271 related articles for article (PubMed ID: 28551752)
1. Behavioural Phenotypes and Neural Circuit Dysfunctions in Mouse Models of Autism Spectrum Disorder.
Ferhat AT; Halbedl S; Schmeisser MJ; Kas MJ; Bourgeron T; Ey E
Adv Anat Embryol Cell Biol; 2017; 224():85-101. PubMed ID: 28551752
[TBL] [Abstract][Full Text] [Related]
2. Altered mGluR5-Homer scaffolds and corticostriatal connectivity in a Shank3 complete knockout model of autism.
Wang X; Bey AL; Katz BM; Badea A; Kim N; David LK; Duffney LJ; Kumar S; Mague SD; Hulbert SW; Dutta N; Hayrapetyan V; Yu C; Gaidis E; Zhao S; Ding JD; Xu Q; Chung L; Rodriguiz RM; Wang F; Weinberg RJ; Wetsel WC; Dzirasa K; Yin H; Jiang YH
Nat Commun; 2016 May; 7():11459. PubMed ID: 27161151
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Environmental enrichment modulates affiliative and aggressive social behaviour in the neuroligin-3 R451C mouse model of autism spectrum disorder.
Burrows EL; Koyama L; May C; Hill-Yardin EL; Hannan AJ
Pharmacol Biochem Behav; 2020 Aug; 195():172955. PubMed ID: 32474162
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. What we can learn from a genetic rodent model about autism.
Möhrle D; Fernández M; Peñagarikano O; Frick A; Allman B; Schmid S
Neurosci Biobehav Rev; 2020 Feb; 109():29-53. PubMed ID: 31887338
[TBL] [Abstract][Full Text] [Related]
7. The behavioural phenotype of Potocki-Lupski syndrome: a cross-syndrome comparison.
Bissell S; Wilde L; Richards C; Moss J; Oliver C
J Neurodev Disord; 2018 Jan; 10(1):2. PubMed ID: 29329513
[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. Disrupted circuits in mouse models of autism spectrum disorder and intellectual disability.
Golden CE; Buxbaum JD; De Rubeis S
Curr Opin Neurobiol; 2018 Feb; 48():106-112. PubMed ID: 29222989
[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]
11. Genetic control of social behavior: Lessons from mutant mice.
Provenzano G; Chelini G; Bozzi Y
Behav Brain Res; 2017 May; 325(Pt B):237-250. PubMed ID: 27825935
[TBL] [Abstract][Full Text] [Related]
12. Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
Shibutani M; Horii T; Shoji H; Morita S; Kimura M; Terawaki N; Miyakawa T; Hatada I
Int J Mol Sci; 2017 Aug; 18(9):. PubMed ID: 28867767
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Neural Connectivity Evidence for a Categorical-Dimensional Hybrid Model of Autism Spectrum Disorder.
Elton A; Di Martino A; Hazlett HC; Gao W
Biol Psychiatry; 2016 Jul; 80(2):120-128. PubMed ID: 26707088
[TBL] [Abstract][Full Text] [Related]
15. Ketamine administration in early postnatal life as a tool for mimicking Autism Spectrum Disorders core symptoms.
Bove M; Schiavone S; Tucci P; Sikora V; Dimonte S; Colia AL; Morgese MG; Trabace L
Prog Neuropsychopharmacol Biol Psychiatry; 2022 Jul; 117():110560. PubMed ID: 35460811
[TBL] [Abstract][Full Text] [Related]
16. CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
Katayama Y; Nishiyama M; Shoji H; Ohkawa Y; Kawamura A; Sato T; Suyama M; Takumi T; Miyakawa T; Nakayama KI
Nature; 2016 Sep; 537(7622):675-679. PubMed ID: 27602517
[TBL] [Abstract][Full Text] [Related]
17. Modeling of autism genetic variations in mice: focusing on synaptic and microcircuit dysfunctions.
Qiu S; Aldinger KA; Levitt P
Dev Neurosci; 2012; 34(2-3):88-100. PubMed ID: 22572629
[TBL] [Abstract][Full Text] [Related]
18. Advances in understanding the pathophysiology of autism spectrum disorders.
Yenkoyan K; Grigoryan A; Fereshetyan K; Yepremyan D
Behav Brain Res; 2017 Jul; 331():92-101. PubMed ID: 28499914
[TBL] [Abstract][Full Text] [Related]
19. Altered functional organization within the insular cortex in adult males with high-functioning autism spectrum disorder: evidence from connectivity-based parcellation.
Yamada T; Itahashi T; Nakamura M; Watanabe H; Kuroda M; Ohta H; Kanai C; Kato N; Hashimoto RI
Mol Autism; 2016; 7():41. PubMed ID: 27713815
[TBL] [Abstract][Full Text] [Related]
20. Development of an autism severity score for mice using Nlgn4 null mutants as a construct-valid model of heritable monogenic autism.
El-Kordi A; Winkler D; Hammerschmidt K; Kästner A; Krueger D; Ronnenberg A; Ritter C; Jatho J; Radyushkin K; Bourgeron T; Fischer J; Brose N; Ehrenreich H
Behav Brain Res; 2013 Aug; 251():41-9. PubMed ID: 23183221
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
