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Identification of the Kelch Family Protein Nd1-L as a Novel Molecular Interactor of KRIT1
Loss-of-function mutations of the KRIT1 gene (CCM1) have been associated with the Cerebral Cavernous Malformation (CCM) disease, which is characterized by serious alterations of brain capillary architecture. The KRIT1 protein contains multiple interaction domains and motifs, suggesting that it might...
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| Hlavní autoři: | , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3435375/ https://ncbi.nlm.nih.gov/pubmed/22970292 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0044705 |
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