These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 23656912)

  • 1. Maternal nutrient restriction in the ewe from early to midgestation programs reduced steroidogenic enzyme expression and tended to reduce progesterone content of corpora lutea, as well as circulating progesterone in nonpregnant aged female offspring.
    Long NM; Tuersunjiang N; George LA; Lemley CO; Ma Y; Murdoch WJ; Nathanielsz PW; Ford SP
    Reprod Biol Endocrinol; 2013 May; 11():34. PubMed ID: 23656912
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Luteal expression of steroidogenic factor-1 mRNA during the estrous cycle and in response to luteotropic and luteolytic stimuli in ewes.
    Juengel JL; Larrick TL; Meberg BM; Niswender GD
    Endocrine; 1998 Dec; 9(3):227-32. PubMed ID: 10221587
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The effect of early to mid-gestational nutrient restriction on female offspring fertility and hypothalamic-pituitary-adrenal axis response to stress.
    Long NM; Nijland MJ; Nathanielsz PW; Ford SP
    J Anim Sci; 2010 Jun; 88(6):2029-37. PubMed ID: 20190172
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic merit for fertility traits in Holstein cows: V. Factors affecting circulating progesterone concentrations.
    Moore SG; Scully S; Browne JA; Fair T; Butler ST
    J Dairy Sci; 2014 Sep; 97(9):5543-57. PubMed ID: 24952779
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Human chorionic gonadotropin increases serum progesterone, number of corpora lutea and angiogenic factors in pregnant sheep.
    Coleson MP; Sanchez NS; Ashley AK; Ross TT; Ashley RL
    Reproduction; 2015 Jul; 150(1):43-52. PubMed ID: 25861798
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Corpora lutea in superovulated ewes fed different planes of nutrition.
    Kraisoon A; Redmer DA; Bass CS; Navanukraw C; Dorsam ST; Valkov V; Reyaz A; Grazul-Bilska AT
    Domest Anim Endocrinol; 2018 Jan; 62():16-23. PubMed ID: 28886590
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The expression of ovine placental lactogen, StAR and progesterone-associated steroidogenic enzymes in placentae of overnourished growing adolescent ewes.
    Lea RG; Wooding P; Stewart I; Hannah LT; Morton S; Wallace K; Aitken RP; Milne JS; Regnault TR; Anthony RV; Wallace JM
    Reproduction; 2007 Apr; 133(4):785-96. PubMed ID: 17504922
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hormonal regulation of messenger ribonucleic acid encoding steroidogenic acute regulatory protein in ovine corpora lutea.
    Juengel JL; Meberg BM; Turzillo AM; Nett TM; Niswender GD
    Endocrinology; 1995 Dec; 136(12):5423-9. PubMed ID: 7588291
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cytochromes P-450scc, P-450(17)alpha, adrenodoxin, and reduced nicotinamide adenine dinucleotide phosphate-cytochrome P-450 reductase in bovine follicles and corpora lutea. Changes in specific contents during the ovarian cycle.
    Rodgers RJ; Waterman MR; Simpson ER
    Endocrinology; 1986 Apr; 118(4):1366-74. PubMed ID: 3004911
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Stimulatory effect of LH, PGE2 and progesterone on StAR protein, cytochrome P450 cholesterol side chain cleavage and 3beta hydroxysteroid dehydrogenase gene expression in bovine luteal cells.
    Rekawiecki R; Nowik M; Kotwica J
    Prostaglandins Other Lipid Mediat; 2005 Dec; 78(1-4):169-84. PubMed ID: 16303614
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Loss of luteotropic prostaglandin E plays an important role in the regulation of luteolysis in women.
    Nio-Kobayashi J; Kudo M; Sakuragi N; Iwanaga T; Duncan WC
    Mol Hum Reprod; 2017 May; 23(5):271-281. PubMed ID: 28333263
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effects of endocannabinoid 1 and 2 (CB1; CB2) receptor agonists on luteal weight, circulating progesterone, luteal mRNA for luteinizing hormone (LH) receptors, and luteal unoccupied and occupied receptors for LH in vivo in ewes.
    Tsutahara NM; Weems YS; Arreguin-Arevalo JA; Nett TM; LaPorte ME; Uchida J; Pang J; McBride T; Randel RD; Weems CW
    Prostaglandins Other Lipid Mediat; 2011 Feb; 94(1-2):17-24. PubMed ID: 21109016
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Effect of dose of prostaglandin F(2alpha) on steroidogenic components and oligonucleosomes in ovine luteal tissue.
    Juengel JL; Haworth JD; Rollyson MK; Silva PJ; Sawyer HR; Niswender GD
    Biol Reprod; 2000 Apr; 62(4):1047-51. PubMed ID: 10727276
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Luteal expression of cytochrome P450 side-chain cleavage, steroidogenic acute regulatory protein, 3beta-hydroxysteroid dehydrogenase, and 20alpha-hydroxysteroid dehydrogenase genes in late pregnant rats: effect of luteinizing hormone and RU486.
    Stocco CO; Chedrese J; Deis RP
    Biol Reprod; 2001 Oct; 65(4):1114-9. PubMed ID: 11566732
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Role of luteinizing hormone in the expression of cholesterol side-chain cleavage cytochrome P450 and 3 beta-hydroxysteroid dehydrogenase, delta 5-4 isomerase messenger ribonucleic acids in the primate corpus luteum.
    Ravindranath N; Little-Ihrig L; Benyo DF; Zeleznik AJ
    Endocrinology; 1992 Nov; 131(5):2065-70. PubMed ID: 1425410
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Corpus luteum function following single and double ovulation during estrous cycle in Sanjabi ewes.
    Shabankareh HK; Habibizad J; Torki M
    Anim Reprod Sci; 2009 Sep; 114(4):362-9. PubMed ID: 19042100
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The influence of the ovulation rate on ultrasonically determined ovine corpus luteum morphometry and progesterone concentrations in cyclic and early pregnant sheep.
    Kaulfuss KH; Moritz S; Giucci E
    Dtsch Tierarztl Wochenschr; 2003 Jun; 110(6):249-54. PubMed ID: 12866258
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maternal undernutrition during early to midgestation programs tissue-specific alterations in the expression of the glucocorticoid receptor, 11beta-hydroxysteroid dehydrogenase isoforms, and type 1 angiotensin ii receptor in neonatal sheep.
    Whorwood CB; Firth KM; Budge H; Symonds ME
    Endocrinology; 2001 Jul; 142(7):2854-64. PubMed ID: 11416004
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Effect of luteinizing hormone (LH), pregnancy-specific protein B (PSPB), or arachidonic acid (AA) on secretion of progesterone and prostaglandins (PG) E (PGE; PGE(1) and PGE(2)) and F(2alpha) (PGF(2alpha)) by ovine corpora lutea of the estrous cycle or pregnancy in vitro.
    Weems YS; Kim L; Humphreys V; Tsuda V; Blankfein R; Wong A; Weems CW
    Prostaglandins Other Lipid Mediat; 2007 Nov; 84(3-4):163-73. PubMed ID: 17991618
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Effects of indomethacin, luteinizing hormone (LH), prostaglandin E2 (PGE2), trilostane, mifepristone, ethamoxytriphetol (MER-25) on secretion of prostaglandin E (PGE), prostaglandin F2alpha (PGF2alpha) and progesterone by ovine corpora lutea of pregnancy or the estrous cycle.
    Kim L; Weems YS; Bridges PJ; LeaMaster BR; Ching L; Vincent DL; Weems CW
    Prostaglandins Other Lipid Mediat; 2001 Mar; 63(4):189-203. PubMed ID: 11305696
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.