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Plos One|December 5, 2013
Mammalian target of rapamycin complex I (mTORC1) activity in ras homologue enriched in brain (Rheb)-deficient mouse embryonic fibroblastsMarlous J Groenewoud, Susan M I Goorden, Jorien Kassies, et al.Cell|November 6, 2008
Neurofibromin regulation of ERK signaling modulates GABA release and learningYijun Cui, Rui M Costa, Geoffrey G Murphy, et al.Journal of Proteomics|November 11, 2017
Improvement of ubiquitylation site detection by Orbitrap mass spectrometryLennart van der Wal, Karel Bezstarosti, Karen A Sap, et al.Human Molecular Genetics|September 4, 2020
Conserved UBE3A subcellular distribution between human and mice is facilitated by non-homologous isoformsF Isabella Zampeta, Monica Sonzogni, Eva Niggl, et al.Frontiers in Cellular Neuroscience|January 10, 2018
Modulation of Murine Olivary Connexin 36 Gap Junctions by PKA and CaMKIIPaolo Bazzigaluppi, Sheena C Isenia, Elize D Haasdijk, et al.Molecular and Cellular Biology|February 16, 2011
Rheb is essential for murine developmentSusanna M I Goorden, Marianne Hoogeveen-Westerveld, Caroline Cheng, et al.Molecular Autism|August 28, 2025
UBE3A reinstatement restores behaviorand proteome in an Angelman syndrome mouse model of imprinting defectsClaudia Milazzo, Ramanathan Narayanan, Solveig Badillo, et al.Molecular Psychiatry|February 6, 2026
UBE3A isoform-selective and non-selective contributions to Angelman syndrome phenotypesJoseph C Krzeski, Edwin J Mientjes, Matthew C Judson, et al.Cerebellum (London, England)|October 8, 2010
Motor learning in children with neurofibromatosis type ILianne C Krab, Arja de Goede-Bolder, Femke K Aarsen, et al.Human Molecular Genetics|February 19, 2021
Loss of nuclear UBE3A activity is the predominant cause of Angelman syndrome in individuals carrying UBE3A missense mutationsStijn N V Bossuyt, A Mattijs Punt, Ilona J de Graaf, et al.Pageof 13