<--- Back to Details
First PageDocument Content
Gene expression / Messenger RNA / Nonsense mutation / Polyadenylation / Internal ribosome entry site / FMR1 / Iron response element / Point mutation / MicroRNA / Biology / Genetics / RNA
Date: 2009-03-09 08:24:28
Gene expression
Messenger RNA
Nonsense mutation
Polyadenylation
Internal ribosome entry site
FMR1
Iron response element
Point mutation
MicroRNA
Biology
Genetics
RNA

Biol. Cell[removed], 251–262 (Printed in Great Britain) Review

Add to Reading List

Source URL: www.biolcell.org

Download Document from Source Website

File Size: 402,29 KB

Share Document on Facebook

Similar Documents

Trinucleotide repeat disorders / Autism / Neurogenetic disorders / Fragile X syndrome / Pediatrics / Syndromes / FMR1 / Fragile X-associated tremor/ataxia syndrome / Dynamic mutation / Myotonic dystrophy / FXS / Polymerase chain reaction

FMR1, HTT and DM1 Repeat Screening by LightCycler Samuel S. CHONG, PhD Associate Professor Department of Pediatrics, Yong Loo Lin School of Medicine, National University of

DocID: 1oY4g - View Document

Neurological disorders / Psychiatry / Fragile X syndrome / Mental retardation / Pediatrics / Syndromes / Jim Cantore / FMR1 / Causes of autism / Health / Autism / Abnormal psychology

FRAXA Research Foundation FRAXA Board of Directors All directors are parents of children with Fragile X FRAXA’s mission is to find effective treatments

DocID: 1agjY - View Document

Genetics / Neurological disorders / Syndromes / Pervasive developmental disorders / Fragile X syndrome / Pediatrics / FMR1 / Chromosomal fragile site / Disability / Health / Medicine / Autism

Fragile X Syndrome First described Martin & Bell (1943): families with sex-linked inheritance for learning difficulties & characteristic physical features. Lubsidentified the chromosome fragile site just above th

DocID: 1aa7P - View Document

FMR1 / Genes / Fragile X syndrome / Messenger RNA / Arc / Gene expression / Biology / Genetics / Molecular biology

The Journal of Neuroscience, April 13, 2011 • 31(15):5693–5698 • 5693 Brief Communications Fragile X Mental Retardation Protein Regulates Protein Expression and mRNA Translation of the Potassium Channel

DocID: 17FYe - View Document

Neurophysiology / FMR1 / Fragile X syndrome / Long-term potentiation / Long-term depression / Synaptic plasticity / Synaptic scaling / AMPA receptor / Metaplasticity / Biology / Neuroscience / Nervous system

The Brugada syndrome mutation A39V does not affect surface expression of neuronal rat Cav1.2 channels

DocID: 15CZr - View Document