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Search Results to Emily G. Farrow

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One or more keywords matched the following items that are connected to Farrow, Emily

Item TypeName
Concept Receptor, Fibroblast Growth Factor, Type 1
Academic Article Extended mutational analyses of FGFR1 in osteoglophonic dysplasia.
Academic Article Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosis.
Academic Article Hypophosphatemia with elevations in serum fibroblast growth factor 23 in a child with Jansen's metaphyseal chondrodysplasia.
Academic Article A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic features.
Academic Article Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic rickets.
Academic Article Initial FGF23-mediated signaling occurs in the distal convoluted tubule.
Academic Article Altered renal FGF23-mediated activity involving MAPK and Wnt: effects of the Hyp mutation.
Academic Article Neonatal iron deficiency causes abnormal phosphate metabolism by elevating FGF23 in normal and ADHR mice.
Academic Article Recent advances in renal phosphate handling.
Academic Article Parathyroid hormone receptor signaling in osteocytes increases the expression of fibroblast growth factor-23 in vitro and in vivo.
Academic Article Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice.
Academic Article Miscellaneous non-inflammatory musculoskeletal conditions. Hyperphosphatemic familial tumoral calcinosis (FGF23, GALNT3 and aKlotho).
Academic Article Circulating aKlotho influences phosphate handling by controlling FGF23 production.
Academic Article Erythropoietin stimulates murine and human fibroblast growth factor-23, revealing novel roles for bone and bone marrow.
Academic Article Autoimmune hyperphosphatemic tumoral calcinosis in a patient with FGF23 autoantibodies.

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  • Fibroblast Growth Factor 1