The beginning of becoming a human—insights from researchers
A new review paper was published in advance by Aging, titled "The beginning of becoming a human."
May 9, 2024
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A new review paper was published in advance by Aging, titled "The beginning of becoming a human."
May 9, 2024
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New research from City, University of London and the University of Southampton highlights the importance of Healthy Start for low-income families and outlines several recommendations for local and national governments to ...
May 7, 2024
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Metachromatic leukodystrophy is a rare genetic disorder that mainly affects young children and results in severe neurological symptoms accompanied by a loss of motor and intellectual capacities. At Paris Brain Institute, ...
Apr 22, 2024
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Neuropeptides, which are broadly considered to modulate synaptic communication, can have unique and life-long effects on brain development, particularly the wiring of neuronal circuits.
Apr 23, 2024
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For years, Kasia Lipska, MD, MHS, associate professor of medicine (endocrinology) at Yale School of Medicine (YSM), has been advocating for affordable pricing of insulin, an essential —and sometimes lifesaving—drug for ...
Apr 29, 2024
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A new research paper was published in Aging titled, "A novel deep proteomic approach in human skeletal muscle unveils distinct molecular signatures affected by aging and resistance training."
May 1, 2024
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Why do some young children struggle to sit through a story one day but not the next? Why do they rush impulsively into one activity but not another? Parents and teachers often focus on individual differences as they prepare ...
Apr 24, 2024
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A gene previously linked to intellectual disability has been found to regulate learning and memory in mice. The gene, called KDM5B has previously been linked to some intellectual disability disorders and autism. In the general ...
May 8, 2024
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First linked to mutations in the CHD7 gene in 2004, CHARGE syndrome is a rare genetic disorder occurring in approximately 1 in 8,500 to 15,000 births. According to the National Institute of Health (NIH), CHARGE syndrome is ...
May 7, 2024
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Mutations in the MAGEL2 gene, which cause Schaaf-Yang syndrome (SYS)—an ultra-rare disease that affects neuronal and cognitive development—generate truncated, non-functional proteins that tend to accumulate in the cell ...
May 7, 2024
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