256 related articles for article (PubMed ID: 24906954)
1. A MicroRNA Profile in Fmr1 Knockout Mice Reveals MicroRNA Expression Alterations with Possible Roles in Fragile X Syndrome.
Liu T; Wan RP; Tang LJ; Liu SJ; Li HJ; Zhao QH; Liao WP; Sun XF; Yi YH; Long YS
Mol Neurobiol; 2015; 51(3):1053-63. PubMed ID: 24906954
[TBL] [Abstract][Full Text] [Related]
2. microRNAs and Fragile X Syndrome.
Lin SL
Adv Exp Med Biol; 2015; 888():107-21. PubMed ID: 26663181
[TBL] [Abstract][Full Text] [Related]
3. ICAM5 as a Novel Target for Treating Cognitive Impairment in Fragile X Syndrome.
Pei YP; Wang YY; Liu D; Lei HY; Yang ZH; Zhang ZW; Han M; Cheng K; Chen YS; Li JQ; Cheng GR; Xu L; Wu QM; McClintock SM; Yang Y; Zhang Y; Zeng Y
J Neurosci; 2020 Feb; 40(6):1355-1365. PubMed ID: 31882402
[TBL] [Abstract][Full Text] [Related]
4. Identification of messenger RNAs and microRNAs associated with fragile X mental retardation protein.
Duan R; Jin P
Methods Mol Biol; 2006; 342():267-76. PubMed ID: 16957381
[TBL] [Abstract][Full Text] [Related]
5. Fragile X mental retardation protein replacement restores hippocampal synaptic function in a mouse model of fragile X syndrome.
Zeier Z; Kumar A; Bodhinathan K; Feller JA; Foster TC; Bloom DC
Gene Ther; 2009 Sep; 16(9):1122-9. PubMed ID: 19571888
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Proteome profiling of the prefrontal cortex of Fmr1 knockout mouse reveals enhancement of complement and coagulation cascades.
Gao MM; Shi H; Yan HJ; Long YS
J Proteomics; 2023 Mar; 274():104822. PubMed ID: 36646274
[TBL] [Abstract][Full Text] [Related]
9. Lysine acetylome profiling in mouse hippocampus and its alterations upon FMRP deficiency linked to abnormal energy metabolism.
Wu YY; Yang C; Yan HJ; Lu P; Zhang L; Feng WC; Long YS
J Proteomics; 2022 Oct; 269():104720. PubMed ID: 36089189
[TBL] [Abstract][Full Text] [Related]
10. Synaptic vesicle dynamic changes in a model of fragile X.
Broek JAC; Lin Z; de Gruiter HM; van 't Spijker H; Haasdijk ED; Cox D; Ozcan S; van Cappellen GWA; Houtsmuller AB; Willemsen R; de Zeeuw CI; Bahn S
Mol Autism; 2016; 7():17. PubMed ID: 26933487
[TBL] [Abstract][Full Text] [Related]
11. Fragile X protein family member FXR1P is regulated by microRNAs.
Cheever A; Blackwell E; Ceman S
RNA; 2010 Aug; 16(8):1530-9. PubMed ID: 20519410
[TBL] [Abstract][Full Text] [Related]
12. Involvement of FMRP in Primary MicroRNA Processing via Enhancing Drosha Translation.
Wan RP; Zhou LT; Yang HX; Zhou YT; Ye SH; Zhao QH; Gao MM; Liao WP; Yi YH; Long YS
Mol Neurobiol; 2017 May; 54(4):2585-2594. PubMed ID: 26993298
[TBL] [Abstract][Full Text] [Related]
13. Macro role(s) of microRNAs in fragile X syndrome?
Li X; Jin P
Neuromolecular Med; 2009; 11(3):200-7. PubMed ID: 19669947
[TBL] [Abstract][Full Text] [Related]
14. Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome.
Till SM; Wijetunge LS; Seidel VG; Harlow E; Wright AK; Bagni C; Contractor A; Gillingwater TH; Kind PC
Hum Mol Genet; 2012 May; 21(10):2143-56. PubMed ID: 22328088
[TBL] [Abstract][Full Text] [Related]
15. Identification of differentially expressed microRNAs and their target genes in the hippocampal tissues of Fmr1 knockout mice.
Zhang M; Li X; Xiao D; Lu T; Qin B; Zheng Z; Zhang Y; Liu Y; Yan T; Han X
Am J Transl Res; 2020; 12(3):813-824. PubMed ID: 32269714
[TBL] [Abstract][Full Text] [Related]
16. Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice.
Iliff AJ; Renoux AJ; Krans A; Usdin K; Sutton MA; Todd PK
Hum Mol Genet; 2013 Mar; 22(6):1180-92. PubMed ID: 23250915
[TBL] [Abstract][Full Text] [Related]
17. Whole genome microarray analysis of gene expression in subjects with fragile X syndrome.
Bittel DC; Kibiryeva N; Butler MG
Genet Med; 2007 Jul; 9(7):464-72. PubMed ID: 17666893
[TBL] [Abstract][Full Text] [Related]
18. Involvement of Phosphodiesterase 2A Activity in the Pathophysiology of Fragile X Syndrome.
Maurin T; Melancia F; Jarjat M; Castro L; Costa L; Delhaye S; Khayachi A; Castagnola S; Mota E; Di Giorgio A; Servadio M; Drozd M; Poupon G; Schiavi S; Sardone L; Azoulay S; Ciranna L; Martin S; Vincent P; Trezza V; Bardoni B
Cereb Cortex; 2019 Jul; 29(8):3241-3252. PubMed ID: 30137253
[TBL] [Abstract][Full Text] [Related]
19. NMD abnormalities during brain development in the Fmr1-knockout mouse model of fragile X syndrome.
Kurosaki T; Sakano H; Pröschel C; Wheeler J; Hewko A; Maquat LE
Genome Biol; 2021 Nov; 22(1):317. PubMed ID: 34784943
[TBL] [Abstract][Full Text] [Related]
20. Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.
Myrick LK; Deng PY; Hashimoto H; Oh YM; Cho Y; Poidevin MJ; Suhl JA; Visootsak J; Cavalli V; Jin P; Cheng X; Warren ST; Klyachko VA
Proc Natl Acad Sci U S A; 2015 Jan; 112(4):949-56. PubMed ID: 25561520
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
