Results 121 to 130 of about 109,973,714 (148)

Personalized Follow Up and Genetic Diagnosis Update of FMR1-Related Conditions: A Change in Diagnosis, Prognosis and Expectations. [PDF]

open access: yesInt J Mol Sci
Roche-Martínez A   +5 more
europepmc   +1 more source

Altered ECM deposition and cell adhesion signaling in a human cortical organoid model of fragile X syndrome. [PDF]

open access: yesMol Brain
Havusha-Laufer S   +9 more
europepmc   +1 more source

RNA-Based Therapeutics in Genetic Neurodevelopmental Disorders: Bridging Molecular Genetics and Precision Medicine. [PDF]

open access: yesInt J Mol Sci
Focșa IO   +11 more
europepmc   +1 more source

Genetic Reduction of the Translational Repressors FMRP and 4E-BP2 Preserves Memory in Mouse Models of Alzheimer's Disease. [PDF]

open access: yesAging Cell
Ribeiro FC   +11 more
europepmc   +1 more source

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

Characterizing Populations Based on Proximity to a Fragile X Syndrome Specialty Clinic. [PDF]

open access: yesAm J Intellect Dev Disabil
Ogunsola HY   +7 more
europepmc   +1 more source

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