News: genetics
Genetics, not lack of oxygen, causes cerebral palsy in quarter of cases
The world’s largest study of cerebral palsy (CP) genetics has discovered genetic defects are most likely responsible for more than a quarter of cases in Chinese children, rather than a lack of oxygen at birth as previously thought.
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Funding boost to help reduce surgery side effects
A pilot trial is now underway to reduce the side effects experienced by patients who require a general anaesthetic and pain relief during surgery.
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Major cerebral palsy gene revealed
Researchers from the ³ÉÈË´óƬ have identified the gene that is the most common genetic cause of cerebral palsy, increasing the chances of finding better treatments for the debilitating disease.
Oldest clinical case of a rare genetic condition discovered
A group of international researchers including experts from the ³ÉÈË´óƬ has uncovered evidence of a genetic condition that gives men an extra X chromosome, reporting the oldest clinical case of Klinefelter Syndrome to date.
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New research to block the action of damaged genes may reverse rare and devastating childhood illnesses
In a new published in Nature Portfolio Journal of Genomic Medicine this month, a team of researchers led by Adelaide University has outlined a first step in developing the DNA tools to switch off the progression of some of the toughest and previously most mysterious neurological disorders.
DNA editing technique provides new tool for disease research and gene therapy
Researchers at the ³ÉÈË´óƬ, the South Australian Health and Medical Research Institute (SAHMRI) and CSIRO have developed a new technique to edit genes in living cells with unprecedented efficiency.Â
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Genetics behind a quarter of cerebral palsy cases
At least a quarter of children with cerebral palsy have a clinically important genetic finding and 50 per cent of these will have immediate implications for their care, a new study from the ³ÉÈË´óƬ has found.
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Study confirms genetic link in cerebral palsy
An international research team including the ³ÉÈË´óƬ has found further evidence that rare gene mutations can cause cerebral palsy, findings which could lead to earlier diagnosis and new treatments for this devastating movement disorder.
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Ancient DNA paints genetic portrait of Andes civilisations
An international team of researchers including the ³ÉÈË´óƬ, has completed the first large-scale study of DNA belonging to ancient humans of the central Andes in South America and found early genetic differences between groups of nearby regions, and surprising genetic continuity over thousands of years.
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New technique delivers complete DNA sequences of chromosomes inherited from mother and father
An international team of scientists led by the ³ÉÈË´óƬ’s Davies Research Centre has shown that it is possible to disentangle the DNA sequences of the chromosomes inherited from the mother and the father, to create true diploid genomes from a single individual.
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