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.
361 related articles for article (PubMed ID: 30610205)
1. An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function. Wang L; Pang K; Han K; Adamski CJ; Wang W; He L; Lai JK; Bondar VV; Duman JG; Richman R; Tolias KF; Barth P; Palzkill T; Liu Z; Holder JL; Zoghbi HY Mol Psychiatry; 2020 Oct; 25(10):2534-2555. PubMed ID: 30610205 [TBL] [Abstract][Full Text] [Related]
2. Targeting of δ-catenin to postsynaptic sites through interaction with the Shank3 N-terminus. Hassani Nia F; Woike D; Martens V; Klüssendorf M; Hönck HH; Harder S; Kreienkamp HJ Mol Autism; 2020 Oct; 11(1):85. PubMed ID: 33115499 [TBL] [Abstract][Full Text] [Related]
3. SHANK3 Mutations Associated with Autism and Schizophrenia Lead to Shared and Distinct Changes in Dendritic Spine Dynamics in the Developing Mouse Brain. Huang C; Voglewede MM; Ozsen EN; Wang H; Zhang H Neuroscience; 2023 Sep; 528():1-11. PubMed ID: 37532012 [TBL] [Abstract][Full Text] [Related]
4. Pharmacological enhancement of mGlu5 receptors rescues behavioral deficits in SHANK3 knock-out mice. Vicidomini C; Ponzoni L; Lim D; Schmeisser MJ; Reim D; Morello N; Orellana D; Tozzi A; Durante V; Scalmani P; Mantegazza M; Genazzani AA; Giustetto M; Sala M; Calabresi P; Boeckers TM; Sala C; Verpelli C Mol Psychiatry; 2017 May; 22(5):689-702. PubMed ID: 27021819 [TBL] [Abstract][Full Text] [Related]
5. Transcriptional determinism and stochasticity contribute to the complexity of autism-associated SHANK family genes. Lu X; Ni P; Suarez-Meade P; Ma Y; Forrest EN; Wang G; Wang Y; Quiñones-Hinojosa A; Gerstein M; Jiang YH Cell Rep; 2024 Jul; 43(7):114376. PubMed ID: 38900637 [TBL] [Abstract][Full Text] [Related]
6. Shank3 mutation in a mouse model of autism leads to changes in the S-nitroso-proteome and affects key proteins involved in vesicle release and synaptic function. Amal H; Barak B; Bhat V; Gong G; Joughin BA; Wang X; Wishnok JS; Feng G; Tannenbaum SR Mol Psychiatry; 2020 Aug; 25(8):1835-1848. PubMed ID: 29988084 [TBL] [Abstract][Full Text] [Related]
7. Shank3 mutation impairs glutamate signaling and myelination in ASD mouse model and human iPSC-derived OPCs. Fischer I; Shohat S; Leichtmann-Bardoogo Y; Nayak R; Wiener G; Rosh I; Shemen A; Tripathi U; Rokach M; Bar E; Hussein Y; Castro AC; Chen G; Soffer A; Schokoroy-Trangle S; Elad-Sfadia G; Assaf Y; Schroeder A; Monteiro P; Stern S; Maoz BM; Barak B Sci Adv; 2024 Oct; 10(41):eadl4573. PubMed ID: 39392881 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. The Role of Thioredoxin System in Shank3 Mouse Model of Autism. Bazbaz W; Kartawy M; Hamoudi W; Ojha SK; Khaliulin I; Amal H J Mol Neurosci; 2024 Sep; 74(4):90. PubMed ID: 39347996 [TBL] [Abstract][Full Text] [Related]
10. Adult restoration of Shank3 expression rescues selective autistic-like phenotypes. Mei Y; Monteiro P; Zhou Y; Kim JA; Gao X; Fu Z; Feng G Nature; 2016 Feb; 530(7591):481-4. PubMed ID: 26886798 [TBL] [Abstract][Full Text] [Related]
12. Disrupted extracellular matrix and cell cycle genes in autism-associated Shank3 deficiency are targeted by lithium. Ioannidis V; Pandey R; Bauer HF; Schön M; Bockmann J; Boeckers TM; Lutz AK Mol Psychiatry; 2024 Mar; 29(3):704-717. PubMed ID: 38123724 [TBL] [Abstract][Full Text] [Related]
13. SHANK3 gene mutations associated with autism facilitate ligand binding to the Shank3 ankyrin repeat region. Mameza MG; Dvoretskova E; Bamann M; Hönck HH; Güler T; Boeckers TM; Schoen M; Verpelli C; Sala C; Barsukov I; Dityatev A; Kreienkamp HJ J Biol Chem; 2013 Sep; 288(37):26697-708. PubMed ID: 23897824 [TBL] [Abstract][Full Text] [Related]
14. Increased rates of cerebral protein synthesis in Shank3 knockout mice: Implications for a link between synaptic protein deficit and dysregulated protein synthesis in autism spectrum disorder/intellectual disability. Torossian A; Saré RM; Loutaev I; Smith CB Neurobiol Dis; 2021 Jan; 148():105213. PubMed ID: 33276083 [TBL] [Abstract][Full Text] [Related]
15. Autism-associated mutations in ProSAP2/Shank3 impair synaptic transmission and neurexin-neuroligin-mediated transsynaptic signaling. Arons MH; Thynne CJ; Grabrucker AM; Li D; Schoen M; Cheyne JE; Boeckers TM; Montgomery JM; Garner CC J Neurosci; 2012 Oct; 32(43):14966-78. PubMed ID: 23100419 [TBL] [Abstract][Full Text] [Related]
16. Inhibition of Trpv4 rescues circuit and social deficits unmasked by acute inflammatory response in a Shank3 mouse model of Autism. Tzanoulinou S; Musardo S; Contestabile A; Bariselli S; Casarotto G; Magrinelli E; Jiang YH; Jabaudon D; Bellone C Mol Psychiatry; 2022 Apr; 27(4):2080-2094. PubMed ID: 35022531 [TBL] [Abstract][Full Text] [Related]
17. A cross-talk between nitric oxide and the glutamatergic system in a Shank3 mouse model of autism. Hamoudi W; Tripathi MK; Ojha SK; Amal H Free Radic Biol Med; 2022 Aug; 188():83-91. PubMed ID: 35716826 [TBL] [Abstract][Full Text] [Related]
18. Autism-associated Bucher M; Niebling S; Han Y; Molodenskiy D; Hassani Nia F; Kreienkamp HJ; Svergun D; Kim E; Kostyukova AS; Kreutz MR; Mikhaylova M Elife; 2021 May; 10():. PubMed ID: 33945465 [TBL] [Abstract][Full Text] [Related]
19. Influence of maternal zinc supplementation on the development of autism-associated behavioural and synaptic deficits in offspring Shank3-knockout mice. Vyas Y; Lee K; Jung Y; Montgomery JM Mol Brain; 2020 Aug; 13(1):110. PubMed ID: 32758248 [TBL] [Abstract][Full Text] [Related]
20. Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder. Kabitzke PA; Brunner D; He D; Fazio PA; Cox K; Sutphen J; Thiede L; Sabath E; Hanania T; Alexandrov V; Rasmusson R; Spooren W; Ghosh A; Feliciano P; Biemans B; Benedetti M; Clayton AL Genes Brain Behav; 2018 Jan; 17(1):4-22. PubMed ID: 28753255 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]