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NameEmailPhD ProgramResearch InterestPublications
Edwards, Whitney

EMAIL
PUBLICATIONS

PHD PROGRAM
Cell Biology & Physiology

RESEARCH INTEREST
Cardiovascular Biology, Cardiovascular Disease, Cell Biology, Cell Signaling, Developmental Biology, Developmental Disorders, Disease, Genetic Basis of Disease, Metabolism, Molecular Biology, Molecular Mechanisms of Disease

Our lab aims to identify the fundamental molecular mechanisms underlying heart development and congenital heart disease. Our multifaceted approach includes primary cardiac cell culture, genetic mouse models, biochemical/molecular studies, and transcriptomics. Additionally, we employ proteomics-based methods to investigate 1) protein expression dynamics, 2) protein interaction networks, and 3) post-translational modifications (PTMs) in heart development. Current research projects focus on investigating the function of two essential PTMs in cardiogenesis: protein prenylation and palmitoylation.

Chen, Gang
WEBSITE
EMAIL
PUBLICATIONS

PHD PROGRAM
Cell Biology & Physiology

RESEARCH INTEREST
Cell Biology, Developmental Biology, Molecular Biology, Molecular Mechanisms of Disease, Pulmonary Research, Regenerative Medicine, Respiratory Physiology & Infections, Signal Transduction, Stem Cells

We use cutting edge technology to study pathogenesis of human pulmonary diseases including cystic fibrosis, Job’s syndrome, idiopathic pulmonary fibrosis by both human specimens, mouse genetic models, with a goal of finding the therapies. Recently, we developed a serial of lung epithelial-lineage tracing systems, providing the powerful tools for identify mechanisms of lung disease involved in post-acute sequelae SARS-CoV-2 infection, also known as “long COVID”, in collaboration with Dr. Ralph Baric’s Lab at UNC-CH.

Rosenthal, Adam
WEBSITE
EMAIL
PUBLICATIONS

PHD PROGRAM
Microbiology & Immunology

RESEARCH INTEREST
Bacteriology, Molecular Biology, Pathogenesis & Infection, Systems Biology

Our lab uses a systems biology approach to study phenotypic heterogeneity in bacteria. We develop tools that quantify single cell bacterial transcription. We then compare dynamic measurements during vegetative growth and infection to identify regulators of gene expression and mechanisms that bacteria use to coordinate community organization. With this data we want to understand the role of heterogeneity and noise in infectious disease.

Walls, Alex

EMAIL

PHD PROGRAM

RESEARCH INTEREST
Bacteriology, Molecular Biology, Pathogenesis & Infection

Toomer, Drew

EMAIL

PHD PROGRAM

RESEARCH INTEREST
Cancer Biology, Molecular Biology, Pathology

Szymanski, Rachel

EMAIL

PHD PROGRAM

RESEARCH INTEREST
Genomics, Molecular Biology

Salcido, Ryan

EMAIL

PHD PROGRAM

RESEARCH INTEREST
Developmental Biology, Genetics, Molecular Biology

Puller, Gabby

EMAIL

PHD PROGRAM

RESEARCH INTEREST
Bacteriology, Biochemistry, Molecular Biology

Prida Ajo, Gisselle

EMAIL

PHD PROGRAM

RESEARCH INTEREST
Genetics, Molecular Biology, Structural Biology

Madden, Ethan

EMAIL

PHD PROGRAM

RESEARCH INTEREST
Biomaterials, Genetics, Molecular Biology