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Topic:Estrous Cycle

The estrous cycle in horses is a recurring reproductive cycle that mares undergo, typically during the breeding season. This cycle is characterized by a series of hormonal changes that prepare the mare for potential conception. The cycle is divided into two main phases: estrus and diestrus. During estrus, the mare is receptive to mating, and ovulation occurs. In contrast, the diestrus phase is a period when the mare is not receptive to a stallion. The regulation of the estrous cycle involves a complex interplay of hormones such as estrogen, progesterone, luteinizing hormone, and follicle-stimulating hormone. Understanding the estrous cycle is important for effective breeding management and reproductive health in horses. This page compiles peer-reviewed research studies and scholarly articles that explore the physiology, hormonal regulation, and implications of the estrous cycle in equine reproduction.
Changes in PGF2alpha secretion during prolonged luteal phase in mares.
Journal of reproduction and fertility. Supplement    January 1, 2000   Issue 56 305-315 
Kindahl H, Odensvik K, Hansen B, Daels PF.The aim of this study was to characterize changes in PGF2alpha secretion in mares with persistent corpora lutea that were induced by administering altrenogest during oestrus. In Expt 1, PGF2alpha secretion was compared among mares undergoing normal oestrous cycles (n=7) and mares undergoing prolonged luteal phases (n=6), using the mean 15-ketodihydro-PGF2alpha (PGFM) plasma concentrations, peak PGFM concentrations and number of PGFM surges each day, from day 12 to day 16 of the luteal phase. In Expt 2, oxytocin-induced PGF2alpha secretion was characterized on days 13 and 16 of the luteal phase...
Uncoupling of the equine reproductive axes during transition into anoestrus.
Journal of reproduction and fertility. Supplement    January 1, 2000   Issue 56 153-161 
Nequin LG, King SS, Roser JF, Soderstrom BL, Carnevale EM, Neumann KR.The reproductive activity of light horse mares (n=12) was monitored each day from 3 September until 29 January, or until the mares entered anoestrus, by behaviour evaluation, ultrasonography and blood sampling. Follicles, corpora lutea and ovulation, as well as oestradiol, progesterone, and LH and FSH concentrations, were analysed to determine a reproductive profile for the transition into anoestrus. The results of the present study indicate that light horse mares progress through four phases during the autumn transition into anoestrus: (i) normal cycles; (ii) aberrant cycles; (iii) anovulatio...
Ovarian secretion of inhibin in mares.
Journal of reproduction and fertility. Supplement    January 1, 2000   Issue 56 239-245 
Tanaka Y, Nagamine N, Nambo Y, Nagata S, Nagaoka K, Tsunoda N, Taniyama H, Yoshihara T, Oikawa M, Watanabe G, Taya K.In mares, circulating immunoreactive inhibin concentrations increase during the follicular phase and decrease at the start of the LH surge. Thereafter, sharp increases in circulating immunoreactive inhibin concentrations, the 'ovulatory increase', are observed during ovulation. In the present study, the cellular sources and molecular form of ovarian inhibin were investigated to determine the mechanism responsible for this unique ovulatory increase. Three sizes of ovarian follicles (small, 30 mm in diameter) were selected. Inhibin alpha-subunit was localized by immunohistochemistry to the gran...
Oxytocin administration prolongs luteal function in cyclic mares.
Journal of reproduction and fertility    January 1, 2000   Volume 116, Issue 2 315-320 doi: 10.1530/jrf.0.1160315
Stout TA, Lamming GE, Allen WR.Recent evidence indicates that, in mares, as in the domestic ruminants, oxytocin and its endometrial receptor play important roles in stimulating the pulsatile releases of prostaglandin F2 alpha from the endometrium that effect luteolysis. In the present experiment, continuous administration of oxytocin by subcutaneous minipump to five mares during days 8-20 after ovulation abolished luteolysis in four of them, while all four of the control mares infused similarly with saline underwent luteolysis at the expected time. When oxytocin administration began on day 10, instead of on day 8, after ovu...
Influence of the dopamine antagonist domperidone on the vernal transition in seasonally anoestrous mares.
Journal of reproduction and fertility. Supplement    January 1, 2000   Issue 56 185-193 
Brendemuehl JP, Cross DL.The aim of the present study was to determine the effect of prolonged administration of the dopamine antagonist domperidone on follicular development, ovulation and endocrine profiles in anoestrous mares. Anoestrous mares (n=16) were maintained under natural photoperiod and ambient temperature. Eight of the mares were treated with domperidone each day from 15 January until the first ovulation of the year. The mean number and size of follicles > or =20 mm in diameter were significantly greater in domperidone-treated mares than in control mares by day 14 of treatment. The day of first ovulati...
Immunolocalization of oxytocin and neurophysin in the mare uterus.
Journal of reproduction and fertility. Supplement    January 1, 2000   Issue 56 289-296 
Watson ED, Buckingham J, Björkstén T, Nikolakopoulos E.The presence of oxytocin in the mare uterus was determined by radioimmunoassay of tissue extracts and uterine lavage fluid, and by immunohistochemistry. Samples were obtained from mares during the oestrous cycle and on day 14 of pregnancy. Immunoreactive oxytocin was detected in extracts of endometrium and myometrium, and in uterine lavage fluid. In tissue sections, the luminal epithelium, the epithelium of the superficial, but not deep, glands, blood vessel walls and myometrium all stained positively for oxytocin, whereas only the luminal epithelium and epithelium of the superficial glands st...
Ovulation synchrony after follicle ablation in mares.
Journal of reproduction and fertility. Supplement    January 1, 2000   Issue 56 257-269 
Bergfelt DR, Adams GP.Two experiments were performed to determine the efficacy of ultrasound-guided transvaginal follicle ablation for synchronizing ovarian function in mares. The experiments were initiated at random stages of the oestrous cycle in control (nonablated) and follicle-ablated mares. On day 0, all follicles > or =10 mm in diameter were punctured, aspirated and curettaged in ablated mares, and, on day 4, two doses of PGF2alpha were administered with a 12 h interval between the doses to both ablated and nonablated (control) mares. In Expt 1, hCG was administered to the ablated mares on the first or se...
Estimation of sodium and potassium concentrations in the uterine fluid of mares by microdialysis and ion chromatography.
Journal of reproduction and fertility. Supplement    January 1, 2000   Issue 56 327-332 
Waelchli RO, Jaworski T, Ruddock WD, Betteridge KJ.Equine blastocyst fluid has a lower [Na+], a higher [K+] and a lower osmolality than does normal blood serum. Based on the assumptions that the sodium pump is primarily responsible for fluid accumulation and that ions transported actively into the blastocyst increase blastocyst osmolality above that of the external medium, we hypothesized that the [Na+] and the osmolality of mare uterine fluid are lower than those of blastocyst fluid. Microdialysis and ion chromatography were used to estimate [Na+] and [K+] of uterine fluid. Mares (n=10) were used for in vivo measurements at different stages o...
The uterus as a source of oxytocin in cyclic mares.
Journal of reproduction and fertility. Supplement    January 1, 2000   Issue 56 281-287 
Stout TA, Lamming GE, Allen WR.In a recent study, continuous administration of oxytocin by subcutaneous minipump to mares from day 8 to 20 after ovulation prevented luteolysis in most of the treated but none of the control mares, indicating a role for oxytocin in cyclical luteolysis in mares. In the present study, measurement of oxytocin concentrations in uterine flushings recovered from nine mares during days 14-18 after ovulation gave values that were many times higher than those measured concurrently in peripheral plasma. Furthermore, intrauterine administration of oxytocin to four mares on day 14 after ovulation stimula...
A detailed study of hormonal profiles in mares at luteolysis.
Journal of reproduction and fertility. Supplement    January 1, 2000   Issue 56 271-279 
Shand N, Irvine CH, Turner JE, Alexander SL.Jugular blood samples were collected at 4 h intervals from six mares during an oestrous cycle to study the hormonal events that occur around the time of luteolysis. Blood samples from day 10 (day 0 = ovulation) until day 3 of oestrus were assayed for prostaglandin metabolite 13,14-dihydro-15-keto PGF2alpha (PGFM), oxytocin, prolactin, progesterone and oestrogen conjugates. PGF2alpha (0.5 or 1.5 mg) was administered to six mid-dioestrous mares and the oxytocin and prolactin responses were measured. One to five large (peak > or =2 x nadir) pulses of PGFM, oxytocin and prolactin were detected ...
Role of luteinizing hormone in follicle deviation based on manipulating progesterone concentrations in mares.
Biology of reproduction    November 26, 1999   Volume 61, Issue 6 1492-1498 doi: 10.1095/biolreprod61.6.1492
Gastal EL, Bergfelt DR, Nogueira GP, Gastal MO, Ginther OJ.The effects of several doses of progesterone on FSH and LH concentrations were used to study the role of the gonadotropins on deviation in growth rates of the two largest follicles during the establishment of follicle dominance. Progesterone was given to pony mares at a daily dose rate of 0 mg (controls), 30 mg (low dose), 100 mg (intermediate dose), and 300 mg (high dose). All follicles > or = 6 mm were ablated at Day 10 (Day 0 = ovulation) to initiate a new follicular wave; prostaglandin F(2alpha) was given to induce luteolysis, and progesterone was given from Days 10 to 24. The low dose ...
A selective increase in circulating inhibin and inhibin pro-alphaC at the time of ovulation in the mare.
The American journal of physiology    November 24, 1999   Volume 277, Issue 5 E870-E875 doi: 10.1152/ajpendo.1999.277.5.E870
Nagaoka K, Nambo Y, Nagamine N, Nagata SI, Tanaka Y, Shinbo H, Tsunoda N, Taniyama H, Watanabe G, Groome NP, Taya K.The relationship between a selective increase in circulating immunoreactive (ir)-inhibin and the time of ovulation was investigated in mares. Concentrations of plasma ir-inhibin were measured every 4 h during the periovulatory period. Inhibin pro-alphaC, a precursor protein of the inhibin alpha-subunit, was also measured. The changes in ir-inhibin and inhibin pro-alphaC in circulation were parallel. Concentrations of both ir-inhibin and inhibin pro-alphaC in the plasma increased at the same time when ovulatory follicles ruptured, and the peak levels of circulating ir-inhibin and inhibin pro-al...
Cell proliferation patterns in the equine endometrium throughout the non-pregnant reproductive cycle.
Journal of reproduction and fertility    October 3, 1999   Volume 116, Issue 1 167-175 doi: 10.1530/jrf.0.1160167
Gerstenberg C, Allen WR, Stewart F.Immunohistochemical detection of the proliferation marker Ki-67 antigen was used to monitor mitotic activity in the endometrium of mares. The monoclonal antibody MIB1 was validated for use on equine tissues by demonstrating its reaction with activated peripheral blood lymphocytes, and endometrial biopsies were recovered from 26 non-pregnant mares at selected stages during the reproductive cycle. The proportion of positively stained nuclei was counted in five random areas on each histological section to determine the percentage and type of proliferating cells. Multiplication rates in the types ...
Dual regulation of promoter II- and promoter 1f-derived cytochrome P450 aromatase transcripts in equine granulosa cells during human chorionic gonadotropin-induced ovulation: a novel model for the study of aromatase promoter switching.
Endocrinology    August 28, 1999   Volume 140, Issue 9 4133-4141 doi: 10.1210/endo.140.9.6951
Boerboom D, Kerban A, Sirois J.Estradiol biosynthesis is a key biochemical trait of developing follicles. To study its regulation in equine follicles, the objectives of this study were to clone and determine the structure of equine cytochrome P450 aromatase (P450AROM), and characterize the regulation of P450AROM and P450 17alpha-hydroxylase/C17-20 lyase (P45017alpha) messenger RNAs (mRNAs) in vivo in equine preovulatory follicles isolated during hCG-induced ovulation. Two distinct P450AROM complementary DNAs (cDNAs) were isolated from an equine preovulatory follicle cDNA library. One clone was 2682 bp in length and included...
Experimental assumption of dominance by a smaller follicle and associated hormonal changes in mares.
Biology of reproduction    August 24, 1999   Volume 61, Issue 3 724-730 doi: 10.1095/biolreprod61.3.724
Gastal EL, Gastal MO, Ginther OJ.A two-follicle model was used to study the nature of selection of the dominant follicle in mares by ablating neither or one of the two follicles on the day the larger follicle reached >/= 20 mm (Day 0). The larger follicle became the dominant follicle in all mares in which both follicles (n = 8) or only the larger follicle (n = 10) was retained. When only the smaller follicle (n = 9) was retained, it became dominant and ovulated in six mares and became atretic in three mares; the difference in diameter between the two follicles on Day 0 was less (p < 0.01) in mares in which the retained ...
Follicle deviation and intrafollicular and systemic estradiol concentrations in mares.
Biology of reproduction    June 22, 1999   Volume 61, Issue 1 31-39 doi: 10.1095/biolreprod61.1.31
Gastal EL, Gastal MO, Wiltbank MC, Ginther OJ.By definition, follicle deviation begins on the day the two largest follicles of a wave begin to differ in growth rates. The relationships between follicle deviation and intrafollicular and systemic estradiol concentrations were studied in ponies, using a two-follicle model in which all but the two largest follicles were ablated. A 20-microliter sample of follicular fluid was obtained from each of the two follicles by transvaginal ultrasonography. In experiment 1, the two follicles were sampled when the larger follicle reached 15 mm. No differences (p > 0.05) in post-sampling follicle chara...
Oxytocin-neurophysin I mRNA abundance in equine uterine endometrium.
Domestic animal endocrinology    May 27, 1999   Volume 16, Issue 3 183-192 doi: 10.1016/s0739-7240(99)00008-9
Behrendt-Adam CY, Adams MH, Simpson KS, McDowell KJ.A positive-feedback loop between luteal oxytocin and uterine prostaglandin F2 alpha (PGF) is a major signal for luteolysis in ruminants. Likewise, uterine PGF causes luteolysis in mares, but the involvement of oxytocin in this process is unclear. We wanted: 1) to determine if the oxytocin-neurophysin I (OT-NP I) gene is transcribed into mRNA in the endometrium of mares; and, if so, 2) to analyze relative changes in abundance of endometrial OT-NP I mRNA throughout the estrous cycle and during early stages of pregnancy. Endometrial biopsies were obtained from nonbred mares during estrus, and 5, ...
Intrafollicular content of luteinizing hormone receptor, alpha-inhibin, and aromatase in relation to follicular growth, estrous cycle stage, and oocyte competence for in vitro maturation in the mare.
Biology of reproduction    April 20, 1999   Volume 60, Issue 5 1120-1127 doi: 10.1095/biolreprod60.5.1120
Goudet G, Belin F, Bézard J, Gérard N.The intrafollicular content of LH receptor, alpha-inhibin, and aromatase are known good indicators of follicular status. We investigated the amounts of these proteins in granulosa and cumulus cells in relation to oocyte competence for in vitro maturation, follicular growth, and estrous cycle stage in the mare. Follicular punctures were performed 34 h after an injection of crude equine gonadotropins, either during the follicular phase, at the end of the follicular phase, or during the luteal phase. The cumulus-oocyte complex, granulosa cells, and follicular fluid of follicles larger than 5 mm w...
The effects of equine somatotropin (eST) on follicular development and circulating plasma hormone profiles in cyclic mares treated during different stages of the estrous cycle.
Domestic animal endocrinology    March 19, 1999   Volume 16, Issue 1 57-67 doi: 10.1016/s0739-7240(98)00046-0
Cochran RA, Leonardi-Cattolica AA, Sullivan MR, Kincaid LA, Leise BS, Thompson DL, Godke RA.The effects of exogenous equine somatotropin (eST) administration on ovarian activity and plasma hormone levels were evaluated on horse and pony mares. The objectives of this study were to determine the effects of eST on follicular development and circulating concentrations of leutinizing hormone (LH), estradiol, progesterone, and insulin-like growth factor I (IGF-I) in cyclic horse and pony mares. Sixteen mares received daily injections (i.m.) of eST at a concentration of 25 micrograms/kg body weight on either Days 6 through 12 (Treatment A) or 13 through 19 (Treatment B) postovulation. In ad...
[Follicular dynamics after treatment with hCG for ovulation induction in mares].
Tierarztliche Praxis. Ausgabe G, Grosstiere/Nutztiere    March 17, 1999   Volume 27, Issue 1 47-51 
Bollwein H, Braun J.In this study the use of hCG for induction of ovulation is described. Factors such as follicle diameter at the time of administration of hCG (3000 IE hCG i.v.), follicular growth after hCG and the rate of double ovulations were evaluated. A total of 168 mares presented for artificial insemination were used. In 249 estrous periods hCG was given to mares exhibiting standing estrous when a minimum follicle diameter of 30 mm and a well developed edema of the endometrium could be detected by ultrasonography. In nine estrous periods ovulation occurred within 24 hours after hCG. The majority of mares...
Human chorionic gonadotropin induces an inverse regulation of steroidogenic acute regulatory protein messenger ribonucleic acid in theca interna and granulosa cells of equine preovulatory follicles.
Endocrinology    February 2, 1999   Volume 140, Issue 2 667-674 doi: 10.1210/endo.140.2.6499
Kerban A, Boerboom D, Sirois J.The time- and gonadotropin-dependent regulation of steroidogenic acute regulatory protein (StAR) has not been characterized in vivo in preovulatory follicles of large monoovulatory species or sexually mature animals. The objectives of this study were to clone equine StAR and describe the regulation of its messenger RNA (mRNA) in equine follicles after the administration of an ovulatory dose of hCG. The screening of an equine follicle complementary DNA (cDNA) library with a mouse StAR cDNA probe revealed two forms of equine StAR that differ only in the length of their 3'-untranslated region (3'...
Morphology of the oocyte-follicular connection in the mare.
Anatomy and embryology    January 30, 1999   Volume 199, Issue 1 21-28 doi: 10.1007/s004290050205
Brück I, Greve T, Hyttel P.The present study characterised the oocyte-follicular connection (i.e., oocyte fixation site) in Graafian follicles of the mare morphologically. Antral follicles were dissected in toto from ovaries obtained from oestrous, dioestrous and transitional mares after slaughter. The location of the cumulus oophorus complex in relation to the ovulation fossa, the width and density of the blood vessels surrounding the cumulus oophorus complex, the relative dimensions and histological aspects of the cumulus oophorus were investigated. For ultrastructural analysis of the junctional regions, cumulus-oocyt...
Gonadotrophin profiles and dioestrous pulsatile release patterns in mares as determined by collection of jugular blood at 4 h intervals throughout an oestrous cycle.
Journal of reproduction and fertility    December 23, 1998   Volume 113, Issue 2 315-322 doi: 10.1530/jrf.0.1130315
Irvine CH, Turner JE, Alexander SL, Shand N, van Noordt S.In mares, dioestrous FSH profiles based on once-a-day sampling are variable; however, the pulsatility of plasma FSH, which has been suggested by limited windows of intensive sampling, may contribute to this variability. Jugular blood from six mares was sampled at 4 h intervals throughout an ovulatory cycle to determine cyclic FSH and LH patterns more accurately and to measure gonadotrophin pulse frequency during dioestrus. Synchronous pulses of FSH and LH occurred regularly in all mares between day 4 and day 12 (ovulation = day 0) with a mean (+/- SEM) frequency of 1.9 +/- 0.1 (FSH) or 1.6 +/-...
Endometrial oxytocin receptor and uterine prostaglandin secretion in mares during the oestrous cycle and early pregnancy.
Journal of reproduction and fertility    December 23, 1998   Volume 113, Issue 2 173-179 doi: 10.1530/jrf.0.1130173
Starbuck GR, Stout TA, Lamming GE, Allen WR, Flint AP.Circulating concentrations of 13,14-dihydro-15-ketoprostaglandin F2 alpha (PGFM) were measured before and after administration of oxytocin and after endometrial biopsy, with or without uterine flushing performed per vaginam, on days 10, 14 and 18 after ovulation in nine pregnant and nine cyclic mares. Concentrations of oxytocin receptor were measured in endometrial biopsy samples. Neither pregnancy status nor time after ovulation affected basal PGFM concentrations. PGFM concentrations were increased after oxytocin administration on each of the days studied in cyclic mares; on day 14 the mean r...
The effect of dietary protein on reproduction in the mare. V. Endocrine changes and conception during the early post partum period.
Journal of the South African Veterinary Association    December 16, 1998   Volume 69, Issue 3 81-88 doi: 10.4102/jsava.v69i3.822
van Niekerk FE, van Niekerk CH.Pregnant Anglo-Arab and Thoroughbred mares (n = 24) were divided randomly according to age and breed into 4 groups of 6 mares each from approximately 6 weeks before their expected foaling date. Diets received by the 4 groups varied in essential amino-acid and total protein contents. Serum progestagen, FSH and LH concentrations were determined from the day of parturition until foal heat and during the 1st oestrous cycle following foal heat. Serum progestagen, FSH and LH concentrations did not differ between the treatment groups. Progestagen concentrations were high (mean = 7.0: 5.2-16.4 ng/ml) ...
Inhibin secretion in the mare: localization of inhibin alpha, betaA, and betaB subunits in the ovary.
Biology of reproduction    November 26, 1998   Volume 59, Issue 6 1392-1398 doi: 10.1095/biolreprod59.6.1392
Nagamine N, Nambo Y, Nagata S, Nagaoka K, Tsunoda N, Taniyama H, Tanaka Y, Tohei A, Watanabe G, Taya K.To determine the source of circulating inhibin and estradiol-17beta during the estrous cycle in mares, the cellular localization of the inhibin alpha, betaA, and betaB subunits and aromatase in the ovary was determined by immunohistochemistry. Concentrations of immunoreactive (ir-) inhibin, estradiol-17beta, progesterone, LH, and FSH in peripheral blood were also measured during the estrous cycle in mares. Immunohistochemically, inhibin alpha subunits were localized in the granulosa cells of small and large follicles and in the theca interna cells of large follicles, whereas inhibin betaA and ...
Gonadotropin response to naloxone in the mare: effect of time of year and reproductive status.
Biology of reproduction    October 22, 1998   Volume 59, Issue 5 1195-1199 doi: 10.1095/biolreprod59.5.1195
Davison LA, McManus CJ, Fitzgerald BP.In the mare, endogenous opioids have been implicated in the suppression of gonadotropin secretion during seasonal anestrus (AN). The present study tested whether continuation of reproductive activity during the nonbreeding season (NBS) reflects the absence of a seasonal shift in opioid tone compared to what occurs in AN mares. During the NBS, 11 AN and 8 luteal-phase mares received 0.1, 0.05, 0. 025 mg/kg naloxone (NAL) or vehicle on alternate days. Whereas cycling mares responded to all dosages of NAL, AN mares responded only to the higher dosages for FSH, and LH failed to increase at any dos...
Ultrasonic evaluation for the time of ovulation in ewes treated with norgestomet and norgestomet followed by pregnant mare’s serum gonadotropin.
Journal of animal science    October 22, 1998   Volume 76, Issue 9 2235-2238 doi: 10.2527/1998.7692235x
Cardwell BE, Fitch GQ, Geisert RD.Progestogens and follicular stimulants have proved reasonably successful for estrus synchronization, but time of ovulation relative to removal of the progestogen is not clearly established. We monitored time of ovulation in ewes following synchronized estrus. Ovaries of 40 Dorset and Rambouillet x Dorset ewes were evaluated during the spring and fall (20/replicate). Ewes were randomly assigned to one of two treatment groups (n = 20/group): implant-only (I) ewes received a norgestomet implant for 10 d; and implant + PMSG (PI) ewes received a norgestomet implant for 10 d with an i.m. injection o...
Controlled-release products for the control of the estrus cycle in cattle, sheep, goats, deer, pigs, and horses.
Critical reviews in therapeutic drug carrier systems    September 15, 1998   Volume 15, Issue 4 285-379 
Rathbone MJ, Macmillan KL, Jöchle W, Boland MP, Inskeep EK.This paper describes the estrus cycles of a number of livestock breeds and reviews the controlled-release drug delivery systems that are currently available for the purpose of controlled breeding. The bovine estrus cycle is reviewed in detail, and the estrus cycles of other species are described in a manner that highlights similarities and differences between species. Pertinent formulation and pharmacokinetic information about current drug delivery systems is presented and discussed, and recent advances in this area are also described.
Oocyte competence for in vitro maturation is associated with histone H1 kinase activity and is influenced by estrous cycle stage in the mare.
Biology of reproduction    August 1, 1998   Volume 59, Issue 2 456-462 doi: 10.1095/biolreprod59.2.456
Goudet G, Bézard J, Belin F, Duchamp G, Palmer E, Gérard N.The in vitro maturation rate of equine oocytes remains low, regardless of culture conditions. Our objective was to determine the reasons for failure of equine oocytes to resume meiosis during in vitro maturation and to ascertain the influence of the estrous cycle stage on meiotic competence. In 10 cyclic mares, 7 ultrasound-guided follicular punctures were performed alternately during the follicular phase (group DF; n = 3 punctures), at the end of the follicular phase (group EF; n = 2), and during the luteal phase (group DL; n = 2). We evaluated the competence of the oocytes for in vitro matur...
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