248 related articles for article (PubMed ID: 18606860)
1. Targeted disruption of Pten in ovarian granulosa cells enhances ovulation and extends the life span of luteal cells.
Fan HY; Liu Z; Cahill N; Richards JS
Mol Endocrinol; 2008 Sep; 22(9):2128-40. PubMed ID: 18606860
[TBL] [Abstract][Full Text] [Related]
2. Cell type-specific targeted mutations of Kras and Pten document proliferation arrest in granulosa cells versus oncogenic insult to ovarian surface epithelial cells.
Fan HY; Liu Z; Paquet M; Wang J; Lydon JP; DeMayo FJ; Richards JS
Cancer Res; 2009 Aug; 69(16):6463-72. PubMed ID: 19679546
[TBL] [Abstract][Full Text] [Related]
3. Oocyte-specific deletion of Pten in mice reveals a stage-specific function of PTEN/PI3K signaling in oocytes in controlling follicular activation.
Jagarlamudi K; Liu L; Adhikari D; Reddy P; Idahl A; Ottander U; Lundin E; Liu K
PLoS One; 2009 Jul; 4(7):e6186. PubMed ID: 19587782
[TBL] [Abstract][Full Text] [Related]
4. CRL4DCAF1 is required in activated oocytes for follicle maintenance and ovulation.
Yu C; Xu YW; Sha QQ; Fan HY
Mol Hum Reprod; 2015 Feb; 21(2):195-205. PubMed ID: 25371539
[TBL] [Abstract][Full Text] [Related]
5. Specific disruption of Tsc1 in ovarian granulosa cells promotes ovulation and causes progressive accumulation of corpora lutea.
Huang L; Wang ZB; Jiang ZZ; Hu MW; Lin F; Zhang QH; Luo YB; Hou Y; Zhao Y; Fan HY; Schatten H; Sun QY
PLoS One; 2013; 8(1):e54052. PubMed ID: 23335988
[TBL] [Abstract][Full Text] [Related]
6. Conjugated linoleic acids attenuate FSH- and IGF1-stimulated cell proliferation; IGF1, GATA4, and aromatase expression; and estradiol-17β production in buffalo granulosa cells involving PPARγ, PTEN, and PI3K/Akt.
Sharma I; Singh D
Reproduction; 2012 Sep; 144(3):373-83. PubMed ID: 22733801
[TBL] [Abstract][Full Text] [Related]
7. Expression and function of PAIRBP1 within gonadotropin-primed immature rat ovaries: PAIRBP1 regulation of granulosa and luteal cell viability.
Peluso JJ; Pappalardo A; Losel R; Wehling M
Biol Reprod; 2005 Aug; 73(2):261-70. PubMed ID: 15814896
[TBL] [Abstract][Full Text] [Related]
8. Alterations of circadian clockworks during differentiation and apoptosis of rat ovarian cells.
Chu G; Yoshida K; Narahara S; Uchikawa M; Kawamura M; Yamauchi N; Xi Y; Shigeyoshi Y; Hashimoto S; Hattori MA
Chronobiol Int; 2011 Jul; 28(6):477-87. PubMed ID: 21797776
[TBL] [Abstract][Full Text] [Related]
9. Either Kras activation or Pten loss similarly enhance the dominant-stable CTNNB1-induced genetic program to promote granulosa cell tumor development in the ovary and testis.
Richards JS; Fan HY; Liu Z; Tsoi M; Laguë MN; Boyer A; Boerboom D
Oncogene; 2012 Mar; 31(12):1504-20. PubMed ID: 21860425
[TBL] [Abstract][Full Text] [Related]
10. PTEN and Akt expression during growth of human ovarian follicles.
Goto M; Iwase A; Ando H; Kurotsuchi S; Harata T; Kikkawa F
J Assist Reprod Genet; 2007 Nov; 24(11):541-6. PubMed ID: 17999178
[TBL] [Abstract][Full Text] [Related]
11. Involvement of Fas antigen in ovarian follicular atresia and luteolysis.
Sakamaki K; Yoshida H; Nishimura Y; Nishikawa S; Manabe N; Yonehara S
Mol Reprod Dev; 1997 May; 47(1):11-8. PubMed ID: 9110309
[TBL] [Abstract][Full Text] [Related]
12. The orphan nuclear receptor Nr5a2 is essential for luteinization in the female mouse ovary.
Bertolin K; Gossen J; Schoonjans K; Murphy BD
Endocrinology; 2014 May; 155(5):1931-43. PubMed ID: 24552399
[TBL] [Abstract][Full Text] [Related]
13. Microtubular dynamics in granulosa cells of periovulatory follicles and granulosa-derived (large) lutein cells of sheep: relationships to the steroidogenic folliculo-luteal shift and functional luteolysis.
Murdoch WJ
Biol Reprod; 1996 May; 54(5):1135-40. PubMed ID: 8722636
[TBL] [Abstract][Full Text] [Related]
14. Estrogen promotes luteolysis by redistributing prostaglandin F2α receptors within primate luteal cells.
Kim SO; Markosyan N; Pepe GJ; Duffy DM
Reproduction; 2015 May; 149(5):453-64. PubMed ID: 25687410
[TBL] [Abstract][Full Text] [Related]
15. Luteal granulosa cells from natural cycles are more capable of maintaining their viability, steroidogenic activity and LH receptor expression than those of stimulated IVF cycles.
Bildik G; Akin N; Seyhan A; Esmaeilian Y; Yakin K; Keles I; Balaban B; Ata B; Urman B; Oktem O
Hum Reprod; 2019 Feb; 34(2):345-355. PubMed ID: 30520979
[TBL] [Abstract][Full Text] [Related]
16. Prolonged luteal activity in mares--a semantic quagmire.
Ginther OJ
Equine Vet J; 1990 May; 22(3):152-6. PubMed ID: 2193807
[TBL] [Abstract][Full Text] [Related]
17. Loss of the proapoptotic BH3-only protein BCL-2 modifying factor prolongs the fertile life span in female mice.
Liew SH; Vaithiyanathan K; Cook M; Bouillet P; Scott CL; Kerr JB; Strasser A; Findlay JK; Hutt KJ
Biol Reprod; 2014 Apr; 90(4):77. PubMed ID: 24571986
[TBL] [Abstract][Full Text] [Related]
18. Hormonal and immunological characterization of the 32 kilodalton ovarian-specific protein.
Parmer TG; McLean MP; Duan WR; Nelson SE; Albarracin CT; Khan I; Gibori G
Endocrinology; 1992 Nov; 131(5):2213-21. PubMed ID: 1425419
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Ovarian follicular and luteal physiology.
Channing CP; Schaerf FW; Anderson LD; Tsafriri A
Int Rev Physiol; 1980; 22():117-201. PubMed ID: 6248477
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]