PubMed for id: 2296

Year	Number of Results
1993	1
1994	1
1995	1
1996	1
1997	2
1998	2
1999	1
2000	2
2001	7
2002	7
2003	6
2004	4
2005	1
2006	7
2007	8
2008	9
2009	13
2010	7
2011	11
2012	13
2013	7
2014	11
2015	18
2016	19
2017	18
2018	21
2019	14
2020	23
2021	22
2022	13
2023	5
2024	2

1

Research progress on the regulatory mechanisms of FOXC1 expression in cancers and its role in drug resistance.

Yang Y, Li W, Yang H, Zhang Y, Zhang S, Xu F, Hao Y, Cao W, Du G, Wang J. Yang Y, et al. Gene. 2024 Mar 1;897:148079. doi: 10.1016/j.gene.2023.148079. Epub 2023 Dec 13. Gene. 2024. PMID: 38101711 Review.

2

FoxC1 activates limbal epithelial stem cells following corneal epithelial debridement.

Yang W, Lee SK, Lehmann OJ, Wu Z, Hiriyanna S, Swaroop A, Lavker RM, Peng H, Kume T. Yang W, et al. Exp Eye Res. 2023 Sep;234:109599. doi: 10.1016/j.exer.2023.109599. Epub 2023 Jul 22. Exp Eye Res. 2023. PMID: 37488009

3

Spectrum of white matter abnormalities associated with FOXC1-related disorders in two unrelated cases.

Tabassum T, Maria Daniela D, La Piana R. Tabassum T, et al. Am J Med Genet C Semin Med Genet. 2023 Jun;193(2):167-171. doi: 10.1002/ajmg.c.32051. Epub 2023 May 31. Am J Med Genet C Semin Med Genet. 2023. PMID: 37255026

4

Somatic FOXC1 insertion mutation remodels the immune microenvironment and promotes the progression of childhood acute lymphoblastic leukemia.

Wang Y, Ma X, Huang J, Yang X, Kang M, Sun X, Li H, Wu Y, Zhang H, Zhu Y, Xue Y, Fang Y. Wang Y, et al. Cell Death Dis. 2022 May 3;13(5):431. doi: 10.1038/s41419-022-04873-y. Cell Death Dis. 2022. PMID: 35504885 Free PMC article.

5

Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1.

Ahmed MR, Sethna S, Krueger LA, Yang MB, Hufnagel RB. Ahmed MR, et al. Genes (Basel). 2022 Feb 24;13(3):411. doi: 10.3390/genes13030411. Genes (Basel). 2022. PMID: 35327965 Free PMC article.

6

FOXC1.

Li M, Lv H, Zhong S, Zhou S, Lu H, Yang W. Li M, et al. Arch Pathol Lab Med. 2022 Aug 1;146(8):994-1003. doi: 10.5858/arpa.2021-0039-OA. Arch Pathol Lab Med. 2022. PMID: 34784418 Free article.

7

Identification and functional study of FOXC1 variants in Chinese families with glaucoma.

Wang X, Liu X, Li Y, Yang B, Sun X, Yang P, Zhong Z, Chen J. Wang X, et al. Am J Med Genet A. 2022 Feb;188(2):540-547. doi: 10.1002/ajmg.a.62551. Epub 2021 Nov 6. Am J Med Genet A. 2022. PMID: 34741396

8

[FOXC1 Knockdown Reverses Gefitinib Resistance in Non-small Cell Lung Cancer].

Peng C, Li P, Yang M, Chen D, Huang Y. Peng C, et al. Zhongguo Fei Ai Za Zhi. 2021 Aug 20;24(8):538-547. doi: 10.3779/j.issn.1009-3419.2021.103.11. Epub 2021 Aug 2. Zhongguo Fei Ai Za Zhi. 2021. PMID: 34334155 Free PMC article. Chinese.

9

Loss of FOXC1 contributes to the corneal epithelial fate switch and pathogenesis.

Li M, Zhu L, Liu J, Huang H, Guo H, Wang L, Li L, Gu S, Tan J, Zhong J, Wang B, Mao Z, Fan Y, Liu C, Yuan J, Ouyang H. Li M, et al. Signal Transduct Target Ther. 2021 Jan 8;6(1):5. doi: 10.1038/s41392-020-00378-2. Signal Transduct Target Ther. 2021. PMID: 33414365 Free PMC article.

10

FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma.

Or L, Barkana Y, Hecht I, Weiner C, Einan-Lifshitz A, Pras E. Or L, et al. Exp Eye Res. 2020 Nov;200:108220. doi: 10.1016/j.exer.2020.108220. Epub 2020 Sep 6. Exp Eye Res. 2020. PMID: 32905845

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