These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
373 related articles for article (PubMed ID: 9763493)
1. Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome. DeLorey TM; Handforth A; Anagnostaras SG; Homanics GE; Minassian BA; Asatourian A; Fanselow MS; Delgado-Escueta A; Ellison GD; Olsen RW J Neurosci; 1998 Oct; 18(20):8505-14. PubMed ID: 9763493 [TBL] [Abstract][Full Text] [Related]
2. Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3. Jiang YH; Pan Y; Zhu L; Landa L; Yoo J; Spencer C; Lorenzo I; Brilliant M; Noebels J; Beaudet AL PLoS One; 2010 Aug; 5(8):e12278. PubMed ID: 20808828 [TBL] [Abstract][Full Text] [Related]
3. GABA and epileptogenesis: comparing gabrb3 gene-deficient mice with Angelman syndrome in man. DeLorey TM; Olsen RW Epilepsy Res; 1999 Sep; 36(2-3):123-32. PubMed ID: 10515160 [TBL] [Abstract][Full Text] [Related]
5. GABAA receptor beta3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in beta3 subunit levels, EEG, and behavior. Liljelund P; Handforth A; Homanics GE; Olsen RW Brain Res Dev Brain Res; 2005 Jun; 157(2):150-61. PubMed ID: 15878204 [TBL] [Abstract][Full Text] [Related]
6. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Samaco RC; Hogart A; LaSalle JM Hum Mol Genet; 2005 Feb; 14(4):483-92. PubMed ID: 15615769 [TBL] [Abstract][Full Text] [Related]
7. Angelman syndrome: correlations between epilepsy phenotypes and genotypes. Minassian BA; DeLorey TM; Olsen RW; Philippart M; Bronstein Y; Zhang Q; Guerrini R; Van Ness P; Livet MO; Delgado-Escueta AV Ann Neurol; 1998 Apr; 43(4):485-93. PubMed ID: 9546330 [TBL] [Abstract][Full Text] [Related]
8. Angelman syndrome and severe infections in a patient with de novo 15q11.2-q13.1 deletion and maternally inherited 2q21.3 microdeletion. Neubert G; von Au K; Drossel K; Tzschach A; Horn D; Nickel R; Kaindl AM Gene; 2013 Jan; 512(2):453-5. PubMed ID: 23124039 [TBL] [Abstract][Full Text] [Related]
9. Mouse models of Angelman syndrome, a neurodevelopmental disorder, display different brain regional GABA(A) receptor alterations. Sinkkonen ST; Homanics GE; Korpi ER Neurosci Lett; 2003 Apr; 340(3):205-8. PubMed ID: 12672542 [TBL] [Abstract][Full Text] [Related]
10. Strain-dependence of the Angelman Syndrome phenotypes in Ube3a maternal deficiency mice. Born HA; Dao AT; Levine AT; Lee WL; Mehta NM; Mehra S; Weeber EJ; Anderson AE Sci Rep; 2017 Aug; 7(1):8451. PubMed ID: 28814801 [TBL] [Abstract][Full Text] [Related]
11. Angelman syndrome reviewed from a neurophysiological perspective. The UBE3A-GABRB3 hypothesis. Dan B; Boyd SG Neuropediatrics; 2003 Aug; 34(4):169-76. PubMed ID: 12973656 [TBL] [Abstract][Full Text] [Related]
17. Synaptic clustering differences due to different GABRB3 mutations cause variable epilepsy syndromes. Shi YW; Zhang Q; Cai K; Poliquin S; Shen W; Winters N; Yi YH; Wang J; Hu N; Macdonald RL; Liao WP; Kang JQ Brain; 2019 Oct; 142(10):3028-3044. PubMed ID: 31435640 [TBL] [Abstract][Full Text] [Related]
18. From electrophysiology to chromatin: a bottom-up approach to Angelman syndrome. Dan B; Servais L; Boyd SG; Wagstaff J; Cheron G Ann N Y Acad Sci; 2004 Dec; 1030():599-611. PubMed ID: 15659843 [TBL] [Abstract][Full Text] [Related]
19. [The GABAA receptor beta 3-subunit gene (GABRB3) as a candidate responsible for central nerve disturbances in Angelman syndrome (AS)]. Saitoh S; Niikawa N Nihon Rinsho; 1993 Sep; 51(9):2409-13. PubMed ID: 8411721 [TBL] [Abstract][Full Text] [Related]
20. Genotype-Phenotype Correlations in Angelman Syndrome. Yang L; Shu X; Mao S; Wang Y; Du X; Zou C Genes (Basel); 2021 Jun; 12(7):. PubMed ID: 34203304 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]