MIT neuroscientists have made a breakthrough in treating fragile X syndrome by leveraging a novel neurotransmitter signaling ...
Scheduled Feeding improved sleep/wake rhythms in the Fmr1 KO mutants.
MIT researchers suggests a potential molecular strategy for treating fragile X syndrome by enhancing NMDA subunit function.
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A clinical research team from the LKS Faculty of Medicine, the University of Hong Kong (HKUMed), and international genetic researchers led a global research study using multi-omics analysis and ...
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News Medical on MSNTargeting FGFR mutations offers new hope for bone repair in skeletal disordersGain-of-function mutations in fibroblast growth factor receptor (FGFR) genes are known to cause a range of skeletal disorders ...
Many neurodivergent women face late diagnoses, masking, and self-doubt. Overcoming impostor feelings means embracing identity ...
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