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Researchers identify a new mechanism that may halt Huntington’s disease progression

Huntington’s disease (HD) affects around 1 in every 10,000 people in the UK. There is currently no cure for HD […]

A Spotlight On: The Minority Coalition for Precision Medicine – Michael Friend

Michael Friend is the co-founder and CEO of the Minority Coalition for Precision Medicine, which aims to eradicate health disparities […]

Novel telomerase regulator may be involved in ageing and cancer

Researchers have discovered a repetitive and highly variable DNA sequence that regulates telomerase activity, illuminating a genetic and molecular basis […]

Patient Perspectives: Maddie Stoodley – Gaucher’s Association Ambassador and UK Board Member

Maddie Stoodley is a rare disease patient and Gaucher’s Association Ambassador and UK board member. Stoodley was diagnosed at 16 […]

Scientists uncover the molecular mechanisms behind spindle elongation in human cells

A recent study on human cell division has revealed the two motor proteins that are responsible for spindle elongation during […]

Reimagine neuroscience with single cell and spatial multiomics

The nervous system is a complex system made up of a plethora of cell types. Neurological disorders represent a leading cause […]

UVR causes rare type of eye cancer

According to research funded by Cancer Research UK and others, ultraviolet radiation (UVR) has been found to cause a rare […]

Genomics week in brief: Week ending 3rd October

Don’t worry! We are back again for the second week bringing you the latest genomics updates over the past week. […]

“The one where an episode is stored on DNA”

Twist Bioscience last month announced that for the first time, an episode of a Netflix Original Series has been stored […]

Biologically-validated AI is how scientists are realising the full potential of single-cell RNA sequencing

The promise of single-cell gene expression data Genomic data are an excellent source of novel disease biomarkers and targets. In […]