Citations for
1FOXL1
Foxl1 promotes liver repair following cholestatic injury in mice.
Sackett SD, Gao Y, Shin S, Esterson YB, Tsingalia A, Hurtt RS, Brondell K, Kaestner KH, Greenbaum LE.
Lab Invest ab Invest. 2009 Oct 19. [Epub ahead of print] 2009
2FOXF1, FOXL1
FoxF1 and FoxL1 link hedgehog signaling and the control of epithelial proliferation in the developing stomach and intestine.
Madison BB, McKenna LB, Dolson D, Epstein DJ, Kaestner KH.
J Biol Chem 284(9):5936-44. Epub 2008 Dec 2. 2009
3FOXL1
Foxl1 is a mesenchymal Modifier of Min in carcinogenesis of stomach and colon.
Perreault N, Sackett SD, Katz JP, Furth EE, Kaestner KH.
Genes Dev 19(3):311-5. Epub 2005 Jan 13. 2005
4FOXL1
Reduction of SNAP25 in acid secretion defect of Foxl1-/- gastric parietal cells.
Kato Y, Fukamachi H, Takano-Maruyama M, Aoe T, Murahashi Y, Horie S, Suzuki Y, Saito Y, Koseki H, Ohno H.
Biochem Biophys Res Commun 320(3):766-72. 2004
5FOXL1
Mesenchymal transcription factor Fkh6 is essential for the development and differentiation of parietal cells.
Fukamachi H, Fukuda K, Suzuki M, Furumoto T, Ichinose M, Shimizu S, Tsuchiya S, Horie S, Suzuki Y, Saito Y, Watanabe K, Taniguchi M, Koseki H.
Biochem Biophys Res Commun 280(4):1069-76. 2001
6FOXC2, FOXL1, LPDD
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.
Fang J, Dagenais SL, Erickson RP, Arlt MF, Glynn MW, Gorski JL, Seaver LH, Glover TW.
Am J Hum Genet 67(6):1382-8. 2000
7FOXC2, FOXL1
Clustered arrangement of winged helix genes fkh-6 and MFH-1: possible implications for mesoderm development.
Kaestner KH, Bleckmann SC, Monaghan AP, Schlondorff J, Mincheva A, Lichter P, Schutz G.
Development 122(6):1751-8. 1996
8FOXC1, FOXD1, FOXD4, FOXE3, FOXF1, FOXI1, FOXL1
Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending.
Pierrou S, Hellqvist M, Samuelsson L, Enerback S, Carlsson P.
EMBO J 13(20) : 5002-12. 1994