Zhuxi Huang
Shanghai, China
Last Updated: 09/26/2026
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Found 8 publications
New CHARGE Syndrome Mouse Models Reveal the Contribution of the Enzymatic Activity of CHD7 in Pathogenesis.
Journal: Genesis (New York, N.Y. : 2000)
Published: July 28, 2025
ATPase-deficient CHD7 disease variant disrupts neural development via chromatin dysregulation.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: June 12, 2025
Histone H3K36 methyltransferases NSD1 and SETD2 are required for brain development.
Journal: Human genetics
Published: January 06, 2025
Generation and characterization of Chd7-iCreERT2-tdTomato mice.
Journal: Genesis (New York, N.Y. : 2000)
Published: September 17, 2023
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.
Journal: Frontiers in neuroscience
Published: June 07, 2022
CHD7 in oocytes is essential for female fertility.
Journal: Annals of translational medicine
Published: January 14, 2022
Showing 1-8 of 8
Last Updated: 09/26/2026