Aerobic glycolysis, the process by which cells transform glucose into lactate, is key for eye development in mammals, according to a new Northwestern Medicine study published in Nature Communications.
Jul 14, 2023
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Sensory cells in the vagus nerve can detect and locate food in the esophagus. Their signals help transport the food onward to the stomach. Signal failure leads to swallowing disorders, say a team led by Carmen Birchmeier ...
May 26, 2023
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A cleft lip or palate arises from the combined effects of genes and inflammatory risk factors experienced during pregnancy, such as smoking or infections, finds a new study led by UCL researchers.
May 24, 2023
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A new type of developmental disability caused by mutations in a gene known as CBX1 has been discovered by a UT Southwestern Medical Center researcher and his colleagues. The findings, reported in Genetics in Medicine, offer ...
May 17, 2023
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CU Boulder researchers have discovered a protein's crucial role in helping breast and ovarian tumors survive and thrive and have found that suppressing that protein kills cancer cells without harming healthy ones.
Apr 13, 2023
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What if doctors could break down conditions like autism into their key symptoms, map these symptoms to "hotspots" in the brain, and then treat those areas directly with brain stimulation? If it bears out, such an approach ...
Mar 31, 2023
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Virginia Tech researchers studying brain development have identified a molecule that is critical in developing the stress response, a finding that sheds new light on the potential cause of mental health conditions such as ...
Feb 16, 2023
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Universitätsmedizin Berlin, the Max Planck Institute for Molecular Genetics (MPIMG), and the University Hospital Schleswig-Holstein (UKSH) have investigated in detail how BPTA syndrome, an extremely rare hereditary condition, ...
Feb 8, 2023
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25
There is a large degree of overlap between the genetic causes of autism and ADHD. Now, researchers from Aarhus University have found gene variants, which increase the risk of developing only one of the diagnoses and not the ...
Oct 4, 2022
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Genetic variation affecting developmental genes not previously linked to urethral development may contribute to a congenital condition that is the most common cause of kidney failure in young males, a study published today ...
Sep 20, 2022
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