292 related articles for article (PubMed ID: 32731855)
1. Genetic background mutations drive neural circuit hyperconnectivity in a fragile X syndrome model.
Kennedy T; Rinker D; Broadie K
BMC Biol; 2020 Jul; 18(1):94. PubMed ID: 32731855
[TBL] [Abstract][Full Text] [Related]
2. Neuron-Specific FMRP Roles in Experience-Dependent Remodeling of Olfactory Brain Innervation during an Early-Life Critical Period.
Golovin RM; Vest J; Broadie K
J Neurosci; 2021 Feb; 41(6):1218-1241. PubMed ID: 33402421
[TBL] [Abstract][Full Text] [Related]
3. Neural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinase.
Siller SS; Broadie K
Dis Model Mech; 2011 Sep; 4(5):673-85. PubMed ID: 21669931
[TBL] [Abstract][Full Text] [Related]
4. ESCRT-III Membrane Trafficking Misregulation Contributes To Fragile X Syndrome Synaptic Defects.
Vita DJ; Broadie K
Sci Rep; 2017 Aug; 7(1):8683. PubMed ID: 28819289
[TBL] [Abstract][Full Text] [Related]
5. In vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylation.
Coffee RL; Williamson AJ; Adkins CM; Gray MC; Page TL; Broadie K
Hum Mol Genet; 2012 Feb; 21(4):900-15. PubMed ID: 22080836
[TBL] [Abstract][Full Text] [Related]
6. Neuron class-specific requirements for Fragile X Mental Retardation Protein in critical period development of calcium signaling in learning and memory circuitry.
Doll CA; Broadie K
Neurobiol Dis; 2016 May; 89():76-87. PubMed ID: 26851502
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P.
Coffee RL; Tessier CR; Woodruff EA; Broadie K
Dis Model Mech; 2010; 3(7-8):471-85. PubMed ID: 20442204
[TBL] [Abstract][Full Text] [Related]
9. Wnd/DLK Is a Critical Target of FMRP Responsible for Neurodevelopmental and Behavior Defects in the Drosophila Model of Fragile X Syndrome.
Russo A; DiAntonio A
Cell Rep; 2019 Sep; 28(10):2581-2593.e5. PubMed ID: 31484070
[TBL] [Abstract][Full Text] [Related]
10. Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila.
Friedman SH; Dani N; Rushton E; Broadie K
Dis Model Mech; 2013 Nov; 6(6):1400-13. PubMed ID: 24046358
[TBL] [Abstract][Full Text] [Related]
11. Fragile X Mental Retardation Protein Restricts Small Dye Iontophoresis Entry into Central Neurons.
Kennedy T; Broadie K
J Neurosci; 2017 Oct; 37(41):9844-9858. PubMed ID: 28887386
[TBL] [Abstract][Full Text] [Related]
12. GABAergic circuit dysfunction in the Drosophila Fragile X syndrome model.
Gatto CL; Pereira D; Broadie K
Neurobiol Dis; 2014 May; 65():142-59. PubMed ID: 24423648
[TBL] [Abstract][Full Text] [Related]
13. Temporal requirements of the fragile X mental retardation protein in the regulation of synaptic structure.
Gatto CL; Broadie K
Development; 2008 Aug; 135(15):2637-48. PubMed ID: 18579676
[TBL] [Abstract][Full Text] [Related]
14. Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder models.
Gatto CL; Broadie K
Front Synaptic Neurosci; 2010; 2():4. PubMed ID: 21423490
[TBL] [Abstract][Full Text] [Related]
15. Spontaneous motor-behavior abnormalities in two
Andrew DR; Moe ME; Chen D; Tello JA; Doser RL; Conner WE; Ghuman JK; Restifo LL
J Neurogenet; 2021 Mar; 35(1):1-22. PubMed ID: 33164597
[TBL] [Abstract][Full Text] [Related]
16. Fragile X Mental Retardation Protein Regulates Activity-Dependent Membrane Trafficking and
Sears JC; Broadie K
Front Mol Neurosci; 2017; 10():440. PubMed ID: 29375303
[TBL] [Abstract][Full Text] [Related]
17. Fragile X mental retardation protein is required for programmed cell death and clearance of developmentally-transient peptidergic neurons.
Gatto CL; Broadie K
Dev Biol; 2011 Aug; 356(2):291-307. PubMed ID: 21596027
[TBL] [Abstract][Full Text] [Related]
18.
Trajković J; Makevic V; Pesic M; Pavković-Lučić S; Milojevic S; Cvjetkovic S; Hagerman R; Budimirovic DB; Protic D
Genes (Basel); 2022 Dec; 14(1):. PubMed ID: 36672829
[TBL] [Abstract][Full Text] [Related]
19. Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models.
Doll CA; Broadie K
Front Cell Neurosci; 2014; 8():30. PubMed ID: 24570656
[TBL] [Abstract][Full Text] [Related]
20. Insulin signaling misregulation underlies circadian and cognitive deficits in a Drosophila fragile X model.
Monyak RE; Emerson D; Schoenfeld BP; Zheng X; Chambers DB; Rosenfelt C; Langer S; Hinchey P; Choi CH; McDonald TV; Bolduc FV; Sehgal A; McBride SMJ; Jongens TA
Mol Psychiatry; 2017 Aug; 22(8):1140-1148. PubMed ID: 27090306
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
