Jingying Wu

600 Yi Shan Road
Shanghai, 200233, China

Last Updated: 09/26/2026

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Found 16 publications

Microglia replacement halts the progression of microgliopathy in mice and humans.

Microglia replacement halts the progression of microgliopathy in mice and humans.

Journal: Science (New York, N.Y.)
Published: July 10, 2025

Case Report: A pharmacist-led precision therapy framework for managing invasive fungal infection in CSF1R-Related leukoencephalopathy post Allo-HSCT.

Case Report: A pharmacist-led precision therapy framework for managing invasive fungal infection in CSF1R-Related leukoencephalopathy post Allo-HSCT.

Journal: Frontiers in pharmacology
Published: July 01, 2025

Reply to: Heterogeneity of CSF1R-RD: Genes, Environment, or Both?

Reply to: Heterogeneity of CSF1R-RD: Genes, Environment, or Both?

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: May 17, 2024

Heterozygous KCNJ10 Variants Affecting Kir4.1 Channel Cause Paroxysmal Kinesigenic Dyskinesia.

Heterozygous KCNJ10 Variants Affecting Kir4.1 Channel Cause Paroxysmal Kinesigenic Dyskinesia.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: March 16, 2024

The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China.

The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 18, 2023

Adult-onset neuronal intranuclear inclusion disease related retinal degeneration: a Chinese case series.

Adult-onset neuronal intranuclear inclusion disease related retinal degeneration: a Chinese case series.

Journal: Frontiers in medicine
Published: March 17, 2023

Episodic Neurological Dysfunction in X-Linked Charcot-Marie-Tooth Disease: Expansion of the Phenotypic and Genetic Spectrum.

Episodic Neurological Dysfunction in X-Linked Charcot-Marie-Tooth Disease: Expansion of the Phenotypic and Genetic Spectrum.

Journal: Journal of clinical neurology (Seoul, Korea)
Published: March 17, 2023

An AARS1 variant identified to cause adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia.

An AARS1 variant identified to cause adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia.

Journal: Translational neurodegeneration
Published: December 06, 2022

DNA hypermethylation of NOTCH2NLC in neuronal intranuclear inclusion disease: a case-control study.

DNA hypermethylation of NOTCH2NLC in neuronal intranuclear inclusion disease: a case-control study.

Journal: Journal of neurology
Published: March 31, 2022

Altered intrinsic brain activity in patients with CSF1R-related leukoencephalopathy.

Altered intrinsic brain activity in patients with CSF1R-related leukoencephalopathy.

Journal: Brain imaging and behavior
Published: January 24, 2022

Generation of an human induced pluripotent stem cell JTUi007-A from a patient with CSF1R-related leukoencephalopathy carrying heterozygous p.Ile794Thr mutation in CSF1R gene.

Generation of an human induced pluripotent stem cell JTUi007-A from a patient with CSF1R-related leukoencephalopathy carrying heterozygous p.Ile794Thr mutation in CSF1R gene.

Journal: Stem cell research
Published: September 03, 2021

Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome.

Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome.

Journal: Metabolic brain disease
Published: July 31, 2021
Showing 1-12 of 16

Last Updated: 09/26/2026