Ning Cheng

This study examines stimulus-specific adaptation in the auditory cortex of FMR1-KO mice, finding reduced adaptation in male KO mice compared to WT and female KO mice.

This study compares EEG signals in female Fragile X Syndrome mouse models and wild-type controls across ages, finding increased gamma power and altered coupling but discrepancies in other biomarkers.

This study investigates the role of Fmr1 in spinal cord circuits and finds that motor impairments in FXS may arise from supraspinal dysfunction rather than intrinsic spinal defects.

This study examines EEG alterations in juvenile female Fmr1 knockout mice on a C57Bl/6J background, finding increased gamma power and reduced alpha power compared to wild-type controls.

This study shows that auditory hypersensitivity is present in both female and male FMR1-KO mice, with developmental and sex differences in auditory processing at the central nucleus of the inferior colliculus.

This study examines auditory maturation and audiogenic seizure susceptibility in Fmr1 knockout mice, finding hyperexcitability and altered brainstem responses linked to seizures.

This study evaluates gap-induced prepulse inhibition and habituation in FMR1-KO mice during early development, finding sex differences and developmental changes in auditory responses.

This study examines social behavior and cortical activity in juvenile Fmr1 knockout and heterozygous mice, revealing sex- and genotype-dependent differences in social interactions and oscillatory brain activity.

The paper investigates how h- and Na+/K+ pump currents contribute to episodic and continuous rhythmic activities in spinal motor networks using computational models and experimental validation.