Toward peptide-based protein replacement in fragile X syndrome: Evaluating the N-tat strategy
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
A crotamina, neurotoxina isolada a partir da peçonha de Crotalus durissus terrificus (cascavel sul-americana), foi a primeira proteína estudada no Brasil sob o aspecto bioquímico e farmacológico.
Carlos Alberto Vieira +5 more
doaj
The role of FMR1 mRNA structure on the efficiency of non-canonical translation of toxic polyglycine protein. [PDF]
Niewiadomska D +4 more
europepmc +1 more source
Mis-spliced FMR1 transcripts in human fragile X syndrome neural progenitors and neurons. [PDF]
Hourani SM +4 more
europepmc +1 more source
GABAergic neurons exhibit subtype-specific changes in the developing somatosensory cortex of a rat model of Fragile X Syndrome. [PDF]
Sumera A +4 more
europepmc +1 more source
Translatome profiling reveals opposing alterations in inhibitory and excitatory neurons of fragile X mice and identifies EPAC2 as a therapeutic target. [PDF]
Suresh A +13 more
europepmc +1 more source
<i>Fmr1</i> Deletion and Early-Life Stress Interact to Increase Cell Proliferation and Glial Populations at the Expense of Immature Neurons in the Adult Dentate Gyrus. [PDF]
Latchney SE +4 more
europepmc +1 more source
Mapping RNA-Binding Proteins on the Ribosome by Tethered Micrococcal Nuclease. [PDF]
Yao CY, Joseph S.
europepmc +1 more source

