Genetics

Study identifies genetic change in autism-related gene

A new study from Bradley Hospital has identified a genetic change in a recently identified autism-associated gene, which may provide further insight into the causes of autism. The study, now published online in the Journal ...

Diseases, Conditions, Syndromes

Hope for children with TSC, a genetic tumor disorder

Although it is rare, tuberous sclerosis complex (TSC) can be a difficult and frightening diagnosis for parents and children. The genetic disorder causes nonmalignant tumors to form in many different organs, including the ...

Medical research

Zebrafish help identify mutant gene in rare muscle disease

Zebrafish with very weak muscles helped scientists decode the elusive genetic mutation responsible for Native American myopathy, a rare, hereditary muscle disease that afflicts Native Americans in North Carolina.

Medical research

Animals in research: Zebrafish

Zebrafish are probably not the first creatures that come to mind when it comes to animals that are valuable for medical research.

Neuroscience

Advance in tuberous sclerosis brain science

Doctors often diagnose tuberous sclerosis complex (TSC) based on the abnormal growths the genetic disease causes in organs around the body. Those overt anatomical structures, however, belie the microscopic and mysterious ...

Diabetes

UCSB researchers perform pioneering research on Type 2 diabetes

– While legions of medical researchers have been looking to understand the genetic basis of disease and how mutations may affect human health, a group of biomedical researchers at UC Santa Barbara is studying the metabolism ...

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