No treatments are currently available to cure Parkinson’s disease. Better understanding the genetic foundation of this condition can help researchers find ways to slow or halt its progression.
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FTD leads to changes in personality and behavior. Understanding its genetic and molecular causes could lead to new ways to treat neurodegenerative diseases.
In Canada, 14.4 per cent of South Asians have Type 2 diabetes, the highest prevalence of any other ethnic group in the country. Why is this population so disproportionately affected by diabetes?
One enzyme plays a key role in how tumor cells replicate and divide indefinitely. Identifying the genes that give these cells their immortality could provide new drug targets to treat cancer.
Neutralising antibodies aren’t the only game in town.
Changes in our environment can reveal previously hidden mutations in our DNA with potentially good and bad consequences.
Natural selection isn’t the only factor deciding human evolution.
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”.
Why was one gene mutation that affects hair, teeth, sweat glands and breasts ubiquitous among ice age Arctic people? New research points to the advantage it provided for ancestors of Native Americans.
More and more evidence shows evolution isn’t as random as often thought.
In 2030, there is a boom in precision medicine, where diseases – from cancer to dementia – are defined and targeted more specifically with a focus on their molecular makeup.
Comparing genomes of more than 200,000 people, researchers identified genetic variants that are less common in older people, suggesting natural selection continues to weed out disadvantageous traits.
Some animals seem to have missing genes – but the reality is a lot more intriguing.
Converting a DNA sequence into an audio could help us learn something useful about it, like where mutations occur.
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.
How do scientists figure out when evolutionary events – like species splitting away from a common ancestor – happened? It turns out our DNA is a kind of molecular clock, keeping time via genetic changes.
A cryptic part of DNA helps keep a species’ mutations in check until they become useful.
Scientists have discovered that a single gene may reveal a weakness in the development of schizophrenia that could help doctors prevent the condition.
What produces the differences between men and women? Are they trivial or profound? Are they genetic or environmental, or both? And are men really closer genetically to chimpanzees than to women?
What if you could take a simple test to reveal your individual risk of developing a range of cancers and hundreds of other diseases?
Principais colaboradores
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Medical Oncologist and Laboratory Head, WEHI (Walter and Eliza Hall Institute of Medical Research)
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Deputy Vice-Chancellor Academic Quality and Professor of Molecular Biology, UNSW Sydney
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Professor of Law & Adjunct Professor, Faculty of Medicine Dentistry and Health Sciences, The University of Melbourne
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Research Assistant Professor in Neuroscience, The University of Western Australia
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Bennett Chair of Autism, Telethon Kids Institute, The University of Western Australia
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Emeritus Professor of Law, University of Tasmania
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Chair Precision Medicine, Monash University
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PhD Candidate & Research Fellow, University of Tasmania
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Senior Research Fellow, Pathology, The University of Melbourne
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Honorary Fellow, Department of Pathology, The University of Melbourne
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Institute Manager, Órama - Institute for Mental Health and Wellbeing, Flinders University
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Adjunct Professor, Australian Centre for Health Law Research, School of Law, Queensland University of Technology
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Jenny Graves é um amigo do The Conversation.
Distinguished Professor of Genetics and Vice Chancellor's Fellow, La Trobe University
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Professor of Oncology, Head of the RMH Familial Cancer Centre and Joint Head, Breast Cancer Laboratory, WEHI (Walter and Eliza Hall Institute of Medical Research)
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Professor of Genomics, The University of Melbourne
