MeSH tree: L01.462.750
A CU Anschutz study exploring more than 10,000 youth suicides suggests gaps in the system are costing kids' lives, pointing to a critical need for new approaches in responding to the national crisis.
Jul 20, 2026
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Variants of sexually transmitted Shigella—a bacterial infection that causes bloody or prolonged diarrhea and can lead to severe dehydration—are causing more disease and becoming increasingly antibiotic-resistant among sections ...
Jul 9, 2026
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A new study, co-led by Mathias Schmidt from the Max Planck Institute of Psychiatry in Munich and Juan Pablo Lopez from Karolinska Institutet in Sweden, focused on the FKBP5 gene and its encoded protein, FKBP51, a well-established ...
Jul 7, 2026
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New research to be presented today at the annual conference of the European Society of Human Genetics shows that a cancer patient's genetic ancestry can have a significant effect both on how their disease progresses and their ...
Jun 14, 2026
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Patients with COVID-19 can show several different antiviral immune response patterns, which may influence how the disease develops. This is shown in a new study from Karolinska Institutet, published in Genome Medicine, highlighting ...
Jun 12, 2026
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To better understand what drives the emergence of symptoms in Rett syndrome, researchers at Baylor College of Medicine and the Duncan Neurological Research Institute (Duncan NRI) at Texas Children's Hospital took a closer ...
Jun 10, 2026
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For patients diagnosed with IDH-mutant glioma, an incurable brain tumor that often affects adults in their 30s and 40s, treatment typically works at first. However, the cancer almost always returns, and when it does, it frequently ...
Jun 9, 2026
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People with problematic Internet use are unconsciously drawn to certain types of online content. These findings could help researchers develop targeted training programs to support people with problematic Internet use.
Jun 2, 2026
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A brief research report reviewed the prior authorization rules for Aetna, Humana, and UnitedHealthcare and found little consistency in their prior authorization rules. The findings highlight a fragmented system that may contribute ...
May 18, 2026
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UCLA Health researchers have identified a potential drug target for treating Fragile X syndrome, the most common genetic cause of intellectual disability and autism that affects roughly one in 2,000 boys.
May 18, 2026
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