol. Obstet. – 2012. – Vol. 285,№ 2. – P. 535–540.166. Elevatedseruminterleukin-1βlevelsandinterleukin-1β-to-interleukin-1 receptor antagonist ratio 1 week after embryo transfer are associatedwith ectopic pregnancy / J.
Lekovich, G. Doulaveris, T. Orfanelli [et al.] // Fertilityand Sterility. – 2015. – Vol. 104, Iss. 5. – P. 1190–1194.167. Embryonic implantation in mice is blocked by interleukin-1 receptorantagonist / C. Simon, A. Frances, G. N. Piquette [et al.] // Endocrinology. – 1994.– Vol. 134. – P. 521–528.168. Embryonic regulation of integrins beta 3, alpha 4, and alpha 1 inhuman endometrial epithelial cells in vitro / C. Simon, M. J. Gimeno, A.
![](https://s.studizba.com/z.php?f=/templates/si/i/noavatar.png&w=100&h=100&t=1"){kind=avatar}
