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    Glossary FOXC1

    gene encoding a transcription factor crucial for tissue development

    FOXC1, or Forkhead Box C1, is a gene that encodes a transcription factor involved in the regulation of gene expression. This protein plays a crucial role in the development of various tissues, including the eyes, heart, and kidneys. Mutations in the FOXC1 gene can lead to developmental disorders such as Axenfeld-Rieger syndrome, which can affect the eyes and other parts of the body.

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    Research 10 of 897

    1. Foxc1 reinforces quiescence in self-renewing hair follicle stem cells Science · 2016 · 142 citations
    2. Transcription factor FOXC1 positively regulates SFRP1 expression in androgenetic alopecia Experimental Cell Research · 2021
    3. Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis Genes & development · 2010 · 95 citations
    4. FOXE1, A New Transcriptional Target of GLI2 Is Expressed in Human Epidermis and Basal Cell Carcinoma Journal of Investigative Dermatology · 2004 · 92 citations
    5. FOXO1, TGF-β Regulation and Wound Healing International Journal of Molecular Sciences · 2014 · 87 citations
    6. FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program Frontiers in Immunology · 2013 · 69 citations
    7. The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation 2010 · 68 citations
    8. Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation Developmental Biology · 2008 · 67 citations
    9. Evidence That the Satin Hair Mutant Gene Foxq1 Is among Multiple and Functionally Diverse Regulatory Targets for Hoxc13 during Hair Follicle Differentiation 2006 · 65 citations
    10. FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice 2004 · 58 citations
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