A Chinese scientist claims he edited the DNA of twin girls during an in vitro fertilization procedure.
CI Photos / Shutterstock.com
A Chinese scientist has revealed he edited the DNA of twin girls born through in vitro fertilization. These girls are designed to be resistant to HIV. Is the edit a medical necessity or an enhancement?
Symptoms for Huntington's disease typically only start to be experienced in mid-adulthood.
A standee of the movie ‘Rampage’ at a theater in Bangkok, Thailand. Scientists in the film used CRISPR to create a monster.
By Sarunyu L/shutterstock.com
CRISPR has been hailed as the an editing tool that can delete inherited mutations and cure disease. But recent papers suggest that the technique may be too dangerous for use in human therapies.
Specially designed computer games might improve the lives of people with Huntington's disease.
Gone since 1936, and ailing since long before that.
Tasmanian Museum and Art Gallery
The new Tasmanian tiger genome reveals some fascinating facts about this extinct marsupial, including why they were so similar to dogs, and how they were growing more vulnerable to genetic disease.
About 3% of babies are born with birth defects, when there is a problem with how they develop in the womb.
We still don't know what's behind four out of every five birth defects. But that can change.
Human genome editing raises a lot of questions.
Gene sequence image via www.shutterstock.com.
A new report from the National Academies of Science and Medicine outlines conditions that have to be met before gene editing that results in heritable genomic changes can be considered.
History shows how scientists and the public tried to understand hereditary cancer risk well before we had the technology to discover mutations and test for genetic disorders.
Genetic therapy might be able to reverse the harmful effects of sickle cell anaemia.
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.
Families share genes but that doesn’t mean no individual in a family should be accorded privacy about their genetic tests.
When a family member dies from a disease caused by a genetic mutation, doctors have to decide whether to share the deceased person's test results with the rest of the family.
Helpful viruses get protected by decoy viruses in the bloodstream.
The presence of foreign objects, like viruses, in our bloodstream is usually a bad thing. Evolution has created some extremely efficient immune cells that patrol the blood, seeking out material that should…
Researchers have found the missing genetic material that explains haemophilia. Haemophilia B is a genetic disorder that disrupts…
New research could help reclassify common psychiatric disorders that are related to the brain.
Scientists have linked common genetic markers with major psychiatric disorders including autism and schizophrenia, in the…
If policymakers understood what drives people to drink sugary drinks, they make take a different approach.
Policymakers should understand the urge to drink soft drinks is genetically determined, rather than being solely a lifestyle…
Researchers investigating thyroid, pituitary and testicular function have made an unintentional discovery of an X chromosome-linked…
Depending on the condition a couple risk passing to their child, testing can be offered as carrier screening.
Marriages between people who are related is more common than you might think. Unlike what many people think, their offspring are not doomed to birth defects or medical problems. In fact, unless they both…
The mitochondrial genome is passed on by mothers – defects and all.
Media outlets have been reporting that scientists are planning to “create designer babies” with three parents. Professor Justin St John, Director of the Centre for Reproduction and Development at Monash…