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Development, validation and application of a two-site enzyme-linked immunosorbent assay for activin-ABThe anti-epileptic drug valproic acid (VPA) inhibits steroidogenesis in bovine theca and granulosa cells in vitroThe effect of a null mutation in the follicle-stimulating hormone receptor gene on mouse reproductionImmunohistochemical localization of inhibin/activin alpha, betaA and betaB subunits and follistatin in bovine oocytes during in vitro maturation and fertilization.Alterations in intrafollicular regulatory factors and apoptosis during selection of follicles in the first follicular wave of the bovine estrous cycle.Enzyme immunoassays for inhibins, activins and follistatins.Follicle wave growth in cattle.Transcriptomal profiling of bovine ovarian granulosa and theca interna cells in primary culture in comparison with their in vivo counterparts.Functional link between bone morphogenetic proteins and insulin-like peptide 3 signaling in modulating ovarian androgen productionThe global effect of follicle-stimulating hormone and tumour necrosis factor α on gene expression in cultured bovine ovarian granulosa cells.Evidence for the involvement of central conversion of testosterone to oestradiol-17 beta in the regulation of luteinizing hormone secretion in the cockerel.Chicken ovulation cycle.Functional significance of the signal transduction pathways Akt and Erk in ovarian follicles: in vitro and in vivo studies in cattle and sheep.Variations in hypothalamic luteinizing hormone releasing hormone content and release in vitro and plasma concentrations of luteinizing hormone and testosterone in developing cockerels.Bone morphogenetic protein (BMP) ligands and receptors in bovine ovarian follicle cells: actions of BMP-4, -6 and -7 on granulosa cells and differential modulation of Smad-1 phosphorylation by follistatin.Higher gonadotrophin surge-attenuating factor bioactivity is found in small follicles from superovulated women.Differential control of immunoreactive alpha-inhibin and progesterone production by marmoset luteal cells in vitro: evidence for a paracrine action of alpha-inhibin on basal and gonadotropin-stimulated progesterone production.Follicular expression of pro-inflammatory cytokines tumour necrosis factor-α (TNFα), interleukin 6 (IL6) and their receptors in cattle: TNFα, IL6 and macrophages suppress thecal androgen production in vitro.Bone morphogenetic protein-6 enhances gonadotrophin-dependent progesterone and inhibin secretion and expression of mRNA transcripts encoding gonadotrophin receptors and inhibin/activin subunits in chicken granulosa cells.Modulatory effects of gonadotrophins and insulin-like growth factor on the secretion of inhibin A and progesterone by granulosa cells from chicken preovulatory (F1-F3) follicles.Differential effects of activin A on basal and gonadotrophin-induced secretion of inhibin A and progesterone by granulosa cells from preovulatory (F1-F3) chicken follicles.Changes in expression of bone morphogenetic proteins (BMPs), their receptors and inhibin co-receptor betaglycan during bovine antral follicle development: inhibin can antagonize the suppressive effect of BMPs on thecal androgen production.Modulation of sex hormone secretion in cows by acute infection with bovine viral diarrhoea virus.Effects of bovine follicular fluid on gonadotrophin secretion in intact and chronically ovariectomized ewes before and after desensitization of pituitary gonadotrophs to gonadotrophin-releasing hormone.Changes in plasma inhibin A levels during sexual maturation in the female chicken and the effects of active immunization against inhibin alpha-subunit on reproductive hormone profiles and ovarian function.The effect of gonadotrophins with differing LH/FSH ratios on the secretion of the various species of inhibin in women receiving IVF.Ovarian expression of insulin-like peptide 3 (INSL3) and its receptor (RXFP2) during development of bovine antral follicles and corpora lutea and measurement of circulating INSL3 levels during synchronized estrous cycles.Effects of ovarian follicle ablation on FSH, oestradiol and inhibin A concentrations and growth of other follicles in sheep.Women with poor response to IVF have lowered circulating gonadotrophin surge-attenuating factor (GnSAF) bioactivity during spontaneous and stimulated cycles.Day 5 inhibin B levels in a treatment cycle are predictive of IVF outcome.Attenuation by an opioid agonist of the oestradiol-induced LH surge in anoestrous ewes and its reversal by naloxone.Involvement of endogenous opioid peptides in the neuroendocrine response of ewe lambs to the introduction of a ram.The reproductive response of rams to thyroidectomy: mediation by impaired inhibin feedback rather than a change in LH pulsatility.Influence of mutations affecting gonadotropin production or responsiveness on expression of inhibin subunit mRNA and protein in the mouse ovary.Variation in the ovarian reserve is linked to alterations in intrafollicular estradiol production and ovarian biomarkers of follicular differentiation and oocyte quality in cattle.Variation in pituitary expression of mRNAs encoding the putative inhibin co-receptor (betaglycan) and type-I and type-II activin receptors during the chicken ovulatory cycle.Differential expression of mRNAs encoding the putative inhibin co-receptor (betaglycan) and activin type-I and type-II receptors in preovulatory and prehierarchical follicles of the laying hen ovary.Relationship between follicle size and gonadotrophin surge attenuating factor (GnSAF) bioactivity during spontaneous cycles in women.Active immunisation against inhibin promotes a recurrent increase in litter size in sheep.The effect of ovarian reserve and receptor signalling on granulosa cell apoptosis during human follicle development.
P50
Q24323986-FC4C3BAB-6689-4DA2-ACA3-9D69DEAE5F50Q28485144-A3848D40-E70B-46C3-A61D-069E4DEFBCB4Q28591260-357D7B17-88DE-4AA9-BB9A-16A71248822DQ30892168-71366299-140A-47FC-BE36-20B75C481D4AQ32023717-00AB7A79-3D01-4912-BF41-8C935897829FQ34307673-A6743E13-56D8-4A1F-8C61-28B0D7908BC3Q34782526-EB376FD6-963F-4083-9371-C5F1F7C7CC91Q36304225-95445403-5452-4CF1-A799-1422DC7EE2C2Q36762746-1B249C09-0721-4D14-8B40-5870389C2D39Q37532504-3886BA5E-3770-4894-8B01-75B834DFF440Q38354360-2456AA08-86D1-4031-8F3B-5BECAE3195C4Q40199271-3BD431B9-4E49-4DEB-99C3-DA8CEBD98C58Q42107580-BAD750D4-BCC9-4A9A-B84F-B1362BF980A1Q42455218-56F3A2A3-B0F5-4C62-8474-E2DA08CD56DFQ42459550-619B7AD1-F227-4791-ADCA-131951909B39Q42493215-2BE00BAA-01AB-4D93-B2BE-0FC91AB07252Q42497055-96D62F0F-D642-47ED-9A2C-E6C22A629CD9Q42508765-852BB2EF-3A01-46ED-8BA8-45A5FB86D87FQ42516584-CFFB23EA-0283-4400-B15F-2AF5C2BCB064Q42517935-D3F50A76-2EAF-4FA3-9C1D-D11922E270A3Q42527588-9C361FB2-EC4D-4EF2-9202-2902E0DCDE6FQ42925837-AA8A672A-F27A-45AC-B5AF-3673A207479AQ43036793-C0743200-BE66-49A8-945C-0ACB8DE0C955Q43412591-EDCA0148-9ABC-44DC-AB44-2CA5ECCB01AEQ43513844-19BC964B-E9CC-4BC9-AD05-2B19CC6D980AQ43626630-DC54A396-6E29-48DE-9ADC-A83083478876Q43730421-A31F492C-7DBD-4EFE-A8D9-A1FC3FF3B6DCQ43899030-0DE0585A-0D4A-4427-84D1-4EFB09DE19FEQ43899609-E5BAFDBE-6E6B-42C8-99B0-C848EBFC5570Q44013164-953781A9-F446-4A11-8E24-5866609EB3B0Q44339192-D8CDE627-5767-4494-9787-DC19BC48B264Q44345715-19AE24FA-D5D3-47D4-80DB-52567FE09D86Q44581474-63B1FBE1-E661-4DB9-823C-04BEEFF5D701Q44962205-9A0DF7C9-6646-46DC-BED4-7C8FDDA0C5C2Q46151084-52AB892E-DF7C-443A-A1EA-8F7C561F00BCQ46681265-78C3DCB9-E900-4EB3-A9D1-419320429762Q46930582-917559EB-059F-4575-9B2D-66E3F5300CF4Q47207561-9C154FDC-8977-4101-AF12-8229AF34CD39Q47381749-ED5C8700-5AD1-4CE9-B304-32C919F56B19Q47429038-D387C404-89A9-421C-9B0C-73EDDD628D6D
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Knight PG
@ast
Knight PG
@es
Knight PG
@nl
Knight PG
@sl
Philip G. Knight
@en
type
label
Knight PG
@ast
Knight PG
@es
Knight PG
@nl
Knight PG
@sl
Philip G. Knight
@en
altLabel
Knight PG
@en
Phil G Knight
@en
prefLabel
Knight PG
@ast
Knight PG
@es
Knight PG
@nl
Knight PG
@sl
Philip G. Knight
@en
P106
P21
P31
P496
0000-0003-0300-1554
P569
2000-01-01T00:00:00Z