Salk Institute
Birth Defects
Birth Defects
Birth Defects Birth Defects

Birth defect is a catchall term used to describe physical malformations, functional abnormalities and metabolic malfunctions present at the time of birth. Some birth defects are the result of environmental influences, some genetic and some the combination of the two. What can we do to reduce the odds of genetic birth defects? This is a question that Salk scientists address everyday. They are looking at:

  • The process by which control systems regulate chromosome duplication during meiosis (the process by which sperm and eggs are produced). This information is critical to understanding how genetic instability can lead to birth defects and miscarriages.
  • The Notch Pathway, a signaling system involved in the embryonic segmentation process. Segmentation is one of the first steps in the development of the spinal cord, limbs and organs. When the system is not working correctly, embryos can develop a variety of defects that can lead to fused vertebrae, congenital scoliosis and other spinal deformities. It can also lead to defects in other organ systems.
  • The molecular events that guide the formation of the embryonic nervous system with an eye towards identifying miscues. This work, which is fundamental to understanding how the nervous system is wired, may some day lead to methods for correcting abnormal neurodegenerative conditions.
  • The fundamental principles that control the specification and connectivity of spinal neurons involved in locomotion. This research could lead to treatments for movement-related birth defects as well as motor neuron diseases such as Lou Gehrig's disease.
  • How genes control the development of the nervous system. This work could lead to the discovery of genes critical to the development of the human brain. It could also lead to techniques for preventing, diagnosing, or treating birth defects that involve the brain.
  • Development of gene therapy methods that could cure genetic based birth defects. New methodologies use modified Human Immunodeficiency Virus (HIV) to ferry therapeutic genes into cells with defective genes. The modified virus is no longer harmful to humans. Additional work is being done to improve the targeting capability of viral vectors so they infect only specific types of cells. These methods hold tremendous promise for treating hemophilia, cystic fibrosis, color blindness and other genetic eye diseases.
Beverly M. Emerson
Professor
Regulatory Biology Laboratory
Edwin K. Hunter Chair

Ronald M. Evans
Professor and Director
Gene Expression Laboratory
Howard Hughes Medical Institute Investigator
March of Dimes Chair in Molecular and Developmental Biology

Martyn D. Goulding
Professor
Molecular Neurobiology Laboratory
Frederick W. and Joanna J. Mitchell Chair

Juan Carlos Izpisua Belmonte
Professor
Gene Expression Laboratory
Roger Guillemin Chair

Christopher R. Kintner
Professor
Molecular Neurobiology Laboratory
Rita and Richard Atkinson Chair

Greg Lemke
Professor
Molecular Neurobiology Laboratory
Françoise Gilot-Salk Chair

Dennis D. M. O'Leary
Professor
Molecular Neurobiology Laboratory
Vincent J. Coates Chair in Molecular Neurobiology

Catherine Rivier
Professor Emerita
Clayton Foundation Laboratories for Peptide Biology

Jean E. F. Rivier
Professor
Clayton Foundation Laboratories for Peptide Biology
Dr. Frederik Paulsen Chair in Neurosciences

John B. Thomas
Professor
Molecular Neurobiology Laboratory

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