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 ...

Genetics

Gene discoveries give hope against 'Brittle bone' disease

(HealthDay)—Mutations in a gene involved in bone development appear to cause certain severe forms of bone loss, a finding that could lead to new therapies for the common bone-thinning disorder osteoporosis, researchers ...

Autism spectrum disorders

Epigenetic changes shed light on biological mechanism of autism

Scientists from King's College London have identified patterns of epigenetic changes involved in autism spectrum disorder (ASD) by studying genetically identical twins who differ in autism traits. The study, published in ...

Autism spectrum disorders

Autism model in mice linked with genetics

For the first time, researchers have linked autism in a mouse model of the disease with abnormalities in specific regions of the animals' chromosomes. The regions contain genes associated with aberrant brain development and ...

page 37 from 40