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Myelin protein zero (P0)- and Wnt1-Cre marked muscle resident neural crest-derived mesenchymal progenitor cells give rise to heterotopic ossification in mouse models
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作者 Chengzhu Zhao Yoshiko Inada +6 位作者 Kazuya Sekiguchi Kyosuke Hino Megumi Nishio Yasuhiro Yamada Shuichi Matsuda Junya Toguchida Makoto Ikeya 《Genes & Diseases》 SCIE CSCD 2023年第3期731-734,共4页
Heterotopic ossification(HO)describes bone formation at non-skeletal sites and results from traumatic injury,surgery,or genetic disease such as fibrodysplasia ossificans progressiva(FOP).1,2 Although it is known that ... Heterotopic ossification(HO)describes bone formation at non-skeletal sites and results from traumatic injury,surgery,or genetic disease such as fibrodysplasia ossificans progressiva(FOP).1,2 Although it is known that BMP signaling regulates HO,knowledge about the developmental origin of the osteogenic progenitors responsible for the BMP-associated metamorphosis is comparably less.With the use of transgenic mice and labelled neural crest-derived cell,3 we found myelin protein zero(P0,or MPZ)-and Wnt1-lineage cells give rise to BMP-7 induced adult ectopic cartilage and bone. 展开更多
关键词 PROGENITOR OSSIFICATION neural
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