1. Gougeon A. Regulation of ovarian follicular development in primates: facts and hypotheses. Endocr Rev. 1996. 17:121–155.
2. McGee EA, Hsueh AJW. Initial and cyclic recruitment of ovarian follicles. Endocr Rev. 2000. 21:200–214.
3. Park CE, Cha KY, Kim K, Lee KA. Expression of cell cycle regulatory genes during primordial-primary follicle transition in the mouse ovary. Fertil Steril. 2005. 83:410–418.
4. Pan H, O'Brien MJ, Wigglesworth K, Eppig JJ, Schultz RM. Transcript profiling during mouse oocyte development and the effect of gonadotropin priming and development in vitro. Dev Biol. 2005. 286:493–506.
5. Braw-Tal R. The initiation of follicle growth: the oocyte or the somatic cells. Mol Cell Endocrinol. 2002. 187:11–18.
6. Eppig JJ, Wigglesworth K, Pendola FL. The mammalian oocyte orchestrates the rate of ovarian follicular development. Proc Natl Acad Sci U S A. 2002. 99:2890–2894.
7. Eppig JJ. Oocyte control of ovarian follicular development and function in mammals. Reproduction. 2001. 122:829–838.
8. Albertini DF, Sanfins A, Combelles CM. Origins and manifestations of oocyte maturation competencies. Reprod Biomed Online. 2003. 6:410–415.
10. Yoon SJ, Kim KH, Chung HM, Choi DH, Lee WS, Cha KY, Lee KA. Gene expression profiling of early follicular development in primordial, primary, and secondary follicles. Fertil Steril. 2006. 85:193–203.
11. Yoon SJ, Chung HM, Cha KY, Kim NH, Lee KA. Identification of differential gene expression in germinal vesicle vs. metaphase II mouse oocytes by using annealing control primers. Fertil Steril. 2005. 83:1293–1296.
12. Millar JB, Russel P. The cdc25 M-phase inducer: an unconventional protein phosphatase. Cell. 1992. 68:407–410.
13. Mueller PR, Coleman TR, Dunphy WG. Cell cycle regulation of a Xenopus wee1-like kinase. Mol Biol Cell. 1995. 6:119–134.
14. Park CE, Kim YH, Jeon EH, Cha KY, Lee SH, Lee KA. Expression of wee1 and its related cell cycle components in mouse early stage follicles. Cells Tissues Organs. 2004. 177:221–228.
15. Couzin J. Breakthrough of the year. Science. 2002. 298:2295–2297.
16. Kim VN. RNA interference in functional genomics and medicine. J Korean Med Sci. 2003. 18:309–318.
17. Denli AM, Hannon GJ. RNAi: an ever-growing puzzle. Trends Biochem Sci. 2003. 28:196–201.
18. Hannon GJ. RNA interference. Nature. 2002. 418:244–251.
19. Gil J, Esteban M. Induction of apoptosis by the dsRNA-dependent protein kinase (PKR): mechanism of action. Apoptosis. 2000. 5:107–114.
20. Elbashir SM, Lendeckel W, Tuschl T. RNA interference is mediated by 21- and 22-nucleotide RNAs. Genes Dev. 2001. 15:188–200.
21. Wianny F, Zernicka-Goetz M. Specific interference with gene function by double-stranded RNA in early mouse development. Nat Cell Biol. 2000. 2:70–75.
22. Svoboda P, Stein P, Hayashi H, Schultz RM. Selective reduction of dormant maternal mRNAs in mouse oocytes by RNA interference. Development. 2000. 127:4147–4156.
23. Park CE, Shin MR, Jeon EH, Cha KY, Lee SH, Kim K, Kim NH, Lee KA. Oocyte-selective expression of MT transposon-like element, clone MTi7 and its role in oocyte maturation and embryo development. Mol Reprod Dev. 2004. 69:365–374.
24. Yoon SJ, Koo DB, Park JS, Choi KH, Han YM, Lee KA. Identify the role of cytosolic malate dehydrogenase in the oocyte maturation and embryo development
using RNA interference. Fertil Steril (in revision).
25. Yoon SJ, Chung HM, Cha KY, Kim NH, Lee KA. Differentially expressed mRNA profiles between immature germinal vesicle (GV) and mature metaphase II (MII) mouse oocytes. Dev Reprod. 2004. 8:35–42.