MeSH tree: D12.776.422.316.762
Gautam Dongre's two children in India and Pascazia Mazeze's son in Tanzania live with an inherited blood disorder that turns blood cells into instruments of pain.
Dec 14, 2023
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Many type 2 diabetes cases could be avoided by adopting a healthy lifestyle. A plant-based diet has been shown to play a key role in this. As demonstrated in a study led by Tilman Kühn from MedUni Vienna's Center for Public ...
Dec 11, 2023
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Researchers from Tokyo Metropolitan University have measured how oxygenated hemoglobin levels in the blood change in infants' brains in response to touch. Using spectroscopy methods with external sensors placed on the scalp ...
Dec 11, 2023
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The Food and Drug Administration is expected to decide by Dec. 8 on a new therapy to treat sickle cell disease using gene editing technology called CRISPR, which stands for clustered regularly interspaced short palindromic ...
Dec 8, 2023
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Researchers at St Vincent's Institute of Medical Research (SVI) in Melbourne have shown that a commonly prescribed rheumatoid arthritis drug can suppress the progression of type 1 diabetes.
Dec 6, 2023
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A great number of health problems, and consequently the medical treatments for them, involve how blood flows through the body. Heart attacks are caused by restricted blood flow to the heart muscle. Many symptoms of diabetes ...
Dec 1, 2023
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A randomized trial of eight volunteers spent a week exposed to reduced oxygen levels that simulated high altitude in a residential hypoxia facility, to see if breathing less oxygen could benefit their physical health.
Nov 30, 2023
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Researchers from multiple institutions in China have found a way to use gene editing to reactivate dormant fetal oxygen-transporting proteins in adult blood cells to potentially reverse a wide range of blood disorders.
Researchers have shown for the first time that hemoglobin, a protein found in red blood cells where it binds oxygen, is also present in the epidermis, our skin's outermost body tissue. The study, which appears in the Journal ...
Nov 17, 2023
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Britain's medicines regulator has authorized the world's first gene therapy treatment for sickle cell disease, in a move that could offer relief to thousands of people with the crippling disease in the U.K.
Nov 16, 2023
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