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4. Gastrointestinal dysfunction in patients and mice expressing the autism-associated R451C mutation in neuroligin-3. Hosie S; Ellis M; Swaminathan M; Ramalhosa F; Seger GO; Balasuriya GK; Gillberg C; Råstam M; Churilov L; McKeown SJ; Yalcinkaya N; Urvil P; Savidge T; Bell CA; Bodin O; Wood J; Franks AE; Bornstein JC; Hill-Yardin EL Autism Res; 2019 Jul; 12(7):1043-1056. PubMed ID: 31119867 [TBL] [Abstract][Full Text] [Related]
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7. Shared synaptic pathophysiology in syndromic and nonsyndromic rodent models of autism. Baudouin SJ; Gaudias J; Gerharz S; Hatstatt L; Zhou K; Punnakkal P; Tanaka KF; Spooren W; Hen R; De Zeeuw CI; Vogt K; Scheiffele P Science; 2012 Oct; 338(6103):128-32. PubMed ID: 22983708 [TBL] [Abstract][Full Text] [Related]
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9. Not all neuroligin 3 and 4X missense variants lead to significant functional inactivation. Xu X; Hu Z; Zhang L; Liu H; Cheng Y; Xia K; Zhang X Brain Behav; 2017 Sep; 7(9):e00793. PubMed ID: 28948087 [TBL] [Abstract][Full Text] [Related]
10. Genetic background effects in Neuroligin-3 mutant mice: Minimal behavioral abnormalities on C57 background. Jaramillo TC; Escamilla CO; Liu S; Peca L; Birnbaum SG; Powell CM Autism Res; 2018 Feb; 11(2):234-244. PubMed ID: 29028156 [TBL] [Abstract][Full Text] [Related]
11. Do known mutations in neuroligin genes (NLGN3 and NLGN4) cause autism? Talebizadeh Z; Bittel DC; Veatch OJ; Butler MG; Takahashi TN; Miles JH J Autism Dev Disord; 2004 Dec; 34(6):735-6. PubMed ID: 15679194 [No Abstract] [Full Text] [Related]
12. Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autism. Avdjieva-Tzavella DM; Todorov TP; Todorova AP; Kirov AV; Hadjidekova SP; Rukova BB; Litvinenko IO; Hristova-Naydenova DN; Tincheva RS; Toncheva DI Genet Couns; 2012; 23(4):505-11. PubMed ID: 23431752 [TBL] [Abstract][Full Text] [Related]
13. A Hemizygous 370 Kilobase Microduplication at Xq13.1 in a Three-Year-Old Boy With Autism and Speech Delay. Gumus E Fetal Pediatr Pathol; 2019 Jun; 38(3):239-244. PubMed ID: 30757938 [TBL] [Abstract][Full Text] [Related]
14. Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands. Vincent JB; Kolozsvari D; Roberts WS; Bolton PF; Gurling HM; Scherer SW Am J Med Genet B Neuropsychiatr Genet; 2004 Aug; 129B(1):82-4. PubMed ID: 15274046 [TBL] [Abstract][Full Text] [Related]
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16. Mice with an autism-associated R451C mutation in neuroligin-3 show a cautious but accurate response style in touchscreen attention tasks. Burrows EL; May C; Hill T; Churliov L; Johnson KA; Hannan AJ Genes Brain Behav; 2022 Jan; 21(1):e12757. PubMed ID: 34085373 [TBL] [Abstract][Full Text] [Related]
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19. Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection. Blasi F; Bacchelli E; Pesaresi G; Carone S; Bailey AJ; Maestrini E; Am J Med Genet B Neuropsychiatr Genet; 2006 Apr; 141B(3):220-1. PubMed ID: 16508939 [TBL] [Abstract][Full Text] [Related]
20. Gamma Oscillation Dysfunction in mPFC Leads to Social Deficits in Neuroligin 3 R451C Knockin Mice. Cao W; Lin S; Xia QQ; Du YL; Yang Q; Zhang MY; Lu YQ; Xu J; Duan SM; Xia J; Feng G; Xu J; Luo JH Neuron; 2018 Mar; 97(6):1253-1260.e7. PubMed ID: 29503190 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]