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The Institute for Childhood and Neglected Diseases

Colleagues explore
the use of non-invasive imaging technologies to monitor intracellular pathways
for biological clocks in plants and animals |
The Institute for Childhood and Neglected Diseases (ICND) was established to
apply cutting edge research to understand the basic mechanisms underlying diseases
of childhood and orphan diseases that lack efficacious treatments. Diseases of
both categories often affect populations in developing countries, where the health
infrastructure may be too poor to support major research efforts on these problems.
Examples of such diseases include malaria, epilepsy, mental retardation, cystic
fibrosis, chronic pain, and sleep disorders. The human and economic costs of
these diseases are staggering. According to the World Health Organization, each
year, the microorganism that causes malaria infects 300 million people, and the
disease kills approximately 1 million people. About 90% of the people who have
malaria are in Africa, where the annual costs associated with the disease are
$12 billion. Malaria is the leading cause of childhood mortality in African countries.
Epilepsy is another widespread and costly disease, affecting about 2.3 million
Americans and accounts for $12.5 billion in medical costs and reduced productivity
each year.
Mental retardation is another condition that affects children everywhere;
about 1% of American children 3 to 10 years old have mental retardation. During
the 1995–1996 school year, about 600,000 6- to 21-year-olds with mental retardation
in the United States received special educational services, at a cost of about
$3.3 billion.
Housed in a brand-new, state-of-the-art, 54,000-square-foot building on the
east side of the TSRI campus, the ICND is a focus group within TSRI for young
scientists who are working in areas relevant to the ICND mission. The concept
of the ICND grew out of conversations in 1996 and 1997 among TSRI president Richard
Lerner; John Moores, who was interested in supporting research on illnesses that
affect people in developing countries; and the brothers Bernard and Marc Chase,
who were interested in supporting research on childhood diseases. John and Rebecca
Moores, Bill Bauce, and other automobile enthusiasts donated a number of vintage
automobiles, which were auctioned to support the ICND. The Moores went on to
contribute a valuable coin collection, as well as pledging $5 million to be awarded
over 5 years.
The Human Genome Project has led to a deeper understanding than ever before
of the mechanisms underlying human disease. The ability to study the draft mouse
and human genomes in parallel is providing an unprecendented opportunity to create
a roadmap for assigning a physiological function to all of the 35,000-45,000
human genes. This formidable challenge requires complex multidisciplinary approaches
that create and implement the most powerful research tools available. Investigators
at the ICND use genomics, proteomics and advanced microscopic imaging technologies,
develop many novel transgenic animal models, and aggressively apply these technologies
in an effort to understand the mechanisms of action of a variety of diseases—malaria,
mental retardation, neurodegenerative diseases, neuropathic pain, deafness, sleep
disorders, migraines, and epilepsy, for example—and to devise treatments for
these maladies. ICND scientists plan to systematically study not only the genes
themselves that are associated with these diseases but also the interactions
between the genes in living model systems. ICND researchers have already been
recognized by the international scientific community during the first two years
of their existence. In December of 2002, three of the highly prized Science magazines' Top
Ten Breakthroughs of the Year were results produced by ICND researchers working
on the malarial genome, mechanisms of pain perception and processes important
for sleep disorders and seasonal depression. This remarkable level of achievement
speaks to the investment made in these research areas, and bodes well for further
rapid progress in the near future.
| Faculty |
Areas of Research |
William E. Balch,
Ph.D.
Professor
Department of Cell Biology |
Protein trafficking and the molecular basis for the hereditary
childhood disease cystic fibrosis. |
Kristin Baldwin, Ph.D.
Assistant Professor Department of Cell Biology |
Molecular biology of the sense of smell, genetic mechanisms governing neural circuit development in the olfactory system and cortex. |
Mark Mayford, Ph.D.
Associate Professor
Department of Cell Biology |
Molecular basis of cognitive function, including learning and
memory disabilities and mental retardation. |
Ulrich Mueller,
Ph.D.
Associate Professor
Department of Cell Biology |
Molecular cell biology of mechanosensory perception and childhood
deafness. |
Ardem Patapoutian,
Ph.D.
Assistant Professor
Department of Cell Biology |
Ion channels and receptors involved in nociception and neuropathic
pain. |
Elizabeth Winzeler,
Ph.D.
Assistant Professor
Department of Cell Biology |
Functional genomic approaches to identifying targets in the malarial
parasite Plasmodium. |
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