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Select item 110567031.

FOXL2 and NR5A1 induce human fibroblasts into steroidogenic ovarian granulosa‐like cells

Fan Wen, Yuxi Ding, Mingming Wang, Jing Du, Shen Zhang, Kehkooi Kee

Cell Prolif. 2024 May; 57(5): e13589. Published online 2024 Jan 8. doi: 10.1111/cpr.13589

PMCID:: PMC11056703

Abstract Article PDF–10M

Select item 107496742.

Deletion of cis-regulatory Element in FOXL2 Promoter in a Chinese Family of Type II Blepharophimosis-ptosis-epicanthus Inversus Syndrome with Polydactyly

Qin Shen, Xiaojun Zhao, Yongrong Ji, Peiwei Chai

J Craniofac Surg. 2024 Jan-Feb; 35(1): e52–e56. Published online 2023 Nov 8. doi: 10.1097/SCS.0000000000009801

PMCID:: PMC10749674

Abstract Article PDF–411K

Select item 106290093.

Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family

Zhi-Bo Lin, Zhen-Ji Chen, Hui Yang, Xing-Ru Ding, Jin Li, An-Peng Pan, Hai-Sen Sun, A.-Yong Yu, Shi-Hao Chen

BMC Ophthalmol. 2023; 23: 446. Published online 2023 Nov 7. doi: 10.1186/s12886-023-03189-5

PMCID:: PMC10629009

Abstract Article PDF–1.5M

Select item 103975094.

ERK1/2-SOX9/FOXL2 axis regulates ovarian steroidogenesis and favors the follicular–luteal transition

Vijay Simha Baddela, Marten Michaelis, Xuelian Tao, Dirk Koczan, Jens Vanselow

Life Sci Alliance. 2023 Oct; 6(10): e202302100. Published online 2023 Aug 2. doi: 10.26508/lsa.202302100

PMCID:: PMC10397509

Abstract Article PDF–3.3M

Select item 103261215.

Incidental FOXL2 mutated adult granulosa cell tumour of the ovary with thecoma-like foci

Anne Kristin Fischer, Birgid Schömig-Markiefka, Carina Heydt, Dominik Ratiu, Peter Mallmann, Jörn Meinel, Reinhard Büttner, Dietmar Schmidt, Alexander Quaas

Virchows Arch. 2023; 483(1): 117–124. Published online 2022 Nov 18. doi: 10.1007/s00428-022-03452-y

PMCID:: PMC10326121

Abstract Article PDF–2.2M

Select item 97559996.

Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract

Bixia Zheng, Steve Seltzsam, Chunyan Wang, Luca Schierbaum, Sophia Schneider, Chen-Han Wilfred Wu, Rufeng Dai, Dervla M Connaughton, Makiko Nakayama, Nina Mann, Natasa Stajic, Shrikant Mane, Stuart B Bauer, Velibor Tasic, Hyun Joo Nam, Shirlee Shril, Friedhelm Hildebrandt

Nephrol Dial Transplant. 2022 Oct; 37(10): 1833–1843. Published online 2021 Sep 2. doi: 10.1093/ndt/gfab253

PMCID:: PMC9755999

Abstract Article PDF–1.8M

Select item 94108757.

FOXL2 and FOXA1 cooperatively assemble on the TP53 promoter in alternative dimer configurations

Yuri Choi, Yongyang Luo, Seunghwa Lee, Hanyong Jin, Hye-Jin Yoon, Yoonsoo Hahn, Jeehyeon Bae, Hyung Ho Lee

Nucleic Acids Res. 2022 Aug 26; 50(15): 8929–8946. Published online 2022 Aug 3. doi: 10.1093/nar/gkac673

PMCID:: PMC9410875

Abstract Article PDF–5.3M

Select item 82783228.

Mutant FOXL2^C134W highjacks SMAD4 and SMAD2/3 to drive adult granulosa cell tumors

Stine E. Weis-Banke, Mads Lerdrup, Daniela Kleine-Kohlbrecher, Faizaan Mohammad, Simone Sidoli, Ole N. Jensen, Toshihiko Yanase, Tomoko Nakamura, Akira Iwase, Anthe Stylianou, Nadeem R. Abu-Rustum, Carol Aghajanian, Robert Soslow, Arnaud Da Cruz Paula, Richard P. Koche, Britta Weigelt, Jesper Christensen, Kristian Helin, Paul A.C. Cloos

Cancer Res. Author manuscript; available in PMC 2021 Jul 14.

Published in final edited form as: Cancer Res. 2020 Sep 1; 80(17): 3466–3479. Published online 2020 Jul 8. doi: 10.1158/0008-5472.CAN-20-0259

PMCID:: PMC8278322

Abstract Article PDF–2.5M

Select item 80729969.

Adult‐type granulosa cell tumor of the ovary: a FOXL2‐centric disease

Jessica A Pilsworth, Dawn R Cochrane, Samantha J Neilson, Bahar H Moussavi, Daniel Lai, Aslı D Munzur, Janine Senz, Yi Kan Wang, Sina Zareian, Ali Bashashati, Adele Wong, Jacqueline Keul, Annette Staebler, Hannah S van Meurs, Hugo M Horlings, Stefan Kommoss, Friedrich Kommoss, Esther Oliva, Anniina EM Färkkilä, Blake Gilks, David G Huntsman

J Pathol Clin Res. 2021 May; 7(3): 243–252. Published online 2021 Jan 11. doi: 10.1002/cjp2.198

PMCID:: PMC8072996

Abstract Article PDF–629K

Select item 800904810.

Impact of cytosine methylation on DNA binding specificities of human transcription factors

Yimeng Yin, Ekaterina Morgunova, Arttu Jolma, Eevi Kaasinen, Biswajyoti Sahu, Syed Khund-Sayeed, Pratyush K. Das, Teemu Kivioja, Kashyap Dave, Fan Zhong, Kazuhiro R. Nitta, Minna Taipale, Alexander Popov, Paul A. Ginno, Silvia Domcke, Jian Yan, Dirk Schübeler, Charles Vinson, Jussi Taipale

Science. Author manuscript; available in PMC 2021 Mar 30.

Published in final edited form as: Science. 2017 May 5; 356(6337): eaaj2239. doi: 10.1126/science.aaj2239

PMCID:: PMC8009048

Abstract Article PDF–2.6M

Select item 800791311.

Functional Studies of Novel FOXL2 Variants in Chinese Families With Blepharophimosis–Ptosis–Epicanthus Inversus Syndrome

Fang Li, Huifang Chen, Yefei Wang, Jie Yang, Yixiong Zhou, Xin Song, Jiayan Fan

Front Genet. 2021; 12: 616112. Published online 2021 Mar 16. doi: 10.3389/fgene.2021.616112

PMCID:: PMC8007913

Abstract Article PDF–3.3M

Select item 799857512.

The Genetic and Clinical Features of FOXL2-Related Blepharophimosis, Ptosis and Epicanthus Inversus Syndrome

Cécile Méjécase, Chandni Nigam, Mariya Moosajee, John C. Bladen

Genes (Basel) 2021 Mar; 12(3): 364. Published online 2021 Mar 4. doi: 10.3390/genes12030364

PMCID:: PMC7998575

Abstract Article PDF–781K

Select item 773760613.

An alternative miRISC targets a cancer‐associated coding sequence mutation in FOXL2

Eunkyoung Shin, Hanyong Jin, Dae‐Shik Suh, Yongyang Luo, Hye‐Jeong Ha, Tae Heon Kim, Yoonsoo Hahn, Seogang Hyun, Kangseok Lee, Jeehyeon Bae

EMBO J. 2020 Dec 15; 39(24): e104719. Published online 2020 Nov 20. doi: 10.15252/embj.2020104719

Correction in:: EMBO J. 2021 Aug 16; 40(16): e108163.

PMCID:: PMC7737606

Abstract Article PDF–3.7M

Select item 745513914.

Ovarian granulosa cell tumor characterization identifies FOXL2 as an immunotherapeutic target

Stefano Pierini, Janos L. Tanyi, Fiona Simpkins, Erin George, Mireia Uribe-Herranz, Ronny Drapkin, Robert Burger, Mark A. Morgan, Andrea Facciabene

JCI Insight. 2020 Aug 20; 5(16): e136773. Published online 2020 Aug 20. doi: 10.1172/jci.insight.136773

PMCID:: PMC7455139

Abstract Article PDF–7.4M

Select item 721893715.

FOXL2 expression might be a novel prognostic biomarker in patients with laryngeal squamous cell carcinoma

Jun Ge, Li Jiang, Yuke Tian, Min Zheng, Meiling Huang, Juan Li

J Int Med Res. 2020 Apr; 48(4): 0300060520919252. Published online 2020 Apr 28. doi: 10.1177/0300060520919252

PMCID:: PMC7218937

Abstract Article PDF–646K

Select item 718160816.

FOXL2 directs DNA double-strand break repair pathways by differentially interacting with Ku

Hanyong Jin, Boeun Lee, Yongyang Luo, Yuri Choi, Eui-Hwan Choi, Hong Jin, Kee-Beom Kim, Sang Beom Seo, Yong-Hak Kim, Hyung Ho Lee, Keun Pil Kim, Kangseok Lee, Jeehyeon Bae

Nat Commun. 2020; 11: 2010. Published online 2020 Apr 24. doi: 10.1038/s41467-020-15748-1

PMCID:: PMC7181608

Abstract Article PDF–4.8M

Select item 700063417.

A novel FOXL2 mutation in two infertile patients with blepharophimosis–ptosis–epicanthus inversus syndrome

Jingmei Hu, Hanni Ke, Wei Luo, Yajuan Yang, Hongli Liu, Guangyu Li, Yingying Qin, Jinlong Ma, Shidou Zhao

J Assist Reprod Genet. 2020 Jan; 37(1): 223–229. Published online 2019 Dec 10. doi: 10.1007/s10815-019-01651-2

PMCID:: PMC7000634

Abstract Article PDF–1.5M

Select item 667014018.

Premature ovarian insufficiency as a variable feature of blepharophimosis, ptosis, and epicanthus inversus syndrome associated with c.223C > T p.(Leu75Phe) FOXL2 mutation: a case report

Barbara Grzechocińska, Damian Warzecha, Maria Wypchło, Rafal Ploski, Mirosław Wielgoś

BMC Med Genet. 2019; 20: 132. Published online 2019 Jul 31. doi: 10.1186/s12881-019-0865-0

PMCID:: PMC6670140

Abstract Article PDF–1.1M

Select item 642009719.

H4K20me0 recognition by BRCA1-BARD1 directs homologous recombination in sister chromatids

Kyosuke Nakamura, Giulia Saredi, Jordan R. Becker, Benjamin M. Foster, Nhuong V. Nguyen, Tracey Beyer, Laura C. Cesa, Peter A. Faull, Saulius Lukauskas, Thomas Frimurer, J. Ross Chapman, Till Bartke, Anja Groth

Nat Cell Biol. Author manuscript; available in PMC 2019 Aug 25.

Published in final edited form as: Nat Cell Biol. 2019 Mar; 21(3): 311–318. Published online 2019 Feb 25. doi: 10.1038/s41556-019-0282-9

PMCID:: PMC6420097

Article PDF–1.7M

Select item 623815120.

FOXL2^C134W-Induced CYP19 Expression via Cooperation With SMAD3 in HGrC1 Cells

Martina Belli, Nahoko Iwata, Tomoko Nakamura, Akira Iwase, Dwayne Stupack, Shunichi Shimasaki

Endocrinology. 2018 Apr; 159(4): 1690–1703. Published online 2018 Feb 19. doi: 10.1210/en.2017-03207

PMCID:: PMC6238151

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