Wenshu Xiangwei

No.5 Le Yuan Road
Daxing, 102627, China

Last Updated: 09/26/2026

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Found 15 publications

Tamibarotene promotes differentiation of neuroblastoma SH-SY5Y cells into neurons, which is associated with activation of the PI3K/AKT signaling pathway.

Tamibarotene promotes differentiation of neuroblastoma SH-SY5Y cells into neurons, which is associated with activation of the PI3K/AKT signaling pathway.

Journal: BMC neuroscience

Published: February 03, 2025

De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor.

De novo GRIN variants in M3 helix associated with neurological disorders control channel gating of NMDA receptor.

Journal: Cellular and molecular life sciences : CMLS

Published: May 23, 2023

Clinical and functional consequences of GRIA variants in patients with neurological diseases.

Clinical and functional consequences of GRIA variants in patients with neurological diseases.

Journal: Cellular and molecular life sciences : CMLS

Published: May 10, 2023

GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications.

GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications.

Journal: Journal of neurology

Published: July 14, 2021

A de novo GRIN1 Variant Associated With Myoclonus and Developmental Delay: From Molecular Mechanism to Rescue Pharmacology.

A de novo GRIN1 Variant Associated With Myoclonus and Developmental Delay: From Molecular Mechanism to Rescue Pharmacology.

Journal: Frontiers in genetics

Published: April 12, 2021

Phenotypic spectrum of patients with GABRB2 variants: from mild febrile seizures to severe epileptic encephalopathy.

Phenotypic spectrum of patients with GABRB2 variants: from mild febrile seizures to severe epileptic encephalopathy.

Journal: Developmental medicine and child neurology

Published: May 26, 2020

Negative allosteric modulation of GluN1/GluN3 NMDA receptors.

Negative allosteric modulation of GluN1/GluN3 NMDA receptors.

Journal: Neuropharmacology

Published: November 01, 2019

The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus.

The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: September 27, 2019

De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseases.

De novo GRIN variants in NMDA receptor M2 channel pore-forming loop are associated with neurological diseases.

Journal: Human mutation

Published: March 25, 2019

Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation.

Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation.

Journal: Gene

Published: February 11, 2019

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy.

Journal: Brain : a journal of neurology

Published: January 14, 2019

Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies.

Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies.

Journal: Brain : a journal of neurology

Published: August 06, 2018

Showing 1-12 of 15

Last Updated: 09/26/2026