Abstract

Landmark advances in skeletal biology have arisen mainly from the identification of disease-causing mutations and the advent of rapid and selective gene-targeting technologies to phenocopy human disease in mice. Here, we discuss work on newly identified mechanisms controlling the remodeling of bone, communication of bone cells with cells of other lineages, and crosstalk between bone and vital organs as these relate to the therapeutic targeting of the skeleton.

Original languageEnglish
Pages (from-to)701-718
Number of pages18
JournalEndocrine Reviews
Volume39
Issue number5
DOIs
StatePublished - 1 Oct 2018

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