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OSTM1 Bone Defect Reveals an Intercellular Hematopoietic Crosstalk
The most severe form of bone autosomal recessive osteopetrosis both in humans and in the gray-lethal (gl/gl) mouse is caused by mutations in the Ostm1 gene. Although osteopetrosis is usually associated with a defect in the hematopoietic-derived osteoclast cells, this study determined that Ostm1 is e...
Wedi'i Gadw mewn:
| Prif Awduron: | , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
American Society for Biochemistry and Molecular Biology
2008
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2662145/ https://ncbi.nlm.nih.gov/pubmed/18790735 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M805242200 |
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