As we enter an era where once incurable diseases become curable, be prepared for some challenging debates about how to pay for gene therapy and the value of a human life.
Academic rigour, journalistic flair
Articles on Gene therapy
Displaying 21 - 40 of 45 articles
Scientists worldwide are calling for a moratorium on gene editing in germline cells. But what is a germline cell? How does it differ from other cells in our body? Why does it matter if we edit them?
If those who survive are the fittest, does that also make them the best? And if so, is engineering ‘better’ babies just evolution, or another step in a long history of eugenics?
Once genetic lesions for diseases such as cystic fibrosis and haemophilia were identified, the idea of replacing or correcting defective genes grew into what we now call “gene therapy”.
In a completely new approach to treating addiction, researchers use genetically engineered skin cells to inactivate cocaine and block cravings and addiction in mice.
An increasing list of rare diseases can now be treated with gene therapy. But we need to figure out a way to make them affordable.
One big challenge for gene therapies is delivering DNA or RNA safely to cells inside patients’ bodies. New nanoparticles could be an improvement over the current standard – repurposed viruses.
A successful gene therapy for the leading cause of sight loss in children is being reviewed by the FDA.
The gene therapy CTL019 induced complete remission in 90% of patients.
A new research paper reports dangerous side effects in CRISPR-edited mice. Some scientists are pushing back, placing blame for the unwanted mutations on the experiment, not the technique.
Researchers are starting to harness the potential of this much-hyped gene editing technique – with coming applications in medicine, biology and agriculture.
A report released by the US National Academies of Science and Medicine underscores the potential of gene editing and acknowledges the sensitivities in managing the ethical dimensions.
Cystic fibrosis (CF) affects around 3,000 people in Australia and 70,000 worldwide. It’s an inherited disease caused by a mutation in a single gene called CFTR.
How new therapies could prove a headache for the world of sport.
A toddler from London has had gene therapy for leukaemia and it seems to have worked. But why have breakthroughs taken so long?
Until more is understood, it’s sensible to limit experimentation that would make changes to germ line cells that would be passed on to future generations.
Gene therapy is allowing us to switch on natural beneficial mutations to counteract the effects of negative mutations in diseases such as sickle cell anaemia.
That genetic editing techniques have become as straightforward as they have poses questions for how we want them to be used.
When you buy a diet coke, or any other consumables containing the artificial sweetener aspartame, you’ll see a warning against consuming the product if you have phenylketonuria, an inherited metabolic…
Viruses have traditionally been mankind’s enemies, causing disease and often mutating out of the reach of our medicines. But now a new technology is conscripting them into doing good. Viral vectors show…
Job Board
-
Deputy Social Media Producer
-
Research Fellow /Senior Research Fellow – Implementation Science
-
Associate Professor, Occupational Therapy
-
GRAINS RESEARCH AND DEVELOPMENT CORPORATION CHAIRPERSON
-
Faculty of Law - Academic Appointment Opportunities
Top contributors
-
Deputy Vice-Chancellor Academic Quality and Professor of Molecular Biology, UNSW Sydney
-
Doctoral Student in Biochemistry, University of Washington
-
Researcher, L’Université d’Ottawa/University of Ottawa
-
Honorary Fellow at Department of Pharmacology and Therapeutics, The University of Melbourne
-
Senior research fellow, University of Adelaide
-
Lecturer, UNSW Sydney
-
Professor of Bioethics, University of Sydney
-
Professor of Ethics, Keele University
-
Ph.D. Candidate in Chemical Biology, Harvard University
-
Associate Professor in Physiology, Exercise and Nutrition, University of Stirling
-
Scientific Director of the Kidscan Childrens Cancer Research Charity, University of Salford
-
Chief Medical Scientist and Team Leader, CF Airway Research Group, University of Adelaide
-
Presidential Professor and Director of Graduate Studies for biology programs; Director, Cellular & Behavioral Neurobiology Graduate Program, University of Oklahoma
-
Postdoctoral Research Fellow in Materials Science and Engineering, Stanford University
-
Senior Research Fellow, Melbourne Centre for the Study of Higher Education, University of Melbourne, The University of Melbourne
