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Items: 1 to 20 of 22

1.

Amplification of R-spondin1 signaling induces granulosa cell fate defects and cancers in mouse adult ovary.

De Cian MC, Pauper E, Bandiera R, Vidal VP, Sacco S, Gregoire EP, Chassot AA, Panzolini C, Wilhelm D, Pailhoux E, Youssef SA, de Bruin A, Teerds K, Schedl A, Gillot I, Chaboissier MC.

Oncogene. 2017 Jan 12;36(2):208-218. doi: 10.1038/onc.2016.191. Epub 2016 Jun 6.

2.

Constitutive Activation of PI3K in Oocyte Induces Ovarian Granulosa Cell Tumors.

Kim SY, Ebbert K, Cordeiro MH, Romero MM, Whelan KA, Suarez AA, Woodruff TK, Kurita T.

Cancer Res. 2016 Jul 1;76(13):3851-61. doi: 10.1158/0008-5472.CAN-15-3358. Epub 2016 May 9.

PMID:
27197196
3.

Insights into granulosa cell tumors using spontaneous or genetically engineered mouse models.

Kim SY.

Clin Exp Reprod Med. 2016 Mar;43(1):1-8. doi: 10.5653/cerm.2016.43.1.1. Epub 2016 Mar 31. Review.

4.

Deletion of Arid1a in Reproductive Tract Mesenchymal Cells Reduces Fertility in Female Mice.

Wang X, Khatri S, Broaddus R, Wang Z, Hawkins SM.

Biol Reprod. 2016 Apr;94(4):93. doi: 10.1095/biolreprod.115.133637. Epub 2016 Mar 9.

5.

The role of WNT signaling in adult ovarian folliculogenesis.

Hernandez Gifford JA.

Reproduction. 2015 Oct;150(4):R137-48. doi: 10.1530/REP-14-0685. Epub 2015 Jun 30. Review.

6.

FOXO1/3 and PTEN Depletion in Granulosa Cells Promotes Ovarian Granulosa Cell Tumor Development.

Liu Z, Ren YA, Pangas SA, Adams J, Zhou W, Castrillon DH, Wilhelm D, Richards JS.

Mol Endocrinol. 2015 Jul;29(7):1006-24. doi: 10.1210/me.2015-1103. Epub 2015 Jun 10.

7.

The absence of ER-β results in altered gene expression in ovarian granulosa cells isolated from in vivo preovulatory follicles.

Binder AK, Rodriguez KF, Hamilton KJ, Stockton PS, Reed CE, Korach KS.

Endocrinology. 2013 Jun;154(6):2174-87. doi: 10.1210/en.2012-2256. Epub 2013 Apr 11.

8.

MLH1-silenced and non-silenced subgroups of hypermutated colorectal carcinomas have distinct mutational landscapes.

Donehower LA, Creighton CJ, Schultz N, Shinbrot E, Chang K, Gunaratne PH, Muzny D, Sander C, Hamilton SR, Gibbs RA, Wheeler D.

J Pathol. 2013 Jan;229(1):99-110. doi: 10.1002/path.4087.

9.

Consequences of RAS and MAPK activation in the ovary: the good, the bad and the ugly.

Fan HY, Liu Z, Mullany LK, Richards JS.

Mol Cell Endocrinol. 2012 Jun 5;356(1-2):74-9. doi: 10.1016/j.mce.2011.12.005. Epub 2011 Dec 16. Review.

10.

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 22;31(12):1504-20. doi: 10.1038/onc.2011.341. Epub 2011 Aug 22.

11.

The Wnt inhibitory factor 1 (WIF1) is targeted in glioblastoma and has a tumor suppressing function potentially by induction of senescence.

Lambiv WL, Vassallo I, Delorenzi M, Shay T, Diserens AC, Misra A, Feuerstein B, Murat A, Migliavacca E, Hamou MF, Sciuscio D, Burger R, Domany E, Stupp R, Hegi ME.

Neuro Oncol. 2011 Jul;13(7):736-47. doi: 10.1093/neuonc/nor036. Epub 2011 Jun 3.

12.

Beta-catenin (CTNNB1) promotes preovulatory follicular development but represses LH-mediated ovulation and luteinization.

Fan HY, O'Connor A, Shitanaka M, Shimada M, Liu Z, Richards JS.

Mol Endocrinol. 2010 Aug;24(8):1529-42. doi: 10.1210/me.2010-0141. Epub 2010 Jul 7.

13.

WNT4/beta-catenin pathway maintains female germ cell survival by inhibiting activin betaB in the mouse fetal ovary.

Liu CF, Parker K, Yao HH.

PLoS One. 2010 Apr 29;5(4):e10382. doi: 10.1371/journal.pone.0010382.

14.

WNT4 is required for normal ovarian follicle development and female fertility.

Boyer A, Lapointe E, Zheng X, Cowan RG, Li H, Quirk SM, DeMayo FJ, Richards JS, Boerboom D.

FASEB J. 2010 Aug;24(8):3010-25. doi: 10.1096/fj.09-145789. Epub 2010 Apr 6.

15.

Minireview: physiological and pathological actions of RAS in the ovary.

Fan HY, Richards JS.

Mol Endocrinol. 2010 Feb;24(2):286-98. doi: 10.1210/me.2009-0251. Epub 2009 Oct 30. Review.

16.

Muscle satellite cells are a functionally heterogeneous population in both somite-derived and branchiomeric muscles.

Ono Y, Boldrin L, Knopp P, Morgan JE, Zammit PS.

Dev Biol. 2010 Jan 1;337(1):29-41. doi: 10.1016/j.ydbio.2009.10.005. Epub 2009 Oct 14.

17.

The mammalian ovary from genesis to revelation.

Edson MA, Nagaraja AK, Matzuk MM.

Endocr Rev. 2009 Oct;30(6):624-712. doi: 10.1210/er.2009-0012. Epub 2009 Sep 23. Review.

18.

Conditional deletion of beta-catenin mediated by Amhr2cre in mice causes female infertility.

Hernandez Gifford JA, Hunzicker-Dunn ME, Nilson JH.

Biol Reprod. 2009 Jun;80(6):1282-92. doi: 10.1095/biolreprod.108.072280. Epub 2009 Jan 28.

19.

Dicer1 is essential for female fertility and normal development of the female reproductive system.

Hong X, Luense LJ, McGinnis LK, Nothnick WB, Christenson LK.

Endocrinology. 2008 Dec;149(12):6207-12. doi: 10.1210/en.2008-0294. Epub 2008 Aug 14.

20.

Synergistic effects of Pten loss and WNT/CTNNB1 signaling pathway activation in ovarian granulosa cell tumor development and progression.

Laguë MN, Paquet M, Fan HY, Kaartinen MJ, Chu S, Jamin SP, Behringer RR, Fuller PJ, Mitchell A, Doré M, Huneault LM, Richards JS, Boerboom D.

Carcinogenesis. 2008 Nov;29(11):2062-72. doi: 10.1093/carcin/bgn186. Epub 2008 Aug 6.

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