Mark Schultz, PhD
Assistant Professor
Department
Pediatrics
Understanding and developing therapeutics for rare pediatric genetic disorders.
Biography
The Schultz laboratory studies protein homeostasis and the underlying genetic causes of rare inherited childhood diseases. We leverage induced pluripotent stem cells (iPSCs), iPSC derived neurons/hepatocytes, and mouse models to study and modulate protein folding/degradation.
Research areas
- Human Genetics
- Medical Genetics
- Molecular Genetics