A novel inhibitor rescues cerebellar defects in a zebrafish model of Down syndrome–associated kinase Dyrk1A overexpression
Author:
Funder
German Research Foundation
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference71 articles.
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2. A human homologue of Drosophila minibrain (Mnb) is expressed in the neuronal regions affected in Down syndrome and maps to the critical region;Guimerâ;Hum. Mol. Genet.,1996
3. Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome;Smith;Nat. Genet.,1997
4. The Down syndrome-related protein kinase DYRK1A phosphorylates p27Kip1 and Cyclin D1 and induces cell cycle exit and neuronal differentiation;Soppa;Cell Cycle,2014
5. Minibrain drives the dacapo-dependent cell cycle exit of neurons in the Drosophila brain by promoting asense and prospero expression;Shaikh;Development,2016
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Lifelong regeneration of cerebellar Purkinje cells after induced cell ablation in zebrafish;eLife;2023-04-12
2. Proteomic profiling reveals mitochondrial dysfunction in the cerebellum of transgenic mice overexpressing DYRK1A, a Down syndrome candidate gene;Frontiers in Molecular Neuroscience;2022-12-15
3. Lifelong regeneration of cerebellar Purkinje neurons after induced cell ablation in zebrafish;2022-05-10
4. Differential maturation and chaperone dependence of the paralogous protein kinases DYRK1A and DYRK1B;Scientific Reports;2022-02-14
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