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Characterization of the interaction between anthrax toxin and its cellular receptors
Mutations in capillary morphogenesis gene 2 (CMG2), one of the two closely related proteins that act as anthrax toxin receptors, cause two rare human autosomal recessive conditions, juvenile hyaline fibromatosis (JHF) and infantile systemic hyalinosis (ISH). Here we demonstrate that CMG2 proteins wi...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2459336/ https://ncbi.nlm.nih.gov/pubmed/17381430 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1462-5822.2006.00845.x |
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