Zhaokun Wang

No. 4, Jianshe North Road, Chenghua District
Chengdu, 610054, China

Last Updated: 09/26/2026

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Found 14 publications

PDA-AR: Progressive low-light facial expression recognition via multi-level alignment.

PDA-AR: Progressive low-light facial expression recognition via multi-level alignment.

Journal: Neural networks : the official journal of the International Neural Network Society
Published: October 30, 2025

TSPYL5 Promotes Triple-Negative Breast Cancer Metastasis by Antagonizing USP10-Mediated PTEN Stabilization to Unleash a ZEB1-Dependent EMT Program.

TSPYL5 Promotes Triple-Negative Breast Cancer Metastasis by Antagonizing USP10-Mediated PTEN Stabilization to Unleash a ZEB1-Dependent EMT Program.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: October 14, 2025

TSPYL5-driven G3BP1 nuclear membrane translocation facilitates p53 cytoplasm sequestration via accelerating RanBP2-mediated p53 sumoylation and nuclear export in neuroblastoma.

TSPYL5-driven G3BP1 nuclear membrane translocation facilitates p53 cytoplasm sequestration via accelerating RanBP2-mediated p53 sumoylation and nuclear export in neuroblastoma.

Journal: Cell death & disease
Published: August 05, 2024

Evidence based on Mendelian randomization and colocalization analysis strengthens causal relationships between structural changes in specific brain regions and risk of amyotrophic lateral sclerosis.

Evidence based on Mendelian randomization and colocalization analysis strengthens causal relationships between structural changes in specific brain regions and risk of amyotrophic lateral sclerosis.

Journal: Frontiers in neuroscience
Published: November 06, 2023

Mendelian randomization study revealed a gut microbiota-neuromuscular junction axis in myasthenia gravis.

Mendelian randomization study revealed a gut microbiota-neuromuscular junction axis in myasthenia gravis.

Journal: Scientific reports
Published: October 25, 2023

SCN5A-L256del and L1621F exhibit loss-of-function properties related to autosomal recessive congenital cardiac disorders presenting as sick sinus syndrome, dilated cardiomyopathy, and sudden cardiac death.

SCN5A-L256del and L1621F exhibit loss-of-function properties related to autosomal recessive congenital cardiac disorders presenting as sick sinus syndrome, dilated cardiomyopathy, and sudden cardiac death.

Journal: Gene
Published: October 20, 2023

Nonsense suppression induces read-through of a novel BMPR1A variant in a Chinese family with hereditary colorectal cancer.

Nonsense suppression induces read-through of a novel BMPR1A variant in a Chinese family with hereditary colorectal cancer.

Journal: Annals of human genetics
Published: October 18, 2023

NR0B1 augments sorafenib resistance in hepatocellular carcinoma through promoting autophagy and inhibiting apoptosis.

NR0B1 augments sorafenib resistance in hepatocellular carcinoma through promoting autophagy and inhibiting apoptosis.

Journal: Cancer science
Published: June 21, 2023

Primary azoospermia factor C duplication associated with spermatogenic impariment: a case-control study based on Y-chromosome haplogrouping in a Han Chinese population.

Primary azoospermia factor C duplication associated with spermatogenic impariment: a case-control study based on Y-chromosome haplogrouping in a Han Chinese population.

Journal: Andrology
Published: March 24, 2023

Mouse Tspyl5 promotes spermatogonia proliferation through enhancing Pcna-mediated DNA replication.

Mouse Tspyl5 promotes spermatogonia proliferation through enhancing Pcna-mediated DNA replication.

Journal: Reproduction, fertility, and development
Published: March 22, 2023

A novel missense variant c.71G > T (p.Gly24Val) of the CRYBA4 gene contributes to autosomal-dominant congenital cataract in a Chinese family.

A novel missense variant c.71G > T (p.Gly24Val) of the CRYBA4 gene contributes to autosomal-dominant congenital cataract in a Chinese family.

Journal: International ophthalmology
Published: November 22, 2021

Identification of novel single-nucleotide variants altering RNA splicing of PKD1 and PKD2.

Identification of novel single-nucleotide variants altering RNA splicing of PKD1 and PKD2.

Journal: Journal of human genetics
Published: March 08, 2021
Showing 1-12 of 14

Last Updated: 09/26/2026