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.
220 related articles for article (PubMed ID: 32503885)
1. Kirrel3-Mediated Synapse Formation Is Attenuated by Disease-Associated Missense Variants. Taylor MR; Martin EA; Sinnen B; Trilokekar R; Ranza E; Antonarakis SE; Williams ME J Neurosci; 2020 Jul; 40(28):5376-5388. PubMed ID: 32503885 [TBL] [Abstract][Full Text] [Related]
2. The intellectual disability gene Kirrel3 regulates target-specific mossy fiber synapse development in the hippocampus. Martin EA; Muralidhar S; Wang Z; Cervantes DC; Basu R; Taylor MR; Hunter J; Cutforth T; Wilke SA; Ghosh A; Williams ME Elife; 2015 Nov; 4():e09395. PubMed ID: 26575286 [TBL] [Abstract][Full Text] [Related]
3. Examining Hippocampal Mossy Fiber Synapses by 3D Electron Microscopy in Wildtype and Kirrel3 Knockout Mice. Martin EA; Woodruff D; Rawson RL; Williams ME eNeuro; 2017; 4(3):. PubMed ID: 28670619 [TBL] [Abstract][Full Text] [Related]
4. Autism and Intellectual Disability-Associated KIRREL3 Interacts with Neuronal Proteins MAP1B and MYO16 with Potential Roles in Neurodevelopment. Liu YF; Sowell SM; Luo Y; Chaubey A; Cameron RS; Kim HG; Srivastava AK PLoS One; 2015; 10(4):e0123106. PubMed ID: 25902260 [TBL] [Abstract][Full Text] [Related]
6. Neph2/Kirrel3 regulates sensory input, motor coordination, and home-cage activity in rodents. Völker LA; Maar BA; Pulido Guevara BA; Bilkei-Gorzo A; Zimmer A; Brönneke H; Dafinger C; Bertsch S; Wagener JR; Schweizer H; Schermer B; Benzing T; Hoehne M Genes Brain Behav; 2018 Nov; 17(8):e12516. PubMed ID: 30133126 [TBL] [Abstract][Full Text] [Related]
7. IL-1 receptor accessory protein-like 1 associated with mental retardation and autism mediates synapse formation by trans-synaptic interaction with protein tyrosine phosphatase δ. Yoshida T; Yasumura M; Uemura T; Lee SJ; Ra M; Taguchi R; Iwakura Y; Mishina M J Neurosci; 2011 Sep; 31(38):13485-99. PubMed ID: 21940441 [TBL] [Abstract][Full Text] [Related]
8. Modular Splicing Is Linked to Evolution in the Synapse-Specificity Molecule Kirrel3. Traenkner D; Shennib O; Johnson A; Weinbrom A; Taylor MR; Williams ME eNeuro; 2023 Dec; 10(12):. PubMed ID: 37977826 [TBL] [Abstract][Full Text] [Related]
9. Detection of autism spectrum disorder-related pathogenic trio variants by a novel structure-based approach. Rao S; Sadybekov A; DeWitt DC; Lipka J; Katritch V; Herring BE Mol Autism; 2024 Apr; 15(1):12. PubMed ID: 38566250 [TBL] [Abstract][Full Text] [Related]
10. Neurotrophin-3 Enhances the Synaptic Organizing Function of TrkC-Protein Tyrosine Phosphatase σ in Rat Hippocampal Neurons. Ammendrup-Johnsen I; Naito Y; Craig AM; Takahashi H J Neurosci; 2015 Sep; 35(36):12425-31. PubMed ID: 26354911 [TBL] [Abstract][Full Text] [Related]
11. Dissection of synapse induction by neuroligins: effect of a neuroligin mutation associated with autism. Chubykin AA; Liu X; Comoletti D; Tsigelny I; Taylor P; Südhof TC J Biol Chem; 2005 Jun; 280(23):22365-74. PubMed ID: 15797875 [TBL] [Abstract][Full Text] [Related]
12. Comprehensive expression pattern of kin of irregular chiasm-like 3 in the adult mouse brain. Hisaoka T; Komori T; Fujimoto K; Kitamura T; Morikawa Y Biochem Biophys Res Commun; 2021 Jul; 563():66-72. PubMed ID: 34062388 [TBL] [Abstract][Full Text] [Related]
14. Establishment of transgenic fluorescent mice for labeling synapses and screening synaptogenic adhesion molecules. Yang L; Zhang J; Liu S; Zhang Y; Wang L; Wang X; Wang S; Li K; Wei M; Zhang C Elife; 2024 Mar; 13():. PubMed ID: 38450720 [TBL] [Abstract][Full Text] [Related]
15. Identification of Protein Tyrosine Phosphatase Receptor Type O (PTPRO) as a Synaptic Adhesion Molecule that Promotes Synapse Formation. Jiang W; Wei M; Liu M; Pan Y; Cao D; Yang X; Zhang C J Neurosci; 2017 Oct; 37(41):9828-9843. PubMed ID: 28871037 [TBL] [Abstract][Full Text] [Related]
16. TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function. Ba W; Yan Y; Reijnders MR; Schuurs-Hoeijmakers JH; Feenstra I; Bongers EM; Bosch DG; De Leeuw N; Pfundt R; Gilissen C; De Vries PF; Veltman JA; Hoischen A; Mefford HC; Eichler EE; Vissers LE; Nadif Kasri N; De Vries BB Hum Mol Genet; 2016 Mar; 25(5):892-902. PubMed ID: 26721934 [TBL] [Abstract][Full Text] [Related]
17. A Rare Variant Identified Within the GluN2B C-Terminus in a Patient with Autism Affects NMDA Receptor Surface Expression and Spine Density. Liu S; Zhou L; Yuan H; Vieira M; Sanz-Clemente A; Badger JD; Lu W; Traynelis SF; Roche KW J Neurosci; 2017 Apr; 37(15):4093-4102. PubMed ID: 28283559 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Abnormal behaviours relevant to neurodevelopmental disorders in Kirrel3-knockout mice. Hisaoka T; Komori T; Kitamura T; Morikawa Y Sci Rep; 2018 Jan; 8(1):1408. PubMed ID: 29362445 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]