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The Journal of Biological Chemistry|July 11, 2012
Ca(2+)/calmodulin-dependent protein kinase IIα (αCaMKII) controls the activity of the dopamine transporter: implications for Angelman syndromeThomas Steinkellner, Jae-Won Yang, Therese R Montgomery, et al.
Molecular Psychiatry|March 10, 2022
A cross-species spatiotemporal proteomic analysis identifies UBE3A-dependent signaling pathways and targetsNikhil J Pandya, Sonja Meier, Stefka Tyanova, et al.
Nature Neuroscience|January 30, 2007
Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of alphaCaMKII inhibitory phosphorylationGeeske M van Woerden, Karen D Harris, Mohammad Reza Hojjati, et al.
World Journal of Clinical Cases|February 7, 2024
Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndromeWiem Manoubi, Marwa Mahdouani, Dorra Hmida, et al.
ACS Chemical Neuroscience|February 25, 2026
Phosphoproteomic Analysis of Cortical Tissue from Mice Lacking Both CaMKIIα and CaMKIIβ Identifies Novel In Vivo SubstratesPomme M F Rigter, Karel Bezstarosti, Oguz Can Koc, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 10, 2003
Derangements of hippocampal calcium/calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndromeEdwin J Weeber, Yong-Hui Jiang, Ype Elgersma, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|March 23, 2025
The effect of lamotrigine on cortical inhibition and plasticity in Neurofibromatosis type 1: Exploratory analysis of a randomized controlled trial (NF1-EXCEL)Myrthe J Ottenhoff, Anouk Heuvelmans, Jesminne Castricum, et al.
Plos One|March 30, 2012
Functional gene-expression analysis shows involvement of schizophrenia-relevant pathways in patients with 22q11 deletion syndromeNico J M van Beveren, Lianne C Krab, Sigrid Swagemakers, et al.
The Journal of Clinical Investigation|October 21, 2015
Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome modelCaroline F Bruinsma, Martijn Schonewille, Zhenyu Gao, et al.
Molecular Genetics & Genomic Medicine|September 5, 2020
A novel UBE3A sequence variant identified in eight related individuals with neurodevelopmental delay, results in a phenotype which does not match the clinical criteria of Angelman syndromeAmber Geerts-Haages, Stijn N V Bossuyt, Inge den Besten, et al.
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