Hereditary angioedema gene therapy hope
A CRISPR-based genome therapy has shown promising results for patients with a rare genetic swelling disorder
This author has yet to write their bio.Meanwhile lets just say that we are proud Alison Emm contributed a whooping 12 entries.
A CRISPR-based genome therapy has shown promising results for patients with a rare genetic swelling disorder
NHS England has launched a testing service for people with Jewish ancestry to see if they carry a potentially harmful BRCA variant
The use of the targeted therapy has been expanded to include certain types of breast, prostate, ovarian, fallopian tube and primary peritoneal cancers
A new RNA-based therapy for Alzheimer’s disease that’s in clinical trial phase could be the first of its kind to use ‘gene silencing’ for the condition
The UK has approved a new type of gene therapy for the blood disorders sickle cell disease and beta-thalassaemia, a world-first using CRISPR technology
A new gene therapy is being trialled for children with a rare form of deafness caused by variants in the OTOF gene
This winter sees the start of the Generation Study, which will explore the benefits and challenges of sequencing the genomes of 100,000 newborns
After years of research, a fully annotated sequence of the human Y chromosome has been published. We celebrate this breakthrough with a few key facts
The UK is no sun-drenched paradise, but skin cancer is common among the population. As summer ends, we consider new research that may offer an explanation as to why
The way in which rare diseases are investigated has been opened up by whole genome sequencing. We look at its impact on both clinicians and patients
In the second part of our pharmacogenomics blog series, we look at how new research could lead to a more effective application of drugs
Curiosity, patience, and the humble pea plant are three fundamental factors that have allowed us to sequence an entire human genome in 24 hours
Developing people
for health and
healthcare
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