CDKL5 kinase controls transcription‐coupled responses to DNA damage

Mutations in the gene encoding the CDKL5 kinase are among the most common genetic causes of childhood epilepsy and can also give rise to the severe neurodevelopmental condition CDD (CDKL5 deficiency disorder). Despite its importance for human health, the phosphorylation targets and cellular roles of...

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Detalles Bibliográficos
Autores principales: Khanam, Taran, Muñoz, Ivan, Weiland, Florian, Carroll, Thomas, Morgan, Michael, Borsos, Barbara N, Pantazi, Vasiliki, Slean, Meghan, Novak, Miroslav, Toth, Rachel, Appleton, Paul, Pankotai, Tibor, Zhou, Houjiang, Rouse, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634139/
https://www.ncbi.nlm.nih.gov/pubmed/34605059
http://dx.doi.org/10.15252/embj.2021108271

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634139/
https://www.ncbi.nlm.nih.gov/pubmed/34605059
http://dx.doi.org/10.15252/embj.2021108271

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