Weijun Feng

Shanghai, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 24 publications

New CHARGE Syndrome Mouse Models Reveal the Contribution of the Enzymatic Activity of CHD7 in Pathogenesis.

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

Inhibition of BRG1 suppresses the progression of glioblastoma via repressing oligodendrocyte genes.

Inhibition of BRG1 suppresses the progression of glioblastoma via repressing oligodendrocyte genes.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: June 24, 2025

ATPase-deficient CHD7 disease variant disrupts neural development via chromatin dysregulation.

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.

Histone H3K36 methyltransferases NSD1 and SETD2 are required for brain development.

Journal: Human genetics

Published: January 06, 2025

Ablation of dysmorphic neurons is a safe and effective treatment for focal cortical dysplasia II.

Ablation of dysmorphic neurons is a safe and effective treatment for focal cortical dysplasia II.

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

Published: November 08, 2024

Identifying the Pathogenicity of a Novel NPRL3 Missense Mutation Using Personalized Cortical Organoid Model of Focal Cortical Dysplasia.

Identifying the Pathogenicity of a Novel NPRL3 Missense Mutation Using Personalized Cortical Organoid Model of Focal Cortical Dysplasia.

Journal: Journal of molecular neuroscience : MN

Published: November 02, 2024

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

Chromatin modification abnormalities by CHD7 and KMT2C loss promote medulloblastoma progression.

Chromatin modification abnormalities by CHD7 and KMT2C loss promote medulloblastoma progression.

Journal: Cell reports

Published: July 18, 2024

Mutation of CHD7 impairs the output of neuroepithelium transition that is reversed by the inhibition of EZH2.

Mutation of CHD7 impairs the output of neuroepithelium transition that is reversed by the inhibition of EZH2.

Journal: Molecular psychiatry

Published: June 11, 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

A spectrum of AKT3 activating mutations cause focal malformations of cortical development (FMCDs) in cortical organoids.

A spectrum of AKT3 activating mutations cause focal malformations of cortical development (FMCDs) in cortical organoids.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: December 17, 2023

Generation and characterization of Chd7-iCreERT2-tdTomato mice.

Generation and characterization of Chd7-iCreERT2-tdTomato mice.

Journal: Genesis (New York, N.Y. : 2000)

Published: September 17, 2023

Showing 1-12 of 24

Last Updated: 09/26/2026