444 related articles for article (PubMed ID: 31860442)
1. FMRP has a cell-type-specific role in CA1 pyramidal neurons to regulate autism-related transcripts and circadian memory.
Sawicka K; Hale CR; Park CY; Fak JJ; Gresack JE; Van Driesche SJ; Kang JJ; Darnell JC; Darnell RB
Elife; 2019 Dec; 8():. PubMed ID: 31860442
[TBL] [Abstract][Full Text] [Related]
2. FMRP regulates mRNAs encoding distinct functions in the cell body and dendrites of CA1 pyramidal neurons.
Hale CR; Sawicka K; Mora K; Fak JJ; Kang JJ; Cutrim P; Cialowicz K; Carroll TS; Darnell RB
Elife; 2021 Dec; 10():. PubMed ID: 34939924
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Selective Deletion of Astroglial FMRP Dysregulates Glutamate Transporter GLT1 and Contributes to Fragile X Syndrome Phenotypes In Vivo.
Higashimori H; Schin CS; Chiang MS; Morel L; Shoneye TA; Nelson DL; Yang Y
J Neurosci; 2016 Jul; 36(27):7079-94. PubMed ID: 27383586
[TBL] [Abstract][Full Text] [Related]
5. Fragile X Mental Retardation Protein Bidirectionally Controls Dendritic I
Brandalise F; Kalmbach BE; Mehta P; Thornton O; Johnston D; Zemelman BV; Brager DH
J Neurosci; 2020 Jul; 40(27):5327-5340. PubMed ID: 32467357
[TBL] [Abstract][Full Text] [Related]
6. Activity-dependent regulation of release probability at excitatory hippocampal synapses: a crucial role of fragile X mental retardation protein in neurotransmission.
Wang XS; Peng CZ; Cai WJ; Xia J; Jin D; Dai Y; Luo XG; Klyachko VA; Deng PY
Eur J Neurosci; 2014 May; 39(10):1602-12. PubMed ID: 24646437
[TBL] [Abstract][Full Text] [Related]
7. Conserved hippocampal cellular pathophysiology but distinct behavioural deficits in a new rat model of FXS.
Till SM; Asiminas A; Jackson AD; Katsanevaki D; Barnes SA; Osterweil EK; Bear MF; Chattarji S; Wood ER; Wyllie DJ; Kind PC
Hum Mol Genet; 2015 Nov; 24(21):5977-84. PubMed ID: 26243794
[TBL] [Abstract][Full Text] [Related]
8. FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism.
Darnell JC; Van Driesche SJ; Zhang C; Hung KY; Mele A; Fraser CE; Stone EF; Chen C; Fak JJ; Chi SW; Licatalosi DD; Richter JD; Darnell RB
Cell; 2011 Jul; 146(2):247-61. PubMed ID: 21784246
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Genetic upregulation of BK channel activity normalizes multiple synaptic and circuit defects in a mouse model of fragile X syndrome.
Deng PY; Klyachko VA
J Physiol; 2016 Jan; 594(1):83-97. PubMed ID: 26427907
[TBL] [Abstract][Full Text] [Related]
11. The role of fragile X mental retardation protein in major mental disorders.
Fatemi SH; Folsom TD
Neuropharmacology; 2011 Jun; 60(7-8):1221-6. PubMed ID: 21108954
[TBL] [Abstract][Full Text] [Related]
12. Alterations in CA1 hippocampal synapses in a mouse model of fragile X syndrome.
Jawaid S; Kidd GJ; Wang J; Swetlik C; Dutta R; Trapp BD
Glia; 2018 Apr; 66(4):789-800. PubMed ID: 29274095
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Normal CA1 Place Fields but Discoordinated Network Discharge in a Fmr1-Null Mouse Model of Fragile X Syndrome.
Talbot ZN; Sparks FT; Dvorak D; Curran BM; Alarcon JM; Fenton AA
Neuron; 2018 Feb; 97(3):684-697.e4. PubMed ID: 29358017
[TBL] [Abstract][Full Text] [Related]
16. The role of reduced expression of fragile X mental retardation protein in neurons and increased expression in astrocytes in idiopathic and syndromic autism (duplications 15q11.2-q13).
Wegiel J; Brown WT; La Fauci G; Adayev T; Kascsak R; Kascsak R; Flory M; Kaczmarski W; Kuchna I; Nowicki K; Martinez-Cerdeno V; Wisniewski T; Wegiel J
Autism Res; 2018 Oct; 11(10):1316-1331. PubMed ID: 30107092
[TBL] [Abstract][Full Text] [Related]
17. 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]
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. 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]
20. Voltage-Independent SK-Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of
Deng PY; Carlin D; Oh YM; Myrick LK; Warren ST; Cavalli V; Klyachko VA
J Neurosci; 2019 Jan; 39(1):28-43. PubMed ID: 30389838
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]