718 related articles for article (PubMed ID: 26637167)
1. Fmrp Interacts with Adar and Regulates RNA Editing, Synaptic Density and Locomotor Activity in Zebrafish.
Shamay-Ramot A; Khermesh K; Porath HT; Barak M; Pinto Y; Wachtel C; Zilberberg A; Lerer-Goldshtein T; Efroni S; Levanon EY; Appelbaum L
PLoS Genet; 2015 Dec; 11(12):e1005702. PubMed ID: 26637167
[TBL] [Abstract][Full Text] [Related]
2. Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse.
Filippini A; Bonini D; Lacoux C; Pacini L; Zingariello M; Sancillo L; Bosisio D; Salvi V; Mingardi J; La Via L; Zalfa F; Bagni C; Barbon A
RNA Biol; 2017 Nov; 14(11):1580-1591. PubMed ID: 28640668
[TBL] [Abstract][Full Text] [Related]
3. Modulation of dADAR-dependent RNA editing by the Drosophila fragile X mental retardation protein.
Bhogal B; Jepson JE; Savva YA; Pepper AS; Reenan RA; Jongens TA
Nat Neurosci; 2011 Oct; 14(12):1517-24. PubMed ID: 22037499
[TBL] [Abstract][Full Text] [Related]
4. The RNA binding protein fragile X mental retardation protein promotes myelin sheath growth.
Doll CA; Yergert KM; Appel BH
Glia; 2020 Mar; 68(3):495-508. PubMed ID: 31626382
[TBL] [Abstract][Full Text] [Related]
5. Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules.
El Fatimy R; Davidovic L; Tremblay S; Jaglin X; Dury A; Robert C; De Koninck P; Khandjian EW
PLoS Genet; 2016 Jul; 12(7):e1006192. PubMed ID: 27462983
[TBL] [Abstract][Full Text] [Related]
6. Deletion of Fmr1 in parvalbumin-expressing neurons results in dysregulated translation and selective behavioral deficits associated with fragile X syndrome.
Kalinowska M; van der Lei MB; Kitiashvili M; Mamcarz M; Oliveira MM; Longo F; Klann E
Mol Autism; 2022 Jun; 13(1):29. PubMed ID: 35768828
[TBL] [Abstract][Full Text] [Related]
7. Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses.
Antar LN; Li C; Zhang H; Carroll RC; Bassell GJ
Mol Cell Neurosci; 2006; 32(1-2):37-48. PubMed ID: 16631377
[TBL] [Abstract][Full Text] [Related]
8. microRNAs and Fragile X Syndrome.
Lin SL
Adv Exp Med Biol; 2015; 888():107-21. PubMed ID: 26663181
[TBL] [Abstract][Full Text] [Related]
9. STEP inhibition reverses behavioral, electrophysiologic, and synaptic abnormalities in Fmr1 KO mice.
Chatterjee M; Kurup PK; Lundbye CJ; Hugger Toft AK; Kwon J; Benedict J; Kamceva M; Banke TG; Lombroso PJ
Neuropharmacology; 2018 Jan; 128():43-53. PubMed ID: 28943283
[TBL] [Abstract][Full Text] [Related]
10. Metabotropic glutamate receptor activation regulates fragile x mental retardation protein and FMR1 mRNA localization differentially in dendrites and at synapses.
Antar LN; Afroz R; Dictenberg JB; Carroll RC; Bassell GJ
J Neurosci; 2004 Mar; 24(11):2648-55. PubMed ID: 15028757
[TBL] [Abstract][Full Text] [Related]
11. Fragile X mental retardation protein modulates the stability of its m6A-marked messenger RNA targets.
Zhang F; Kang Y; Wang M; Li Y; Xu T; Yang W; Song H; Wu H; Shu Q; Jin P
Hum Mol Genet; 2018 Nov; 27(22):3936-3950. PubMed ID: 30107516
[TBL] [Abstract][Full Text] [Related]
12. Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies.
Dury AY; El Fatimy R; Tremblay S; Rose TM; Côté J; De Koninck P; Khandjian EW
PLoS Genet; 2013 Oct; 9(10):e1003890. PubMed ID: 24204304
[TBL] [Abstract][Full Text] [Related]
13. Abnormal neuronal morphology and neurochemistry in the auditory brainstem of Fmr1 knockout rats.
Ruby K; Falvey K; Kulesza RJ
Neuroscience; 2015 Sep; 303():285-98. PubMed ID: 26166728
[TBL] [Abstract][Full Text] [Related]
14. Expression of fragile X mental retardation-1 gene with nuclear export signal mutation changes the expression profiling of mouse cerebella immortal neuronal cell.
Hu L; Chen Y; Evers S; Shen Y
Proteomics; 2005 Oct; 5(15):3979-90. PubMed ID: 16130171
[TBL] [Abstract][Full Text] [Related]
15. Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.
Han K; Chen H; Gennarino VA; Richman R; Lu HC; Zoghbi HY
Hum Mol Genet; 2015 Apr; 24(7):1813-23. PubMed ID: 25432536
[TBL] [Abstract][Full Text] [Related]
16. Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 gene.
van 't Padje S; Engels B; Blonden L; Severijnen LA; Verheijen F; Oostra BA; Willemsen R
Dev Genes Evol; 2005 Apr; 215(4):198-206. PubMed ID: 15818485
[TBL] [Abstract][Full Text] [Related]
17. Analysis of FMR1 deletion in a subpopulation of post-mitotic neurons in mouse cortex and hippocampus.
Amiri A; Sanchez-Ortiz E; Cho W; Birnbaum SG; Xu J; McKay RM; Parada LF
Autism Res; 2014 Feb; 7(1):60-71. PubMed ID: 24408886
[TBL] [Abstract][Full Text] [Related]
18. Metabotropic glutamate receptors and fragile x mental retardation protein: partners in translational regulation at the synapse.
Ronesi JA; Huber KM
Sci Signal; 2008 Feb; 1(5):pe6. PubMed ID: 18272470
[TBL] [Abstract][Full Text] [Related]
19. Post-translational modifications of the Fragile X Mental Retardation Protein in neuronal function and dysfunction.
Prieto M; Folci A; Martin S
Mol Psychiatry; 2020 Aug; 25(8):1688-1703. PubMed ID: 31822816
[TBL] [Abstract][Full Text] [Related]
20. Fmr1 deficiency promotes age-dependent alterations in the cortical synaptic proteome.
Tang B; Wang T; Wan H; Han L; Qin X; Zhang Y; Wang J; Yu C; Berton F; Francesconi W; Yates JR; Vanderklish PW; Liao L
Proc Natl Acad Sci U S A; 2015 Aug; 112(34):E4697-706. PubMed ID: 26307763
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
