| 1 |
2019 |
Role of FGF10/FGFR2b Signaling in Mouse Digestive Tract Development, Repair and Regeneration Following Injury. |
FGF10, Fgfr2b, SBR |
| 2 |
2018 |
LHX2 Mediates the FGF-to-SHH Regulatory Loop during Limb Development. |
AER, Shh, ZPA |
| 3 |
2016 |
Fgf regulates dedifferentiation during skeletal muscle regeneration in adult zebrafish. |
EOM, p-ERK |
| 4 |
2016 |
Mechanism of FGF receptor dimerization and activation. |
TM |
| 5 |
2016 |
Sonic hedgehog protein regulates fibroblast growth factor 8 expression in metanephric explant culture from BALB/c mice: Possible mechanisms associated with renal morphogenesis. |
SHH |
| 6 |
2015 |
Attenuating endogenous Fgfr2b ligands during bleomycin-induced lung fibrosis does not compromise murine lung repair. |
Dox, DTG, PN, STG |
| 7 |
2015 |
Control of hepatocyte proliferation and survival by Fgf receptors is essential for liver regeneration in mice. |
Fgfr |
| 8 |
2015 |
Expression of Fgf23 in activated dendritic cells and macrophages in response to immunological stimuli in mice. |
NF-kappaB, TNF-alpha |
| 9 |
2015 |
Fgf signaling controls the telencephalic distribution of Fgf-expressing progenitors generated in the rostral patterning center. |
RPC |
| 10 |
2015 |
Fgf-signaling-dependent Sox9a and Atoh1a regulate otic neural development in zebrafish. |
SAG |
| 11 |
2014 |
Distal expression of sprouty (spry) genes during Xenopus laevis limb development and regeneration. |
AER, Spry, spry |
| 12 |
2014 |
Fgfr signaling is required as the early eye field forms to promote later patterning and morphogenesis of the eye. |
POM |
| 13 |
2014 |
Fgfr1 inactivation in the mouse telencephalon results in impaired maturation of interneurons expressing parvalbumin. |
GE, GFP, MGE |
| 14 |
2013 |
Angiotensin II-induced cardiac hypertrophy and fibrosis are promoted in mice lacking Fgf16. |
--- |
| 15 |
2013 |
Fgf3 and Fgf10a work in concert to promote maturation of the epibranchial placodes in zebrafish. |
EB |
| 16 |
2013 |
Tbx2 terminates shh/fgf signaling in the developing mouse limb bud by direct repression of gremlin1. |
BMP, GREM1, Shh |
| 17 |
2012 |
Spry1 and spry2 are essential for development of the temporomandibular joint. |
RTK, Spry, TMJ |
| 18 |
2011 |
Expression of fibroblast growth factors (Fgfs) in murine tooth development. |
--- |
| 19 |
2011 |
Role of fibroblast growth factor receptor signaling in kidney development. |
MM, UB |
| 20 |
2011 |
Role of fibroblast growth factor receptor signaling in kidney development. |
Fgfrl1, MM, UB |
| 21 |
2011 |
The physical basis of FGFR3 response to fgf1 and fgf2. |
FGFRs |
| 22 |
2011 |
The role of fibroblast growth factors on the differentiation of vaginal epithelium of neonatal mice. |
Fgfr2IIIb, KRT14, Trp63 |
| 23 |
2010 |
Evolution of developmental regulation in the vertebrate FgfD subfamily. |
CNEs |
| 24 |
2010 |
Hormone-like (endocrine) Fgfs: their evolutionary history and roles in development, metabolism, and disease. |
Fgfr |
| 25 |
2009 |
Fgf receptor 3 activation promotes selective growth and expansion of occipitotemporal cortex. |
Fgfr3 |
| 26 |
2009 |
Fibroblast growth factor 21 regulates lipolysis in white adipose tissue but is not required for ketogenesis and triglyceride clearance in liver. |
KO |
| 27 |
2009 |
Loss of connexin43-mediated gap junctional coupling in the mesenchyme of limb buds leads to altered expression of morphogens in mice. |
BMP2, Cx43, ODDD, Shh |
| 28 |
2008 |
Regulated addition of new myocardial and epicardial cells fosters homeostatic cardiac growth and maintenance in adult zebrafish. |
--- |
| 29 |
2007 |
Complex regulation of cyp26a1 creates a robust retinoic acid gradient in the zebrafish embryo. |
RA |
| 30 |
2007 |
Expression of chick Fgf19 and mouse Fgf15 orthologs is regulated in the developing brain by Fgf8 and Shh. |
ZLI |
| 31 |
2007 |
Fgf-dependent otic induction requires competence provided by Foxi1 and Dlx3b. |
--- |
| 32 |
2007 |
Fgf19 expression patterns in the developing chick inner ear. |
--- |
| 33 |
2007 |
Patterning the dorsal telencephalon: a role for sonic hedgehog? |
Gli3R, Shh |
| 34 |
2007 |
Role of fibroblast growth factor receptor signaling in kidney development. |
--- |
| 35 |
2007 |
The Fgf families in humans, mice, and zebrafish: their evolutional processes and roles in development, metabolism, and disease. |
Fgfr |
| 36 |
2006 |
Fgf16 is essential for pectoral fin bud formation in zebrafish. |
AER, SHH, ZPA |
| 37 |
2006 |
Fgf21 is essential for haematopoiesis in zebrafish. |
--- |
| 38 |
2006 |
Stomach development is dependent on fibroblast growth factor 10/fibroblast growth factor receptor 2b-mediated signaling. |
--- |
| 39 |
2005 |
Comprehensive expression atlas of fibroblast growth factors and their receptors generated by a novel robotic in situ hybridization platform. |
ISH |
| 40 |
2005 |
Fgf8 drives myogenic progression of a novel lateral fast muscle fibre population in zebrafish. |
--- |
| 41 |
2005 |
Fibroblast growth factor signaling in tumorigenesis. |
--- |
| 42 |
2005 |
Stimulation of cell motility by a viral fibroblast growth factor homolog: proposal for a role in viral pathogenesis. |
AcMNPV, RNA |
| 43 |
2004 |
A crucial role for fibroblast growth factor signaling in embryonic mammary gland development. |
--- |
| 44 |
2004 |
Evolution of the Fgf and Fgfr gene families. |
--- |
| 45 |
2004 |
Fgf and Bmp signals repress the expression of Bapx1 in the mandibular mesenchyme and control the position of the developing jaw joint. |
BMPs, RAP |
| 46 |
2004 |
Fgf signaling induces posterior neuroectoderm independently of Bmp signaling inhibition. |
BMPs |
| 47 |
2004 |
fgf17b, a novel member of Fgf family, helps patterning zebrafish embryos. |
chd, lft1 |
| 48 |
2003 |
Fibroblast growth factors (FGFS) increase breast tumor growth rate, metastases, blood flow, and oxygenation without significant change in vascular density. |
--- |
| 49 |
2003 |
The IIIb isoform of fibroblast growth factor receptor 2 is required for proper growth and branching of pancreatic ductal epithelium but not for differentiation of exocrine or endocrine cells. |
Fgfr2b |
| 50 |
2002 |
Fgf8 and Fgf3 are required for zebrafish ear placode induction, maintenance and inner ear patterning. |
ace |
| 51 |
2002 |
Transforming growth factor-beta3 (Tgf-beta3) down-regulates Tgf-beta3 receptor type I (Tbetar-I) during rescue of cranial sutures from osseous obliteration. |
BMPs, Tbetar-I, Tgf-beta3, TGF-betas |
| 52 |
2001 |
Fibroblast growth factor signalling in mouse mammary gland development. |
--- |
| 53 |
2001 |
Fibroblast growth factors in regenerating limbs of Ambystoma: cloning and semi-quantitative RT-PCR expression studies. |
--- |
| 54 |
2001 |
Misexpression of Fgf-4 in the chick limb inhibits myogenesis by down-regulating Frek expression. |
mFgf-4 |
| 55 |
2000 |
Ace/Fgf8 is required for forebrain commissure formation and patterning of the telencephalon. |
CNS |
| 56 |
2000 |
Roles for Fgf signaling during zebrafish fin regeneration. |
FGFR1 |
| 57 |
1999 |
A subset of fibroblast growth factors (Fgfs) promote survival, but Fgf-8b specifically promotes astroglial differentiation of rat cortical precursor cells. |
--- |
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