Iron deficiency drives an autosomal dominant hypophosphatemic rickets (ADHR) phenotype in fibroblast growth factor-23 (Fgf23) knock-in mice

Autosomal dominant hypophosphatemic rickets (ADHR) is unique among the disorders involving Fibroblast growth factor 23 (FGF23) because individuals with R176Q/W and R179Q/W mutations in the FGF23 (176)RXXR(179)/S(180) proteolytic cleavage motif can cycle from unaffected status to delayed onset of dis...

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Bibliografiset tiedot
Päätekijät: Farrow, Emily G., Yu, Xijie, Summers, Lelia J., Davis, Siobhan I., Fleet, James C., Allen, Matthew R., Robling, Alexander G., Stayrook, Keith R., Jideonwo, Victoria, Magers, Martin J., Garringer, Holly J., Vidal, Ruben, Chan, Rebecca J., Goodwin, Charles B., Hui, Siu L., Peacock, Munro, White, Kenneth E.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: National Academy of Sciences 2011
Aiheet:
PNAS Plus
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3219119/
https://ncbi.nlm.nih.gov/pubmed/22006328
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1110905108
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