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Generation of an immunodeficient mouse model of tcirg1-deficient autosomal recessive osteopetrosis
BACKGROUND: Autosomal recessive osteopetrosis is a rare skeletal disorder with increased bone density due to a failure in osteoclast bone resorption. In most cases, the defect is cell-autonomous, and >50% of patients bear mutations in the TCIRG1 gene, encoding for a subunit of the vacuolar proton...
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| I publikationen: | Bone Rep |
|---|---|
| Huvudupphovsmän: | , , , , , , , , , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Elsevier
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6953598/ https://ncbi.nlm.nih.gov/pubmed/31938717 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bonr.2020.100242 |
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