Adams GP, Matteri RL, Kastelic JP, Ko JC, Ginther OJ. Association between surges of follicle-stimulating hormone and the emergence of follicular waves in heifers. J Reprod Fertil. 1992;94(1):177–88.
Ginther OJ, Kastelic JP, Knopf L. Compositions and characteristics of follicular waves during the bovine estrous cycle. Anim Reprod Sci. 1989;20:187–200.
Ginther OJ, Knopf L, Kastelic JP. Temporal associations among ovarian events in cattle during oestrous cycles with two and three follicular waves. J Reprod Fertil. 1989;87(1):223–30.
Jaiswal RS, Singh J, Marshall L, Adams GP. Repeatability of 2-wave and 3-wave patterns of ovarian follicular development during the bovine estrous cycle. Theriogenology. 2009;72(1):81–90.
Adams GP, Matteri RL, Ginther OJ. Effect of progesterone on ovarian follicles, emergence of follicular waves and circulating follicle-stimulating hormone in heifers. J Reprod Fertil. 1992;96(2):627–40.
Savio JD, Thatcher WW, Morris GR, Entwistle K, Drost M, Mattiacci MR. Effects of induction of low plasma progesterone concentrations with a progesterone-releasing intravaginal device on follicular turnover and fertility in cattle. J Reprod Fertil. 1993;98(1):77–84.
Mihm M, Baguisi A, Boland MP, Roche JF. Association between the duration of dominance of the ovulatory follicle and pregnancy rate in beef heifers. J Reprod Fertil. 1994;102(1):123–30.
Lee CN, Cook DL, Parfet JR, Smith CA, Youngquist RS, Garverick HA. Induction of persistent ovarian follicular structures following administration of progesterone near the onset of estrus in dairy cattle. J Dairy Sci. 1988;71(12):3505–8.
Noble KM, Tebble JE, Harvey D, Dobson H. Ultrasonography and hormone profiles of persistent ovarian follicles (cysts) induced with low doses of progesterone in cattle. J Reprod Fertil. 2000;120(2):361–6.
Ahmad N, Townsend EC, Dailey RA, Inskeep EK. Relationships of hormonal patterns and fertility to occurrence of two or three waves of ovarian follicles, before and after breeding, in beef cows and heifers. Anim Reprod Sci. 1997;49(1):13–28.
Bleach EC, Glencross RG, Knight PG. Association between ovarian follicle development and pregnancy rates in dairy cows undergoing spontaneous oestrous cycles. Reproduction. 2004;127(5):621–9.
Knopf L, Kastelic JP, Schallenberger E, Ginther OJ. Ovarian follicular dynamics in heifers: test of two-wave hypothesis by ultrasonically monitoring individual follicles. Domest Anim Endocrinol. 1989;6(2):111–9.
Townson DH, Tsang PC, Butler WR, Frajblat M, Griel LC Jr, Johnson CJ, Milvae RA, Niksic GM, Pate JL. Relationship of fertility to ovarian follicular waves before breeding in dairy cows. J Anim Sci. 2002;80(4):1053–8.
Dias FC, Mapletoft RJ, Kastelic JP, Adams GP, Colazo MG, Stover BC, Dochi O, Singh J. Effect of length of progesterone exposure during ovulatory wave development on pregnancy rate. Theriogenology. 2012;77(2):437–44.
Dias FC, Costa E, Adams GP, Mapletoft RJ, Kastelic JP, Dochi O, Singh J. Effect of duration of growing phase of ovulatory follicles on oocyte competence in superstimulated cattle. Reprod Fertil Dev. 2012;25(3):523–30.
Garcia Guerra A, Tribulo A, Yapura J, Singh J, Mapletoft RJ. Effect of length of superstimulatory treatment protocol on ovarian response and number of transferable embryos in beef cattle. Theriogenology. 2012;78(2):353–60.
Dadarwal D, Honparkhe M, Dias FC, Alce T, Lessard C, Singh J. Effect of superstimulation protocols on nuclear maturation and distribution of lipid droplets in bovine oocytes. Reprod Fertil Dev. 2015;27(8):1137–46.
Carabatsos MJ, Sellitto C, Goodenough DA, Albertini DF. Oocyte-granulosa cell heterologous gap junctions are required for the coordination of nuclear and cytoplasmic meiotic competence. Dev Biol. 2000;226(2):167–79.
Eppig JJ. Analysis of mouse oogenesis in vitro. Oocyte isolation and the utilization of exogenous energy sources by growing oocytes. J Exp Zool. 1976;198(3):375–82.
Haghighat N, Van Winkle LJ. Developmental change in follicular cell-enhanced amino acid uptake into mouse oocytes that depends on intact gap junctions and transport system Gly. J Exp Zool. 1990;253(1):71–82.
Thomas FH, Vanderhyden BC. Oocyte-granulosa cell interactions during mouse follicular development: regulation of kit ligand expression and its role in oocyte growth. Reprod Biol Endocrinol. 2006;4:19.
De La Fuente R, Eppig JJ. Transcriptional activity of the mouse oocyte genome: companion granulosa cells modulate transcription and chromatin remodeling. Dev Biol. 2001;229(1):224–36.
Dias FC, Khan MI, Adams GP, Sirard MA, Singh J. Granulosa cell function and oocyte competence: super-follicles, super-moms and super-stimulation in cattle. Anim Reprod Sci. 2014;149(1–2):80–9.
Dias FC, Khan MI, Sirard MA, Adams GP, Singh J. Differential gene expression of granulosa cells after ovarian superstimulation in beef cattle. Reproduction. 2013;146(2):181–91.
Dias FC, Dadarwal D, Adams GP, Mrigank H, Mapletoft RJ, Singh J. Length of the follicular growing phase and oocyte competence in beef heifers. Theriogenology. 2013;79(8):1177–83.
Garcia Guerra A, Tribulo A, Yapura J, Adams GP, Singh J, Mapletoft RJ. Lengthened superstimulatory treatment in cattle: evidence for rescue of follicles within a wave rather than continuous recruitment of new follicles. Theriogenology. 2015;84(3):467–76.
Bergfelt DR, Lightfoot KC, Adams GP. Ovarian synchronization following ultrasound-guided follicular ablation in heifers. Theriogenology. 1994;42:895–907.
Singh J, Pierson RA, Adams GP. Ultrasound image attributes of bovine ovarian follicles and endocrine and functional correlates. J Reprod Fertil. 1998;112(1):19–29.
Blazejczyk M, Miron M, Nadon R. FlexArray: a statistical data analysis software for gene expression microarrays. In. Montreal, Canada: Genome Quebec; 2007.
Smyth GK. Limma: linear models for microarray data. In: Gentleman R, Carey V, Huber W, irizarry R, Springer DS, editors. Bioinformatics and computational biology solutions using R and Bioconductor. New York: Springer; 2005. p. 473.
Smyth GK. Linear models and empirical bayes methods for assessing differential expression in microarray experiments. Stat Appl Genet Mol Biol. 2004;3(1):3.
Pfaffl MW, Horgan GW, Dempfle L. Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic Acids Res. 2002;30(9):e36.
Gilbert I, Robert C, Vigneault C, Blondin P, Sirard MA. Impact of the LH surge on granulosa cell transcript levels as markers of oocyte developmental competence in cattle. Reproduction. 2012;143(6):735–47.
Gilbert I, Robert C, Dieleman S, Blondin P, Sirard MA. Transcriptional effect of the LH surge in bovine granulosa cells during the peri-ovulation period. Reproduction. 2011;141(2):193–205.
Ndiaye K, Fayad T, Silversides DW, Sirois J, Lussier JG. Identification of downregulated messenger RNAs in bovine granulosa cells of dominant follicles following stimulation with human chorionic gonadotropin. Biol Reprod. 2005;73(2):324–33.
Agca C, Ries JE, Kolath SJ, Kim JH, Forrester LJ, Antoniou E, Whitworth KM, Mathialagan N, Springer GK, Prather RS, et al. Luteinization of porcine preovulatory follicles leads to systematic changes in follicular gene expression. Reproduction. 2006;132(1):133–45.
Wu LL, Russell DL, Norman RJ, Robker RL. Endoplasmic reticulum (ER) stress in cumulus-oocyte complexes impairs pentraxin-3 secretion, mitochondrial membrane potential (DeltaPsi m), and embryo development. Mol Endocrinol. 2012;26(4):562–73.
Zhang X, Jafari N, Barnes RB, Confino E, Milad M, Kazer RR. Studies of gene expression in human cumulus cells indicate pentraxin 3 as a possible marker for oocyte quality. Fertil Steril. 2005;83(Suppl 1):1169–79.
Diouf MN, Sayasith K, Lefebvre R, Silversides DW, Sirois J, Lussier JG. Expression of phospholipase A2 group IVA (PLA2G4A) is upregulated by human chorionic gonadotropin in bovine granulosa cells of ovulatory follicles. Biol Reprod. 2006;74(6):1096–103.
Duffy DM, Seachord CL, Dozier BL. An ovulatory gonadotropin stimulus increases cytosolic phospholipase A2 expression and activity in granulosa cells of primate periovulatory follicles. J Clin Endocrinol Metab. 2005;90(10):5858–65.
Shimada M, Hernandez-Gonzalez I, Gonzalez-Robayna I, Richards JS. Paracrine and autocrine regulation of epidermal growth factor-like factors in cumulus oocyte complexes and granulosa cells: key roles for prostaglandin synthase 2 and progesterone receptor. Mol Endocrinol. 2006;20(6):1352–65.
Pall M, Friden BE, Brannstrom M. Induction of delayed follicular rupture in the human by the selective COX-2 inhibitor rofecoxib: a randomized double-blind study. Hum Reprod. 2001;16(7):1323–8.
Hester KE, Harper MJ, Duffy DM. Oral administration of the cyclooxygenase-2 (COX-2) inhibitor meloxicam blocks ovulation in non-human primates when administered to simulate emergency contraception. Hum Reprod. 2010;25(2):360–7.
Bridges PJ, Komar CM, Fortune JE. Gonadotropin-induced expression of messenger ribonucleic acid for cyclooxygenase-2 and production of prostaglandins E and F2alpha in bovine preovulatory follicles are regulated by the progesterone receptor. Endocrinology. 2006;147(10):4713–22.
Davis BJ, Lennard DE, Lee CA, Tiano HF, Morham SG, Wetsel WC, Langenbach R. Anovulation in cyclooxygenase-2-deficient mice is restored by prostaglandin E2 and interleukin-1beta. Endocrinology. 1999;140(6):2685–95.
Liu J, Carriere PD, Dore M, Sirois J. Prostaglandin G/H synthase-2 is expressed in bovine preovulatory follicles after the endogenous surge of luteinizing hormone. Biol Reprod. 1997;57(6):1524–31.
Takahashi T, Morrow JD, Wang H, Dey SK. Cyclooxygenase-2-derived prostaglandin E(2) directs oocyte maturation by differentially influencing multiple signaling pathways. J Biol Chem. 2006;281(48):37117–29.
Fayad T, Lefebvre R, Nimpf J, Silversides DW, Lussier JG. Low-density lipoprotein receptor-related protein 8 (LRP8) is upregulated in granulosa cells of bovine dominant follicle: molecular characterization and spatio-temporal expression studies. Biol Reprod. 2007;76(3):466–75.
Vaknin KM, Lazar S, Popliker M, Tsafriri A. Role of meiosis-activating sterols in rat oocyte maturation: effects of specific inhibitors and changes in the expression of lanosterol 14alpha-demethylase during the preovulatory period. Biol Reprod. 2001;64(1):299–309.
Robker RL, Richards JS. Hormone-induced proliferation and differentiation of granulosa cells: a coordinated balance of the cell cycle regulators cyclin D2 and p27Kip1. Mol Endocrinol. 1998;12(7):924–40.
Robker RL, Richards JS. Hormonal control of the cell cycle in ovarian cells: proliferation versus differentiation. Biol Reprod. 1998;59(3):476–82.
van Montfoort AP, Geraedts JP, Dumoulin JC, Stassen AP, Evers JL, Ayoubi TA. Differential gene expression in cumulus cells as a prognostic indicator of embryo viability: a microarray analysis. Mol Hum Reprod. 2008;14(3):157–68.
Carriere PD, Harvey D, Cooke GM. The role of pregnenolone-metabolizing enzymes in the regulation of oestradiol biosynthesis during development of the first wave dominant follicle in the cow. J Endocrinol. 1996;149(2):233–42.
Dieleman SJ, Bevers MM, Poortman J, van Tol HT. Steroid and pituitary hormone concentrations in the fluid of preovulatory bovine follicles relative to the peak of LH in the peripheral blood. J Reprod Fertil. 1983;69(2):641–9.
Dieleman SJ, Kruip TA, Fontijne P, de Jong WH, van der Weyden GC. Changes in oestradiol, progesterone and testosterone concentrations in follicular fluid and in the micromorphology of preovulatory bovine follicles relative to the peak of luteinizing hormone. J Endocrinol. 1983;97(1):31–42.
Lingenfelter BM, Dailey RA, Inskeep EK, Vernon MW, Poole DH, Rhinehart JD, Yao J. Microarray analysis of gene expression in granulosal cells from persistent follicles in cattle. Anim Reprod Sci. 2008;104(2–4):405–13.
Lingenfelter BM, Dailey RA, Inskeep EK, Vernon MW, Poole DH, Rhinehart JD, Yao J. Changes of maternal transcripts in oocytes from persistent follicles in cattle. Mol Reprod Dev. 2007;74(3):265–72.
Blondin P, Sirard MA. Oocyte and follicular morphology as determining characteristics for developmental competence in bovine oocytes. Mol Reprod Dev. 1995;41(1):54–62.
Blondin P, Coenen K, Guilbault LA, Sirard MA. In vitro production of bovine embryos: developmental competence is acquired before maturation. Theriogenology. 1997;47(5):1061–75.
Salamone DF, Adams GP, Mapletoft RJ. Changes in the cumulus-oocyte complex of subordinate follicles relative to follicular wave status in cattle. Theriogenology. 1999;52(4):549–61.
Barnes FL, Sirard MA. Oocyte maturation. Semin Reprod Med. 2000;18(2):123–31.