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Published in 2018 at "Journal of Bone and Mineral Research"
DOI: 10.1002/jbmr.3327
Abstract: Osteocytes remodel their surrounding perilacunar matrix and canalicular network to maintain skeletal homeostasis. Perilacunar/canalicular remodeling is also thought to play a role in determining bone quality. X‐linked hypophosphatemia (XLH) is characterized by elevated serum fibroblast…
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Keywords:
perilacunar canalicular;
canalicular remodeling;
perilacunar;
hyp mice ... See more keywords
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Published in 2023 at "Journal of the Endocrine Society"
DOI: 10.1210/jendso/bvad022
Abstract: Abstract Context X-linked hypophosphatemia (XLH) is a genetic disease, causing life-long hypophosphatemia due to overproduction of fibroblast growth factor 23 (FGF23). XLH is associated with Chiari malformations, cranial synostosis, and syringomyelia. FGF23 signals through FGFR1c…
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Keywords:
production;
hyp mice;
xlh;
csf production ... See more keywords