Shijun Wei

Key Laboratory For Experimental Teratology Of The Ministry Of Education
Jinan, China

Last Updated: 09/26/2026

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Found 10 publications

SMEK1 ablation promotes glucose uptake and improves obesity-related metabolic dysfunction via AMPK signaling pathway.

SMEK1 ablation promotes glucose uptake and improves obesity-related metabolic dysfunction via AMPK signaling pathway.

Journal: American journal of physiology. Endocrinology and metabolism

Published: April 03, 2024

Ppp4r3a deficiency leads to depression-like behaviors in mice by modulating the synthesis of synaptic proteins.

Ppp4r3a deficiency leads to depression-like behaviors in mice by modulating the synthesis of synaptic proteins.

Journal: Disease models & mechanisms

Published: October 28, 2021

Lack of WDFY4 Aggravates Ovalbumin-Induced Asthma via Enhanced Th2 Cell Differentiation.

Lack of WDFY4 Aggravates Ovalbumin-Induced Asthma via Enhanced Th2 Cell Differentiation.

Journal: International archives of allergy and immunology

Published: January 28, 2021

Deficiency in WDFY4 reduces the number of CD8+ T cells via reactive oxygen species-induced apoptosis.

Deficiency in WDFY4 reduces the number of CD8+ T cells via reactive oxygen species-induced apoptosis.

Journal: Molecular immunology

Published: January 22, 2021

Correction to: A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus.

Correction to: A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus.

Journal: Journal of clinical immunology

Published: August 01, 2020

A SMOC2 variant inhibits BMP signaling by competitively binding to BMPR1B and causes growth plate defects.

A SMOC2 variant inhibits BMP signaling by competitively binding to BMPR1B and causes growth plate defects.

Journal: Bone

Published: June 09, 2020

A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus.

A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus.

Journal: Journal of clinical immunology

Published: September 13, 2019

ORMDL3 and its implication in inflammatory disorders.

ORMDL3 and its implication in inflammatory disorders.

Journal: International journal of rheumatic diseases

Published: June 08, 2018

WDFY4 Is Involved in Symptoms of Systemic Lupus Erythematosus by Modulating B Cell Fate via Noncanonical Autophagy.

WDFY4 Is Involved in Symptoms of Systemic Lupus Erythematosus by Modulating B Cell Fate via Noncanonical Autophagy.

Journal: Journal of immunology (Baltimore, Md. : 1950)

Published: March 19, 2018

Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth 2.

Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth 2.

Journal: Neuro-degenerative diseases

Published: July 10, 2017

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Last Updated: 09/26/2026