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Biology of Reproduction, ISSN 0006-3363, 2015, Volume 92, Issue 1
ABSTRACT Although the various members of the fibroblast growth factor (FGF) family are generally mitotic, one member, FGF18, has been shown to increase the... 
apoptosis | FGF | PUMA | caspase | estradiol
Journal Article
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 07/2017, Volume 114, Issue 29, pp. 7505 - 7512
Journal Article
Journal Article
FEBS letters, ISSN 0014-5793, 01/2016, Volume 590, Issue 1, pp. 53 - 67
Mechanisms underlying the association between fibroblastic growth factor 23 (FGF‐23) and inflammation are uncertain. We found that FGF‐23 was markedly... 
macrophages | interferon gamma | 1,25(OH)2D | Klotho | lipopolysaccharide | FGF‐23 | 1,25(OH) | FGF-23
Journal Article
Critical reviews in oncology/hematology, ISSN 1040-8428, 2017, Volume 113, pp. 256 - 267
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2009, Volume 107, Issue 1, pp. 407 - 412
Fibroblast growth factor (FGF) 23 inhibits renal phosphate reabsorption by activating FGF receptor (FGFR) 1c in a Klotho-dependent fashion. The phosphaturic... 
Phosphates | Proteins | Phosphorylation | Excretion | Kidneys | Rickets | Hypophosphatemia | Fibroblast growth factors | Kidney diseases | Binding sites | FGF23 C-terminal peptide | Endogenous inhibitor of FGF23 | Binary FGF receptor 1c-klotho complex | Composite FGF receptor 1c-klotho interface | FGF23 antagonist | FAMILIAL TUMORAL CALCINOSIS | RICKETS | binary FGF receptor 1c-Klotho complex | SECRETED KLOTHO PROTEIN | INDUCED OSTEOMALACIA | MULTIDISCIPLINARY SCIENCES | PEX GENE | TRANSCRIPTS ENCODING MEMBRANE | endogenous inhibitor of FGF23 | IN-VIVO | composite FGF receptor 1c-Klotho interface | FIBROBLAST GROWTH FACTOR-23 | CHRONIC KIDNEY-DISEASE | INTRAVENOUS PHOSPHATE | Protein Structure, Tertiary | Cell Line | Membrane Proteins - genetics | Humans | Mice, Inbred C57BL | Opossums | Glucuronidase - metabolism | Peptides - genetics | Receptor, Fibroblast Growth Factor, Type 1 - metabolism | Fibroblast Growth Factors - genetics | Rats | Hypophosphatemia - metabolism | Receptor, Fibroblast Growth Factor, Type 1 - genetics | Rats, Sprague-Dawley | Kidney Tubules - cytology | Fibroblast Growth Factors - metabolism | Multiprotein Complexes - metabolism | Animals | Peptides - metabolism | Glucuronidase - genetics | Signal Transduction - physiology | Membrane Proteins - metabolism | Mice | Mitogen-Activated Protein Kinases - metabolism | Physiological aspects | Care and treatment | Research | Growth factor receptors | Biological Sciences
Journal Article
The EMBO Journal, ISSN 0261-4189, 02/2011, Volume 30, Issue 4, pp. 783 - 795
The epithelial–mesenchymal transition (EMT) is a crucial event in wound healing, tissue repair, and cancer progression in adult tissues. Here, we demonstrate... 
FGF‐2 | TGF‐β | δEF1 | FGF receptor | EMT | FGF-2 | TGF-β | CELLS | dEF1 | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | INDUCTION | IDENTIFICATION | SUPPRESSION | FIBROBLASTS | CELL BIOLOGY | PROSTATE ADENOCARCINOMA | COREPRESSORS | TGF-beta | TUMOR-GROWTH | PROGRESSION | Neoplasms - metabolism | Protein Binding - genetics | Myofibroblasts - physiology | Epithelial-Mesenchymal Transition - physiology | Homeodomain Proteins - metabolism | Humans | Actins - metabolism | Fibroblast Growth Factor 2 - pharmacology | Epithelial-Mesenchymal Transition - drug effects | Epithelial-Mesenchymal Transition - genetics | Actins - genetics | DNA-Binding Proteins - metabolism | Myofibroblasts - metabolism | Cell Differentiation - genetics | Protein Isoforms - metabolism | Neoplasms - genetics | Protein Binding - drug effects | Receptors, Fibroblast Growth Factor - genetics | Fibroblast Growth Factor 2 - metabolism | Gene Expression Regulation, Neoplastic - drug effects | Cell Differentiation - physiology | Neoplasm Invasiveness | Alternative Splicing - genetics | Cells, Cultured | Transforming Growth Factor beta - physiology | Alcohol Oxidoreductases - metabolism | Signal Transduction - genetics | Myofibroblasts - drug effects | Protein Isoforms - physiology | Transcription Factors - metabolism | Transforming Growth Factor beta - pharmacology | Alternative Splicing - drug effects | Cell Differentiation - drug effects | Models, Biological | Receptors, Fibroblast Growth Factor - metabolism | Neoplasms - pathology | Protein Isoforms - genetics | Zinc Finger E-box-Binding Homeobox 1
Journal Article
The Journal of biological chemistry, ISSN 1083-351X, 2017, Volume 292, Issue 46, pp. 18961 - 18972
Cytoglobin (CYGB) belongs to the mammalian globin family and is exclusively expressed in hepatic stellate cells (HSCs) in the liver. In addition to its... 
FAT-STORING CELLS | OXIDATIVE STRESS | hepatic stellate cell (HSC) | RAT | liver | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | LIVER FIBROSIS | KINASE | TRANSCRIPTION | c-Jun N-terminal kinase (JNK) | cytoglobin | FIBROGENESIS | PROLIFERATION | MECHANISMS | fibroblast growth factor (FGF) | fibrosis | Molecular Bases of Disease
Journal Article
Diabetes (New York, N.Y.), ISSN 1939-327X, 2006, Volume 55, Issue 9, pp. 2470 - 2478
Journal Article