Name Peter Tishler | ||
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Time capsule tuesday letter reading by peter tishler md division of genetics video bwh
Peter Verveer Tishler, M.D. (born July 18, 1937) is a researcher in human genetics and orphan diseases, educator, and clinician especially in the areas of genetic diseases, including polycystic kidney disease, chronic obstructive pulmonary disease, Fabry disease, and the porphyrias.
Contents
- Time capsule tuesday letter reading by peter tishler md division of genetics video bwh
- Biography
- Selected publications
- References
Time capsule tuesday letter reading by peter tishler md division of genetics video bwh
Biography
Tishler was born on July 18, 1937 in New Jersey to Max Tishler and Elizabeth M. Verveer.
Tishler attended public schools and Harvard College where he majored in biochemistry. He wrote his senior thesis on carboxypeptidase, in the lab of Dr. C.J. Fu at the Jimmy Fund, graduating cum laude in 1959.
Tishler attended Yale School of Medicine and graduated in 1962. While at Yale, Tishler began working with the Thorndike Memorial Laboratory at Boston City Hospital from 1963 to 1977.
William B. Castle, discoverer of intrinsic factor, introduced him to Sidney H. Ingbar with whom Tishler began work on the metabolic actions of thyroid hormone. Maxwell Finland contributed to Tishler’s scientific and clinical work. Tishler’s interest in genetics arose from his laboratory research in the study of thyroid function in patients with phenylketonuria.
During the Vietnam War, Tishler worked as a Public Health Service officer at the National Institutes of Health. In the following years, he continued his basic laboratory work, but also was concerned with genetics and medicine in the terms of population and epidemiology. He was also involved in familial studies of hypertension at one of the first community health centers in the U.S., East Boston Neighborhood Health Center.