Sclerostin antibody improves phosphate metabolism hormones, bone formation rates, and bone mass in adult Hyp mice

X-linked hypophosphatemia (XLH) is caused by a loss-of-function mutation in the phosphate regulating gene with homology to endopeptidase located on the X chromosome (PHEX). Loss of functional PHEX results in elevated fibroblast growth factor 23 (FGF23), impaired phosphate reabsorption, and inhibited...

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Bibliografische gegevens
Hoofdauteurs: Carpenter, Kelsey A., Davison, Reid, Shakthivel, Shruti, Anderson, Kyle D., Ko, Frank C., Ross, Ryan D.
Formaat: Text
Taal:Engels
Gepubliceerd in: 2021
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Online toegang:https://pmc.ncbi.nlm.nih.gov/articles/PMC8671249/
https://pubmed.ncbi.nlm.nih.gov/34537437
http://dx.doi.org/10.1016/j.bone.2021.116201
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