Pages that link to "Q34100256"
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The following pages link to Altered mRNA transport, docking, and protein translation in neurons lacking fragile X mental retardation protein (Q34100256):
Displaying 50 items.
- The molecular basis of cognitive deficits in pervasive developmental disorders (Q26991872) (← links)
- The FMRP regulon: from targets to disease convergence (Q27014002) (← links)
- Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules (Q27308310) (← links)
- A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons. (Q28079929) (← links)
- Fragile X related protein 1 clusters with ribosomes and messenger RNAs at a subset of dendritic spines in the mouse hippocampus (Q28505448) (← links)
- DSCR1 interacts with FMRP and is required for spine morphogenesis and local protein synthesis (Q28506537) (← links)
- Uncoupling of the endocannabinoid signalling complex in a mouse model of fragile X syndrome (Q28585288) (← links)
- Computational identification of new structured cis-regulatory elements in the 3'-untranslated region of human protein coding genes (Q28727243) (← links)
- Both Maintenance and Avoidance of RNA-Binding Protein Interactions Constrain Coding Sequence Evolution (Q30398026) (← links)
- From FMRP function to potential therapies for fragile X syndrome (Q30410502) (← links)
- Gestational and early postnatal hypothyroidism alters VGluT1 and VGAT bouton distribution in the neocortex and hippocampus, and behavior in rats. (Q30417259) (← links)
- Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders (Q30458768) (← links)
- Maternal genetic mutations as gestational and early life influences in producing psychiatric disease-like phenotypes in mice (Q30475378) (← links)
- G-quadruplex RNA structure as a signal for neurite mRNA targeting (Q30502060) (← links)
- Fragile X mental retardation protein is required for programmed cell death and clearance of developmentally-transient peptidergic neurons (Q30502814) (← links)
- Impaired cognitive discrimination and discoordination of coupled theta-gamma oscillations in Fmr1 knockout mice (Q30713841) (← links)
- Functionally diverse dendritic mRNAs rapidly associate with ribosomes following a novel experience (Q34163285) (← links)
- Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected]. (Q34318418) (← links)
- A role for dendritic translation of CaMKIIα mRNA in olfactory plasticity (Q34328699) (← links)
- The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge (Q35170163) (← links)
- Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders (Q35196556) (← links)
- Smaug1 mRNA-silencing foci respond to NMDA and modulate synapse formation (Q35636583) (← links)
- Nxf7 deficiency impairs social exploration and spatio-cognitive abilities as well as hippocampal synaptic plasticity in mice (Q35837309) (← links)
- Single-molecule insights into mRNA dynamics in neurons (Q35889984) (← links)
- Fmr1 deficiency promotes age-dependent alterations in the cortical synaptic proteome. (Q36008447) (← links)
- RNA imaging in living cells - methods and applications (Q36189974) (← links)
- High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters (Q36239937) (← links)
- Genetic removal of p70 S6 kinase 1 corrects molecular, synaptic, and behavioral phenotypes in fragile X syndrome mice (Q36342394) (← links)
- New X-chromosomal interactors of dFMRP regulate axonal and synaptic morphology of brain neurons in Drosophila melanogaster (Q36384227) (← links)
- Targeting of ribosomal protein S6 to dendritic spines by in vivo high frequency stimulation to induce long-term potentiation in the dentate gyrus (Q36506661) (← links)
- Neuronal profilins in health and disease: Relevance for spine plasticity and Fragile X syndrome. (Q36742801) (← links)
- Resources for the Comprehensive Discovery of Functional RNA Elements (Q36820981) (← links)
- Crystal structure of a dimerization domain of human Caprin-1: insights into the assembly of an evolutionarily conserved ribonucleoprotein complex consisting of Caprin-1, FMRP and G3BP1 (Q37006982) (← links)
- Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila (Q37287441) (← links)
- Imaging Single-mRNA Localization and Translation in Live Neurons (Q37575755) (← links)
- Glucocorticoid receptors are localized to dendritic spines and influence local actin signaling (Q37680042) (← links)
- Imaging mRNA and protein interactions within neurons (Q37695976) (← links)
- Translation in astrocyte distal processes sets molecular heterogeneity at the gliovascular interface. (Q37724151) (← links)
- Messengers, motors and mysteries: sorting of eukaryotic mRNAs by cytoskeletal transport (Q37936481) (← links)
- Control of cytoplasmic mRNA localization (Q37943793) (← links)
- RNA-binding proteins involved in RNA localization and their implications in neuronal diseases (Q38019564) (← links)
- Dendritic protein synthesis in the normal and diseased brain (Q38069393) (← links)
- The many functions of mRNA localization during normal development and disease: from pillar to post (Q38152421) (← links)
- Fragile X syndrome: a preclinical review on metabotropic glutamate receptor 5 (mGluR5) antagonists and drug development (Q38162720) (← links)
- Nervous translation, do you get the message? A review of mRNPs, mRNA-protein interactions and translational control within cells of the nervous system (Q38222192) (← links)
- Integrated transcriptome analysis of human iPS cells derived from a fragile X syndrome patient during neuronal differentiation (Q38441936) (← links)
- Memory Takes Time (Q38654326) (← links)
- Anatomy and Cell Biology of Autism Spectrum Disorder: Lessons from Human Genetics (Q38678076) (← links)
- MeCP2 deficiency is associated with reduced levels of tubulin acetylation and can be restored using HDAC6 inhibitors (Q38957608) (← links)
- FMRP regulates miR196a-mediated repression of HOXB8 via interaction with the AGO2 MID domain (Q39004678) (← links)