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Search results 1301 to 1400 out of 2229 for Fgfr3

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Type Details Score
Publication
First Author: Santos-Ocampo S
Year: 1996
Journal: J Biol Chem
Title: Expression and biological activity of mouse fibroblast growth factor-9.
Volume: 271
Issue: 3
Pages: 1726-31
Publication
First Author: Avivi A
Year: 1992
Journal: Oncogene
Title: Promoter region of the murine fibroblast growth factor receptor 2 (bek/KGFR) gene.
Volume: 7
Issue: 10
Pages: 1957-62
Publication
First Author: Murali SK
Year: 2016
Journal: PLoS Biol
Title: Excessive Osteocytic Fgf23 Secretion Contributes to Pyrophosphate Accumulation and Mineralization Defect in Hyp Mice.
Volume: 14
Issue: 4
Pages: e1002427
Publication
First Author: Choi D
Year: 2017
Journal: Circ Res
Title: ORAI1 Activates Proliferation of Lymphatic Endothelial Cells in Response to Laminar Flow Through Krüppel-Like Factors 2 and 4.
Volume: 120
Issue: 9
Pages: 1426-1439
Publication
First Author: Barnard JC
Year: 2005
Journal: Endocrinology
Title: Thyroid hormones regulate fibroblast growth factor receptor signaling during chondrogenesis.
Volume: 146
Issue: 12
Pages: 5568-80
Publication
First Author: Dorry SJ
Year: 2020
Journal: Am J Respir Cell Mol Biol
Title: FGFR2 Is Required for AEC2 Homeostasis and Survival after Bleomycin-induced Lung Injury.
Volume: 62
Issue: 5
Pages: 608-621
Publication      
First Author: Kobayashi T
Year: 2023
Journal: bioRxiv
Title: Reduced glycolysis links resting zone chondrocyte proliferation in the growth plate.
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein
Organism: Mus musculus/domesticus
Length: 535  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 1319  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 309  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 1068  
Fragment?: false
Publication  
First Author: Ratzan EM
Year: 2020
Journal: Development
Title: Fgf8 genetic labeling reveals the early specification of vestibular hair cell type in mouse utricle.
Volume: 147
Issue: 22
Publication  
First Author: Campbell DP
Year: 2016
Journal: Sci Rep
Title: Canonical Notch signaling plays an instructive role in auditory supporting cell development.
Volume: 6
Pages: 19484
Publication
First Author: Zhang J
Year: 2018
Journal: Eur J Neurosci
Title: ERBB2 signaling drives supporting cell proliferation in vitro and apparent supernumerary hair cell formation in vivo in the neonatal mouse cochlea.
Volume: 48
Issue: 10
Pages: 3299-3316
Publication
First Author: Li XJ
Year: 2022
Journal: Sci Adv
Title: Follistatin promotes LIN28B-mediated supporting cell reprogramming and hair cell regeneration in the murine cochlea.
Volume: 8
Issue: 6
Pages: eabj7651
Publication
First Author: Hu NY
Year: 2020
Journal: Neurosci Bull
Title: Expression Patterns of Inducible Cre Recombinase Driven by Differential Astrocyte-Specific Promoters in Transgenic Mouse Lines.
Volume: 36
Issue: 5
Pages: 530-544
Publication
First Author: Reilly JF
Year: 2000
Journal: J Biol Chem
Title: Association of fibroblast growth factor receptor 1 with the adaptor protein Grb14. Characterization of a new receptor binding partner.
Volume: 275
Issue: 11
Pages: 7771-8
Publication
First Author: Ong SH
Year: 2000
Journal: Mol Cell Biol
Title: FRS2 proteins recruit intracellular signaling pathways by binding to diverse targets on fibroblast growth factor and nerve growth factor receptors.
Volume: 20
Issue: 3
Pages: 979-89
Publication
First Author: Karlsson T
Year: 1995
Journal: Oncogene
Title: Molecular interactions of the Src homology 2 domain protein Shb with phosphotyrosine residues, tyrosine kinase receptors and Src homology 3 domain proteins.
Volume: 10
Issue: 8
Pages: 1475-83
Publication
First Author: Schlessinger J
Year: 2000
Journal: Mol Cell
Title: Crystal structure of a ternary FGF-FGFR-heparin complex reveals a dual role for heparin in FGFR binding and dimerization.
Volume: 6
Issue: 3
Pages: 743-50
Publication
First Author: Li C
Year: 2005
Journal: Development
Title: FGFR1 function at the earliest stages of mouse limb development plays an indispensable role in subsequent autopod morphogenesis.
Volume: 132
Issue: 21
Pages: 4755-64
Publication
First Author: Itoh N
Year: 1990
Journal: Biochem Biophys Res Commun
Title: The complete amino acid sequence of the shorter form of human basic fibroblast growth factor receptor deduced from its cDNA.
Volume: 169
Issue: 2
Pages: 680-5
Publication
First Author: Riley BM
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Impaired FGF signaling contributes to cleft lip and palate.
Volume: 104
Issue: 11
Pages: 4512-7
Publication
First Author: Dixon MJ
Year: 2011
Journal: Nat Rev Genet
Title: Cleft lip and palate: understanding genetic and environmental influences.
Volume: 12
Issue: 3
Pages: 167-78
Protein Domain
Type: Domain
Description: Fibroblast growth factors (FGFs) [, ]are a family of multifunctional proteins, often referred to as 'promiscuous growth factors' due to their diverse actions on multiple cell types [, ]. FGFs are mitogens, which stimulate growth or differentiation of cells of mesodermal or neuroectodermal origin. The function of FGFs in developmental processes include mesoderm induction, anterior-posterior patterning, limb development, and neural induction and development. In mature tissues, they are involved in diverse processes including keratinocyte organisation and wound healing [, , , , , ]. FGF involvement is critical during normal development of both vertebrates and invertebrates, and irregularities in their function leads to a range of developmental defects [, , , ]. Fibroblast growth factors are heparin-binding proteins and interactions with cell-surface-associated heparan sulfate proteoglycans have been shown to be essential for FGF signal transduction. FGFs have internal pseudo-threefold symmetry (β-trefoil topology) []. There are currently over 20 different FGF family members that have been identified in mammals, all of which are structurally related signaling molecules [, ]. They exert their effects through four distinct membrane fibroblast growth factor receptors (FGFRs), FGFR1 to FGFR4 [], which belong to the tyrosine kinase superfamily. Upon binding to FGF, the receptors dimerize and their intracellular tyrosine kinase domains become active [].The FGFRs consist of an extracellular ligand-binding domain composed of three immunoglobulin-like domains (D1-D3), a single transmembrane helix domain, and an intracellular domain with tyrosine kinase activity []. The three immunoglobin(Ig)-like domains, D1, D2, and D3, present a stretch of acidic amino acids (known as the acid box) between D1 and D2. This acid box can participate in the regulation of FGF binding to the FGFR. Immunoglobulin-like domains D2 and D3 are sufficient for FGF binding. FGFR family members differ from one another in their ligandaffinities and tissue distribution [, ]. Most FGFs can bind to several different FGFR subtypes. Indeed, FGF1 is sometimes referred to as the universal ligand, as it is capable of activating all of the different FGFRs []. However, there are some exceptions. For example, FGF7 only interacts with FGFR2 []and FGF18 was recently shown to only activate FGFR3 []. Fibroblast growth factor receptor 1 (FGFR1) binds both acidic and basic fibroblast growth factors and is involved in limb induction []. FGFR1 has been shown to be associated with Pfeiffer syndrome [], and cleft lip and/or palate [, ]. Fibroblast growth factor receptor 1 has been shown to interact with growth factor receptor-bound protein 14 (GRB14) [], Src homology 2 domain containing adaptor protein B (SHB) [], fibroblast growth factor receptor substrate 2 (FRS2)[]and fibroblast growth factor 1 (FGF1) [, ].This entry represents the catalytic domain of FGFR1.
Protein Domain
Type: Family
Description: Fibroblast growth factors (FGFs) [, ]are a family of multifunctional proteins, often referred to as 'promiscuous growth factors' due to their diverse actions on multiple cell types [, ]. FGFs are mitogens, which stimulate growth or differentiation of cells of mesodermal or neuroectodermal origin. The function of FGFs in developmental processes include mesoderm induction, anterior-posterior patterning, limb development, and neural induction and development. In mature tissues, they are involved in diverse processes including keratinocyte organisation and wound healing [, , , , , ]. FGF involvement is critical during normal development of both vertebrates and invertebrates, and irregularities in their function leads to a range of developmental defects [, , , ]. Fibroblast growth factors are heparin-binding proteins and interactions with cell-surface-associated heparan sulfate proteoglycans have been shown to be essential for FGF signal transduction. FGFs have internal pseudo-threefold symmetry (β-trefoil topology) []. There are currently over 20 different FGF family members that have been identified in mammals, all of which are structurally related signaling molecules [, ]. They exert their effects through four distinct membrane fibroblast growth factor receptors (FGFRs), FGFR1 to FGFR4 [], which belong to the tyrosine kinase superfamily. Upon binding to FGF, the receptors dimerize and their intracellular tyrosine kinase domains become active [].The FGFRs consist of an extracellular ligand-binding domain composed of three immunoglobulin-like domains (D1-D3), a single transmembrane helix domain, and an intracellular domain with tyrosine kinase activity []. The three immunoglobin(Ig)-like domains, D1, D2, and D3, present a stretch of acidic amino acids (known as the acid box) between D1 and D2. This acid box can participate in the regulation of FGF binding to the FGFR. Immunoglobulin-like domains D2 and D3 are sufficient for FGF binding. FGFR family members differ from one another in their ligand affinities and tissue distribution [, ]. Most FGFs can bind to several different FGFR subtypes. Indeed, FGF1 is sometimes referred to as the universal ligand, as it is capable of activating all of the different FGFRs []. However, there are some exceptions. For example, FGF7 only interacts with FGFR2 []and FGF18 was recently shown to only activate FGFR3 []. This entry represents the fibroblast growth factor receptor family.
Publication  
First Author: Barbosa M
Year: 2021
Journal: Front Cell Dev Biol
Title: Recovery of Depleted miR-146a in ALS Cortical Astrocytes Reverts Cell Aberrancies and Prevents Paracrine Pathogenicity on Microglia and Motor Neurons.
Volume: 9
Pages: 634355
Publication
First Author: Shu CC
Year: 2016
Journal: Arthritis Rheumatol
Title: Ablation of Perlecan Domain 1 Heparan Sulfate Reduces Progressive Cartilage Degradation, Synovitis, and Osteophyte Size in a Preclinical Model of Posttraumatic Osteoarthritis.
Volume: 68
Issue: 4
Pages: 868-79
Protein
Organism: Mus musculus/domesticus
Length: 91  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 104  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 200  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 208  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 30  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 208  
Fragment?: false
Publication
First Author: Duchesne L
Year: 2006
Journal: J Biol Chem
Title: N-glycosylation of fibroblast growth factor receptor 1 regulates ligand and heparan sulfate co-receptor binding.
Volume: 281
Issue: 37
Pages: 27178-89
Publication
First Author: Hughes SE
Year: 1997
Journal: J Histochem Cytochem
Title: Differential expression of the fibroblast growth factor receptor (FGFR) multigene family in normal human adult tissues.
Volume: 45
Issue: 7
Pages: 1005-19
Publication
First Author: Cotton LM
Year: 2008
Journal: Endocr Rev
Title: Cellular signaling by fibroblast growth factors (FGFs) and their receptors (FGFRs) in male reproduction.
Volume: 29
Issue: 2
Pages: 193-216
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein
Organism: Mus musculus/domesticus
Length: 589  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 358  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 380  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 309  
Fragment?: false
Protein  
Organism: Mus musculus/domesticus
Length:  
Publication
First Author: Wu Y
Year: 2023
Journal: Neuron
Title: Hepatic soluble epoxide hydrolase activity regulates cerebral Aβ metabolism and the pathogenesis of Alzheimer's disease in mice.
Volume: 111
Issue: 18
Pages: 2847-2862.e10
Publication
First Author: Liu Z
Year: 2012
Journal: J Neurosci
Title: Age-dependent in vivo conversion of mouse cochlear pillar and Deiters' cells to immature hair cells by Atoh1 ectopic expression.
Volume: 32
Issue: 19
Pages: 6600-10
Publication
First Author: Jones MR
Year: 2022
Journal: Cell Mol Life Sci
Title: FGFR2b signalling restricts lineage-flexible alveolar progenitors during mouse lung development and converges in mature alveolar type 2 cells.
Volume: 79
Issue: 12
Pages: 609
Publication  
First Author: Ghimire SR
Year: 2018
Journal: Development
Title: A non-autonomous function of the core PCP protein VANGL2 directs peripheral axon turning in the developing cochlea.
Volume: 145
Issue: 12
Publication
First Author: Matsushita Y
Year: 2022
Journal: Nat Commun
Title: The fate of early perichondrial cells in developing bones.
Volume: 13
Issue: 1
Pages: 7319
Publication
First Author: BonDurant LD
Year: 2017
Journal: Cell Metab
Title: FGF21 Regulates Metabolism Through Adipose-Dependent and -Independent Mechanisms.
Volume: 25
Issue: 4
Pages: 935-944.e4
Protein
Organism: Mus musculus/domesticus
Length: 245  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 109  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 154  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 112  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 245  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 156  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 105  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 159  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 153  
Fragment?: false
Publication
First Author: Skjerpen CS
Year: 2002
Journal: EMBO J
Title: Binding of FGF-1 variants to protein kinase CK2 correlates with mitogenicity.
Volume: 21
Issue: 15
Pages: 4058-69
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus caroli
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus pahari
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus spretus
Publication
First Author: Kwiatkowski BA
Year: 2008
Journal: J Cell Physiol
Title: FGFR4 and its novel splice form in myogenic cells: Interplay of glycosylation and tyrosine phosphorylation.
Volume: 215
Issue: 3
Pages: 803-17
Publication
First Author: Yu C
Year: 2000
Journal: J Biol Chem
Title: Elevated cholesterol metabolism and bile acid synthesis in mice lacking membrane tyrosine kinase receptor FGFR4.
Volume: 275
Issue: 20
Pages: 15482-9
Publication
First Author: Huang X
Year: 2007
Journal: Diabetes
Title: FGFR4 prevents hyperlipidemia and insulin resistance but underlies high-fat diet induced fatty liver.
Volume: 56
Issue: 10
Pages: 2501-10
Publication
First Author: Yu C
Year: 2002
Journal: Am J Pathol
Title: Increased carbon tetrachloride-induced liver injury and fibrosis in FGFR4-deficient mice.
Volume: 161
Issue: 6
Pages: 2003-10
Publication
First Author: Grabner A
Year: 2015
Journal: Cell Metab
Title: Activation of Cardiac Fibroblast Growth Factor Receptor 4 Causes Left Ventricular Hypertrophy.
Volume: 22
Issue: 6
Pages: 1020-32
Publication
First Author: French DM
Year: 2012
Journal: PLoS One
Title: Targeting FGFR4 inhibits hepatocellular carcinoma in preclinical mouse models.
Volume: 7
Issue: 5
Pages: e36713
Publication
First Author: Yu C
Year: 2005
Journal: J Biol Chem
Title: Independent repression of bile acid synthesis and activation of c-Jun N-terminal kinase (JNK) by activated hepatocyte fibroblast growth factor receptor 4 (FGFR4) and bile acids.
Volume: 280
Issue: 18
Pages: 17707-14
Publication
First Author: Seitzer N
Year: 2010
Journal: Cancer Res
Title: A single nucleotide change in the mouse genome accelerates breast cancer progression.
Volume: 70
Issue: 2
Pages: 802-12
Publication  
First Author: Bringuier CM
Year: 2023
Journal: Cells
Title: Up-Regulation of Astrocytic Fgfr4 Expression in Adult Mice after Spinal Cord Injury.
Volume: 12
Issue: 4
Publication
First Author: Ezzat S
Year: 2013
Journal: Cell Metab
Title: The cancer-associated FGFR4-G388R polymorphism enhances pancreatic insulin secretion and modifies the risk of diabetes.
Volume: 17
Issue: 6
Pages: 929-40
Publication
First Author: Nakano-Tateno T
Year: 2014
Journal: Mol Endocrinol
Title: FGFR4 polymorphic variants modulate phenotypic features of Cushing disease.
Volume: 28
Issue: 4
Pages: 525-33
Publication
First Author: Tateno T
Year: 2011
Journal: PLoS Genet
Title: The FGFR4-G388R polymorphism promotes mitochondrial STAT3 serine phosphorylation to facilitate pituitary growth hormone cell tumorigenesis.
Volume: 7
Issue: 12
Pages: e1002400
Publication
First Author: Lutz SZ
Year: 2019
Journal: J Clin Endocrinol Metab
Title: The Gly385(388)Arg Polymorphism of the FGFR4 Receptor Regulates Hepatic Lipogenesis Under Healthy Diet.
Volume: 104
Issue: 6
Pages: 2041-2053