Nuclear Receptors and Genetic Disease

Dr. McCabe began his research career at the age of 15 in the laboratory of Samuel P. Bessman, M.D., in the Pediatric Research Laboratory at the University of Maryland School of Medicine. He received his B.A. with Honors in Biology from The Johns Hopkins University in 1967. As part of his M.D./Ph.D. Program, he earned his Ph.D. in Pharmacology from the University of Southern California in 1972 where he was inducted into both Sigma Xi and Phi Kappa Phi. In 1974, Dr. McCabe was granted an M.D. from the University of Southern California where he was inducted into Alpha Omega Alpha. He completed his Pediatrics Residency at the University of Minnesota Hospitals in 1976.Dr. McCabe served as a Pediatric Metabolism Fellow at the University of Colorado Health Sciences Center from 1976 until 1978. He remained at Colorado as a faculty member in the Department of Pediatrics and the Department of Biochemistry, Biophysics and Genetics. He became Director of the Metabolic Diseases Clinic in 1977 and developed it into a national resource serving 10 states in the Rocky Mountain area. As a Fellow, he discovered Glycerol Kinase Deficiency (GKD). He characterized the biochemistry of this disorder and was the first to recognize GKD as part of a contiguous gene syndrome, Complex Glycerol Kinase Deficiency, including GKD, Duchenne Muscular Dystrophy, and Adrenal Hypoplasia Congenita (AHC). He was the first to show that DNA could be extracted from newborn screening blotters. This discovery was the basis for the use of blotters for molecular genetic diagnosis, forensics including the DNA dog tag, and infectious disease diagnosis.In 1986, Dr. McCabe left Colorado to direct the Robert J. Kleberg, Jr. Clinical Center at the Institute for Molecular Genetics at Baylor College of Medicine. Under his leadership the clinical service became internationally renowned for prenatal genetics, clinical genetics and biochemical genetics. In addition to outpatient clinics, inpatient services were provided to

The Nuclear Receptor Superfamily, T.P. BurrisThyroid Hormone Receptors, U. Dressel and A. BaniahmadEstrogen and Progesterone Receptors, G.F. AllanThe Androgen Receptor, G. Jenster, J. Trapman and A.O. BrinkmanDAX-1 and Related Orphan Receptors, E. Vilain and E.R.B. McCabeThe Vitamin D Receptor, P.N. MacDonald, D.M. Kraichely and A.J. BrownRetinoid Receptors, A.C.-K. Chung and A.J. CooneyMineralocorticoid and Glucocorticoid Receptors, T. Kino, A. Vottero and G.P. ChrousosHepatocyte Nuclear Factor 4a, F.M. Sladek and S.D. SeidelPeroxisome Proliferator-Activated Receptors (PPAR), A. Elbrecht, A. Adams and D.E. MollerCoactivators and Corepressors,D.M. Lonard and Z. Nawaz