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.
488 related articles for article (PubMed ID: 22749736)
1. SHANK3 as an autism spectrum disorder-associated gene. Uchino S; Waga C Brain Dev; 2013 Feb; 35(2):106-10. PubMed ID: 22749736 [TBL] [Abstract][Full Text] [Related]
2. Identification of two novel Shank3 transcripts in the developing mouse neocortex. Waga C; Asano H; Sanagi T; Suzuki E; Nakamura Y; Tsuchiya A; Itoh M; Goto Y; Kohsaka S; Uchino S J Neurochem; 2014 Jan; 128(2):280-93. PubMed ID: 24164323 [TBL] [Abstract][Full Text] [Related]
3. Novel Therapeutic Approach for Autism Spectrum Disorder: Focus on SHANK3. Uchino S; Waga C Curr Neuropharmacol; 2015; 13(6):786-92. PubMed ID: 26511836 [TBL] [Abstract][Full Text] [Related]
4. Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism. Jaramillo TC; Speed HE; Xuan Z; Reimers JM; Liu S; Powell CM Autism Res; 2016 Mar; 9(3):350-75. PubMed ID: 26559786 [TBL] [Abstract][Full Text] [Related]
6. A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes. Xu N; Lv H; Yang T; Du X; Sun Y; Xiao B; Fan Y; Luo X; Zhan Y; Wang L; Li F; Yu Y Orphanet J Rare Dis; 2020 Nov; 15(1):335. PubMed ID: 33256793 [TBL] [Abstract][Full Text] [Related]
7. Developmental profiling of ASD-related shank3 transcripts and their differential regulation by valproic acid in zebrafish. Liu CX; Peng XL; Hu CC; Li CY; Li Q; Xu X Dev Genes Evol; 2016 Nov; 226(6):389-400. PubMed ID: 27562614 [TBL] [Abstract][Full Text] [Related]
8. A blueprint for research on Shankopathies: a view from research on autism spectrum disorder. Carbonetto S Dev Neurobiol; 2014 Feb; 74(2):85-112. PubMed ID: 24218108 [TBL] [Abstract][Full Text] [Related]
9. Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders. Zhu L; Wang X; Li XL; Towers A; Cao X; Wang P; Bowman R; Yang H; Goldstein J; Li YJ; Jiang YH Hum Mol Genet; 2014 Mar; 23(6):1563-78. PubMed ID: 24186872 [TBL] [Abstract][Full Text] [Related]
10. Behavioral Phenotyping of an Improved Mouse Model of Phelan-McDermid Syndrome with a Complete Deletion of the Drapeau E; Riad M; Kajiwara Y; Buxbaum JD eNeuro; 2018; 5(3):. PubMed ID: 30302388 [TBL] [Abstract][Full Text] [Related]
12. Developmental social communication deficits in the Shank3 rat model of phelan-mcdermid syndrome and autism spectrum disorder. Berg EL; Copping NA; Rivera JK; Pride MC; Careaga M; Bauman MD; Berman RF; Lein PJ; Harony-Nicolas H; Buxbaum JD; Ellegood J; Lerch JP; Wöhr M; Silverman JL Autism Res; 2018 Apr; 11(4):587-601. PubMed ID: 29377611 [TBL] [Abstract][Full Text] [Related]
13. A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case. Samogy-Costa CI; Varella-Branco E; Monfardini F; Ferraz H; Fock RA; Barbosa RHA; Pessoa ALS; Perez ABA; Lourenço N; Vibranovski M; Krepischi A; Rosenberg C; Passos-Bueno MR J Neurodev Disord; 2019 Jul; 11(1):13. PubMed ID: 31319798 [TBL] [Abstract][Full Text] [Related]
14. Repetitive behaviors in the Shank1 knockout mouse model for autism spectrum disorder: developmental aspects and effects of social context. Sungur AÖ; Vörckel KJ; Schwarting RK; Wöhr M J Neurosci Methods; 2014 Aug; 234():92-100. PubMed ID: 24820912 [TBL] [Abstract][Full Text] [Related]
15. Association between deletion size and important phenotypes expands the genomic region of interest in Phelan-McDermid syndrome (22q13 deletion syndrome). Sarasua SM; Dwivedi A; Boccuto L; Rollins JD; Chen CF; Rogers RC; Phelan K; DuPont BR; Collins JS J Med Genet; 2011 Nov; 48(11):761-6. PubMed ID: 21984749 [TBL] [Abstract][Full Text] [Related]
16. Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits. Speed HE; Kouser M; Xuan Z; Reimers JM; Ochoa CF; Gupta N; Liu S; Powell CM J Neurosci; 2015 Jul; 35(26):9648-65. PubMed ID: 26134648 [TBL] [Abstract][Full Text] [Related]
17. Phelan McDermid Syndrome: From Genetic Discoveries to Animal Models and Treatment. Harony-Nicolas H; De Rubeis S; Kolevzon A; Buxbaum JD J Child Neurol; 2015 Dec; 30(14):1861-70. PubMed ID: 26350728 [TBL] [Abstract][Full Text] [Related]
18. GABA Neuronal Deletion of Yoo T; Cho H; Lee J; Park H; Yoo YE; Yang E; Kim JY; Kim H; Kim E Front Cell Neurosci; 2018; 12():341. PubMed ID: 30356810 [TBL] [Abstract][Full Text] [Related]