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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Detaylı Bibliyografya
Asıl Yazarlar: 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.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2011
Konular:
PNAS Plus
Online Erişim: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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