Weijia Zeng

State Key Lab Of Genetic Engineering
Shanghai, 200438, China

Last Updated: 09/26/2026

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Found 14 publications

Increased PRSS56 expression is a causal factor and therapeutic target for human axial high myopia.

Increased PRSS56 expression is a causal factor and therapeutic target for human axial high myopia.

Journal: Cell research

Published: June 18, 2025

Aerobic Exercise Affected Lymphocyte Apoptosis by Modulating ROS Release and NLRP3 Inflammasome Activation.

Aerobic Exercise Affected Lymphocyte Apoptosis by Modulating ROS Release and NLRP3 Inflammasome Activation.

Journal: Bulletin of experimental biology and medicine

Published: May 06, 2023

KCTD7 mutations impair the trafficking of lysosomal enzymes through CLN5 accumulation to cause neuronal ceroid lipofuscinoses.

KCTD7 mutations impair the trafficking of lysosomal enzymes through CLN5 accumulation to cause neuronal ceroid lipofuscinoses.

Journal: Science advances

Published: August 03, 2022

Clinical characteristics and early prediction of mortality risk in patients with acute organophosphate poisoning-induced shock.

Clinical characteristics and early prediction of mortality risk in patients with acute organophosphate poisoning-induced shock.

Journal: Frontiers in medicine

Published: July 11, 2022

Identification of Prognostic Factors for Recurrence and Mortality in Patients With Acute Pulmonary Embolism.

Identification of Prognostic Factors for Recurrence and Mortality in Patients With Acute Pulmonary Embolism.

Journal: The heart surgery forum

Published: July 04, 2022

Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes.

Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes.

Journal: Human genomics

Published: July 04, 2022

Biallelic DNAH9 mutations are identified in Chinese patients with defective left-right patterning and cilia-related complex congenital heart disease.

Biallelic DNAH9 mutations are identified in Chinese patients with defective left-right patterning and cilia-related complex congenital heart disease.

Journal: Human genetics

Published: October 12, 2021

Two sides of NNMT in alcoholic and non-alcoholic fatty liver development.

Two sides of NNMT in alcoholic and non-alcoholic fatty liver development.

Journal: Journal of hepatology

Published: November 17, 2020

Biallelic loss of function NEK3 mutations deacetylate α-tubulin and downregulate NUP205 that predispose individuals to cilia-related abnormal cardiac left-right patterning.

Biallelic loss of function NEK3 mutations deacetylate α-tubulin and downregulate NUP205 that predispose individuals to cilia-related abnormal cardiac left-right patterning.

Journal: Cell death & disease

Published: August 09, 2020

Bi-Allelic Mutations in NUP205 and NUP210 Are Associated With Abnormal Cardiac Left-Right Patterning.

Bi-Allelic Mutations in NUP205 and NUP210 Are Associated With Abnormal Cardiac Left-Right Patterning.

Journal: Circulation. Genomic and precision medicine

Published: July 16, 2019

Combined effects of FH (E404D) and ACOX2 (R409H) cause metabolic defects in primary cardiac malignant tumor.

Combined effects of FH (E404D) and ACOX2 (R409H) cause metabolic defects in primary cardiac malignant tumor.

Journal: Cell death discovery

Published: January 08, 2018

Rare mutations in apoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects.

Rare mutations in apoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects.

Journal: Cell death & disease

Published: August 18, 2017

Showing 1-12 of 14

Last Updated: 09/26/2026