Results 111 to 120 of about 14,329 (173)

HK2 drives synaptic dysfunction in fragile X syndrome via epigenetic regulation of H3K18 lactylation. [PDF]

open access: yesFront Pharmacol
Luan Y   +7 more
europepmc   +1 more source

Neonatal expression of human FMRP isoform corrects cortical deficits and improves behavior in a mouse model of fragile X syndrome. [PDF]

open access: yesMol Ther Nucleic Acids
Norman AO   +12 more
europepmc   +1 more source

Massively parallel characterization of RNA G-quadruplex stability and molecular recognition. [PDF]

open access: yesNucleic Acids Res
Martyr JG   +9 more
europepmc   +1 more source

The m⁶A reader YTHDF2 regulates mRNA transport and axon outgrowth in developing neurons. [PDF]

open access: yesNat Commun
Koo B   +19 more
europepmc   +1 more source

Mitochondria-ER contact sites in neurological disorders. [PDF]

open access: yesAnim Cells Syst (Seoul)
Jin Jang E   +4 more
europepmc   +1 more source

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