[Caballero J.N., Gervasi M.G., Veiga M.F., Dalvit G.C., Perez-Martínez S., Cetica P.D., Vazquez-Levin M.H. (2014). Epithelial cadherin is present in bovine oviduct epithelial cells and gametes, and is involved in fertilization-related events. Theriogenology, 81: 1189–1206.]Search in Google Scholar
[Dubé K.N., Smart N. (2018). Thymosin β4 and the vasculature: multiple roles in development, repair and protection against disease. Expert Opin. Biol. Ther., 18: 131–139.]Search in Google Scholar
[Fan Y., Gong Y., Ghosh P.K., Graham L.M., Fox P.L. (2009). Spatial coordination of actin polymerization and ILK-Akt2 activity during endothelial cell migration. Dev. Cell, 16: 661–674.]Search in Google Scholar
[Gajda B., Poniedziałek-Kempny K., Rajska I., Smorąg Z. (2015) Effect of thymosin on in vitro fertilization and developmental competence and quality of pig embryos. Anim. Reprod., 12: 735.]Search in Google Scholar
[Gao F., Zhang J., Wang X., Yang J., Chen D., Huff V., Liu Y.X. (2014). Wt1 functions in ovarian follicle development by regulating granulosa cell differentiation. Hum. Mol. Genet., 23: 333–341.]Search in Google Scholar
[Guimarães A.L., Pereira S.A., Diógenes M.N., Dode M.A. (2016). Effect of insulin-transferrin- selenium (ITS) and l-ascorbic acid (AA) during in vitro maturation on in vitro bovine embryo development. Zygote, 24: 890–899.]Search in Google Scholar
[Guinobert I., Viltard M., Piquemal D., Elalouf J.M., Marti J., Lelièvre-Pégorier M. (2006). Identification of differentially expressed genes between fetal and adult mouse kidney: candidate gene in kidney development. Nephron. Physiol., 102: 81–91.]Search in Google Scholar
[Hall A.K. (1991). Differential expression of thymosin genes in human tumors and in developing human kidney. Int. J. Cancer., 48: 672–677.]Search in Google Scholar
[Hall A.K., Aten R., Behrman H.R. (1991 a). Differential modulation of thymosin genes in the immature rat ovary by gonadotropins. Mol. Cell. Endocrinol., 79: 37–43.10.1016/0303-7207(91)90093-8]Search in Google Scholar
[Hall A.K., Aten R., Behrman H.R. (1991 b). Thymosin gene expression is modulated by pregnant mare’s serum gonadotropin, human chorionic gonadotropin, and prostaglandin F2 alpha in the immature rat ovary. Endocrinology, 128: 951–957.10.1210/endo-128-2-9511989873]Search in Google Scholar
[Hall N.R., O’Grady M.P., Menzies R.A. (1992). Thymic regulation of the hypothalamic-pituitary-gonadal axis. Int. J. Immunopharmacol., 14: 353–359.]Search in Google Scholar
[Hinkel R., El-Aouni C., Olson T., Horstkotte J., Mayer S., Müller S., Willhauck M., Spitzweg C., Gildehaus F.J., Münzing W., Hannappel E., Bock-Marquet-te I., Di Maio J.M., Hatzopoulos A.K., Boekstegers P., Kupatt C. (2008). Thymosin β4 is an essential paracrine factor of embryonic endothelial progenitor cell-mediated cardioprotection. Circulation, 117: 2232–2240.]Search in Google Scholar
[Huang H.C., Hu C.H., Tang M.C., Wang W.S., Chen P.M., Su Y. (2007). Thymosin b4 triggers an epithelial–mesenchymal transition in colorectal carcinoma by upregulating integrin-linked kinase. Oncogene, 26: 2781–2790.]Search in Google Scholar
[Kim S., Kwon J. (2017). Thymosin β4 has a major role in dermal burn wound healing that involves actin cytoskeletal remodelling via heat-shock protein 70. J. Tissue Eng. Regen Med., 11: 1262–1273.]Search in Google Scholar
[Labas V., Teixeira-Gomes A.P., Bouguereau L., Gargaros A., Spina L., Marestaing A., Uzbekova S. (2018). Intact cell MALDI-TOF mass spectrometry on single bovine oocyte and follicular cells combined with top-down proteomics: A novel approach to characterise markers of oocyte maturation. J. Proteomics, 175: 56–74.]Search in Google Scholar
[Lee J.W., Kim H.S., Moon E.Y. (2019). Thymosin β-4 is a novel regulator for primary cilium formation by nephronophthisis 3 in HeLa human cervical cancer cells. Sci. Rep., 2: 6849.]Search in Google Scholar
[Lucas C.G., Remião M.H., Komninou E.R., Domingues W.B., Haas C., Leon P.M., Campos V.F., Ourique A., Guterres S.S., Pohlmann A.R., Basso A.C., Seixas F.K., Beck R.C., Collares T. (2015). Tretinoin-loaded lipid-core nanocapsules decrease reactive oxygen species levels and improve bovine embryonic development during in vitro oocyte maturation. Reprod. Toxicol., 58: 131–139.]Search in Google Scholar
[Namgoong S., Kim N.H. (2016). Roles of actin binding proteins in mammalian oocyte maturation and beyond. Cell Cycle, 15: 1830–1843.]Search in Google Scholar
[Nemolato S., Messana I., Cabras T., Manconi B., Inzitari R., Fanali C., Vento G., Tirone C., Romagnoli C., Riva A., Fanni D., Di Felice E., Faa G., Castagno-la M. (2009). Thymosin beta (4) and beta (10) levels in preterm newborn oral cavity and foetal salivary glands evidence a switch of secretion during foetal development. PLoS One, 4: e5109.]Search in Google Scholar
[Nemolato S., Cabras T., Fanari M.U., Cau F., Fanni D., Gerosa C., Manconi B., Messana I., Castagnola M., Faa G. (2010). Immunoreactivity of thymosin beta 4 in human foetal and adult genitourinary tract. Eur. J. Histochem., 54: e43.]Search in Google Scholar
[Opiela J., Romanek J., Lipiński D., Smorąg Z. (2014). Effect of hyaluronan on developmental competence and quality of oocytes and obtained blastocysts from in vitro maturation of bovine oocytes. Biomed. Res. Int., 519189.]Search in Google Scholar
[Salhab M., Papillier P., Perreau C., Guyader-Joly C., Dupont J., Mermillod P., Uzbekova S. (2010). Thymosins β-4 and β-10 are expressed in bovine ovarian follicles and upregulated in cumulus cells during meiotic maturation. Reprod. Fert. Develop., 22: 1206–1221.]Search in Google Scholar
[Salviano M.B., Collares F.J., Becker B.S., Rodrigues B.A., Rodrigues J.L. (2016). Bovine non-competent oocytes (BCB-) negatively impact the capacity of competent (BCB+) oocytes to undergo in vitro maturation, fertilisation and embryonic development. Zygote, 24: 245–251.]Search in Google Scholar
[Skowronek O., Zdebska N., Opiela J. (2016). The impact of thymosin β4 on bovine oocytes meiotic maturation and DNA fragmentation. Proc. 4th Winter Workshop of the Society for Biology of Reproduction, Zakopane, Poland, 3–5.02.2016, p.36.]Search in Google Scholar
[Takezawa Y., Yoshida K., Miyado K., Sato M., Nakamura A., Kawano N., Saka-kibara K., Kondo T., Harada Y., Ohnami N., Kanai S., Miyado M., Saito H., Takahashi Y., Akutsu H., Umezawa A. (2011). β-catenin is a molecular switch that regulates transition of cell-cell adhesion to fusion. Sci. Rep., 1: 68.]Search in Google Scholar
[Tripurani S.K., Lee K.B., Wang L., Wee G., Smith G.W., Lee Y.S., Latham K.E., Yao J. (2011). A novel functional role for the oocyte-specific transcription factor newborn ovary homeobox (NOBOX) during early embryonic development in cattle. Endocrinology, 152: 1013–1023.]Search in Google Scholar
[Wang W.S., Chen P.M., Hsiao H.L., Wang H.S., Liang W.Y., Su Y. (2004). Overexpression of the thymosin beta-4 gene is associated with increased invasion of SW480 colon carcinoma cells and the distant metastasis of human colorectal carcinoma. Oncogene, 23: 6666–6671.]Search in Google Scholar
[Warzych E., Pers-Kamczyc E., Krzywak A., Dudzińska S., Lechniak D. (2013). Apoptotic index within cumulus cells is a questionable marker of meiotic competence of bovine oocytes matured in vitro. Reprod. Biol., 13: 82–87.]Search in Google Scholar
[Wierzchoś-Hilczer A. (2017). Thymosin β4 structure – multiple biological functions and potential therapeutic applications. Wiad. Zoot., LV: 30–36.]Search in Google Scholar
[Wooldridge L.K., Ealy A.D. (2019). Interleukin-6 increases inner cell mass numbers in bovine embryos. BMC Dev. Biol., 19: 2.]Search in Google Scholar
[Yan H., Wen J., Zhang T., Zheng W., He M., Huang K., Guo Q., Chen Q., Yang Y., Deng G., Xu J., Wei Z., Zhang H., Xia G., Wang C. (2019). Oocyte-derived E-cadherin acts as a multiple functional factor maintaining the primordial follicle pool in mice. Cell Death Dis., 10: 160.]Search in Google Scholar
[Zhao Y., Qiu F., Xu S., Yu L., Fu G. (2011). Thymosin beta 4 activates integrin-linked kinase and decreases endothelial progenitor cells apoptosis under serum deprivation. J. Cell. Physiol., 226: 2798–2806.]Search in Google Scholar