PiN Faculty Member - Louis Kunkel, PhD

Louis Kunkel, PhD

Professor of Pediatrics

Boston Children's Hospital
Center for Life Science, Room 15024.B
3 Blackfan Circle
Boston, MA 02115
Tel: 617-355-6729
Fax: 617-730-0253

The muscular dystrophies are genetically heterogeneous muscle wasting disorders with at least 20 underlying genes, which can be mutated to yield dystrophy. How abnormalities in the proteins encoded by these genes causes the common pathogenesis is still emerging. The identification of many of these genes has lead to a better understanding of how normal muscle functions and the ways in which this normal function can be disturbed. This understanding has lead to viable approaches to therapy including gene and stem cell delivery of normal genes. Muscle is a regenerative tissue and contains mononuclear cells, which are capable of cell proliferation followed by fusion into new muscle myofibers. This regenerative capacity serves as the basis of stem cell therapy for the muscular dystrophies.

The muscular dystrophies are examples of monogenic traits where single genes bare mutations which are fully apparent in all individuals who inherit them. Most common human disease has, as its basis, interplay of genetics and environment. With the emergence of the complete human DNA sequence it is now possible to unravel the genetic component of disorders such as autism, heart disease and cognitive impairment. This is accomplished by the analysis of common variants found in genes which might influence gene or protein activity and such variation may predispose an individual to a particular disease. Finding such associations involves the analysis of many such variations in many normal and diseased individuals. The techniques and analysis of these association experiments are available in the laboratory.

Last Update: 5/12/2014


For a complete listing of publications click here.



© 2016 President and Fellows
of Harvard College