Jingmin M. Wang

Beijing, 102627, China

Last Updated: 09/26/2026

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Found 78 publications

Clinical characterization of SPTBN1, SPTBN2, and SPTBN5 variants: A case series and systematic review.

Clinical characterization of SPTBN1, SPTBN2, and SPTBN5 variants: A case series and systematic review.

Journal: Seizure

Published: January 20, 2026

Clinical characterization and structural modeling of a novel de novo SPTBN1 missense variant in a Chinese child.

Clinical characterization and structural modeling of a novel de novo SPTBN1 missense variant in a Chinese child.

Journal: BMC pediatrics

Published: December 11, 2025

Correction: SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy.

Correction: SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy.

Journal: Acta epileptologica

Published: September 12, 2025

Natural History and Prognostic Factors in Pediatric Alexander Disease: A Cohort Study.

Natural History and Prognostic Factors in Pediatric Alexander Disease: A Cohort Study.

Journal: Pediatric neurology

Published: May 06, 2025

Spatial lipidomics reveals altered lipid profiles in TMEM63A mutant rats with hypomyelination.

Spatial lipidomics reveals altered lipid profiles in TMEM63A mutant rats with hypomyelination.

Journal: Scientific reports

Published: February 20, 2025

Spatiotemporal Expression of IRS-1 During Brain Development and its Role in Neural Stem Cell Differentiation.

Spatiotemporal Expression of IRS-1 During Brain Development and its Role in Neural Stem Cell Differentiation.

Journal: Neuromolecular medicine

Published: January 14, 2025

Compound heterozygous mutations in the SSPOP gene lead to epilepsy and developmental disorders.

Compound heterozygous mutations in the SSPOP gene lead to epilepsy and developmental disorders.

Journal: Brain : a journal of neurology

Published: October 27, 2024

Effects of the Small-Molecule ISRIB on the Rapid and Efficient Myelination of Oligodendrocytes in Human Stem Cell-Derived Cerebral Organoids in Patients With Leukoencephalopathy With Vanishing White Matter.

Effects of the Small-Molecule ISRIB on the Rapid and Efficient Myelination of Oligodendrocytes in Human Stem Cell-Derived Cerebral Organoids in Patients With Leukoencephalopathy With Vanishing White Matter.

Journal: CNS neuroscience & therapeutics

Published: October 20, 2024

Morphological Characteristics and Extracellular Matrix Abnormalities in Astrocytes Derived From iPSCs of Children With Alexander Disease.

Morphological Characteristics and Extracellular Matrix Abnormalities in Astrocytes Derived From iPSCs of Children With Alexander Disease.

Journal: CNS neuroscience & therapeutics

Published: September 14, 2024

SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy.

SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathy.

Journal: Acta epileptologica

Published: May 18, 2024

Bexarotene Promotes Neuroblastoma SH-SY5Y Cell Differentiation to Mature Neurons with Decreased Proliferation.

Bexarotene Promotes Neuroblastoma SH-SY5Y Cell Differentiation to Mature Neurons with Decreased Proliferation.

Journal: Molecular neurobiology

Published: April 04, 2024

Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activation.

Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activation.

Journal: Cerebral cortex (New York, N.Y. : 1991)

Published: March 18, 2024

Showing 1-12 of 78

Last Updated: 09/26/2026