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  • Y chromosome loss causes heart failure and death from cardiovascular disease

    Loss of the Y chromosome in blood cells of men is associated with disease and mortality, but no clear causal relationship has previously been identified. Now, researchers from Uppsala University show in the journal Science that loss of the Y chromosome in white blood cells causes development of fibrosis in the heart, impaired heart function and death from cardiovascular diseases in men.

  • Ancestral genetic variation essential for rapid evolution of Darwin’s finches

    In a study an international team of researchers have identified 28 gene regions that have been particularly important in the evolution of Darwin’s finches. These genetic variants do not represent recent mutations but constitute ancestral genetic variation that has accumulated over time as different species of Darwin’s finches have evolved with striking differences in beak morphology.

  • New hypothesis about crocodiles’ ears may help people with impaired hearing

    Impaired hearing affects billions of people, but crocodiles, who live almost as long and can surpass 70 years of age, have good hearing throughout their lives. One reason is because can create new hair cells, and a research group from Uppsala University is now on the path to finding out why. Hopefully, knowledge from the world of crocodiles will be able to help people with impaired hearing.

  • Municipal housing policy influences refugee reception

    Municipalities can use their local housing policy to influence the intake of refugees and the extent to which refugees are able to settle in the municipality in the long term. While certain municipalities offer refugees permanent housing contracts, others only provide temporary contracts that make it difficult for individuals to stay and establish themselves in the municipality.

  • Iceland volcano eruption opens a rare window into the Earth beneath our feet

    The recent Fagradalsfjall eruption in the southwest of Iceland has enthralled the whole world, including nature lovers and scientists alike. The eruption was especially important as it provided geologists with a unique opportunity to study magmas that were accumulated in a deep crustal magma reservoir but ultimately derived from the Earth’s mantle (below 20 km).

  • Oral contraceptives and hormone therapy increase the risk of stroke

    Oral contraceptives and hormone therapy at menopause increase the risk of stroke. The increased risk is greatest during the first year of treatment and then declines. The study, which is now published in Stroke, is based on data from over a quarter of a million women from the UK Biobank database.

  • New inherited retroviruses identified in the koala genome

    Historic virus infections can be traced in vertebrate genomes. For millions of years, these genomes have been repositories for retroviruses that incorporated their code into germline cells and were inherited as endogenous retroviruses (ERVs). Researchers from Uppsala University now provide new findings about retroviral establishment in the koala genome. The findings are being published in PNAS.

  • Bioarchaeological evidence of very early Islamic burials in the Levant

    A new study combining archaeological, historical and bioarchaeological data provides new insights into the early Islamic period in modern-day Syria. The research team was planning to focus on a much older time period but came across what they believe to be remains of early Muslims in the Syrian countryside.

  • Newly discovered coronavirus common in bank voles

    Researchers from the Zoonosis Science Center at Uppsala University have identified a new coronavirus. Their study of approximately 260 bank voles caught around Grimsö, Örebro County, shows that the virus is well established in Sweden’s red-backed voles. The finding has been published in the journal Viruses.

  • Gene variant influences risk for blood clots in covid patients

    A gene variant in the natural immune system influences the risk for blood clots in the lungs of severely ill COVID-19 patients. This has been documented in a new study by researchers at Uppsala University and Karolinska Institutet that has now been published in Nature Immunology.

  • Rare genetic variants not the major contributing factors to common diseases

    Although some rare genetic variants can increase the risk of disease markedly for a few individuals, the genetic contribution to common diseases is mostly due to a combination of many common genetic variants with small effects. This is shown in a comprehensive study by researchers at Uppsala University and SciLifeLab, published in the journal Nature Communications.

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