Forkhead transcription factors: key players in development and metabolism.
By P. Carlsson, M. Mahlapuu. Developmental Biology, 2002
906 citations recorded by the source corpus.
View Paper: https://www.semanticscholar.org/paper/ac157db0e4bfa24e3006b2c3af91a3efecf5adcd
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- Armando van der Horst
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- I. Wang
Citations in the corpus
- A Transparent Window into Biology: A Primer on Caenorhabditis elegans (2015, background): “The vertebrate FoxA transcription factors are homologous to PHA-4 and are involved in gut development in many species (Carlsson and Mahlapuu 2002).”
- FOXP3 controls regulatory T cell function through cooperation with NFAT. (2006, unknown): “The AP-1 binding sequence in the Il2 promoter ARRE2 site resembles consensus binding sites for forkhead proteins (Carlsson and Mahlapuu, 2002) and for FOXP1 (Wang et al., 2003) (Figure 1C).”
- The epithelial–mesenchymal transition: new insights in signaling, development, and disease (2006, unknown): “Both Twist and Goosecoid regulate FOXC2, which is a transcription factor of the FOX family of forkhead helix-turn-helix DNA-binding proteins that regulates EMT and organ development in multiple tissues (Carlsson and Mahlapuu, 2002).”
- Forkhead Box M1 Regulates the Transcriptional Network of Genes Essential for Mitotic Progression and Genes Encoding the SCF (Skp2-Cks1) Ubiquitin Ligase (2005, background): “The mammalian Forkhead box (Fox) family of transcription factors consists of more than 50 mammalian proteins (9, 26) that share homology in the winged helix DNA binding domain (12, 43).”
- Stressing the role of FoxO proteins in lifespan and disease (2007, background): “Until now, more than 100 members of this evolutionarily conserved transcription factor family have been identified, with roles in development, differentiation, proliferation, apoptosis, stress resistance and metabolism (reviewed in Ref”