References
- Scaramuzzi RJ, Baird DT, Campbell BK, et al. Regulation of folliculogenesis and the determination of ovulation rate in ruminants. Reprod Fertil Dev 2011;23:444-67. https://doi.org/10.1071/RD09161
- Kennedy JP, Worthington CA, Cole ER. The post-natal development of the ovary and uterus of the Merino lamb. J Reprod Fertil 1974;36:275-82. https://doi.org/10.1530/jrf.0.0360275
- Tassell R, Chamley WA, Kennedy JP. Gonadotrophin levels and ovarian development in the neonatal ewe lamb. Aust J Biol Sci 1978;31:267-73. https://doi.org/10.1071/BI9780267
- Sonjaya H, Driancourt MA. Ovarian follicles during infancy in Romanov and Ile-de-France ewe lambs. J Reprod Fertil 1987;81:241-8. https://doi.org/10.1530/jrf.0.0810241
- Rawlings NC, Evans AC, Honaramooz A, Bartlewski PM. Antral follicle growth and endocrine changes in prepubertal cattle, sheep and goats. Anim Reprod Sci 2003;78:259-70. https://doi.org/10.1016/S0378-4320(03)00094-0
- Kelly JM, Kleemann DO, Walker SK. Enhanced efficiency in the production of offspring from 4- to 8-week-old lambs. Theriogenology 2005;63:1876-90. https://doi.org/10.1016/j.theriogenology.2004.09.010
- Gou KM, Guan H, Bai JH, et al. Field evaluation of juvenile in vitro embryo transfer (JIVET) in sheep. Anim Reprod Sci 2009; 112:316-24. https://doi.org/10.1016/j.anireprosci.2008.05.008
- Paramio MT, Izquierdo D. Current status of in vitro embryo production in sheep and goats. Reprod Domest Anim 2014;49 Suppl 4:37-48.
- Amiridis GS, Cseh S. Assisted reproductive technologies in the reproductive management of small ruminants. Anim Reprod Sci 2012;130:152-61. https://doi.org/10.1016/j.anireprosci.2012.01.009
- Ptak G, Loi P, Dattena M, Tischner M, Cappai P. Offspring from one-month-old lambs: studies on the developmental capability of prepubertal oocytes. Biol Reprod 1999;61:1568-74. https://doi.org/10.1095/biolreprod61.6.1568
- Leoni GG, Bebbere D, Succu S, et al. Relations between relative mRNA abundance and developmental competence of ovine oocytes. Mol Reprod Dev 2007;74:249-57. https://doi.org/10.1002/mrd.20442
- Morton KM. Developmental capabilities of embryos produced in vitro from prepubertal lamb oocytes. Reprod Domest Anim 2008; 43 Suppl 2:137-43.
- Leoni GG, Palmerini MG, Satta V, et al. Differences in the kinetic of the first meiotic division and in active mitochondrial distribution between prepubertal and adult oocytes mirror differences in their developmental competence in a sheep model. PLoS One 2015;10:e0124911. https://doi.org/10.1371/journal.pone.0124911
- Hamel M, Dufort I, Robert C, et al. Identification of differentially expressed markers in human follicular cells associated with competent oocytes. Hum Reprod, 2008, 23: 1118-27. https://doi.org/10.1093/humrep/den048
- Dias FC, Khan MI, Sirard MA, Adams GP, Singh J. Differential gene expression of granulosa cells after ovarian superstimulation in beef cattle. Reproduction 2013;146:181-91. https://doi.org/10.1530/REP-13-0114
- Primig M. The bioinformatics tool box for reproductive biology. Biochim Biophys Acta 2012;1822:1880-95. https://doi.org/10.1016/j.bbadis.2012.05.018
- Kang X, Liu G, Liu Y, Xu Q, Zhang M, Fang M. Transcriptome profile at different physiological stages reveals potential mode for curly fleece in Chinese tan sheep. PLoS One 2013;8:e71763. https://doi.org/10.1371/journal.pone.0071763
- Kim D, Pertea G, Trapnell C, Pimentel H, Kelley R, Salzberg SL. TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions. Genome Biol, 2013;14:R36. https://doi.org/10.1186/gb-2013-14-4-r36
- Mortazavi A, Williams BA, Mccue K, Schaeffer L, Wold B. Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nat Methods 2008;5:621-8. https://doi.org/10.1038/nmeth.1226
- Wang L, Feng Z, Wang X, Wang X, Zhang X. DEGseq: an R package for identifying differentially expressed genes from RNA-seq data. Bioinformatics 2010;26:136-8. https://doi.org/10.1093/bioinformatics/btp612
- Bonnet A, Cabau C, Bouchez O, et al. An overview of gene expression dynamics during early ovarian folliculogenesis: specificity of follicular compartments and bi-directional dialog. BMC Genomics 2013;14:904. https://doi.org/10.1186/1471-2164-14-904
- Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 2001;25:402-8. https://doi.org/10.1006/meth.2001.1262
- Clement F, Monniaux D. Multiscale modelling of ovarian follicular selection. Prog Biophys Mol Biol 2013;113:398-408. https://doi.org/10.1016/j.pbiomolbio.2012.12.005
- Hatzirodos N, Irving-Rodgers HF, Hummitzsch K, et al. Transcriptome profiling of granulosa cells of bovine ovarian follicles during growth from small to large antral sizes. BMC Genomics 2014;15:24. https://doi.org/10.1186/1471-2164-15-24
- Conti M, Hsieh M, Park JY, Su YQ. Role of the epidermal growth factor network in ovarian follicles. Mol Endocrinol 2006;20:715-23. https://doi.org/10.1210/me.2005-0185
- Yamashita Y, Shimada M. The release of EGF domain from EGF-like factors by a specific cleavage enzyme activates the EGFRMAPK3/1 pathway in both granulosa cells and cumulus cells during the ovulation process. J Reprod Dev 2012;58:510-4. https://doi.org/10.1262/jrd.2012-056
- Khan DR, Guillemette C, Sirard MA, Richard FJ. Characterization of FSH signalling networks in bovine cumulus cells: a perspective on oocyte competence acquisition. Mol Hum Reprod 2015;21: 688-701. https://doi.org/10.1093/molehr/gav032
- Fujihara M, Comizzoli P, Keefer CL, Wildt DE, Songsasen N. Epidermal growth factor (EGF) sustains in vitro primordial follicle viability by enhancing stromal cell proliferation via MAPK and PI3K pathways in the prepubertal, but not adult, cat ovary. Biol Reprod 2014;90:86.
- Hatzirodos N, Hummitzsch K, Irving-Rodgers HF, et al. Transcriptome profiling of granulosa cells from bovine ovarian follicles during atresia. BMC Genomics 2014;15:40. https://doi.org/10.1186/1471-2164-15-40
- Cao R, Wu WJ, Zhou XL, et al. Expression and preliminary functional profiling of the let-7 family during porcine ovary follicle atresia. Mol Cells 2015;38:304-11. https://doi.org/10.14348/molcells.2015.2122
- Berkholtz CB, Lai BE, Woodruff TK, Shea LD. Distribution of extracellular matrix proteins type I collagen, type IV collagen, fibronectin, and laminin in mouse folliculogenesis. Histochem Cell Biol 2006;126:583-92. https://doi.org/10.1007/s00418-006-0194-1
- Donadeu FX, Fahiminiya S, Esteves CL, et al.Transcriptome profiling of granulosa and theca cells during dominant follicle development in the horse. Biol Reprod 2014;91:111.
- Hiradate Y, Ohtake J, Hoshino Y, Tanemura K, Sato E. Adrenomedullin: a possible regulator of germinal vesicle breakdown. Biochem Biophys Res Commun 2011;415:691-5. https://doi.org/10.1016/j.bbrc.2011.10.139
- Skinner MK, Schmidt M, Savenkova MI, Sadler-Riggleman I, Nilsson EE. Regulation of granulosa and theca cell transcriptomes during ovarian antral follicle development. Mol Reprod Dev 2008;75:1457-72. https://doi.org/10.1002/mrd.20883
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