198 related articles for article (PubMed ID: 18299429)
41. 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]
42. Progesterone regulates FGF10, MET, IGFBP1, and IGFBP3 in the endometrium of the ovine uterus.
Satterfield MC; Hayashi K; Song G; Black SG; Bazer FW; Spencer TE
Biol Reprod; 2008 Dec; 79(6):1226-36. PubMed ID: 18753603
[TBL] [Abstract][Full Text] [Related]
43. Neonatal age and period of estrogen exposure affect porcine uterine growth, morphogenesis, and protein synthesis.
Spencer TE; Wiley AA; Bartol FF
Biol Reprod; 1993 Apr; 48(4):741-51. PubMed ID: 8485238
[TBL] [Abstract][Full Text] [Related]
44. Loss of Runx3 affects ovulation and estrogen-induced endometrial cell proliferation in female mice.
Sakuma A; Fukamachi H; Ito K; Ito Y; Takeuchi S; Takahashi S
Mol Reprod Dev; 2008 Nov; 75(11):1653-61. PubMed ID: 18361415
[TBL] [Abstract][Full Text] [Related]
45. Uterine gland formation in mice is a continuous process, requiring the ovary after puberty, but not after parturition.
Stewart CA; Fisher SJ; Wang Y; Stewart MD; Hewitt SC; Rodriguez KF; Korach KS; Behringer RR
Biol Reprod; 2011 Nov; 85(5):954-64. PubMed ID: 21734259
[TBL] [Abstract][Full Text] [Related]
46. Preputialectomised and intact adult male mice exhibit an elevated urinary ratio of oestradiol to creatinine in the presence of developing females, whilst promoting uterine and ovarian growth of these females.
Khan A; Berger RG; Decatanzaro D
Reprod Fertil Dev; 2009; 21(7):860-8. PubMed ID: 19698290
[TBL] [Abstract][Full Text] [Related]
47. Hysterographic appearance and uterine histology at different stages of the reproductive cycle and after progestagen treatment in the domestic cat.
Chatdarong K; Rungsipipat A; Axnér E; Linde Forsberg C
Theriogenology; 2005 Jul; 64(1):12-29. PubMed ID: 15935839
[TBL] [Abstract][Full Text] [Related]
48. Subfertile female androgen receptor knockout mice exhibit defects in neuroendocrine signaling, intraovarian function, and uterine development but not uterine function.
Walters KA; McTavish KJ; Seneviratne MG; Jimenez M; McMahon AC; Allan CM; Salamonsen LA; Handelsman DJ
Endocrinology; 2009 Jul; 150(7):3274-82. PubMed ID: 19359383
[TBL] [Abstract][Full Text] [Related]
49. Multiple trait genetic evaluation of ewe traits in Icelandic sheep.
Arnason T; Jónmundsson JV
J Anim Breed Genet; 2008 Dec; 125(6):390-6. PubMed ID: 19134074
[TBL] [Abstract][Full Text] [Related]
50. Neonatal exposure to a glyphosate-based herbicide alters the histofunctional differentiation of the ovaries and uterus in lambs.
Alarcón R; Ingaramo PI; Rivera OE; Dioguardi GH; Repetti MR; Demonte LD; Milesi MM; Varayoud J; Muñoz-de-Toro M; Luque EH
Mol Cell Endocrinol; 2019 Feb; 482():45-56. PubMed ID: 30550814
[TBL] [Abstract][Full Text] [Related]
51. Polarized ovaries of the long-tongued bat, Glossophaga soricina: a novel model for studying ovarian development, folliculogenesis, and ovulation.
Komar CM; Zacharachis-Jutz F; Cretekos CJ; Behringer RR; Rasweiler JJ
Anat Rec (Hoboken); 2007 Nov; 290(11):1439-48. PubMed ID: 17929278
[TBL] [Abstract][Full Text] [Related]
52. Uterine differentiation as a foundation for subsequent fertility.
Bartol FF; Wiley AA; Floyd JG; Ott TL; Bazer FW; Gray CA; Spencer TE
J Reprod Fertil Suppl; 1999; 54():287-302. PubMed ID: 10692862
[TBL] [Abstract][Full Text] [Related]
53. Ovine uterine morphogenesis: effects of age and progestin administration and withdrawal on neonatal endometrial development and DNA synthesis.
Bartol FF; Wiley AA; Coleman DA; Wolfe DF; Riddell MG
J Anim Sci; 1988 Nov; 66(11):3000-9. PubMed ID: 3225250
[TBL] [Abstract][Full Text] [Related]
54. Distribution of androgen receptor in the porcine uterus throughout pregnancy.
Słomczyńska M; Duda M; Burek M; Knapczyk K; Czaplicki D; Koziorowski M
Reprod Domest Anim; 2008 Feb; 43(1):35-41. PubMed ID: 18199256
[TBL] [Abstract][Full Text] [Related]
55. Androgen receptor in the ovary of postnatal bank vole females.
Galas J; Slomczynska M; Kwasnik A
Ann N Y Acad Sci; 2005 Apr; 1040():315-9. PubMed ID: 15891050
[TBL] [Abstract][Full Text] [Related]
56. Effect of undernutrition on the uterine environment during maternal recognition of pregnancy in sheep.
Sosa C; Abecia JA; Carriquiry M; Vázquez MI; Fernández-Foren A; Talmon M; Forcada F; Meikle A
Reprod Fertil Dev; 2009; 21(7):869-81. PubMed ID: 19698291
[TBL] [Abstract][Full Text] [Related]
57. Follistatin is essential for normal postnatal development and function of mouse oviduct and uterus.
Holdsworth-Carson SJ; Craythorn RG; Winnall WR; Dhaliwal K; Genovese R; Nowell CJ; Rogers PA; de Kretser DM; Hedger MP; Girling JE
Reprod Fertil Dev; 2015 Sep; 27(7):985-99. PubMed ID: 24630125
[TBL] [Abstract][Full Text] [Related]
58. [Biometric parameters of the uterus, ovaries and levels of 17 beta-estradiol (E2) after delivery in sheep].
Krajnicáková M; Elecko J; Bekeová E; Maracek I; Hendrichovský V
Vet Med (Praha); 1990 Dec; 35(12):747-56. PubMed ID: 2100427
[TBL] [Abstract][Full Text] [Related]
59. Uterine glands: development, function and experimental model systems.
Cooke PS; Spencer TE; Bartol FF; Hayashi K
Mol Hum Reprod; 2013 Sep; 19(9):547-58. PubMed ID: 23619340
[TBL] [Abstract][Full Text] [Related]
60. Emergence of uterine pathology during accelerated biological aging in FSH receptor-haploinsufficient mice.
Danilovich N; Roy I; Sairam MR
Endocrinology; 2002 Sep; 143(9):3618-27. PubMed ID: 12193578
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
