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A new consensus for evaluating CDKL5/STK9‐dependent signalling mechanisms
Mutation or inactivation of CDKL5 kinase is associated with a human neurodevelopmental condition commonly referred to as CDKL5 deficiency disorder.(§) Two recent phosphoproteomics studies identify the first physiological substrates of mammalian CDKL5 and evaluate functional consequences of their pho...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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John Wiley and Sons Inc.
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6293275/ https://www.ncbi.nlm.nih.gov/pubmed/30377159 http://dx.doi.org/10.15252/embj.2018100848 |