Xiaona Wang
Henan Key Laboratory Of Genetic And Developmental Disorders
Zhengzhou, 450018, China
Zhengzhou, 450018, China
Last Updated: 09/26/2026
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Found 19 publications
Ertugliflozin improves animal behaviours associated with oxidative stress and inflammation in a BTBR T + Itpr3tf/J mouse model of autism.
Journal: Brain communications
Published: September 03, 2025
Hypoactivity, abnormal development of dendrites relevant to impaired synaptic transmission of calretinin-expressing interneurons in the medial prefrontal cortex underlies social deficits of mouse model in autism.
Journal: Translational psychiatry
Published: October 26, 2024
Reliability of Serum-Derived Connectome Indicators in Identifying Cirrhosis.
Journal: Journal of proteome research
Published: September 21, 2024
Restoration of nNOS Expression Rescues Autistic-Like Phenotypes Through Normalization of AMPA Receptor-Mediated Neurotransmission.
Journal: Molecular neurobiology
Published: October 28, 2023
GABAB1 receptor knockdown in prefrontal cortex induces behavioral aberrations associated with autism spectrum disorder in mice.
Journal: Brain research bulletin
Published: June 14, 2023
Clinical and genetic analysis of benign familial infantile epilepsy caused by PRRT2 gene variant.
Journal: Frontiers in neurology
Published: January 04, 2023
A de novo low-frequency mosaic variant of KIF1A causes hereditary spastic paraplegia: A literature review.
Journal: Annals of human genetics
Published: October 21, 2022
The GluN2B-Trp373 NMDA Receptor Variant is Associated with Autism-, Epilepsy-Related Phenotypes and Reduces NMDA Receptor Currents in Rats.
Journal: Neurochemical research
Published: November 07, 2021
Last Updated: 09/26/2026