851 related articles for article (PubMed ID: 23235829)
1. FMRP targets distinct mRNA sequence elements to regulate protein expression.
Ascano M; Mukherjee N; Bandaru P; Miller JB; Nusbaum JD; Corcoran DL; Langlois C; Munschauer M; Dewell S; Hafner M; Williams Z; Ohler U; Tuschl T
Nature; 2012 Dec; 492(7429):382-6. PubMed ID: 23235829
[TBL] [Abstract][Full Text] [Related]
2. Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins.
Spencer CM; Serysheva E; Yuva-Paylor LA; Oostra BA; Nelson DL; Paylor R
Hum Mol Genet; 2006 Jun; 15(12):1984-94. PubMed ID: 16675531
[TBL] [Abstract][Full Text] [Related]
3. Identification of FMRP target mRNAs in the developmental brain: FMRP might coordinate Ras/MAPK, Wnt/β-catenin, and mTOR signaling during corticogenesis.
Casingal CR; Kikkawa T; Inada H; Sasaki Y; Osumi N
Mol Brain; 2020 Dec; 13(1):167. PubMed ID: 33323119
[TBL] [Abstract][Full Text] [Related]
4. Molecular and cellular aspects of mental retardation in the Fragile X syndrome: from gene mutation/s to spine dysmorphogenesis.
De Rubeis S; Fernández E; Buzzi A; Di Marino D; Bagni C
Adv Exp Med Biol; 2012; 970():517-51. PubMed ID: 22351071
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancer.
Didiot MC; Tian Z; Schaeffer C; Subramanian M; Mandel JL; Moine H
Nucleic Acids Res; 2008 Sep; 36(15):4902-12. PubMed ID: 18653529
[TBL] [Abstract][Full Text] [Related]
7. microRNAs and Fragile X Syndrome.
Lin SL
Adv Exp Med Biol; 2015; 888():107-21. PubMed ID: 26663181
[TBL] [Abstract][Full Text] [Related]
8. CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.
Ludwig AL; Espinal GM; Pretto DI; Jamal AL; Arque G; Tassone F; Berman RF; Hagerman PJ
Hum Mol Genet; 2014 Jun; 23(12):3228-38. PubMed ID: 24463622
[TBL] [Abstract][Full Text] [Related]
9. Increasing our understanding of human cognition through the study of Fragile X Syndrome.
Cook D; Nuro E; Murai KK
Dev Neurobiol; 2014 Feb; 74(2):147-77. PubMed ID: 23723176
[TBL] [Abstract][Full Text] [Related]
10. HITS-CLIP in various brain areas reveals new targets and new modalities of RNA binding by fragile X mental retardation protein.
Maurin T; Lebrigand K; Castagnola S; Paquet A; Jarjat M; Popa A; Grossi M; Rage F; Bardoni B
Nucleic Acids Res; 2018 Jul; 46(12):6344-6355. PubMed ID: 29668986
[TBL] [Abstract][Full Text] [Related]
11. Neurodevelopmental disorders: Signalling pathways of fragile X syndrome.
Jayaseelan S; Tenenbaum SA
Nature; 2012 Dec; 492(7429):359-60. PubMed ID: 23235826
[No Abstract] [Full Text] [Related]
12. Aberrant RNA translation in fragile X syndrome: From FMRP mechanisms to emerging therapeutic strategies.
Banerjee A; Ifrim MF; Valdez AN; Raj N; Bassell GJ
Brain Res; 2018 Aug; 1693(Pt A):24-36. PubMed ID: 29653083
[TBL] [Abstract][Full Text] [Related]
13. Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequences.
Suhl JA; Chopra P; Anderson BR; Bassell GJ; Warren ST
Hum Mol Genet; 2014 Oct; 23(20):5479-91. PubMed ID: 24876161
[TBL] [Abstract][Full Text] [Related]
14. Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.
Sheridan SD; Theriault KM; Reis SA; Zhou F; Madison JM; Daheron L; Loring JF; Haggarty SJ
PLoS One; 2011; 6(10):e26203. PubMed ID: 22022567
[TBL] [Abstract][Full Text] [Related]
15. A 3' untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR.
Suhl JA; Muddashetty RS; Anderson BR; Ifrim MF; Visootsak J; Bassell GJ; Warren ST
Proc Natl Acad Sci U S A; 2015 Nov; 112(47):E6553-61. PubMed ID: 26554012
[TBL] [Abstract][Full Text] [Related]
16. Biophysical characterization of G-quadruplex forming FMR1 mRNA and of its interactions with different fragile X mental retardation protein isoforms.
Blice-Baum AC; Mihailescu MR
RNA; 2014 Jan; 20(1):103-14. PubMed ID: 24249225
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Discrimination of common and unique RNA-binding activities among Fragile X mental retardation protein paralogs.
Darnell JC; Fraser CE; Mostovetsky O; Darnell RB
Hum Mol Genet; 2009 Sep; 18(17):3164-77. PubMed ID: 19487368
[TBL] [Abstract][Full Text] [Related]
20. Fragile X Mental Retardation Protein positively regulates PKA anchor Rugose and PKA activity to control actin assembly in learning/memory circuitry.
Sears JC; Choi WJ; Broadie K
Neurobiol Dis; 2019 Jul; 127():53-64. PubMed ID: 30771457
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
