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Keywords: FGF10
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Journal Articles
Journal: Development
Development (2019) 146 (2): dev166454.
Published: 16 January 2019
..., localized Fgf10 expression maintains distal Sox9 -expressing epithelial progenitors and promotes basal cell differentiation in the cartilaginous airways. Mesenchymal Fgf10 expression is induced by Wnt signaling but inhibited by Shh signaling, and epithelial Fgf10 signaling activates β-catenin signaling...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2018) 145 (2): dev146829.
Published: 25 January 2018
... are co-expressed distally in the branching epithelium prior to folliculogenesis. The thyroid in Fgf10 null mutants has a normal shape but is severely hypoplastic. Absence of Fgf10 leads to defective branching and disorganized angiofollicular units although Sox9/Fgfr2b expression and the ability of cells...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2017) 144 (18): 3278–3288.
Published: 15 September 2017
... in the embryonic chick. Presumptive hypothalamic cells derive from the rostral diencephalic ventral midline, lie above the prechordal mesendoderm and express Fgf10 . Fgf10 + progenitors undergo anisotropic growth: those displaced rostrally differentiate into anterior cells, then those displaced caudally...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2015) 142 (23): 4056–4067.
Published: 1 December 2015
.... These rudiments expressed the mammary placode markers Wnt10b and Tbx3 and were labeled by antibodies to the mammary mesenchyme markers ERα and androgen receptor. Somitic Fgf10 expression, which is required for normal mammary line formation, was upregulated in mutant cervical somites, and conditional ablation...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2015) 142 (23): 4139–4150.
Published: 1 December 2015
... derives from Fgf10 + progenitor cells, in vivo knockdown of Fgfr2b ligand activity and reduction in Fgf10 expression lead to global reduction in the expression levels of lipofibroblast markers at E18.5. Constitutive Fgfr1b knockouts and mutants with conditional partial inactivation of Fgfr2b in the lung...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2015) 142 (17): 2981–2995.
Published: 1 September 2015
... congenital cystic lung diseases. The cystic lung phenotype in Yy1 mutants can be partly explained by the reduced expression of Shh , a transcriptional target of YY1, in lung endoderm, and the subsequent derepression of mesenchymal Fgf10 expression. Accordingly, SHH supplementation partially rescued the lung...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2014) 141 (17): 3352–3362.
Published: 1 September 2014
... morphogenesis. Basal cells lacking Fgfr2 did not generate an epithelial network owing to a failure in luminal differentiation. Moreover, Fgfr2 null epithelium was unable to undergo ductal branch initiation and elongation due to a deficiency in directional migration. We identified FGF10 and FGF2 as stromal...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2013) 140 (18): 3731–3742.
Published: 15 September 2013
...Thomas Volckaert; Alice Campbell; Erik Dill; Changgong Li; Parviz Minoo; Stijn De Langhe Localized Fgf10 expression in the distal mesenchyme adjacent to sites of lung bud formation has long been thought to drive stereotypic branching morphogenesis even though isolated lung epithelium branches...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2012) 139 (18): 3363–3372.
Published: 15 September 2012
.... We show that pancreatic progenitor-specific ablation of Sox9 during early pancreas development causes pancreas-to-liver cell fate conversion. Sox9 deficiency results in cell-autonomous loss of the fibroblast growth factor receptor (Fgfr) 2b, which is required for transducing mesenchymal Fgf10 signals...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2011) 138 (20): 4465–4473.
Published: 15 October 2011
... of the β-catenin pathway, and that the β-catenin pathway maintains Islet1 expression. These two factors influence each other and function upstream of active proliferation of hindlimb progenitors in the lateral plate mesoderm and the expression of a common factor, Fgf10 . Our data demonstrate that Islet1...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2011) 138 (15): 3331–3340.
Published: 1 August 2011
... been proposed that cardiac fibroblasts are important for growth of the heart during late gestation and are a source of homeostatic factors in the adult. Here, we identify a myocardial to epicardial fibroblast growth factor (FGF) signal, mediated by FGF10 and FGFR2b, that is essential for movement...
Includes: Multimedia, Supplementary data
Journal Articles
Journal: Development
Development (2011) 138 (15): 3307–3317.
Published: 1 August 2011
... and matrix remodeling molecules in Barx2 –/– LGs. In culture, Barx2 regulates expression of matrix metalloproteinases (MMPs) and epithelial cell migration through the extracellular matrix. Fibroblast growth factors are crucial regulators of LG development and we show that Barx2 is required for Fgf10-induced...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2011) 138 (2): 273–282.
Published: 15 January 2011
... a combination of gain- and loss-of-function approaches for FGF10 and SHH, we demonstrate that precise spatio-temporal patterns and appropriate levels of expression of these two signaling molecules in the ventral area are crucial between embryonic day 11.5 and 13.5 for the proper patterning of the cartilage...
Journal Articles
Journal: Development
Development (2010) 137 (22): 3743–3752.
Published: 15 November 2010
... called cervical loops at the base of the incisors. Previous studies have suggested that FGF10, acting mainly through fibroblast growth factor receptor 2b (FGFR2b), is crucial for development of the epithelial stem cell population in mouse incisors. To explore the role of FGFR2b signaling during...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2009) 136 (8): 1387–1396.
Published: 15 April 2009
... and Fgf10 expression in the developing palatal mesenchyme and that specific inactivation of Smo in the palatal mesenchyme indirectly affects palatal epithelial cell proliferation. Together with previous reports that the mesenchymally expressed Fgf10 signals to the palatal epithelium to regulate Shh mRNA...
Includes: Supplementary data
Journal Articles
Journal: Development
Development (2007) 134 (23): 4177–4186.
Published: 1 December 2007
... morphogenesis. Heparanase, an endoglycosidase, colocalized with perlecan in the basement membrane and in epithelial clefts of SMGs. Inhibition of heparanase activity in organ culture decreased branching morphogenesis, and this inhibition was rescued specifically by FGF10 and not by other FGFs. By contrast...
Journal Articles
Journal: Development
Development (2007) 134 (16): 2969–2979.
Published: 15 August 2007
... failure to selectively induce fibroblast growth factor 10 ( Fgf10 ) in the prospective lung region of the foregut. Little is known about the RA-dependent pathways present in the foregut that may be crucial for lung formation. By performing global gene expression analysis of RA-deficient foreguts from...
Journal Articles
Journal: Development
Development (2007) 134 (3): 557–565.
Published: 1 February 2007
.... In the developing seminal vesicles, sustained activation of ERK1/2 was associated with branching morphogenesis and this was absent in svs mutant seminal vesicles. This defect appears to be the immediate downstream effect of partial loss of FGFR2(IIIb)because activation of FGFR2(IIIb) by FGF10 rapidly induced ERK1/2...
Journal Articles
Journal: Development
Development (2007) 134 (1): 93–103.
Published: 1 January 2007
...L. A. Naiche; Virginia E. Papaioannou Tbx4 is a crucial gene in the initiation of hindlimb development and has been reported as a determinant of hindlimb identity and a presumptive direct regulator of Fgf10 in the limb. Using a conditional allele of Tbx4 , we have ablated Tbx4 function before...
Journal Articles
Journal: Development
Development (2006) 133 (8): 1553–1563.
Published: 15 April 2006
... transcripts were co-expressed withΔNp63 in wild-type embryos, but were not detectable in the ectoderm of p63 mutants. In addition, β-catenin and Edar transcripts were significantly reduced in skin ectoderm. We also demonstrate that BMP2, BMP7 and FGF10 are potent inducers of p63 in cultured tissue explants...
Includes: Supplementary data