118 related articles for article (PubMed ID: 34396573)
1. Reply to "An alternative miRISC targets a cancer-associated coding sequence mutation in FOXL2".
Veitia RA; Pilsworth J; Todeschini AL; Huntsman D
EMBO J; 2021 Aug; 40(16):e107517. PubMed ID: 34396573
[TBL] [Abstract][Full Text] [Related]
2. An alternative miRISC targets a cancer-associated coding sequence mutation in FOXL2.
Shin E; Jin H; Suh DS; Luo Y; Ha HJ; Kim TH; Hahn Y; Hyun S; Lee K; Bae J
EMBO J; 2020 Dec; 39(24):e104719. PubMed ID: 33215742
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Functional exploration of the adult ovarian granulosa cell tumor-associated somatic FOXL2 mutation p.Cys134Trp (c.402C>G).
Benayoun BA; Caburet S; Dipietromaria A; Georges A; D'Haene B; Pandaranayaka PJ; L'Hôte D; Todeschini AL; Krishnaswamy S; Fellous M; De Baere E; Veitia RA
PLoS One; 2010 Jan; 5(1):e8789. PubMed ID: 20098707
[TBL] [Abstract][Full Text] [Related]
5. Identification of a novel FOXL2 mutation in a single family with both types of blepharophimosis‑-ptosis-epicanthus inversus syndrome.
Yang L; Li T; Xing Y
Mol Med Rep; 2017 Oct; 16(4):5529-5532. PubMed ID: 28849110
[TBL] [Abstract][Full Text] [Related]
6. Clinical characterization and identification of five novel FOXL2 pathogenic variants in a cohort of 12 Mexican subjects with the syndrome of blepharophimosis-ptosis-epicanthus inversus.
Chacón-Camacho OF; Salgado-Medina A; Alcaraz-Lares N; López-Moreno D; Barragán-Arévalo T; Nava-Castañeda A; Rodríguez-Uribe G; Lieberman E; Rodríguez-Cabrera L; González-Del Angel A; Borbolla AM; Fernández-Hernández L; Graue-Hernández EO; Zenteno JC
Gene; 2019 Jul; 706():62-68. PubMed ID: 31048069
[TBL] [Abstract][Full Text] [Related]
7. FOXL2
Fuller PJ; Nguyen T; Alexiadis M; Chu S
J Pathol; 2022 Jan; 256(1):1-3. PubMed ID: 34687235
[TBL] [Abstract][Full Text] [Related]
8. The Pathognomonic FOXL2 C134W Mutation Alters DNA-Binding Specificity.
Carles A; Trigo-Gonzalez G; Cao Q; Cheng SG; Moksa M; Bilenky M; Huntsman DG; Morin GB; Hirst M
Cancer Res; 2020 Sep; 80(17):3480-3491. PubMed ID: 32641414
[TBL] [Abstract][Full Text] [Related]
9. DICER1 and FOXL2 Mutation Status Correlates With Clinicopathologic Features in Ovarian Sertoli-Leydig Cell Tumors.
Karnezis AN; Wang Y; Keul J; Tessier-Cloutier B; Magrill J; Kommoss S; Senz J; Yang W; Proctor L; Schmidt D; Clement PB; Gilks CB; Huntsman DG; Kommoss F
Am J Surg Pathol; 2019 May; 43(5):628-638. PubMed ID: 30986800
[TBL] [Abstract][Full Text] [Related]
10. FOXL2 and TERT promoter mutation detection in circulating tumor DNA of adult granulosa cell tumors as biomarker for disease monitoring.
Groeneweg JW; Roze JF; Peters EDJ; Sereno F; Brink AGJ; Paijens ST; Nijman HW; van Meurs HS; van Lonkhuijzen LRCW; Piek JMJ; Lok CAR; Monroe GR; van Haaften GW; Zweemer RP
Gynecol Oncol; 2021 Aug; 162(2):413-420. PubMed ID: 34083028
[TBL] [Abstract][Full Text] [Related]
11. The anti-Müllerian hormone (AMH) induces forkhead box L2 (FOXL2) expression in primary culture of human granulosa cells in vitro.
Sacchi S; Marinaro F; Xella S; Marsella T; Tagliasacchi D; La Marca A
J Assist Reprod Genet; 2017 Sep; 34(9):1131-1136. PubMed ID: 28660501
[TBL] [Abstract][Full Text] [Related]
12. A Novel Forkhead Box L2 Missense Mutation, c.1068G>C, in a Chinese Family With Blepharophimosis/Ptosis/ Epicanthus Inversus Syndrome.
Wang S; Ge S; Zhuang A
J Craniofac Surg; 2022 May; 33(3):e238-e240. PubMed ID: 34374675
[TBL] [Abstract][Full Text] [Related]
13. Genomic Disruption of
Niu BB; Tang N; Xu Q; Chai PW
Chin Med J (Engl); 2018 Oct; 131(19):2380-2383. PubMed ID: 30246734
[No Abstract] [Full Text] [Related]
14. FOXL2 Mutation Analysis of Ovarian Sex Cord-Stromal Tumors: Genotype-Phenotype Correlation With Diagnostic Considerations.
Buza N; Wong S; Hui P
Int J Gynecol Pathol; 2018 Jul; 37(4):305-315. PubMed ID: 28700438
[TBL] [Abstract][Full Text] [Related]
15. Rare DICER1 and Absent FOXL2 Mutations Characterize Ovarian Juvenile Granulosa Cell Tumors.
Baillard P; Genestie C; Croce S; Descotes F; Rouleau E; Treilleux I; Gouy S; Morice P; Ray-Coquard I; McCluggage WG; Devouassoux-Shisheboran M
Am J Surg Pathol; 2021 Feb; 45(2):223-229. PubMed ID: 32910017
[TBL] [Abstract][Full Text] [Related]
16. Hypopituitarism in Patients with Blepharophimosis and FOXL2 Mutations.
Castets S; Roucher-Boulez F; Saveanu A; Mallet-Motak D; Chabre O; Amati-Bonneau P; Bonneau D; Girardin C; Morel Y; Villanueva C; Brue T; Reynaud R; Nicolino M
Horm Res Paediatr; 2020; 93(1):30-39. PubMed ID: 32454486
[TBL] [Abstract][Full Text] [Related]
17. FOXL2 Mutation Status in Granulosa Theca Cell Tumors of the Ovary.
Nolan A; Joseph NM; Sangoi AR; Rabban J; Zaloudek C; Garg K
Int J Gynecol Pathol; 2017 Nov; 36(6):568-574. PubMed ID: 28319575
[TBL] [Abstract][Full Text] [Related]
18. A Novel FOXL2 Mutation Implying Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Type I.
Li F; Chai P; Fan J; Wang X; Lu W; Li J; Ge S; Jia R; Zhang H; Fan X
Cell Physiol Biochem; 2018; 45(1):203-211. PubMed ID: 29339661
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Roles of forkhead box protein L2 (foxl2) during gonad differentiation and maintenance in a fish, the olive flounder (Paralichthys olivaceus).
Fan Z; Zou Y; Liang D; Tan X; Jiao S; Wu Z; Li J; Zhang P; You F
Reprod Fertil Dev; 2019 Oct; 31(11):1742-1752. PubMed ID: 31537253
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
