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Fluorescence Resonance Energy Transfer Analysis of Merlin Conformational Changes
Neurofibromatosis type 2 is an inherited autosomal disorder caused by biallelic inactivation of the NF2 tumor suppressor gene. The NF2 gene encodes a 70-kDa protein, merlin, which is a member of the ezrin-radixin-moesin (ERM) family. ERM proteins are believed to be regulated by a transition between...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Microbiology (ASM)
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2798298/ https://ncbi.nlm.nih.gov/pubmed/19884346 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.00248-09 |
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