Zhenxun Wang

Singapore, Singapore

Last Updated: 09/26/2026

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Found 19 publications

One down but many more to go: the state of gene therapy for inherited retinal disease.

One down but many more to go: the state of gene therapy for inherited retinal disease.

Journal: Regenerative medicine
Published: October 07, 2025

Genomic landscape of drug binding and pharmacogenetic variation across diverse populations using SNPdrug3D.

Genomic landscape of drug binding and pharmacogenetic variation across diverse populations using SNPdrug3D.

Journal: Nature communications
Published: December 23, 2024

ZNF395 Is a Hypoxia-Responsive Regulator of Mitochondrial Glutaminolysis in Clear Cell Renal Cell Carcinoma.

ZNF395 Is a Hypoxia-Responsive Regulator of Mitochondrial Glutaminolysis in Clear Cell Renal Cell Carcinoma.

Journal: Cancer research
Published: December 09, 2024

Functionally deficient UBOX5 variants and primary angle-closure glaucoma.

Functionally deficient UBOX5 variants and primary angle-closure glaucoma.

Journal: Nature communications
Published: July 31, 2024

Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk.

Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk.

Journal: Nature aging
Published: May 01, 2024

Induction of a metabolic switch from glucose to ketone metabolism programs ketogenic diet-induced therapeutic vulnerability in lung cancer.

Induction of a metabolic switch from glucose to ketone metabolism programs ketogenic diet-induced therapeutic vulnerability in lung cancer.

Journal: Cell metabolism
Published: October 17, 2023

Rodent genetically modified models of glaucoma.

Rodent genetically modified models of glaucoma.

Journal: Molecular aspects of medicine
Published: July 11, 2023

PARP4 interacts with hnRNPM to regulate splicing during lung cancer progression.

PARP4 interacts with hnRNPM to regulate splicing during lung cancer progression.

Journal: Genome medicine
Published: February 17, 2023

The genetic basis for adult onset glaucoma: Recent advances and future directions.

The genetic basis for adult onset glaucoma: Recent advances and future directions.

Journal: Progress in retinal and eye research
Published: January 04, 2022

Association of the CYP39A1 G204E Genetic Variant with Increased Risk of Glaucoma and Blindness in Patients with Exfoliation Syndrome.

Association of the CYP39A1 G204E Genetic Variant with Increased Risk of Glaucoma and Blindness in Patients with Exfoliation Syndrome.

Journal: Ophthalmology
Published: August 30, 2021

PBRM1-deficient PBAF complexes target aberrant genomic loci to activate the NF-κB pathway in clear cell renal cell carcinoma.

PBRM1-deficient PBAF complexes target aberrant genomic loci to activate the NF-κB pathway in clear cell renal cell carcinoma.

Journal: Nature cell biology
Published: May 25, 2021

Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.

Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.

Journal: JAMA
Published: February 23, 2021
Showing 1-12 of 19

Last Updated: 09/26/2026