Developing therapies

A better understanding of the role of genes in the human body and in disease is suggesting new ways to tackle disease.

News

Image for Patient receives novel gene therapy for type of blindness
The first patient to receive gene therapy for an incurable type of blindness was treated at the John Radcliffe Hospital in Oxford this week as part of a trial funded by the Health Innovation Challenge Fund. 31/10/11
Image for Gene-therapy success for children born without functioning immune system
Researchers at the UCL Institute of Child Health have developed gene-therapy programmes that can successfully treat children born with an inability to fight infections, according to studies published in 'Science Translational Medicine'. 25/08/11
Image for 'Master regulator' gene for obesity and diabetes discovered
Researchers have found that a gene linked to type 2 diabetes and cholesterol levels acts as a 'master regulator', controlling the behaviour of other genes found within fat tissue in the body. 16/05/11
Image for BRAF mutation confirmed as a strong target for cancer drugs
Research has added to the evidence that a genetic mutation found in over 60 per cent of malignant melanomas is an important target for drugs. 10/06/10
Image for Genetic material successfully transferred between two fertilised eggs
Scientists have developed a technique which successfully transfers DNA between human eggs. This could prevent the transmission of mitochondrial diseases. 15/04/10
Image for Genome study takes targeted approach to cancer
The quest for personalised cancer treatments is given a boost today by the announcement of an £8.5 million ($13 million) UK-US alliance, funded by the Wellcome Trust, to find the best treatments for cancers. 23/12/08
Image for Stem cells: Back to basics
A simple switch can reprogram mouse fibroblasts to form embryonic cells capable of making any tissue. 24/08/07
Image for Bypassing mutations with drugs
A new drug bypasses mutations found in diseases such as muscular dystrophy and cystic fibrosis. 17/08/07
Image for Reversing fragile X
Research reveals a potential target for the treatment of fragile X syndrome. 03/08/07
Image for Angelman syndrome problems rescued
Research in mice suggests that many of the deficits associated with Angelman syndrome could be alleviated. 08/02/07
Image for Premature ageing: mending membranes
New research brings hope to people with progerias. 22/08/06
Image for Genomic medicine 'revolution' more likely to be 'evolution', says new report
A new report cautions that people need to be realistic in their expectations regarding the genomic medicine revolution, and recognise that it will be slower in arriving then had been promised. 16/08/06
Image for Novel gene therapy approach: inducing self-repair
Prospects for a new form of gene therapy have been presented at the European Society of Human Genetics conference in Amsterdam. 09/05/06
Image for Researchers reverse memory loss in mice
Researchers have reversed memory loss in mice with significant brain degeneration, a breakthrough that offers hope to people living with Alzheimer's disease. 15/07/05
Image for New report describes UK's progress in gene therapy trials
The Gene Therapy Advisory Committee (GTAC) has published its eleventh annual report. 11/04/05
Image for Gene therapy converts dead bone graft to new, living tissue
Converting foreign bone splints to living bone in mice may lead to help for cancer and trauma patients who suffer with fragile and failing bone grafts. 18/02/05
Image for Stem cells lines created from embryos with genetic diseases
Scientists at a private US fertility clinic have created embryonic stem cell lines from embryos with genetic defects. 15/06/04
Image for Gene therapy trials awarded £4 million
Department of Health announces funding for gene therapy research in the UK. 03/03/04
Image for Targeted DNA vaccine may reverse autoimmune disease
Using DNA vaccines to turn off the immune system in a model of multiple sclerosis. 10/08/03
Image for Gene 'patch' offers treatment hope for Duchenne muscular dystrophy
Antisense therapy overrides genetic defects. 07/07/03
"With the human genome sequenced, some people are expecting personalised medicines within a few years, but the reality is still many years away." David Weatherall
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