Expression pattern of cdkl5 during zebrafish early development: implications for use as model for atypical Rett syndrome
Author:
Funder
Fundação para a Ciência e a Tecnologia
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
http://link.springer.com/article/10.1007/s11033-018-4180-1/fulltext.html
Reference29 articles.
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2. Wang ITJ, Allen M, Goffin D, Zhu X, Fairless AH, Brodkin ES, Siegel SJ, Marsh ED, Blendy JA, Zhou Z (2012) Loss of CDKL5 disrupts kinome profile and event-related potentials leading to autistic-like phenotypes in mice. Proc Natl Acad Sci USA 109(52):21516–21521. https://doi.org/10.1073/pnas.1216988110
3. Amendola E, Zhan Y, Mattucci C, Castroflorio E, Calcagno E, Fuchs C, Lonetti G, Silingardi D, Vyssotski AL, Farley D, Ciani E, Pizzorusso T, Giustetto M, Gross CT (2014) Mapping pathological phenotypes in a mouse model of CDKL5 disorder. PLoS ONE 9(5):e91613. https://doi.org/10.1371/journal.pone.0091613
4. Okuda K, Kobayashi S, Fukaya M, Watanabe A, Murakami T, Hagiwara M, Sato T, Ueno H, Ogonuki N, Komano-Inoue S, Manabe H, Yamaguchi M, Ogura A, Asahara H, Sakagami H, Mizuguchi M, Manabe T, Tanaka T (2017) CDKL5 controls postsynaptic localization of GluN2B-containing NMDA receptors in the hippocampus and regulates seizure susceptibility. Neurobiol Dis 106(Supplement C):158–170. https://doi.org/10.1016/j.nbd.2017.07.002
5. Dooley K, Zon LI (2000) Zebrafish: a model system for the study of human disease. Curr Opin Genet Dev 10(3):252–256. https://doi.org/10.1016/S0959-437X(00)00074-5
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1. Zebrafish in understanding molecular pathophysiology, disease modeling, and developing effective treatments for Rett syndrome;The Journal of Gene Medicine;2024-02
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3. Cdkl5 mutant zebrafish shows skeletal and neuronal alterations mimicking human CDKL5 deficiency disorder;Scientific Reports;2022-06-04
4. Sleep Disorders in Rett Syndrome and Rett-Related Disorders: A Narrative Review;Frontiers in Neurology;2022-03-01
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