
About
Philip Ng is an Associate Professor at Baylor College of Medicine in the Department of Molecular and Human Genetics. He also holds a position in the Program in Translational Biology & Molecular Medicine. His research specializes in gene therapy, particularly using helper-dependent adenoviral vectors (HDAd) for liver and lung diseases.
- BS, University of Toronto
- MS, University of Guelph
- PhD, University of Guelph
- Post-Doctoral Fellowship, McMaster University
Research Focus
Dr. Ng's laboratory develops HDAd vectors for gene therapy, which lack viral genes to improve safety and efficacy. Key areas include:
- Liver-directed therapies for hemophilia, Crigler-Najjar syndrome, and cardiovascular disease
- Lung-directed therapies for cystic fibrosis
- Vector capsid modifications to enhance hepatocyte transduction
- Immune response investigations to refine host-vector interactions
- Gene editing in human-induced pluripotent stem cells (iPSCs) without double-strand breaks
The lab pioneers clinical manufacturing under cGMP and innovative delivery methods like balloon occlusion catheters for targeted therapy in large animals.
Contact
Email: png@bcm.edu
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