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Luteolysis: A Neuroendocrine-Mediated Event
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inferredcites →https://doi.org/10.1002/(sici)1098-2795(199705)47:1<11::aid-mrd2>3.0.co;2-topenalex-snapshot
Involvement of fas antigen in ovarian follicular atresia and luteolysis
inferredcites →https://doi.org/10.1002/9780470718988.ch6openalex-snapshot
The Corpus Luteum of the Guinea Pig
inferredcites →https://doi.org/10.1002/aja.1001540304openalex-snapshot
The corpus luteum of the guinea pig. IV. Fine structure of macrophages during pregnancy and postpartum luteolysis, and the phagocytosis of luteal cells
inferredcites →https://doi.org/10.1002/cber.19340670729openalex-snapshot
Reindarstellung der Hormone aus dem Corpus luteum. (Vorläuf. Mitteil.)
inferredcites →https://doi.org/10.1002/cber.19340670831openalex-snapshot
Zur Isolierung und Charakterisierung des Corpus‐luteum‐Hormons
inferredcites →https://doi.org/10.1002/hlca.193401701111openalex-snapshot
Ein krystallisiertes Hormon aus Corpus luteum. (Vorläufige Mitteilung)
inferredcites →https://doi.org/10.1002/j.1460-2075.1984.tb02139.xopenalex-snapshot
The gene for the hypothalamic peptide hormone oxytocin is highly expressed in the bovine corpus luteum: biosynthesis, structure and sequence analysis.
inferredcites →https://doi.org/10.1006/bbrc.1993.1451openalex-snapshot
Adrenomedullin: A Novel Hypotensive Peptide Isolated from Human Pheochromocytoma
inferredcites →https://doi.org/10.1006/bbrc.1995.2513openalex-snapshot
Molecular Cloning and in Vivo Expression of the Bovine Steroidogenic Acute Regulatory Protein
inferredcites →https://doi.org/10.1007/978-1-4615-9513-7_14openalex-snapshot
Regulation of the Primate Corpus Luteum During Early Pregnancy
inferredcites →https://doi.org/10.1007/978-1-4684-3474-3_65openalex-snapshot
Prostaglandin F2α and Its 13-Dehydro Analogs: Comparative Luteolytic Effects in Vivo
inferredcites →https://doi.org/10.1007/978-1-4684-3474-3_70openalex-snapshot
Demonstration of Luteal Cell Membrane Receptors for Prostaglandin F2α by Ultrastructural and Binding Analysis
inferredcites →https://doi.org/10.1007/978-1-59259-829-8_7openalex-snapshot
Prostaglandins and Leukotrienes
inferredcites →https://doi.org/10.1007/978-3-642-70414-7_5openalex-snapshot
Oxytocin as an Ovarian Hormone
inferredcites →https://doi.org/10.1007/bf00218935openalex-snapshot
Qualitative and quantitative studies on the innervation of the corpus luteum of rat and pig
inferredcites →https://doi.org/10.1007/bf00221861openalex-snapshot
Ultrastructural localisation of oxytocin and neurophysin in the ovine corpus luteum
inferredcites →https://doi.org/10.1007/bf01780004openalex-snapshot
Die Reindarstellung der Hormone aus dem Corpus Luteum
inferredcites →https://doi.org/10.1007/bf02157946openalex-snapshot
The blood flow of the cerebral cortex determined by radioactive krypton85
inferredcites →https://doi.org/10.1007/bf03000210openalex-snapshot
Identification of functional high and low affinity states of the prostaglandin F2 alpha receptor in the ovine corpus luteumin vivo and their role in hormone pulsatility
inferredcites →https://doi.org/10.1016/0002-9378(71)90221-3openalex-snapshot
Human luteal function following hysterectomy as assessed by plasma progestin
inferredcites →https://doi.org/10.1016/0002-9378(72)90616-3openalex-snapshot
The effect of prostaglandin F2α infusion on corpus luteum function
inferredcites →https://doi.org/10.1016/0002-9378(73)90042-2openalex-snapshot
Redistribution of blood flow by prostaglandin F2α in the rabbit ovary
inferredcites →https://doi.org/10.1016/0002-9378(73)90044-6openalex-snapshot
Plasma gonadotropin and ovarian steroid levels in uterovaginal atresia
inferredcites →https://doi.org/10.1016/0002-9378(75)90927-8openalex-snapshot
Levels of prostaglandins F2α and E2 in human endometrium during the menstrual cycle
inferredcites →https://doi.org/10.1016/0002-9378(78)90320-4openalex-snapshot
Endogenous levels of prostaglandin F2α and its main metabolites in plasma and endometrium of normal and dysmenorrheic women
inferredcites →https://doi.org/10.1016/0002-9378(86)90450-3openalex-snapshot
Human ovarian oxytocin: Its source and relationship to steroid hormones
inferredcites →https://doi.org/10.1016/0002-9378(88)90089-0openalex-snapshot
Baboon corpus luteum oxytocin: An intragonadal peptide modulator of luteal function
inferredcites →https://doi.org/10.1016/0002-9378(90)90781-2openalex-snapshot
Oxytocin and vasopressin binding sites in human and bovine ovaries
inferredcites →https://doi.org/10.1016/0002-9378(91)90399-copenalex-snapshot
Oxytocin secretion and human parturition: Pulse frequency and duration increase during spontaneous labor in women
inferredcites →https://doi.org/10.1016/0005-2760(68)90168-9openalex-snapshot
Phospholipid precursors of prostaglandins
inferredcites →https://doi.org/10.1016/0005-2760(76)90224-1openalex-snapshot
Biosynthesis of prostaglandin F2α from arachidonic acid and prostaglandin endoperoxides in the uterus
inferredcites →https://doi.org/10.1016/0005-2760(82)90316-2openalex-snapshot
Species differences in circulating prostaglandin metabolites relevance for the assay of prostaglandin release
inferredcites →https://doi.org/10.1016/0005-2760(94)90186-4openalex-snapshot
Phosphatidylcholine breakdown and signal transduction
inferredcites →https://doi.org/10.1016/0006-291x(76)90337-5openalex-snapshot
Abrogation by prostaglandin F2α of LH-stimulated cyclic AMP accumulation in isolated rat corpora lutea of pregnancy
inferredcites →https://doi.org/10.1016/0006-8993(79)90398-6openalex-snapshot
Cytoplasmic progestin-receptors in guinea pig brain: Characteristics and relationship to the induction of sexual behavior
inferredcites →https://doi.org/10.1016/0006-8993(85)90481-0openalex-snapshot
Estrogen excites oxytocinergic, but not vasopressinergic cells in the paraventricular nucleus of female rat hypothalamus
inferredcites →https://doi.org/10.1016/0014-5793(85)81296-5openalex-snapshot
Ovulation triggers oxytocin gene expression in the bovine ovary
inferredcites →https://doi.org/10.1016/0014-5793(87)81295-4openalex-snapshot
Expression of the oxytocin gene in the large cells of the bovine corpus luteum
inferredcites →https://doi.org/10.1016/0014-5793(94)01198-2openalex-snapshot
Cloning of the rat and human prostaglandin F2α receptors and the expression of the rat prostaglandin F2α receptor
inferredcites →https://doi.org/10.1016/0016-6480(91)90149-zopenalex-snapshot
Prostaglandin-induced secretion of oxytocin and prolactin in red (Cervus elaphus) and Pere David's (Elaphurus davidianus) deer hinds: Evidence for oxytocin of luteal origin
inferredcites →https://doi.org/10.1016/0022-4731(75)90354-4openalex-snapshot
Hormonal and related factors affecting the release of prostaglandin F2α from the uterus
inferredcites →https://doi.org/10.1016/0022-4731(85)90272-9openalex-snapshot
Rapid recovery of nuclear estrogen receptor and oxytocin receptor in the ovine uterus following progesterone withdrawal
inferredcites →https://doi.org/10.1016/0022-4731(87)90190-7openalex-snapshot
Endometrial phospholipase A2 enzymes and their regulation by steroid hormones
inferredcites →https://doi.org/10.1016/0022-4731(87)91039-9openalex-snapshot
Cooxidation of steroidal and non-steroidal estrogens by purified prostaglandin synthase results in a stimulation of prostaglandin formation
inferredcites →https://doi.org/10.1016/0022-4731(89)90266-5openalex-snapshot
Inhibitory effects of the antiprogestin, RU 486, on progesterone actions and luteinizing hormone secretion in pituitary gonadotrophs
inferredcites →https://doi.org/10.1016/0024-3205(71)90213-xopenalex-snapshot
Levels of prostaglandin F2α in the uterine venous blood of sheep during the oestrous cycle
inferredcites →https://doi.org/10.1016/0039-128x(75)90076-8openalex-snapshot
Radioimmunoassay of progesterone, 17-hydroxyprogesterone, estradiol-17β and prostaglandin F in human corpus luteum
inferredcites →https://doi.org/10.1016/0039-128x(84)90047-3openalex-snapshot
The structure of steroids and their diffusion through blood vessel walls in a counter-current system
inferredcites →https://doi.org/10.1016/0090-6980(72)90006-8openalex-snapshot
The effects of exogenous progesterone and estradiol on prostaglandin F levels in ovariectomized ewes
inferredcites →https://doi.org/10.1016/0090-6980(72)90017-2openalex-snapshot
Prostaglandin F2α in the uterus of ewes during early pregnancy
inferredcites →https://doi.org/10.1016/0090-6980(72)90073-1openalex-snapshot
Luteinizing hormone stimulation of ovarian prostaglandin biosynthesis
inferredcites →https://doi.org/10.1016/0090-6980(73)90039-7openalex-snapshot
Induction of premature parturition in goats by prostaglandin F2α administered into the uterine vein
inferredcites →https://doi.org/10.1016/0090-6980(73)90052-xopenalex-snapshot
Steroids in the ovarian venous plasma and F prostaglandins in the peripheral plasma during pseudopregnancy and days 1–9 of pregnancy in the golden hamster
inferredcites →https://doi.org/10.1016/0090-6980(74)90001-xopenalex-snapshot
Prostaglandin F production by granulosa cells from rabbit pre-ovulatory follicles
inferredcites →https://doi.org/10.1016/0090-6980(74)90021-5openalex-snapshot
Effect of oestradiol — 17β and oxytocin treatment on prostaglandin F alpha release in the anoestrous ewe
inferredcites →https://doi.org/10.1016/0090-6980(75)90032-5openalex-snapshot
The synthesis of prostaglandin F by human endometrium in organ culture
inferredcites →https://doi.org/10.1016/0090-6980(75)90051-9openalex-snapshot
Prostaglandin E1 and F2α specific binding in bovine corpora lutea: Comparison with luteolytic effects
inferredcites →https://doi.org/10.1016/0090-6980(75)90102-1openalex-snapshot
Luteolysis induced in pigtail monkeys (Macaca nemestrina) with prostaglandin F2α, ICI 80996 and ICI 81008
inferredcites →https://doi.org/10.1016/0090-6980(75)90114-8openalex-snapshot
A biochemical hypothesis to explain the mechanism of luteal regression
inferredcites →https://doi.org/10.1016/0090-6980(75)90150-1openalex-snapshot
Assessment of possible luteolytic effect of intra-ovarian injection of prostaglandin F2α in the human
inferredcites →https://doi.org/10.1016/0090-6980(76)90035-6openalex-snapshot
Jugular levels of 13,14-dihydro-15-keto-prostaglandin F and progesterone around luteolysis and early pregnancy in the ewe
inferredcites →https://doi.org/10.1016/0090-6980(76)90073-3openalex-snapshot
A study of prostaglandin F2α as the luteolysin in swine: I. Effect of prostaglandin F2α in hysterectomized gilts
inferredcites →https://doi.org/10.1016/0090-6980(76)90074-5openalex-snapshot
Estrogen-induced luteolysis in the rhesus monkey: Reversal with indomethacin
inferredcites →https://doi.org/10.1016/0090-6980(76)90148-9openalex-snapshot
Concentration of prostaglandins F in uterine venous plasma of anesthetized mares during the estrous cycle and early pregnancy
inferredcites →https://doi.org/10.1016/0090-6980(77)90015-6openalex-snapshot
The anatomical basis for a possible counter current exchange mechanism in the human adnex
inferredcites →https://doi.org/10.1016/0090-6980(77)90032-6openalex-snapshot
Prostaglandin F2α specific binding in equine corpora lutea
inferredcites →https://doi.org/10.1016/0090-6980(77)90185-xopenalex-snapshot
Theory of maternal recognition of pregnancy in swine based on estrogen controlled endocrine versus exocrine secretion of prostaglandin F2α by the uterine endometrium
inferredcites →https://doi.org/10.1016/0090-6980(77)90268-4openalex-snapshot
A study of prostaglandin F2α as the luteolysin in swine: II characterization and comparison of prostaglandin F, estrogens and progestin concentrations in utero-ovarian vein plasma of nonpregnant and pregnant gilts
inferredcites →https://doi.org/10.1016/0090-6980(79)90012-1openalex-snapshot
Cyclic AMP formation of isolated human corpora lutea in response to HCG — Interference by PGF2α
inferredcites →https://doi.org/10.1016/0090-6980(79)90059-5openalex-snapshot
Prostaglandins F in uterine and ovarian compartments and in plasma from the uterine vein, ovarian artery and vein, and abdominal aorta of pseudopregnant rats with and without deciduomata
inferredcites →https://doi.org/10.1016/0090-6980(79)90101-1openalex-snapshot
Differential production of prostaglandins within the human uterus
inferredcites →https://doi.org/10.1016/0090-6980(80)90007-6openalex-snapshot
Lipid metabolism and production of progesterone and prostaglandin F during induced regression of porcine corpora lutea
inferredcites →https://doi.org/10.1016/0090-6980(80)90137-9openalex-snapshot
A study of prostaglandin F2α as the luteolysin in swine: V comparison of prostaglandin F, progestins, estrone and estradiol in uterine flushings from pregnant and nonpregnant gilts
inferredcites →https://doi.org/10.1016/0090-6980(81)90163-5openalex-snapshot
Effect of chronic ipsilateral or contralateral intra-uterine infusion of prostaglandin E1 (PGE1) on luteal function of unilaterally ovariectomized ewes
inferredcites →https://doi.org/10.1016/0090-6980(82)90158-7openalex-snapshot
Peripheral plasma concentrations of 13,14-dihydro-15-keto-prostaglandin F2α and progesterone around luteolysis and during early pregnancy in the goat
inferredcites →https://doi.org/10.1016/0090-6980(82)90179-4openalex-snapshot
Embryonic suppression of oxytocin — associated neurophysin release in early pregnant sheep
inferredcites →https://doi.org/10.1016/0090-6980(83)90010-2openalex-snapshot
Metabolism of arachidonic acid by porcine blastocysts and endometrium
inferredcites →https://doi.org/10.1016/0090-6980(83)90074-6openalex-snapshot
Uptake of [3H]-arachidonic acid by human endometrium. Differences between normal and menorrhagic tissue
inferredcites →https://doi.org/10.1016/0090-6980(83)90171-5openalex-snapshot
Corpus luteum regression induced by ultra-low pulses of prostaglandin F2α
inferredcites →https://doi.org/10.1016/0090-6980(84)90080-7openalex-snapshot
An intra-corpus luteum site for the luteolytic action of prostaglandin F2α in the rhesus monkey
inferredcites →https://doi.org/10.1016/0090-6980(87)90097-9openalex-snapshot
Effects of oestradiol, progesterone, hydrocortisone and oxytocin on prostaglandin output from the guinea-pig endometrium maintained in tissue culture
inferredcites →https://doi.org/10.1016/0090-6980(87)90250-4openalex-snapshot
Stimulatory and inhibitory effects of prostaglandins on the gonadotropin-sensitive adenylate cyclase in the monkey corpus luteum
inferredcites →https://doi.org/10.1016/0090-6980(88)90017-2openalex-snapshot
Production of leukotriene B4 by luteal tissues of sheeo treated with prostaglandin F2α
inferredcites →https://doi.org/10.1016/0090-6980(88)90126-8openalex-snapshot
Prostaglandin secretion by perifused porcine endometrium: Further evidence for an endocrine versus exocrine secretion of prostaglandins
inferredcites →https://doi.org/10.1016/0090-6980(88)90276-6openalex-snapshot
Prostaglandin E2 opunteracts the effects of PGF2α in indomethacin treated cycling gilts
inferredcites →https://doi.org/10.1016/0090-6980(90)90027-sopenalex-snapshot
Progesterone induces expression of endometrial messenger RNA encoding for cyclooxygenase (sheep)
inferredcites →https://doi.org/10.1016/0090-6980(92)90084-7openalex-snapshot
desensitization of a high affinity PGF2α receptor in the ovine corpus luteum
inferredcites →https://doi.org/10.1016/0090-6980(93)90039-aopenalex-snapshot
Differential induction of c-jun expression by PGF2-alpha in rat ovary, uterus and adrenal
inferredcites →https://doi.org/10.1016/0090-6980(93)90079-mopenalex-snapshot
Localization of stress protein-70 in ovine corpora lutea during prostaglandin-induced luteolysis
inferredcites →https://doi.org/10.1016/0090-6980(94)90075-2openalex-snapshot
Luteal maintenance during early pregnancy in the pig: Role for prostaglandin E2
inferredcites →https://doi.org/10.1016/0090-6980(94)90094-9openalex-snapshot
Cloning and expression of a cDNA for rat prostaglandin F2α receptor
inferredcites →https://doi.org/10.1016/0090-6980(96)00019-6openalex-snapshot
PLD activation in Chinese hamster ovary (CHO) cells transfected with PGF2α receptor cDNA
inferredcites →https://doi.org/10.1016/0092-8674(92)90123-topenalex-snapshot
Induction of apoptosis in fibroblasts by c-myc protein
inferredcites →https://doi.org/10.1016/0093-691x(82)90176-5openalex-snapshot
Hormonal responses following treatment with different prostaglandin analogues for estrous cycle regulation in cattle
inferredcites →https://doi.org/10.1016/0093-691x(84)90460-6openalex-snapshot
Characterization of intrauterine mobility of the early equine conceptus
inferredcites →https://doi.org/10.1016/0093-691x(96)00099-4openalex-snapshot
Morphological characteristics of the bovine corpus luteum during the estrous cycle and pregnancy
inferredcites →https://doi.org/10.1016/0093-691x(96)00100-8openalex-snapshot
Luteotropic and luteolytic mechanisms in the bovine corpus luteum
inferredcites →https://doi.org/10.1016/0093-691x(96)00101-xopenalex-snapshot
Mechanisms of hormone and growth factor action in the bovine corpus luteum
inferredcites →https://doi.org/10.1016/0093-691x(96)00102-1openalex-snapshot
Intercellular communication in the bovine corpus luteum
inferredcites →https://doi.org/10.1016/0161-4630(81)90071-9openalex-snapshot
Effect of chronic ipsilateral or contralateral intrauterine infusion of prostaglandin E2 (PGE2) on luteal function of unilaterally ovariectomized ewes
inferredcites →https://doi.org/10.1016/0167-5699(90)90035-8openalex-snapshot
Human monocyte chemoattractant protein-1 (MCP-1)
inferredcites →https://doi.org/10.1016/0262-1746(82)90022-1openalex-snapshot
Control of endometrial prostaglandin output during the estrous cycle of the guinea-pig : influence of estradiol 17-β, progesterone, oxytocin and calcium ionophore A23187
inferredcites →https://doi.org/10.1016/0262-1746(86)90212-xopenalex-snapshot
Metabolism of arachidonic acid and synthesis of prostanoids in human endometrium and decidua
inferredcites →https://doi.org/10.1016/0303-7207(79)90073-xopenalex-snapshot
Specific binding of prostaglandin F2α to membranes of rat corpora lutea
inferredcites →https://doi.org/10.1016/0303-7207(89)90179-2openalex-snapshot
Effects of human chorionic gonadotropin, prostaglandin F2α and protein kinase C activators on the cyclic AMP and inositol phosphate second messenger systems in cultured human granulosa-luteal cells
inferredcites →https://doi.org/10.1016/0303-7207(90)90210-yopenalex-snapshot
Cell-specific regulation of progesterone receptor in the female reproductive system
inferredcites →https://doi.org/10.1016/0303-7207(91)90206-8openalex-snapshot
Analyses of ovine corpora lutea for tumor necrosis factor mRNA and bioactivity during prostaglandin-induced luteolysis
inferredcites →https://doi.org/10.1016/0303-7207(93)90205-xopenalex-snapshot
Steroidogenic enzyme activity after acute activation of protein kinase (PK) A and PKC in ovine small and large luteal cells
inferredcites →https://doi.org/10.1016/0303-7207(93)90213-4openalex-snapshot
Mode of action of prostaglandin F2α in human luteinized granulosa cells: role of protein kinase C
inferredcites →https://doi.org/10.1016/0303-7207(94)90158-9openalex-snapshot
Cellular mechanisms of luteolysis
inferredcites →https://doi.org/10.1016/0304-3940(93)90515-mopenalex-snapshot
Central inhibition of nitric oxide synthase preferentially augments release of oxytocin during dehydration
inferredcites →https://doi.org/10.1016/0304-3940(95)12204-4openalex-snapshot
Adrenomedullin-immunoreactive neurons in the paraventricular and supraoptic nuclei of the rat
inferredcites →https://doi.org/10.1016/0378-4320(84)90026-5openalex-snapshot
Prostaglandin production by the uterus of the non-pregnant and early pregnant guinea-pig
inferredcites →https://doi.org/10.1016/0378-4320(84)90027-7openalex-snapshot
Hormone receptor control of pulsatile secretion of PGF2α from the ovine uterus during luteolysis and its abrogation in early pregnancy
inferredcites →https://doi.org/10.1016/0378-4320(84)90030-7openalex-snapshot
Ovarian oxytocin and luteal function in the early pregnant sheep
inferredcites →https://doi.org/10.1016/0378-4320(84)90032-0openalex-snapshot
Levels of prostaglandin F2α metabolites in blood and urine during early pregnancy
inferredcites →https://doi.org/10.1016/0378-4320(84)90033-2openalex-snapshot
Prostaglandin dynamics associated with development of the bovine conceptus
inferredcites →https://doi.org/10.1016/0378-4320(84)90040-xopenalex-snapshot
Hormonal control of early pregnancy in the mare
inferredcites →https://doi.org/10.1016/0378-4320(90)90070-vopenalex-snapshot
Oxytocin plasma levels during spontaneous and cloprostenol-induced luteolysis in sows
inferredcites →https://doi.org/10.1016/0378-4320(92)90096-vopenalex-snapshot
Luteotrophic control of the corpus luteum
inferredcites →https://doi.org/10.1016/0378-4320(92)90097-wopenalex-snapshot
Functional aspects of differentiation and degeneration of the steroidogenic cells of the corpus luteum in domestic ruminants
inferredcites →https://doi.org/10.1016/0739-7240(86)90023-8openalex-snapshot
Effects of pituitary stalk-transection and type of barrier on pituitary and luteal function during the estrous cycle of the ewe
inferredcites →https://doi.org/10.1016/0739-7240(90)90018-uopenalex-snapshot
Luteal oxytocin: characteristics and control of synchronous episodes of oxytocin and PGF2α secretion at luteolysis in ruminants
inferredcites →https://doi.org/10.1016/0739-7240(90)90029-yopenalex-snapshot
Nuclear changes in ovine luteal cells in response to PGF2α
inferredcites →https://doi.org/10.1016/0739-7240(91)90012-9openalex-snapshot
Bovine corpus luteum function after removal of granulosa cells from the preovulatory follicle
inferredcites →https://doi.org/10.1016/0739-7240(95)00065-8openalex-snapshot
Ontogenies of messenger RNA encoding tissue inhibitor of metalloproteinases 1 and 2 within bovine periovulatory follicles and luteal tissue
inferredcites →https://doi.org/10.1016/0922-4106(93)90022-2openalex-snapshot
Photoaffinity labelling and radiation inactivation of the leukotriene B4 receptor in human myeloid cells
inferredcites →https://doi.org/10.1016/0952-3278(95)90115-9openalex-snapshot
The control of prostaglandin production by the endometrium in relation to luteolysis and menstruation
inferredcites →https://doi.org/10.1016/0955-0674(95)80116-2openalex-snapshot
Proteolytic remodeling of extracellular matrix
inferredcites →https://doi.org/10.1016/1043-2760(94)00214-oopenalex-snapshot
Receptors for sex steroids in the primate corpus luteum
inferredcites →https://doi.org/10.1016/b978-0-12-571125-8.50005-3openalex-snapshot
Comparative Aspects of Uterine-Luteal Relationships
inferredcites →https://doi.org/10.1016/b978-0-12-571126-5.50006-6openalex-snapshot
Mechanisms Regulating the Menstrual Cycle in Women
inferredcites →https://doi.org/10.1016/b978-0-12-571127-2.50038-9openalex-snapshot
Factors Affecting the Secretion of Steroids from the Transplanted Ovary in the Sheep
inferredcites →https://doi.org/10.1016/b978-0-12-571130-2.50009-2openalex-snapshot
The Lysosome as a Mediator of Hormone Action
inferredcites →https://doi.org/10.1016/b978-0-12-571137-1.50009-8openalex-snapshot
The Regulation of the Mammalian Corpus Luteum
inferredcites →https://doi.org/10.1016/b978-0-12-571141-8.50005-6openalex-snapshot
Trophic Stimulation of Steroidogenesis: In Search of the Elusive Trigger
inferredcites →https://doi.org/10.1016/b978-0-12-804169-7.00008-8openalex-snapshot
The Posterior Pituitary
inferredcites →https://doi.org/10.1016/s0003-9861(74)80025-1openalex-snapshot
Purification and characterization of porcine relaxin
inferredcites →https://doi.org/10.1016/s0006-291x(75)80080-5openalex-snapshot
Uterine receptor for oxytocin: Effects of estrogen
inferredcites →https://doi.org/10.1016/s0015-0282(16)39132-4openalex-snapshot
Effects of Prostaglandin F2 on Pseudopregnancy and Pregnancy in Mice
inferredcites →https://doi.org/10.1016/s0015-0282(16)41843-1openalex-snapshot
Effects of Indomethacin on Corpus Luteum Function and Pregnancy in Rhesus Monkeys
inferredcites →https://doi.org/10.1016/s0015-0282(16)54719-0openalex-snapshot
Local luteolytic effect of prostaglandin F2 in the human corpus luteum
inferredcites →https://doi.org/10.1016/s0015-0282(16)59050-5openalex-snapshot
Antigonadotropic effect of oxytocin on the isolated human corpus luteum
inferredcites →https://doi.org/10.1016/s0021-9258(17)41942-9openalex-snapshot
Molecular cloning and expression of a cDNA of the bovine prostaglandin F2 alpha receptor.
inferredcites →https://doi.org/10.1016/s0021-9258(17)42265-4openalex-snapshot
Cloning and expression of a cDNA for mouse prostaglandin F receptor.
inferredcites →https://doi.org/10.1016/s0021-9258(18)46930-xopenalex-snapshot
The purification, cloning, and expression of a novel luteinizing hormone-induced mitochondrial protein in MA-10 mouse Leydig tumor cells. Characterization of the steroidogenic acute regulatory protein (StAR).
inferredcites →https://doi.org/10.1016/s0021-9258(19)43455-8openalex-snapshot
Mechanisms Regulating the Concentration and the Conformation of Progesterone Receptor(s) in the Uterus
inferredcites →https://doi.org/10.1016/s0026-895x(25)15378-9openalex-snapshot
Prostaglandin Receptors in NIH 3T3 Cells: Coupling of One Receptor to Adenylate Cyclase and of a Second Receptor to Phospholipase C
inferredcites →https://doi.org/10.1016/s0034-5288(18)32000-9openalex-snapshot
Delayed luteolysis and suppression of the pulsatile release of oxytocin after indomethacin treatment in the goat
inferredcites →https://doi.org/10.1016/s0039-128x(75)90186-5openalex-snapshot
Plasma estrogens, progesterone and chorionic gonadotropin in pregnant rhesus monkeys (Macaca mulatta) after ovariectomy
inferredcites →https://doi.org/10.1016/s0039-128x(80)80006-7openalex-snapshot
Progesterone production by luteal cells isolated from cynomolgus monkeys: Effects of gonadotropin and prolactin during acute incubation and cell culture
inferredcites →https://doi.org/10.1016/s0074-7696(08)62312-8openalex-snapshot
Cell Death: The Significance of Apoptosis
inferredcites →https://doi.org/10.1016/s0090-6980(72)80002-9openalex-snapshot
Prostaglandin F2α: Its effect on the corpus luteum of the menstrual cycle
inferredcites →https://doi.org/10.1016/s0090-6980(72)80003-0openalex-snapshot
Plasma progesterone levels during infusion of prostaglandin F2α in the human
inferredcites →https://doi.org/10.1016/s0090-6980(74)80026-2openalex-snapshot
Prostaglandin F in monkey uterine fluid during the menstrual cycle and following steroid treatment
inferredcites →https://doi.org/10.1016/s0090-6980(74)80027-4openalex-snapshot
Prostaglandin F concentrations in the utero-ovarian venous plasma of the sow during the late luteal phase of the oestrous cycle
inferredcites →https://doi.org/10.1016/s0090-6980(74)80052-3openalex-snapshot
Effects of sequential treatment with estradiol and PGF2α on the length of the primate menstrual cycle
inferredcites →https://doi.org/10.1016/s0090-6980(74)80063-8openalex-snapshot
Prostaglandin receptors in the bovine corpus luteum cell membranes
inferredcites →https://doi.org/10.1016/s0090-6980(75)80016-5openalex-snapshot
Prostaglandin F2α induces release of lysosomal hydrolase from luteinized rat ovarian slices
inferredcites →https://doi.org/10.1016/s0090-6980(76)80008-1openalex-snapshot
Rapid block of gonadotropin uptake by corpora lutea in vivo induced by prostaglandin F2α
inferredcites →https://doi.org/10.1016/s0090-6980(76)80009-3openalex-snapshot
Prostaglandin F and progesterone secretion by porcine endometrium and corpus luteum in vitro
inferredcites →https://doi.org/10.1016/s0090-6980(78)80013-6openalex-snapshot
A study of prostaglandin F2α as the luteolysin in swine: IV an explanation for the luteotrophic effect of estradiol
inferredcites →https://doi.org/10.1016/s0090-6980(80)80039-6openalex-snapshot
Temporal relationship between plasma concentrations of 13,14-dihydro-15-keto-prostaglandin F and neurophysin I/II around luteolysis in sheep
inferredcites →https://doi.org/10.1016/s0090-6980(82)80002-6openalex-snapshot
Phospholipase A2 activity in the rat uterus: Modulation by steroid hormones
inferredcites →https://doi.org/10.1016/s0090-6980(85)80012-5openalex-snapshot
Luteal phase variations in endogenous concentrations of prosta-glandins PGE and PGF and in the capacity for their in vitro formation in the human corpus luteum
inferredcites →https://doi.org/10.1016/s0090-6980(96)00090-1openalex-snapshot
Gap junctional intercellular communication of bovine luteal cells from several stages of the estrous cycle: Effects of prostaglandin F2α, protein kinase C and calcium
inferredcites →https://doi.org/10.1016/s0140-6736(74)90609-6openalex-snapshot
PROSTAGLANDIN-F2α RECEPTOR IN HUMAN CORPORA LUTEA
inferredcites →https://doi.org/10.1016/s0140-6736(82)90441-xopenalex-snapshot
NEUROHYPOPHYSIAL HORMONES IN THE HUMAN OVARY
inferredcites →https://doi.org/10.1016/s0262-1746(83)80006-7openalex-snapshot
Prostaglandin F2α and PGE2 in uterine lymph during the oestrous cycle in sheep
inferredcites →https://doi.org/10.1016/s0303-7207(97)00152-4openalex-snapshot
Temporal expression of urokinase type plasminogen activator, tissue type plasminogen activator, plasminogen activator inhibitor type 1 in rhesus monkey corpus luteum during the luteal maintenance and regression
inferredcites →https://doi.org/10.1016/s0303-7207(97)00166-4openalex-snapshot
Steroidogenic acute regulatory protein: The StAR still shines brightly
inferredcites →https://doi.org/10.1016/s0378-4320(96)01602-8openalex-snapshot
Effect of the rate of progesterone decline at luteolysis on the ovulatory follicles and subsequent estrous cycle length in ewes
inferredcites →https://doi.org/10.1017/cbo9780511529832.016openalex-snapshot
Neurobiological regulation of hormonal response by progestin and estrogen receptors
inferredcites →https://doi.org/10.1017/cbo9780511623493openalex-snapshot
Reproductive Physiology of Marsupials
inferredcites →https://doi.org/10.1017/cbo9781139167727.009openalex-snapshot
Oestrous and menstrual cycles
inferredcites →https://doi.org/10.1017/s0962279900000697openalex-snapshot
Corpus luteum function and regression
inferredcites →https://doi.org/10.1038/200960a0openalex-snapshot
Isolation and Identification of Two Smooth Muscle Stimulants from Menstrual Fluid
inferredcites →https://doi.org/10.1038/216868a0openalex-snapshot
Prostaglandins: Their Disappearance from and Release into the Circulation
inferredcites →https://doi.org/10.1038/223208a0openalex-snapshot
Prostaglandin Antagonists: Synthesis and Smooth Muscle Activity
inferredcites →https://doi.org/10.1038/225600a0openalex-snapshot
Inactivation of Prostaglandins by the Lungs
inferredcites →https://doi.org/10.1038/230243a0openalex-snapshot
Identification of Prostaglandin F2α in the Utero-ovarian Blood of Guinea-pig after Treatment with Oestrogen
inferredcites →https://doi.org/10.1038/230528a0openalex-snapshot
Luteolysis and Ovulation induced by Prostaglandin F2α in the Hamster
inferredcites →https://doi.org/10.1038/249176a0openalex-snapshot
The effect of prostaglandin F2α on ovarian blood flow and corpora lutea regression in the rabbit
inferredcites →https://doi.org/10.1038/297587a0openalex-snapshot
Ovarian secretion of oxytocin is stimulated by prostaglandin
inferredcites →https://doi.org/10.1038/307174a0openalex-snapshot
The establishment and maintenance of pregnancy using in vitro fertilization and embryo donation in a patient with primary ovarian failure
inferredcites →https://doi.org/10.1038/330377a0openalex-snapshot
Interferon-like sequence of ovine trophoblast protein secreted by embryonic trophectoderm
inferredcites →https://doi.org/10.1038/33169openalex-snapshot
Human CD14 mediates recognition and phagocytosis of apoptotic cells
inferredcites →https://doi.org/10.1038/33176openalex-snapshot
Inhibition of oxytocin receptor function by direct binding of progesterone
inferredcites →https://doi.org/10.1038/349617a0openalex-snapshot
Cloning and expression of cDNA for a human thromboxane A2 receptor
inferredcites →https://doi.org/10.1038/361315a0openalex-snapshot
Inositol trisphosphate and calcium signalling
inferredcites →https://doi.org/10.1038/37622openalex-snapshot
Role of cytosolic phospholipase A2 in allergic response and parturition
inferredcites →https://doi.org/10.1038/37635openalex-snapshot
Reduced fertility and postischaemic brain injury in mice deficient in cytosolic phospholipase A2
inferredcites →https://doi.org/10.1038/bjc.1972.33openalex-snapshot
Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics
inferredcites →https://doi.org/10.1038/bjc.1993.40openalex-snapshot
Apoptosis (the 1992 Frank Rose Memorial Lecture)
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4532540openalex-extracted
An Echotextural Evaluation of the Uterus Endometrium in the Early Diagnosis of Pregnancy in Awassi Sheep
inferred← citeshttps://doi.org/10.1002/ajp.22063openalex-snapshot
Contrast Imaging Ultrasound Detects Abnormalities in the Marmoset Ovary
inferred← citeshttps://doi.org/10.1002/ar.a.10182openalex-snapshot
Morphometric analysis of the uterine endometrium of swine on days 12 and 16 postestrus
inferred← citeshttps://doi.org/10.1002/jez.a.10246openalex-snapshot
Changes in localization of immune cells and cytokines in corpora lutea during luteolysis in murine ovaries
inferred← citeshttps://doi.org/10.1002/jez.a.423openalex-snapshot
Effects of tumor necrosis factor‐α on cell proliferation, prostaglandins and matrix‐metalloproteinases production in rat endometrial stromal cells cultured in vitro
inferred← citeshttps://doi.org/10.1002/jez.b.23325openalex-snapshot
Is There Conservation of Vitellogenins in a Placentotrophic Lizard?
inferred← citeshttps://doi.org/10.1002/med.20098openalex-snapshot
Novel cyclooxygenase‐catalyzed bioactive prostaglandin F2α from physiology to new principles in inflammation
inferred← citeshttps://doi.org/10.1002/mrd.10312openalex-snapshot
Soluble Fas (FasB) regulates luteal cell apoptosis during luteolysis in murine ovaries
inferred← citeshttps://doi.org/10.1002/mrd.20849openalex-snapshot
Activator protein 1‐mediated expression of monocyte chemoattractant protein 1 in cultured rat luteal cells
inferred← citeshttps://doi.org/10.1002/mrd.22150openalex-snapshot
Luteoprotective roles of luteinizing hormone are mediated by not only progesterone production but also glucocorticoid conversion in bovine corpus luteum
inferred← citeshttps://doi.org/10.1002/mrd.22332openalex-snapshot
Auto‐amplification system for prostaglandin F2α in bovine corpus luteum
inferred← citeshttps://doi.org/10.1002/mrd.22635openalex-snapshot
Cellular and molecular mechanisms involved in placental separation in the bovine: A review
inferred← citeshttps://doi.org/10.1002/mrd.22999openalex-snapshot
Changes in the expression of prostaglandin family members in bovine corpus luteum during the estrous cycle and pregnancy
inferred← citeshttps://doi.org/10.1002/mrd.23407openalex-snapshot
Heat stress on oocyte or zygote compromises embryo development, impairs interferon tau production and increases reactive oxygen species and oxidative stress in bovine embryos produced in vitro
inferred← citeshttps://doi.org/10.1002/mrd.23678openalex-snapshot
Role of intraluteal and intrauterine prostaglandin signaling in LH‐induced luteolysis in pregnant rats
inferred← citeshttps://doi.org/10.1002/tox.20735openalex-snapshot
Adverse influence of coumestrol on secretory function of bovine luteal cells in the first trimester of pregnancy
inferred← citeshttps://doi.org/10.1007/978-0-387-88186-7_17openalex-snapshot
Prostaglandins and Their Mechanisms of Action in the Cyclic Ovary
inferred← citeshttps://doi.org/10.1007/978-0-387-88186-7_26openalex-snapshot
Molecular Control of Corpus Luteum Function
inferred← citeshttps://doi.org/10.1007/978-1-59259-829-8_7openalex-snapshot
Prostaglandins and Leukotrienes
inferred← citeshttps://doi.org/10.1007/978-3-031-52133-1_75-1openalex-snapshot
The Bovine Estrous Cycle
inferred← citeshttps://doi.org/10.1007/978-3-031-61549-8_75openalex-snapshot
The Bovine Estrous Cycle
inferred← citeshttps://doi.org/10.1007/978-3-031-73079-5_2openalex-snapshot
Ultrasonographic Pregnancy Diagnosis in the Mare
inferred← citeshttps://doi.org/10.1007/978-3-319-15856-3_7openalex-snapshot
Implantation and Establishment of Pregnancy in Ruminants
inferred← citeshttps://doi.org/10.1007/978-3-319-43238-0_2openalex-snapshot
Roles of Hypoxia in Corpus Luteum Formation
inferred← citeshttps://doi.org/10.1007/978-981-19-0116-4_8openalex-snapshot
New Insights into the Mechanism of Maternal Recognition of Pregnancy in Ruminants
inferred← citeshttps://doi.org/10.1007/s004240000466openalex-snapshot
Cytoplasmic Ca2+ at low submicromolar concentration stimulates mitochondrial metabolism in rat luteal cells
inferred← citeshttps://doi.org/10.1007/s00441-007-0531-2openalex-snapshot
Immunolocalization of beclin 1, a bcl-2-binding, autophagy-related protein, in the human ovary: possible relation to life span of corpus luteum
inferred← citeshttps://doi.org/10.1007/s00580-026-03750-wopenalex-snapshot
Consequences of dichlorvos on the oestrous cycle and hormonal profile of the Wistar rat
inferred← citeshttps://doi.org/10.1007/s10059-010-0157-1openalex-snapshot
Bioactive Eicosanoids: Role of Prostaglandin F2α and F2-Isoprostanes in Inflammation and Oxidative Stress Related Pathology
inferred← citeshttps://doi.org/10.1007/s40618-023-02269-zopenalex-snapshot
Role of thyroid stimulating hormone in the maintenance and functioning of the human corpus luteum
inferred← citeshttps://doi.org/10.1016/b0-12-227235-8/00426-0openalex-snapshot
OESTRUS CYCLES | Characteristics
inferred← citeshttps://doi.org/10.1016/b978-0-08-100596-5.01039-8openalex-snapshot
Reproduction, Events and Management: Estrous Cycles: Characteristics
inferred← citeshttps://doi.org/10.1016/b978-0-12-374407-4.00449-0openalex-snapshot
Reproduction, Events and Management | Estrous Cycles: Characteristics
inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00023-5openalex-snapshot
Structure, Function, and Regulation of the Corpus Luteum
inferred← citeshttps://doi.org/10.1016/b978-0-12-800872-0.00009-3openalex-snapshot
Embryo Losses During Nutritional Treatments in Animal Models: Lessons for Humans Embryo Losses and Nutrition in Mammals
inferred← citeshttps://doi.org/10.1016/b978-0-12-803506-1.00037-1openalex-snapshot
Oxytocin and Brain Plasticity
inferred← citeshttps://doi.org/10.1016/b978-0-12-814823-5.00009-xopenalex-snapshot
Ovarian Function During Pregnancy and Lactation
inferred← citeshttps://doi.org/10.1016/b978-0-12-818766-1.00079-9openalex-snapshot
Reproduction, Events and Management: Estrous Cycles: Characteristics
inferred← citeshttps://doi.org/10.1016/b978-0-323-47912-7.00004-4openalex-snapshot
Steroid Hormones and Other Lipid Molecules Involved in Human Reproduction
inferred← citeshttps://doi.org/10.1016/b978-0-443-21477-6.00344-8openalex-snapshot
Pregnancy Recognition Signals With an Emphasis on Ruminants
inferred← citeshttps://doi.org/10.1016/b978-0-7020-7233-8.00001-xopenalex-snapshot
Reproductive Physiology of the Female
inferred← citeshttps://doi.org/10.1016/b978-012053642-9/50006-5openalex-snapshot
The Normal Human Ovary Part I: Reproductive and Endocrine Functions
inferred← citeshttps://doi.org/10.1016/b978-012444562-8/50014-8openalex-snapshot
Prostaglandin Biosynthesis and Action in the Ovary
inferred← citeshttps://doi.org/10.1016/b978-012444562-8/50020-3openalex-snapshot
Apoptosis in Ovarian Development, Function, and Failure
inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50017-8openalex-snapshot
Structure, Function, and Regulation of the Corpus Luteum
inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50063-4openalex-snapshot
OxytocinSynthesis, Secretion, and Reproductive Functions
inferred← citeshttps://doi.org/10.1016/b978-1-4160-4907-4.00006-1openalex-snapshot
Prostaglandins and Other Lipid Mediators in Reproductive Medicine
inferred← citeshttps://doi.org/10.1016/b978-1-4557-2758-2.00006-8openalex-snapshot
Prostaglandins and Other Lipid Mediators in Reproductive Medicine
inferred← citeshttps://doi.org/10.1016/bs.vh.2018.01.001openalex-snapshot
Luteolysis and the Auto-, Paracrine Role of Cytokines From Tumor Necrosis Factor α and Transforming Growth Factor β Superfamilies
inferred← citeshttps://doi.org/10.1016/j.aanat.2005.07.005openalex-snapshot
Unique expression and regulatory mechanisms of EG-VEGF/prokineticin-1 and its receptors in the corpus luteum
inferred← citeshttps://doi.org/10.1016/j.acthis.2018.02.001openalex-snapshot
Expression patterns of claudin-5 and its related signals during luteal regression in pseudopregnant rats: The enhanced effect of additional PGF treatment
inferred← citeshttps://doi.org/10.1016/j.animal.2020.100048openalex-snapshot
The effect of basic fibroblast growth factor 2 on the bovine corpus luteum depends on the stage of the estrous cycle and modulates prostaglandin F2α action
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2004.02.006openalex-snapshot
Endocrine secretion of prostaglandin F2α in cyclic gilts is decreased by intrauterine administration of exogenous oxytocin
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2004.04.014openalex-snapshot
Conceptus signals for establishment and maintenance of pregnancy
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2005.02.003openalex-snapshot
Validation of a 13,14-dihydro-15-keto-PGF2α enzymeimmunoassay and its application for reproductive health monitoring in postpartum buffaloes
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2006.01.009openalex-snapshot
Acute effects of prostaglandin F2α on systemic oxytocin and progesterone concentrations during the mid- or late-luteal phase in mares
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2007.04.016openalex-snapshot
Immunohistochemical demonstration of cyclooxygenase-2 (COX-2) and prostaglandin receptors EP2 and FP expression in the bovine intercaruncular uterine wall around term
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2007.06.026openalex-snapshot
Canine prostaglandin F2α receptor (FP) and prostaglandin F2α synthase (PGFS): Molecular cloning and expression in the corpus luteum
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2008.04.004openalex-snapshot
Effects of melatonin and undernutrition on the viability of ovine embryos during anestrus and the breeding season
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2008.04.006openalex-snapshot
Effect of progesterone and/or estradiol treatments prior to induction of ovulation on subsequent luteal lifespan in anestrous Nelore cows
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2008.04.019openalex-snapshot
Messenger RNA levels of estrogen receptors α and β and progesterone receptors in the cyclic and inseminated/early pregnant sow uterus
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2008.09.016openalex-snapshot
Elevated progesterone concentrations enhance prostaglandin F2α synthesis in dairy cows
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2008.10.013openalex-snapshot
Ovarian and endocrine responses in tropical sheep treated with reduced doses of cloprostenol
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2009.06.021openalex-snapshot
Dynamic progesterone responses to simulation of a natural pulse of a metabolite of prostaglandin F2α in heifers
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2009.12.009openalex-snapshot
Environmental and sow-related factors affecting the duration of farrowing
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2010.02.020openalex-snapshot
Ovarian steroids regulate prostaglandin secretion in the feline endometrium
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2010.05.009openalex-snapshot
Intrapulse changes in progesterone and LH concentrations and luteal blood flow during an estradiol-induced pulse of a metabolite of prostaglandin F2α in heifers
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2010.08.019openalex-snapshot
Circulating hormone concentrations within a pulse of a metabolite of prostaglandin F2α during preluteolysis and early luteolysis in heifers
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2010.10.015openalex-snapshot
Possible involvement of oxytocin and its receptor in the local regulation of prostaglandin secretion in the cat endometrium
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2011.04.012openalex-snapshot
Effects of oestrus induction with progestagens or prostaglandin analogues on ovarian and pituitary function in sheep
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2011.09.013openalex-snapshot
Hormone concentration changes temporally associated with the hour of transition from preluteolysis to luteolysis in mares
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2012.03.007openalex-snapshot
Development of corpus luteum susceptibility to an analog of prostaglandin F2α, throughout the luteal phase in llamas (Lama glama)
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2012.06.014openalex-snapshot
Temporal interrelationships at 15-min intervals among oxytocin, LH, and progesterone during a pulse of a prostaglandin F2α metabolite in heifers
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2012.11.009openalex-snapshot
Short-lived corpora lutea syndrome in anoestrous ewes following 17β-oestradiol or MAP treatments applied before an allogenic sexual stimulation with rams and oestrous ewes
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2014.05.003openalex-snapshot
Does the conceptus of the viviparous lizard Barisia imbricata imbricata participates in the regulation of progesterone production and the control of luteolysis?
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2015.02.007openalex-snapshot
Endometrial expression of selected transcripts in postpartum of primiparous Holstein cows with clinical and subclinical endometritis
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2016.04.012openalex-snapshot
Hormonal concentrations and reproductive performance of Holstein heifers fed Trifolium alexandrinum as a phytoestrogenic roughage
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2018.05.019openalex-snapshot
Effect of different levels of n-3 polyunsaturated fatty acids rich fish oil supplementation on the ovarian and endometrial functions in the goat (Capra hircus)
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2019.106146openalex-snapshot
Suppression of COX-2 mRNA abundance in in vitro cultured goat (Capra hircus) endometrial cells by RNA interference and effect on PGF2-α and PGE2 concentrations
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2020.106589openalex-snapshot
Associations between foetal size and ovarian development in the pig
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2022.107026openalex-snapshot
Expression pattern and cellular localization of two critical non-nuclear progesterone receptors in the ovine corpus luteum during the estrous cycle and early pregnancy
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2023.107264openalex-snapshot
Progesterone-stimulated endometrial cell conditioned media increases in vitro produced bovine embryo blastocyst formation
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2019.734449openalex-snapshot
Comparisons of fecundity and reproductive hormone levels in three populations of Gymnocypris przewalskii
inferred← citeshttps://doi.org/10.1016/j.bbcan.2023.188888openalex-snapshot
Neo-vascularization-based therapeutic perspectives in advanced ovarian cancer
inferred← citeshttps://doi.org/10.1016/j.bbrc.2004.03.167openalex-snapshot
Prostaglandin F2α amplifies tumor necrosis factor-α promoter activity by the FPB prostanoid receptor
inferred← citeshttps://doi.org/10.1016/j.bcp.2005.10.046openalex-snapshot
The effects of prostaglandin F2α treatment on peripheral-type benzodiazepine receptors in the ovary and uterus during pseudopregnancy of rats
inferred← citeshttps://doi.org/10.1016/j.ceca.2004.06.004openalex-snapshot
Prostaglandin F2α potentiates the calcium dependent activation of mitochondrial metabolism in luteal cells
inferred← citeshttps://doi.org/10.1016/j.cyto.2014.02.005openalex-snapshot
Ovarian steroid-dependent tumor necrosis factor-α production and its action on the equine endometrium in vitro
inferred← citeshttps://doi.org/10.1016/j.domaniend.2005.11.006openalex-snapshot
Participation of specific PKC isozymes in the inhibitory effect of ET-1 on progesterone accumulation in cells isolated from early- and mid-phase corpora lutea
inferred← citeshttps://doi.org/10.1016/j.domaniend.2008.02.001openalex-snapshot
Luteotrophic and luteolytic effects of nitric oxide in sheep are dose-dependent in vivo
inferred← citeshttps://doi.org/10.1016/j.domaniend.2009.08.003openalex-snapshot
Evidence for a potential role of neuropeptide Y in ovine corpus luteum function
inferred← citeshttps://doi.org/10.1016/j.domaniend.2010.09.002openalex-snapshot
Concomitance of luteinizing hormone and progesterone oscillations during the transition from preluteolysis to luteolysis in cattle
inferred← citeshttps://doi.org/10.1016/j.domaniend.2010.11.003openalex-snapshot
Tumor necrosis factor-α inhibits the stimulatory effect of luteinizing hormone and prostaglandin E2 on progesterone secretion by the bovine corpus luteum
inferred← citeshttps://doi.org/10.1016/j.domaniend.2011.05.003openalex-snapshot
Effect of dose of estradiol-17β on prominence of an induced 13,14-dihydro-15-keto-PGF2α (PGFM) pulse and relationship of prominence to progesterone, LH, and luteal blood flow in heifers
inferred← citeshttps://doi.org/10.1016/j.domaniend.2015.03.001openalex-snapshot
Lipopolysaccharides, cytokines, and nitric oxide affect secretion of prostaglandins and leukotrienes by bovine mammary gland during experimentally induced mastitis in vivo and in vitro
inferred← citeshttps://doi.org/10.1016/j.domaniend.2016.03.006openalex-snapshot
Early pregnancy in the mare: old concepts revisited
inferred← citeshttps://doi.org/10.1016/j.domaniend.2017.12.004openalex-snapshot
Expression of membrane progestin receptors (mPRs) in the bovine corpus luteum during the estrous cycle and first trimester of pregnancy
inferred← citeshttps://doi.org/10.1016/j.domaniend.2019.02.001openalex-snapshot
Supplemental progesterone induces temporal changes in luteal development and endometrial transcription in beef cattle
inferred← citeshttps://doi.org/10.1016/j.domaniend.2021.106653openalex-snapshot
Unravelling the role of 17β-estradiol on advancing uterine luteolytic cascade in cattle
inferred← citeshttps://doi.org/10.1016/j.domaniend.2025.106939openalex-snapshot
Effectors and predictors of conceptus survival in cattle: What is next?
inferred← citeshttps://doi.org/10.1016/j.etap.2013.09.020openalex-snapshot
Exposure to the endocrine disruptor di(2-ethylhexyl)phthalate affects female reproductive features by altering pulsatile LH secretion
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2007.08.045openalex-snapshot
Effect of the oxytocin antagonist antocin and agonist decomoton on baboon luteal cell production and release of progesterone
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2008.04.029openalex-snapshot
Impact of luteal phase support on pregnancy rates in intrauterine insemination cycles: a prospective randomized study
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2008.11.006openalex-snapshot
Progestogen treatments for cycle management in a sheep model of assisted conception affect the growth patterns, the expression of luteinizing hormone receptors, and the progesterone secretion of induced corpora lutea
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2014.05.002openalex-snapshot
Elevated early follicular progesterone levels and in vitro fertilization outcomes: a prospective intervention study and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2018.02.003openalex-snapshot
Luteal phase support after gonadotropin-releasing hormone agonist triggering: does it still matter?
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2019.10.017openalex-snapshot
Comparison of endometrial prostanoid profiles in three infertile subgroups: the missing part of receptivity?
inferred← citeshttps://doi.org/10.1016/j.jep.2026.122108openalex-snapshot
Investigation of the pharmacodynamic material basis and mechanism of Gexia Zhuyu Decoction in the treatment of primary dysmenorrhea with qi stagnation and blood stasis based on Chinmedomics
inferred← citeshttps://doi.org/10.1016/j.jevs.2013.10.093openalex-snapshot
Ovarian steroid-dependent tumor necrosis factor-α production and its action in equine endometrium in vitro
inferred← citeshttps://doi.org/10.1016/j.jevs.2020.102991openalex-snapshot
Effect of Chronic Administration of Oxytocin on Corpus Luteum Function in Cycling Mares
inferred← citeshttps://doi.org/10.1016/j.jevs.2023.104963openalex-snapshot
Luteal tissue blood flow and side effects of horse-recommended luteolytic doses of dinoprost and cloprostenol in donkeys
inferred← citeshttps://doi.org/10.1016/j.jri.2012.01.004openalex-snapshot
Is cortisol a modulator of interferon tau action in the endometrium during early pregnancy in cattle?
inferred← citeshttps://doi.org/10.1016/j.jtbi.2010.06.005openalex-snapshot
A mathematical model of pregnancy recognition in mammals
inferred← citeshttps://doi.org/10.1016/j.jtbi.2011.02.021openalex-snapshot
A simple mathematical model of the bovine estrous cycle: Follicle development and endocrine interactions
inferred← citeshttps://doi.org/10.1016/j.livprodsci.2005.10.014openalex-snapshot
Postpartum endocrinology and prospects for fertility improvement in the lactating riverine buffalo (Bubalus bubalis) and yak (Poephagus grunniens L.)
inferred← citeshttps://doi.org/10.1016/j.mce.2011.01.002openalex-snapshot
Administration of a gonadotropin-releasing hormone agonist affects corpus luteum vascular stability and development and induces luteal apoptosis in a rat model of ovarian hyperstimulation syndrome
inferred← citeshttps://doi.org/10.1016/j.mce.2011.08.020openalex-snapshot
Early pregnancy induced expression of prostaglandin E2 receptors EP2 and EP4 in the ovine endometrium and regulated by interferon tau through multiple cell signaling pathways
inferred← citeshttps://doi.org/10.1016/j.mce.2013.06.001openalex-snapshot
The progesterone receptor antagonist, onapristone has differential effects on the timing and control of the luteolytic mechanism depending on timing of administration in sheep
inferred← citeshttps://doi.org/10.1016/j.mce.2013.07.005openalex-snapshot
Effects of lysophopatidic acid on tumor necrosis factor α and interferon γ action in the bovine corpus luteum
inferred← citeshttps://doi.org/10.1016/j.plefa.2011.10.008openalex-snapshot
Enhanced prostaglandin F2α formation in human pregnancy and the effect of increased oily fish intake: Results from the Salmon in Pregnancy Study
inferred← citeshttps://doi.org/10.1016/j.pneurobio.2013.09.004openalex-snapshot
Revisiting the roles of progesterone and allopregnanolone in the nervous system: Resurgence of the progesterone receptors
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2004.11.002openalex-snapshot
Uterine region-dependent differences in responsiveness to prostaglandins in the non-pregnant porcine myometrium
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2005.02.001openalex-snapshot
Non-genomic effect of steroids on oxytocin-stimulated intracellular mobilization of calcium and on prostaglandin F2α and E2 secretion from bovine endometrial cells
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2005.03.003openalex-snapshot
Effect of progesterone on the expression of bax and bcl-2 and on caspase activity in bovine luteal cells
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2005.08.002openalex-snapshot
Phytoestrogen metabolites are much more active than phytoestrogens themselves in increasing prostaglandin F2α synthesis via prostaglanin F2α synthase-like 2 stimulation in bovine endometrium
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2005.09.003openalex-snapshot
Regulation of prostaglandin synthesis by interleukin-1α in bovine endometrium during the estrous cycle
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2006.01.002openalex-snapshot
Role of intraluteal prostaglandin F2α, progesterone and oxytocin in basal and pulsatile progesterone release from developing bovine corpus luteum
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2006.03.003openalex-snapshot
Equol and para-ethyl-phenol stimulate prostaglandin F2α secretion in bovine corpus luteum: Intracellular mechanisms of action
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2006.05.008openalex-snapshot
Highly sensitive second antibody format enzymeimmunoassay for determination of 13,14-dihydro-15-keto-PGF2α in blood plasma of mithun (Bos frontalis)
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2006.10.002openalex-snapshot
Endotoxin induces luteal cell apoptosis through the mitochondrial pathway
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2009.08.006openalex-snapshot
The effect of ovarian steroids on oxytocin-stimulated secretion and synthesis of prostaglandins in bovine myometrial cells
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2010.01.002openalex-snapshot
Relationship between concentrations of progesterone, oxytocin, noradrenaline, gene expression and protein level for their receptors in corpus luteum during estrous cycle in the cow
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2012.01.004openalex-snapshot
A new in vivo model for luteolysis using systemic pulsatile infusions of PGF2α
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2015.10.002openalex-snapshot
Lysophosphatidic acid modulates prostaglandin signalling in bovine steroidogenic luteal cells
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2016.12.003openalex-snapshot
Uterine and placental expression of HPGD in cows during pregnancy and release of fetal membranes
inferred← citeshttps://doi.org/10.1016/j.prostaglandins.2018.02.001openalex-snapshot
Effect of dietary n-3 polyunsaturated fatty acid rich fish oil on the endometrial prostaglandin production in the doe ( Capra hircus )
inferred← citeshttps://doi.org/10.1016/j.repbio.2013.12.004openalex-snapshot
Ever-changing cell interactions during the life span of the corpus luteum: Relevance to luteal regression
inferred← citeshttps://doi.org/10.1016/j.repbio.2014.10.004openalex-snapshot
Functional consequences of knocking down porcine prostaglandin synthases in SK-6 swine kidney cell line
inferred← citeshttps://doi.org/10.1016/j.repbio.2016.01.005openalex-snapshot
Pregnancy-associated changes in uterine-luteal relationships in cows: A mini-review
inferred← citeshttps://doi.org/10.1016/j.repbio.2021.100570openalex-snapshot
Loss of luteal sensitivity to luteinizing hormone underlies luteolysis in cattle: A hypothesis
inferred← citeshttps://doi.org/10.1016/j.smallrumres.2010.07.007openalex-snapshot
Assessment of luteal function in goats by ultrasonographic image attribute analysis
inferred← citeshttps://doi.org/10.1016/j.steroids.2006.05.007openalex-snapshot
Inhibition of prostaglandin F2α synthesis and oxytocin receptor by progesterone antagonists in bovine endometrial cells in vitro
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2003.09.005openalex-snapshot
Estrous cycle characteristics, luteal function, secretion of oxytocin (OT) and plasma concentrations of 15-keto-13,14-dihydro-PGF2α (PGF2α-metabolite) after administration of low doses of prostaglandin F2α (PGF2α) in pony mares
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2004.12.003openalex-snapshot
Efficacy of either a single or split treatment of PGF2α after a 14 day melengestrol acetate treatment to synchronize estrus and induce luteolysis in Bos indicus×Bos taurus heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2005.04.015openalex-snapshot
Analysis of gene expression in non-regressed and regressed bovine corpus luteum tissue using a customized ovarian cDNA array
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2006.03.001openalex-snapshot
Expression of enzymes of cyclooxygenase pathway and secretion of prostaglandin E2 and F2α by porcine myometrium during luteolysis and early pregnancy
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2008.03.008openalex-snapshot
Expression of prostaglandin synthesis pathway enzymes in the porcine corpus luteum during the oestrous cycle and early pregnancy
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2008.11.012openalex-snapshot
Postpartum anestrus in dairy cattle
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2009.06.024openalex-snapshot
Concentrations of circulating hormones normalized to pulses of a prostaglandin F2α metabolite during spontaneous luteolysis in mares
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2009.10.008openalex-snapshot
PGFM (13,14-dihydro-15-keto-PGF2α) in pregnant and pseudo-pregnant Iberian lynx: A new noninvasive pregnancy marker for felid species
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2010.02.021openalex-snapshot
Stimulation of pulses of 13,14-dihydro-15-keto-PGF2α (PGFM) with estradiol-17β and changes in circulating progesterone concentrations within a PGFM pulse in heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2010.07.021openalex-snapshot
The transition between preluteolysis and luteolysis in cattle
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2011.03.017openalex-snapshot
Effects of inhibition of prostaglandin F2α biosynthesis during preluteolysis and luteolysis in heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2011.08.016openalex-snapshot
Factors affecting the occurrence of postpartum prolonged luteal activity in clinically healthy high-producing dairy cows
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2011.08.020openalex-snapshot
Induction of PGFM pulses and luteolysis by sequential estradiol-17β treatments in heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2011.10.011openalex-snapshot
Using PGFM (13,14-dihydro-15-keto-prostaglandin F2α) as a non-invasive pregnancy marker for felids
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2011.10.026openalex-snapshot
The end of the tour de force of the corpus luteum in mares
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2011.11.014openalex-snapshot
Role of LH in luteolysis and growth of the ovulatory follicle and estradiol regulation of LH secretion in heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2012.01.001openalex-snapshot
The hour of transition into luteolysis in horses and cattle: A species comparison
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2012.02.024openalex-snapshot
Inhibition of prostaglandin biosynthesis during postluteolysis and effects on CL regression, prolactin, and ovulation in heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2012.03.014openalex-snapshot
Direct effect of PGF2α pulses on PRL pulses, based on inhibition of PRL or PGF2α secretion in heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2012.03.024openalex-snapshot
mRNA transcription of prostaglandin synthases and their products in the equine endometrium in the course of fibrosis
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2012.03.032openalex-snapshot
Compared to dinoprost tromethamine, cloprostenol sodium increased rates of estrus detection, conception and pregnancy in lactating dairy cows on a large commercial dairy
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2012.04.017openalex-snapshot
Advances in modeling of the bovine estrous cycle: Synchronization with PGF2α
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2012.05.021openalex-snapshot
Ovarian and PGF2α responses to stimulation of endogenous PRL pulses during the estrous cycle in mares
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2012.12.003openalex-snapshot
Effect of conceptus on expression of prostaglandin F2α receptor in the porcine endometrium
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2013.02.003openalex-snapshot
Interrelationships among progesterone, LH, and luteal blood flow during a pulse of a PGF2α metabolite and functional role of LH in the progesterone rebound in heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2013.03.025openalex-snapshot
Expression of enzymes and receptors of leukotriene pathway genes in equine endometrium during the estrous cycle and early pregnancy
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2013.05.007openalex-snapshot
Effect of dinoprost and cloprostenol on serum nitric oxide and corpus luteum blood flow during luteolysis in ewes
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2013.05.010openalex-snapshot
Embryonic resorption in context to intragestational corpus luteum regression: A longitudinal ultrasonographic study in the European brown hare (Lepus europaeus PALLAS, 1778)
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2014.10.007openalex-snapshot
Color Doppler provides a reliable and rapid means of monitoring luteolysis in female donkeys
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2014.11.006openalex-snapshot
Oxytocin induction of pulses of a prostaglandin metabolite and luteolysis in mares
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2014.11.008openalex-snapshot
The corpus luteum of the domestic cat: Histologic classification and intraluteal hormone profile
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2015.07.004openalex-snapshot
Effects of intrauterine infusion of Trueperella pyogenes on endometrial mRNA expression of proinflammatory cytokines and luteolytic cascade genes and their association with luteal life span in dairy cows
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2015.09.055openalex-snapshot
Production of prostaglandins in placentae and corpus luteum in pregnant hinds of red deer (Cervus elaphus)
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2016.04.038openalex-snapshot
Mechanisms underlying reduced fertility in anovular dairy cows
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2016.04.051openalex-snapshot
Factors affecting puberty in replacement beef heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2017.02.004openalex-snapshot
Relationship between circulating progesterone at timed-AI and fertility in dairy cows subjected to GnRH-based protocols
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2017.06.008openalex-snapshot
PPAR expression throughout the oestrous cycle in the bovine endometrium
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2017.10.029openalex-snapshot
Early pregnancy diagnosis in ewes by subjective assessment of luteal vascularisation using colour Doppler ultrasonography
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2018.01.010openalex-snapshot
Expression patterns of Toll-like receptors in the ovine corpus luteum during the early pregnancy and prostaglandin F2α-induced luteolysis
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2018.10.026openalex-snapshot
Expression of vitamin D receptor in the porcine uterus and effect of 1,25(OH)2D3 on progesterone and estradiol-17β secretion by uterine tissues in vitro
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2019.04.004openalex-snapshot
Endogenous and exogenous effects of PGF2α during luteolysis in mares
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2020.04.039openalex-snapshot
Luteinizing hormone and ovarian steroids affect in vitro prostaglandin production in the equine myometrium and endometrium
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2020.09.015openalex-snapshot
Partial luteolysis during early diestrus in cattle downregulates VEGFA expression and reduces large luteal cell and corpus luteum sizes and plasma progesterone concentration
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2020.11.013openalex-snapshot
Effect of intramuscular and intravaginal PGE-2 treatment compared to intramuscular oxytocin treatment in eutocic sows on the farrowing performance in a free farrowing system
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2021.02.005openalex-snapshot
Heat stress influences the attenuation of prostaglandin synthesis by interferon tau in bovine endometrial cells
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.01.032openalex-snapshot
Local embryo-mediated changes in endometrial gene expression during embryo mobility in mares
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.06.007openalex-snapshot
Expression patterns of chemokine (C–C motif) ligand 2, prostaglandin F2A receptor and immediate early genes at mRNA level in the bovine corpus luteum after intrauterine treatment with a low dose of prostaglandin F2A
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.10.019openalex-snapshot
Serum progesterone and oxytocinase, and endometrial and luteal gene expression in pregnant, nonpregnant, oxytocin, carbetocin and meclofenamic acid treated mares
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2025.02.014openalex-snapshot
Effects of estradiol on PGF2α synthesis and corpus luteum function during early pregnancy in beef heifers
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2025.117456openalex-snapshot
Phoenixin-14 and its receptor GPR173 in the bovine endometrium: Expression and regulation during the estrous cycle and impact on secretory activity
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2025.117639openalex-snapshot
Evaluation of prostaglandin and injectable progesterone in the early postpartum period on uterine health parameters, follicular dynamics, and fertility in beef cattle
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2025.117734openalex-snapshot
Elevated prostaglandin F2 alpha after the period of embryonic secretion of interferon tau appears to be due to upregulation of uterine synthesis machinery for prostaglandin F2 alpha
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