Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets
Author:
Publisher
Wiley
Subject
Medical Laboratory Technology,Instrumentation,Histology,Anatomy
Reference82 articles.
1. FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome
2. Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG–repeat
3. A Novel RNA-binding Nuclear Protein That Interacts With the Fragile X Mental Retardation (FMR1) Protein
4. A Distinct FMRP Polysomal Population at an Advanced Stage of Mammalian Erythropoiesis
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1. The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study;Journal of Neurodevelopmental Disorders;2022-12
2. Mass Spectrometry for the Study of Autism and Neurodevelopmental Disorders;Advances in Experimental Medicine and Biology;2019
3. Loss of FMRP Impaired Hippocampal Long-Term Plasticity and Spatial Learning in Rats;Frontiers in Molecular Neuroscience;2017-08-28
4. In Silico Analysis of FMR1 Gene Missense SNPs;Cell Biochemistry and Biophysics;2016-02-15
5. Synaptic Plasticity, a Prominent Contributor to the Anxiety in Fragile X Syndrome;Neural Plasticity;2016
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