Results 131 to 140 of about 22,945 (246)

ESCRT-III Membrane Trafficking Misregulation Contributes To Fragile X Syndrome Synaptic Defects

open access: yesScientific Reports, 2017
The leading cause of heritable intellectual disability (ID) and autism spectrum disorders (ASD), Fragile X syndrome (FXS), is caused by loss of the mRNA-binding translational suppressor Fragile X Mental Retardation Protein (FMRP).
Dominic J. Vita, Kendal Broadie
doaj   +1 more source

FMRP-Mediated Axonal Delivery of miR-181d Regulates Axon Elongation by Locally Targeting Map1b and Calm1

open access: yesCell Reports, 2015
Subcellular targeting and local translation of mRNAs are critical for axon development. However, the precise local control of mRNA translation requires investigation.
Bin Wang   +8 more
doaj   +1 more source

ALS-FUS mutation affects the activities of HuD/ELAVL4 and FMRP leading to axon phenotypes in motoneurons [PDF]

open access: gold, 2020
Maria Giovanna Garone   +11 more
openalex   +1 more source

A rapid and dynamic role for FMRP in the plasticity of adult neurons [PDF]

open access: gold, 2023
Daniel G. Gundermann   +2 more
openalex   +1 more source

BDNF Regulates the Expression of Fragile X Mental Retardation Protein mRNA in the Hippocampus

open access: yesNeurobiology of Disease, 2002
Both fragile X mental retardation protein (FMRP) and brain-derived neurotrophic factor (BDNF) are implicated in the maturation of neurons and in the higher cognitive functions.
Maija Castrén   +7 more
doaj   +1 more source

Network assisted analysis to reveal the genetic basis of autism

open access: yes, 2015
While studies show that autism is highly heritable, the nature of the genetic basis of this disorder remains illusive. Based on the idea that highly correlated genes are functionally interrelated and more likely to affect risk, we develop a novel ...
Lei, Jing, Liu, Li, Roeder, Kathryn
core   +1 more source

Toward peptide-based protein replacement in fragile X syndrome: Evaluating the N-tat strategy

open access: yesMedicine in Drug Discovery
Fragile X syndrome (FXS), a leading inherited cause of intellectual disability and autism, arises from loss of the RNA-binding protein FMRP and consequent dysregulation of synaptic mRNA translation.
Oliver A. Kent
doaj   +1 more source

Treatment of Fragile X Syndrome with Cannabidiol: A Case Series Study and Brief Review of the Literature. [PDF]

open access: yes, 2019
Fragile X syndrome (FXS) is an X-linked dominant disorder caused by a mutation in the fragile X mental retardation 1 gene. Cannabidiol (CBD) is an exogenous phytocannabinoid with therapeutic potential for individuals with anxiety, poor sleep, and ...
Bonn-Miller, Marcel   +2 more
core  

The translational regulator dFMRP interacts with epidermal growth factor receptor to regulate apoptosis in Drosophila [PDF]

open access: yes, 2016
poster abstractPosttranscriptional gene regulation is required for all aspects of cellular and tissue development and is a major mechanism underlying many diseases ranging from neurological disorders to cancer.
Sherwood, Jacqueline E.   +2 more
core  

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