Kindlin-2 mediates mechanotransduction in bone by regulating expression of Sclerostin in osteocytes | Communications Biology
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Kindlin-2 mediates mechanotransduction in bone by regulating expression of Sclerostin in osteocytes | Communications Biology
Kindlin-2 deletion in osteoprogenitors causes severe chondrodysplasia and low-turnover osteopenia in mice - ScienceDirect
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Kailyn's Patient Story | Meet Kailyn, a true fighter with osteogenesis imperfecta (OI), a rare genetic disorder that makes her bones as fragile as glass. Despite enduring... | By Baylor Scott &
Claudia Lindner on X: "Our recently published paper on using BoneFinder to assess foot collapse on lateral weight-bearing foot radiographs is now available Open Access: https://t.co/Cd4AXmDqtD The BoneFinder search model generated as
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