...Gabriele Liuzzi; Osvaldo Artimagnella; Simone Frisari; Antonello Mallamaci ABSTRACT Foxg1 masters telencephalic development via a pleiotropic control over its progression. Expressed within the central nervous system (CNS), L1 retrotransposons are implicated in progression of its histogenesis...

... demonstrate that the proliferation of Ecrg4-deficient NSCs was partly maintained by the increased expression of Foxg1. Collectively, these results determine Ecrg4 as a NSC aging factor. * Author for correspondence ( [email protected] ) Competing interests The authors declare no competing...

... is restricted to its medial position is therefore a fundamental patterning issue. Here, we demonstrate that Foxg1 - Lhx2 interactions are crucial for the formation of the hem. Loss of either gene causes a region of the cortical neuroepithelium to transform into hem. We show that FOXG1 regulates Lhx2 expression...

...Martin Roth; Boyan Bonev; Jennefer Lindsay; Robert Lea; Niki Panagiotaki; Corinne Houart; Nancy Papalopulu FoxG1 is a conserved transcriptional repressor that plays a key role in the specification, proliferation and differentiation of the telencephalon, and is expressed from the earliest stages...

...Martine Manuel; Ben Martynoga; Tian Yu; John D. West; John O. Mason; David J. Price Foxg1 is required for development of the ventral telencephalon in the embryonic mammalian forebrain. Although one existing hypothesis suggests that failed ventral telencephalic development in the absence of Foxg1...

..., whereas ipsilateral projections arise from ventrotemporal retina. We investigate how development of these patterns of projection is regulated by the contralateral determinant Foxg1, a forkhead box transcription factor expressed in nasal retina and at the chiasm. In nasal retina, loss of Foxg1 causes...

..., IN 46285, USA 23 9 2005 ©2005. 2005 FGF Vomeronasal organ Neurogenesis Olfactory epithelium Nasal cavity Stem cell Apoptosis Cre recombinase Fgf8 Foxg1 Sox2 Pax6 Mash1 Neurogenin 1 Ncam1 Pyst1 Shh Dlx5 Neuronal progenitor Mouse mutant...

... diencephalon during the formation of the optic chiasm. We report here that in embryos lacking Foxd1,both retinal development and chiasm morphogenesis are disrupted. In the Foxd1 deficient retina, proteins designating the ipsilateral projection, such as Zic2 and EphB1, are missing, and the domain of Foxg1 (BF-1...