Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P
about
Matrix metalloproteinases and minocycline: therapeutic avenues for fragile X syndrome.Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us.Drosophila Cbp53E Regulates Axon Growth at the Neuromuscular JunctionFragile X mental retardation protein is required for programmed cell death and clearance of developmentally-transient peptidergic neurons.Fragile X mental retardation protein regulates translation by binding directly to the ribosomeMicroRNAs miR-30b, miR-30d, and miR-494 regulate human endometrial receptivity.Drosophila modeling of heritable neurodevelopmental disordersA new regulatory function of the region proximal to the RGG box in the fragile X mental retardation proteinNeural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinaseIn vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylationA novel link between FMR gene and the JNK pathway provides clues to possible role in malignant pleural mesothelioma.Crystal structure reveals specific recognition of a G-quadruplex RNA by a β-turn in the RGG motif of FMRP.Two classes of matrix metalloproteinases reciprocally regulate synaptogenesis.Spartin regulates synaptic growth and neuronal survival by inhibiting BMP-mediated microtubule stabilization.Fragile X mental retardation protein regulates trans-synaptic signaling in DrosophilaImpaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models.Fragile X mental retardation protein promotes astrocytoma proliferation via the MEK/ERK signaling pathway.Drosophila melanogaster As a Model Organism to Study RNA Toxicity of Repeat Expansion-Associated Neurodegenerative and Neuromuscular DiseasesFragile X syndrome and model organisms: identifying potential routes of therapeutic intervention.Fragile X syndrome: a preclinical review on metabotropic glutamate receptor 5 (mGluR5) antagonists and drug development.Importance of gene dosage in controlling dendritic arbor formation during development.GABAergic circuit dysfunction in the Drosophila Fragile X syndrome model.A Drosophila model of Fragile X syndrome exhibits defects in phagocytosis by innate immune cells.Molecular and genetic analysis of the Drosophila model of fragile X syndrome.RNA-binding protein FXR2 regulates adult hippocampal neurogenesis by reducing Noggin expression.Fragile X Mental Retardation Protein Regulates Activity-Dependent Membrane Trafficking and Trans-Synaptic Signaling Mediating Synaptic Remodeling.Fragile X Mental Retardation Protein Requirements in Activity-Dependent Critical Period Neural Circuit Refinement.Fragile X related protein 1 (FXR1P) regulates proliferation of adult neural stem cells.Fragile X syndrome: From protein function to therapy.Modeling Fragile X Syndrome in Drosophila.Regulation of Adult Neurogenesis by the Fragile X Family of RNA Binding Proteins
P2860
Q26853083-BB431008-CA62-43A6-9885-9D88F02F9358Q26866506-CFCA8786-393A-4A87-8584-D86BEB7B4D0CQ27302860-BC16EB33-CD7C-41AC-89BF-C3D9D4625ADEQ30502814-67CBE413-2438-412F-A12D-250E83FA8981Q33605244-12B449C7-76DF-41ED-93E0-9D47DF2B863DQ33829568-C8DD2F15-27C0-496D-802A-F0E682FC8134Q34629298-0AB013F1-E9E9-421F-8659-5F6D7D34990DQ35210815-E2AF421C-CD70-412D-A7B3-114E91128FB6Q35232638-4D7BAFE0-47F1-4B86-B595-9B7EDFF0C011Q35688627-999E5543-98EC-40F2-9458-D31A07AC8C2AQ36042626-10F9DADB-0015-4910-9693-D8106CC5EE51Q36120228-7ACC40EC-31A8-4152-8922-295BB43FB6DFQ36497245-D6013BFA-BC50-4B2E-9CBE-B8EEA602434FQ37273587-1C60FC88-52F8-421D-B8D2-7027D082CDA0Q37287441-02388585-0B7C-4BFA-A53F-8266CC3D17A5Q37564195-1A32C0D9-0AB3-4A2E-A81D-271B55ACC252Q37688952-1E7F9F10-62D4-43AA-8942-BD26D41913A8Q37713198-5280D911-CC2F-4D46-9E41-ACA9672F4CF9Q37777539-07B14803-DF04-4238-8A67-2AF295B22110Q38162720-C335D196-F695-425E-B763-F73D86C4B87BQ38537122-C291E80B-9BF1-432A-942A-3E2AB8311457Q38787519-CB3040E9-2442-481D-9986-EDC207A69473Q40323144-C9C007DF-88A9-4DB6-9D56-587DFAC5D1F8Q42063025-603DED7F-9BEB-470B-8BF9-AD2F26FCAC00Q42818864-19A8B18D-BB59-452F-B3BC-5195FDCA945DQ47551369-C0BF8DBF-BC71-449C-9D44-67FC232C2022Q47657806-F772B4D7-3099-410F-B336-065D348ECA7CQ48306723-AC02E4FE-ABA5-43BC-A301-1BC4B5BF1E09Q54782597-1525F804-8BEF-42BB-BDEE-BE79BAA6A418Q55119637-1D51EC3D-2BCB-46E1-A0B9-A9E8CE7F050BQ58790351-4D97B571-F834-4D6B-8CD9-B60DB5F60A66
P2860
Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P
description
2010 nî lūn-bûn
@nan
2010 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Fragile X mental retardation p ...... not shared with FXR1P or FXR2P
@ast
Fragile X mental retardation p ...... not shared with FXR1P or FXR2P
@en
type
label
Fragile X mental retardation p ...... not shared with FXR1P or FXR2P
@ast
Fragile X mental retardation p ...... not shared with FXR1P or FXR2P
@en
prefLabel
Fragile X mental retardation p ...... not shared with FXR1P or FXR2P
@ast
Fragile X mental retardation p ...... not shared with FXR1P or FXR2P
@en
P2093
P2860
P356
P1476
Fragile X mental retardation p ...... not shared with FXR1P or FXR2P
@en
P2093
Charles R Tessier
Elvin A Woodruff
Kendal Broadie
R Lane Coffee
P2860
P304
P356
10.1242/DMM.004598
P577
2010-05-04T00:00:00Z