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Injury of Adult Zebrafish Expressing Acvr1l(Q204D) Does Not Result in Heterotopic Ossification
Fibrodysplasia Ossificans Progressiva (FOP) is a rare, autosomal dominant genetic disorder in humans characterized by the gradual ossification of fibrous tissues, including skeletal muscle, tendons, and ligaments. In humans, mutations in the Type I BMP/TGFβ family member receptor gene, ACVR1, are as...
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| Vydáno v: | Zebrafish |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Mary Ann Liebert, Inc., publishers
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6277083/ https://ncbi.nlm.nih.gov/pubmed/30183553 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/zeb.2018.1611 |
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