Genetics

Discovery of gene defect for allergy and autoimmune diseases

An international team led by a physician from the Karl Landsteiner University for Health Sciences, Krems, describes for the first time a mutation of the IL-33 gene in the human genome that results in multiple allergic disease ...

Oncology & Cancer

New studies clarify which genes may raise breast cancer risk

Two large studies give a much sharper picture of which inherited mutations raise the risk of breast cancer for women without a family history of the disease, and how common these flawed genes are in the general population.

Genetics

The man who is aging too fast

Nobuaki Nagashima was in his mid-20s when he began to feel like his body was breaking down. He was based in Hokkaido, the northernmost prefecture of Japan, where for 12 years he had been a member of the military, vigorously ...

Genetics

New treatment for iron overload on trial

A world-first trial of a treatment for Australia's most common genetic disorder is being led by a University of Queensland researcher.

Genetics

Mutation found in patients without a nose

A mutated gene in patients lacking a nose has been identified by an international team, a first step toward understanding nose development and possible therapies for another condition.

Genetics

Potential autism biomarker found in babies

A biological marker in infants that appears to predict an autism diagnosis has been identified in a small study led by researchers at the Stanford University School of Medicine.

page 51 from 1180