NHLBI

Patients who suffer a longer duration of delirium in the intensive care unit are more likely to experience long-term disability after discharge.

The pulmonary arterial hypertension knowledgebase (PAHKB), developed by Vanderbilt researchers, provides a useful tool for identifying PAH-related genes and signaling pathways relevant to pathogenesis.

A new mouse model reveals gene clusters important in a treatment-resistant form of leukemia.

Variation in the gene for the beta-1 adrenergic receptor increases the risk that a patient will have an abnormal heart rhythm after cardiac surgery.

Using computational tools to search for the genetic basis of what makes us human, Vanderbilt Assistant Professor of Biomedical Informatics Tony Capra and colleagues at the University of California-San Francisco have identified promising candidate regions.

Vanderbilt researchers are studying how mutations in the receptor for light, rhodopsin, cause light blindness.

Importin alpha 5, a member of a family of proteins that “shuttle” other proteins into the nucleus, is a potential new target for drugs to treat inflammatory diseases.