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.
200 related articles for article (PubMed ID: 21862621)
1. Mutant Forkhead L2 (FOXL2) proteins associated with premature ovarian failure (POF) dimerize with wild-type FOXL2, leading to altered regulation of genes associated with granulosa cell differentiation. Kuo FT; Bentsi-Barnes IK; Barlow GM; Pisarska MD Endocrinology; 2011 Oct; 152(10):3917-29. PubMed ID: 21862621 [TBL] [Abstract][Full Text] [Related]
2. Mouse forkhead L2 maintains repression of FSH-dependent genes in the granulosa cell. Kuo FT; Fan K; Bentsi-Barnes I; Barlow GM; Pisarska MD Reproduction; 2012 Oct; 144(4):485-94. PubMed ID: 22847492 [TBL] [Abstract][Full Text] [Related]
3. Human forkhead L2 represses key genes in granulosa cell differentiation including aromatase, P450scc, and cyclin D2. Bentsi-Barnes IK; Kuo FT; Barlow GM; Pisarska MD Fertil Steril; 2010 Jun; 94(1):353-6. PubMed ID: 19917504 [TBL] [Abstract][Full Text] [Related]
4. LATS1 phosphorylates forkhead L2 and regulates its transcriptional activity. Pisarska MD; Kuo FT; Bentsi-Barnes IK; Khan S; Barlow GM Am J Physiol Endocrinol Metab; 2010 Jul; 299(1):E101-9. PubMed ID: 20407010 [TBL] [Abstract][Full Text] [Related]
5. Forkhead l2 is expressed in the ovary and represses the promoter activity of the steroidogenic acute regulatory gene. Pisarska MD; Bae J; Klein C; Hsueh AJ Endocrinology; 2004 Jul; 145(7):3424-33. PubMed ID: 15059956 [TBL] [Abstract][Full Text] [Related]
6. Differential apoptotic and proliferative activities of wild-type FOXL2 and blepharophimosis-ptosis-epicanthus inversus syndrome (BPES)-associated mutant FOXL2 proteins. Kim JH; Bae J J Reprod Dev; 2014 Mar; 60(1):14-20. PubMed ID: 24240106 [TBL] [Abstract][Full Text] [Related]
7. Functional Analysis of a Novel FOXL2 Indel Mutation in Chinese Families with Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Type I. Chai P; Li F; Fan J; Jia R; Zhang H; Fan X Int J Biol Sci; 2017; 13(8):1019-1028. PubMed ID: 28924383 [No Abstract] [Full Text] [Related]
8. Sumoylation of forkhead L2 by Ubc9 is required for its activity as a transcriptional repressor of the Steroidogenic Acute Regulatory gene. Kuo FT; Bentsi-Barnes IK; Barlow GM; Bae J; Pisarska MD Cell Signal; 2009 Dec; 21(12):1935-44. PubMed ID: 19744555 [TBL] [Abstract][Full Text] [Related]
9. Functional study on new FOXL2 mutations found in Chinese patients with blepharophimosis, ptosis, epicanthus inversus syndrome. Zhou L; Wang J; Wang T BMC Med Genet; 2018 Jul; 19(1):121. PubMed ID: 30029625 [TBL] [Abstract][Full Text] [Related]
10. Synergistic activation of the Mc2r promoter by FOXL2 and NR5A1 in mice. Yang WH; Gutierrez NM; Wang L; Ellsworth BS; Wang CM Biol Reprod; 2010 Nov; 83(5):842-51. PubMed ID: 20650879 [TBL] [Abstract][Full Text] [Related]
11. The Genetic and Clinical Features of Méjécase C; Nigam C; Moosajee M; Bladen JC Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33806295 [TBL] [Abstract][Full Text] [Related]
12. Novel FOXL2 mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian insufficiency. Yang XW; He WB; Gong F; Li W; Li XR; Zhong CG; Lu GX; Lin G; Du J; Tan YQ Mol Genet Genomic Med; 2018 Mar; 6(2):261-267. PubMed ID: 29378385 [TBL] [Abstract][Full Text] [Related]
13. Foxl2 up-regulates aromatase gene transcription in a female-specific manner by binding to the promoter as well as interacting with ad4 binding protein/steroidogenic factor 1. Wang DS; Kobayashi T; Zhou LY; Paul-Prasanth B; Ijiri S; Sakai F; Okubo K; Morohashi K; Nagahama Y Mol Endocrinol; 2007 Mar; 21(3):712-25. PubMed ID: 17192407 [TBL] [Abstract][Full Text] [Related]
14. Minireview: roles of the forkhead transcription factor FOXL2 in granulosa cell biology and pathology. Pisarska MD; Barlow G; Kuo FT Endocrinology; 2011 Apr; 152(4):1199-208. PubMed ID: 21248146 [TBL] [Abstract][Full Text] [Related]
15. Aromatase is a direct target of FOXL2: C134W in granulosa cell tumors via a single highly conserved binding site in the ovarian specific promoter. Fleming NI; Knower KC; Lazarus KA; Fuller PJ; Simpson ER; Clyne CD PLoS One; 2010 Dec; 5(12):e14389. PubMed ID: 21188138 [TBL] [Abstract][Full Text] [Related]
16. FOXL2C134W-Induced CYP19 Expression via Cooperation With SMAD3 in HGrC1 Cells. Belli M; Iwata N; Nakamura T; Iwase A; Stupack D; Shimasaki S Endocrinology; 2018 Apr; 159(4):1690-1703. PubMed ID: 29471425 [TBL] [Abstract][Full Text] [Related]
17. FOXL2 Is an Essential Activator of SF-1-Induced Transcriptional Regulation of Anti-Müllerian Hormone in Human Granulosa Cells. Jin H; Won M; Park SE; Lee S; Park M; Bae J PLoS One; 2016; 11(7):e0159112. PubMed ID: 27414805 [TBL] [Abstract][Full Text] [Related]
18. FOXL2: a central transcription factor of the ovary. Georges A; Auguste A; Bessière L; Vanet A; Todeschini AL; Veitia RA J Mol Endocrinol; 2014 Feb; 52(1):R17-33. PubMed ID: 24049064 [TBL] [Abstract][Full Text] [Related]
19. The Genetics and Biology of FOXL2. Tucker EJ Sex Dev; 2022; 16(2-3):184-193. PubMed ID: 34727551 [TBL] [Abstract][Full Text] [Related]
20. Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development. Uda M; Ottolenghi C; Crisponi L; Garcia JE; Deiana M; Kimber W; Forabosco A; Cao A; Schlessinger D; Pilia G Hum Mol Genet; 2004 Jun; 13(11):1171-81. PubMed ID: 15056605 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]