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Search results for: Duchenne Muscular Dystrophy

JAG2 Mutation – New cause for Muscular Dystrophy

A mutation in a previously unexamined Notch ligand, JAG2, is found to cause a rare form of muscular dystrophy (MD) […]

Genome Giants: Kay Davies – Human Geneticist and Professor of Genetics, University of Oxford

Dame Kay Davies is a human geneticist and Professor of Genetics at the University of Oxford. Davies has spent her […]

Genomics week in brief: Week ending 5th June

Another month, another genomics week in brief – full of all the latest genomics news and research from the past […]

Genomics week in brief: Week ending 15th May

In the latest genomics week in brief, we have summarised all of the most recent and exciting genomics news and […]

Just one base at a time

The advancements in base editing, a new genome editing approach, have generated a lot of excitement amongst scientists in recent […]

The UK is developing a new approach to patient-centric precision medicine research

Sano Genetics, Zetta Genomics and Genomics England have partnered to develop a novel system to allow rare disease patients and […]

Genetics Unzipped Podcast: Involving Patients in Genomics Research

“Nothing about me without me!” is the rallying cry for patient involvement in research. In the latest episode of Genetics […]

“Usually, you’re relatively alone in your rare disease community” – Interview with Shelley Simmonds, Patient Advocate for rare diseases

Shelley Simmonds is a patient advocate whose son has Duchenne muscular dystrophy. Duchenne causes muscle weakening and wasting and is […]