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fibroblast growth factor receptors การใช้

ประโยคมือถือ
  • Achondroplasia is a mutation in the fibroblast growth factor receptor 3.
  • Fibroblast growth factor receptor 3 has been shown to interact with FGF1 and FGF9.
  • KGF is a small signaling molecule that binds to fibroblast growth factor receptor 2b ( FGFR2b ).
  • FGF21 stimulates phosphorylation of fibroblast growth factor receptor substrate 2 and ERK1 / 2 in the liver.
  • This syndrome is caused by a mutation in the fibroblast growth factor receptor II, located on chromosome 10.
  • Cancer stem cells of rhabdomyosarcoma have been identified and fibroblast growth factor receptor 3 has been suggested as their marker.
  • They interact with fibroblast growth factor receptor 1, which suggests it may be linked to the modulating of neuronal differentiation.
  • Another is the lab's cloning of FRS2, which is critical for signaling by the Fibroblast growth factor receptor.
  • FGFR1OP2, when fused with the fibroblast growth factor receptor 1 ( FGFR1 ), is shown to cause myeloproliferative syndrome.
  • FGF3 binds to Fibroblast Growth Factor Receptor 3 ( FGFR3 ) to serve as a negative regulator of bone growth during ossification.
  • The study aimed to identify the partner genes to the fibroblast growth factor receptor 1 ( FGFR1 ) involved in the syndrome.
  • She discovered that similar mutations in the same gene, fibroblast growth factor receptor 2 or FGFR2, cause both Jackson Weiss syndrome and Crouzon syndrome.
  • The protein encoded by this gene is a member of the fibroblast growth factor receptor family, where amino acid sequence is highly conserved between members and throughout evolution.
  • Three cell receptors have been described for AAV2 : heparan sulfate proteoglycan ( HSPG ), a V ? 5 integrin and fibroblast growth factor receptor 1 ( FGFR-1 ).
  • The protein encoded by this gene is a member of the fibroblast growth factor receptor ( FGFR ) family, where amino acid sequence is highly conserved between members and throughout evolution.
  • One version of stem cell myeloproliferative disorder is the result of a reciprocal translocation between chromosomes 8 and 9, with the breakpoint associated with fibroblast growth factor receptor 1 and centriolin.
  • These syndromes were tied to mutations in genes that produce proteins called fibroblast growth factor receptors _ molecular antennae that receive chemical signals believed to guide the development of skin, bone and neural tissues.
  • In this study, bFGF was also shown to act on preosteoblasts  in the form of an increased proliferation  after binding to fibroblast growth factor receptor 1 and activating phosphoinositide 3-kinase.
  • The neural cell adhesion molecule N-CAM simultaneously combines with another N-CAM and a fibroblast growth factor receptor to stimulate the tyrosine kinase activity of that receptor to induce the growth of neurites.
  • Once the association between a skeletal disorder and a fibroblast growth factor receptor had been announced, scientists studying other bone diseases leapt on the possibility that their diseases might have something to do with faulty receptors.
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