In collaboration with a foundation that breeds service dogs for the visually impaired, researchers at the School of ...

Affecting 1 in 500 people, hypertrophic cardiomyopathy is a condition in which the walls of the left ventricle, the heart's ...

Researchers have revealed for the first time how a key protein linked to Parkinson's mutates, leads to cell death in the ...

The show is based on the real story of Natalia Grace, a Ukrainian girl born with spondyloepiphyseal dysplasia congenita.

aNew York University, School of Medicine, Department of Psychiatry, New York, NY, USA bNew York University, School of Medicine, Center for Cognitive Neurology, Department of Neurology, New York, NY, ...

A researcher at Michigan State University who has long studied bird colorations said the orange patterns on this snowy owl were likely caused by some type of genetic mutation prompted by an ...

Click your choice to see results and speak your mind. Scientists tapped into a gene mutation in the calcium-signaling pathway of plants to enhance endosymbiosis. This approach was successful in ...

Credit: SciTechDaily.com Scientists have uncovered how mutations in the MeCP2 gene lead to Rett syndrome, a devastating neurological disorder. By removing MeCP2 in adult mice, researchers observed an ...

Researchers found that a unique human variant of the NOVA1 gene, which is absent in Neanderthals and Denisovans, alters vocalization patterns in mice. This suggests that the mutation may have played a ...

Jaime, Todd, and Aaron all inherited a rare PSEN1 gene mutation from their father that ... If most dementia diagnoses are colored in shades of gray, the Bortzes' cases are harshly black and ...

Four young children have gained life-changing improvements in sight following treatment with a pioneering new genetic medicine through UCL Institute of Ophthalmology and Moorfields Eye Hospital ...