519 related articles for article (PubMed ID: 28841651)
1. Functional significance of rare neuroligin 1 variants found in autism.
Nakanishi M; Nomura J; Ji X; Tamada K; Arai T; Takahashi E; Bućan M; Takumi T
PLoS Genet; 2017 Aug; 13(8):e1006940. PubMed ID: 28841651
[TBL] [Abstract][Full Text] [Related]
2. Autism Spectrum Disorder/Intellectual Disability-Associated Mutations in Trio Disrupt Neuroligin 1-Mediated Synaptogenesis.
Tian C; Paskus JD; Fingleton E; Roche KW; Herring BE
J Neurosci; 2021 Sep; 41(37):7768-7778. PubMed ID: 34353896
[TBL] [Abstract][Full Text] [Related]
3. Distortion of the normal function of synaptic cell adhesion molecules by genetic variants as a risk for autism spectrum disorders.
Baig DN; Yanagawa T; Tabuchi K
Brain Res Bull; 2017 Mar; 129():82-90. PubMed ID: 27743928
[TBL] [Abstract][Full Text] [Related]
4. Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment.
Quartier A; Courraud J; Thi Ha T; McGillivray G; Isidor B; Rose K; Drouot N; Savidan MA; Feger C; Jagline H; Chelly J; Shaw M; Laumonnier F; Gecz J; Mandel JL; Piton A
Hum Mutat; 2019 Nov; 40(11):2021-2032. PubMed ID: 31184401
[TBL] [Abstract][Full Text] [Related]
5. Neuroligin 3 R451C mutation alters electroencephalography spectral activity in an animal model of autism spectrum disorders.
Liu JJ; Grace KP; Horner RL; Cortez MA; Shao Y; Jia Z
Mol Brain; 2017 Apr; 10(1):10. PubMed ID: 28385162
[TBL] [Abstract][Full Text] [Related]
6. Canonical versus non-canonical transsynaptic signaling of neuroligin 3 tunes development of sociality in mice.
Yoshida T; Yamagata A; Imai A; Kim J; Izumi H; Nakashima S; Shiroshima T; Maeda A; Iwasawa-Okamoto S; Azechi K; Osaka F; Saitoh T; Maenaka K; Shimada T; Fukata Y; Fukata M; Matsumoto J; Nishijo H; Takao K; Tanaka S; Okabe S; Tabuchi K; Uemura T; Mishina M; Mori H; Fukai S
Nat Commun; 2021 Mar; 12(1):1848. PubMed ID: 33758193
[TBL] [Abstract][Full Text] [Related]
7. Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.
Liu Y; Du Y; Liu W; Yang C; Liu Y; Wang H; Gong X
PLoS One; 2013; 8(2):e56639. PubMed ID: 23468870
[TBL] [Abstract][Full Text] [Related]
8. Autism-associated variants of neuroligin 4X impair synaptogenic activity by various molecular mechanisms.
Yumoto T; Kimura M; Nagatomo R; Sato T; Utsunomiya S; Aoki N; Kitaura M; Takahashi K; Takemoto H; Watanabe H; Okano H; Yoshida F; Nao Y; Tomita T
Mol Autism; 2020 Sep; 11(1):68. PubMed ID: 32873342
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Systematic phenomics analysis of autism-associated genes reveals parallel networks underlying reversible impairments in habituation.
McDiarmid TA; Belmadani M; Liang J; Meili F; Mathews EA; Mullen GP; Hendi A; Wong WR; Rand JB; Mizumoto K; Haas K; Pavlidis P; Rankin CH
Proc Natl Acad Sci U S A; 2020 Jan; 117(1):656-667. PubMed ID: 31754030
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Analysis of four neuroligin genes as candidates for autism.
Ylisaukko-oja T; Rehnström K; Auranen M; Vanhala R; Alen R; Kempas E; Ellonen P; Turunen JA; Makkonen I; Riikonen R; Nieminen-von Wendt T; von Wendt L; Peltonen L; Järvelä I
Eur J Hum Genet; 2005 Dec; 13(12):1285-92. PubMed ID: 16077734
[TBL] [Abstract][Full Text] [Related]
15. DSCAM Deficiency Leads to Premature Spine Maturation and Autism-like Behaviors.
Chen P; Liu Z; Zhang Q; Lin D; Song L; Liu J; Jiao HF; Lai X; Zou S; Wang S; Zhou T; Li BM; Zhu L; Pan BX; Fei E
J Neurosci; 2022 Jan; 42(4):532-551. PubMed ID: 34848499
[TBL] [Abstract][Full Text] [Related]
16. Neurexin gene family variants as risk factors for autism spectrum disorder.
Wang J; Gong J; Li L; Chen Y; Liu L; Gu H; Luo X; Hou F; Zhang J; Song R
Autism Res; 2018 Jan; 11(1):37-43. PubMed ID: 29045040
[TBL] [Abstract][Full Text] [Related]
17. Neuroligins and Neurodevelopmental Disorders: X-Linked Genetics.
Nguyen TA; Lehr AW; Roche KW
Front Synaptic Neurosci; 2020; 12():33. PubMed ID: 32848696
[TBL] [Abstract][Full Text] [Related]
18. [Synapse maturation and autism: learning from neuroligin model mice].
Tabuchi K; Chang W; Asgar NF; Pramanik G
Nihon Shinkei Seishin Yakurigaku Zasshi; 2014 Feb; 34(1):1-4. PubMed ID: 25069265
[TBL] [Abstract][Full Text] [Related]
19. Neuroligin-3: A Circuit-Specific Synapse Organizer That Shapes Normal Function and Autism Spectrum Disorder-Associated Dysfunction.
Uchigashima M; Cheung A; Futai K
Front Mol Neurosci; 2021; 14():749164. PubMed ID: 34690695
[TBL] [Abstract][Full Text] [Related]
20. Social Isolation Alters Social and Mating Behavior in the R451C Neuroligin Mouse Model of Autism.
Burrows EL; Eastwood AF; May C; Kolbe SC; Hill T; McLachlan NM; Churilov L; Hannan AJ
Neural Plast; 2017; 2017():8361290. PubMed ID: 28255463
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]