284 related articles for article (PubMed ID: 35388181)
1. A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling.
Qin Y; Du Y; Chen L; Liu Y; Xu W; Liu Y; Li Y; Leng J; Wang Y; Zhang XY; Feng J; Zhang F; Jin L; Qiu Z; Gong X; Wang H
Mol Psychiatry; 2022 Jul; 27(7):2985-2998. PubMed ID: 35388181
[TBL] [Abstract][Full Text] [Related]
2. Downregulation of mGluR1-mediated signaling underlying autistic-like core symptoms in Shank1 P1812L-knock-in mice.
Qin Y; Zhang XY; Liu Y; Ma Z; Tao S; Li Y; Peng R; Wang F; Wang J; Feng J; Qiu Z; Jin L; Wang H; Gong X
Transl Psychiatry; 2023 Oct; 13(1):329. PubMed ID: 37880287
[TBL] [Abstract][Full Text] [Related]
3. SHANK1 and autism spectrum disorders.
Gong X; Wang H
Sci China Life Sci; 2015 Oct; 58(10):985-90. PubMed ID: 26335738
[TBL] [Abstract][Full Text] [Related]
4. SHANK1 polymorphisms and SNP-SNP interactions among SHANK family: A possible cue for recognition to autism spectrum disorder in infant age.
Qiu S; Li Y; Bai Y; Shi J; Cui H; Gu Y; Ren Y; Zhao Q; Zhang K; Lu M; Wang Y; Li Y; Zhong W; Zhu X; Liu Y; Cheng Y; Qiao Y; Liu Y
Autism Res; 2019 Mar; 12(3):375-383. PubMed ID: 30629339
[TBL] [Abstract][Full Text] [Related]
5. Modeling autism by SHANK gene mutations in mice.
Jiang YH; Ehlers MD
Neuron; 2013 Apr; 78(1):8-27. PubMed ID: 23583105
[TBL] [Abstract][Full Text] [Related]
6. Behavioral phenotypes and neurobiological mechanisms in the Shank1 mouse model for autism spectrum disorder: A translational perspective.
Sungur AÖ; Schwarting RKW; Wöhr M
Behav Brain Res; 2018 Oct; 352():46-61. PubMed ID: 28963042
[TBL] [Abstract][Full Text] [Related]
7. Aberrant cognitive phenotypes and altered hippocampal BDNF expression related to epigenetic modifications in mice lacking the post-synaptic scaffolding protein SHANK1: Implications for autism spectrum disorder.
Sungur AÖ; Jochner MCE; Harb H; Kılıç A; Garn H; Schwarting RKW; Wöhr M
Hippocampus; 2017 Aug; 27(8):906-919. PubMed ID: 28500650
[TBL] [Abstract][Full Text] [Related]
8. Early communication deficits in the Shank1 knockout mouse model for autism spectrum disorder: Developmental aspects and effects of social context.
Sungur AÖ; Schwarting RK; Wöhr M
Autism Res; 2016 Jun; 9(6):696-709. PubMed ID: 26419918
[TBL] [Abstract][Full Text] [Related]
9. Correction: A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling.
Qin Y; Du Y; Chen L; Liu Y; Xu W; Liu Y; Li Y; Leng J; Wang Y; Zhang XY; Feng J; Zhang F; Jin L; Qiu Z; Gong X; Wang H
Mol Psychiatry; 2022 Sep; 27(9):3922. PubMed ID: 35538194
[No Abstract] [Full Text] [Related]
10. 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]
11.
Xi K; Cai SQ; Yan HF; Tian Y; Cai J; Yang XM; Wang JM; Xing GG
J Neurosci; 2023 May; 43(21):3949-3969. PubMed ID: 37037606
[TBL] [Abstract][Full Text] [Related]
12. NEXMIF/KIDLIA Knock-out Mouse Demonstrates Autism-Like Behaviors, Memory Deficits, and Impairments in Synapse Formation and Function.
Gilbert J; O'Connor M; Templet S; Moghaddam M; Di Via Ioschpe A; Sinclair A; Zhu LQ; Xu W; Man HY
J Neurosci; 2020 Jan; 40(1):237-254. PubMed ID: 31704787
[TBL] [Abstract][Full Text] [Related]
13. Autism-associated Shank3 mutations alter mGluR expression and mGluR-dependent but not NMDA receptor-dependent long-term depression.
Lee K; Vyas Y; Garner CC; Montgomery JM
Synapse; 2019 Aug; 73(8):e22097. PubMed ID: 30868621
[TBL] [Abstract][Full Text] [Related]
14. Developmental impaired Akt signaling in the Shank1 and Shank3 double knock-out mice.
Mossa A; Pagano J; Ponzoni L; Tozzi A; Vezzoli E; Sciaccaluga M; Costa C; Beretta S; Francolini M; Sala M; Calabresi P; Boeckers TM; Sala C; Verpelli C
Mol Psychiatry; 2021 Jun; 26(6):1928-1944. PubMed ID: 33402706
[TBL] [Abstract][Full Text] [Related]
15. Sociability and motor functions in Shank1 mutant mice.
Silverman JL; Turner SM; Barkan CL; Tolu SS; Saxena R; Hung AY; Sheng M; Crawley JN
Brain Res; 2011 Mar; 1380():120-37. PubMed ID: 20868654
[TBL] [Abstract][Full Text] [Related]
16. SHANK1 Deletions in Males with Autism Spectrum Disorder.
Sato D; Lionel AC; Leblond CS; Prasad A; Pinto D; Walker S; O'Connor I; Russell C; Drmic IE; Hamdan FF; Michaud JL; Endris V; Roeth R; Delorme R; Huguet G; Leboyer M; Rastam M; Gillberg C; Lathrop M; Stavropoulos DJ; Anagnostou E; Weksberg R; Fombonne E; Zwaigenbaum L; Fernandez BA; Roberts W; Rappold GA; Marshall CR; Bourgeron T; Szatmari P; Scherer SW
Am J Hum Genet; 2012 May; 90(5):879-87. PubMed ID: 22503632
[TBL] [Abstract][Full Text] [Related]
17. The eIF4E homolog 4EHP (eIF4E2) regulates hippocampal long-term depression and impacts social behavior.
Wiebe S; Meng XQ; Kim SH; Zhang X; Lacaille JC; Aguilar-Valles A; Sonenberg N
Mol Autism; 2020 Nov; 11(1):92. PubMed ID: 33225984
[TBL] [Abstract][Full Text] [Related]
18. Comparison of SHANK3 deficiency in animal models: phenotypes, treatment strategies, and translational implications.
Delling JP; Boeckers TM
J Neurodev Disord; 2021 Nov; 13(1):55. PubMed ID: 34784886
[TBL] [Abstract][Full Text] [Related]
19. Juvenile Shank3b deficient mice present with behavioral phenotype relevant to autism spectrum disorder.
Balaan C; Corley MJ; Eulalio T; Leite-Ahyo K; Pang APS; Fang R; Khadka VS; Maunakea AK; Ward MA
Behav Brain Res; 2019 Jan; 356():137-147. PubMed ID: 30134148
[TBL] [Abstract][Full Text] [Related]
20. A Novel Human
Stephenson JR; Wang X; Perfitt TL; Parrish WP; Shonesy BC; Marks CR; Mortlock DP; Nakagawa T; Sutcliffe JS; Colbran RJ
J Neurosci; 2017 Feb; 37(8):2216-2233. PubMed ID: 28130356
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
