Meixin Hu

399 Wanyuan Road
Shanghai, 201102, China

Last Updated: 09/26/2026

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Found 10 publications

Role and Impact of the brsk2 Gene in Zebrafish Retinal Development and Visual Function Characterized by Behavioral, Histological, and Transcriptomic Analyses.

Role and Impact of the brsk2 Gene in Zebrafish Retinal Development and Visual Function Characterized by Behavioral, Histological, and Transcriptomic Analyses.

Journal: International journal of molecular sciences

Published: December 17, 2025

Lead exposure leads to premature neural differentiation via inhibiting Wnt signaling.

Lead exposure leads to premature neural differentiation via inhibiting Wnt signaling.

Journal: Environmental pollution (Barking, Essex : 1987)

Published: August 19, 2024

AAV-mediated Stambp gene replacement therapy rescues neurological defects in a mouse model of microcephaly-capillary malformation syndrome.

AAV-mediated Stambp gene replacement therapy rescues neurological defects in a mouse model of microcephaly-capillary malformation syndrome.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: April 08, 2024

Dynamic Regulation of brsk2 in the Social and Motor Development of Zebrafish: A Developmental Behavior Analysis.

Dynamic Regulation of brsk2 in the Social and Motor Development of Zebrafish: A Developmental Behavior Analysis.

Journal: International journal of molecular sciences

Published: August 30, 2023

Behavioral and Sensory Deficits Associated with Dysfunction of GABAergic System in a Novel shank2-Deficient Zebrafish Model.

Behavioral and Sensory Deficits Associated with Dysfunction of GABAergic System in a Novel shank2-Deficient Zebrafish Model.

Journal: International journal of molecular sciences

Published: November 25, 2022

A single-cell atlas reveals the heterogeneity of meningeal immunity in a mouse model of Methyl CpG binding protein 2 deficiency.

A single-cell atlas reveals the heterogeneity of meningeal immunity in a mouse model of Methyl CpG binding protein 2 deficiency.

Journal: Frontiers in immunology

Published: September 28, 2022

Novel compound heterozygous mutation in STAMBP causes a neurodevelopmental disorder by disrupting cortical proliferation.

Novel compound heterozygous mutation in STAMBP causes a neurodevelopmental disorder by disrupting cortical proliferation.

Journal: Frontiers in neuroscience

Published: June 07, 2022

Deleterious Variation in BR Serine/Threonine Kinase 2 Classified a Subtype of Autism.

Deleterious Variation in BR Serine/Threonine Kinase 2 Classified a Subtype of Autism.

Journal: Frontiers in molecular neuroscience

Published: March 26, 2022

Adaptive Immune Deficiency Impairs Neural Activity After Training and Retrieval.

Adaptive Immune Deficiency Impairs Neural Activity After Training and Retrieval.

Journal: Frontiers in neuroscience

Published: July 11, 2021

A Novel Method of Synthesis of Fluorescent Carbon Dots for Supersensitive and Selective Detection of Cancer Markers.

A Novel Method of Synthesis of Fluorescent Carbon Dots for Supersensitive and Selective Detection of Cancer Markers.

Journal: Journal of nanoscience and nanotechnology

Published: September 08, 2018

Showing 1-10 of 10

Last Updated: 09/26/2026