Researchers in China have successfully restored the vision of mice with retinitis pigmentosa, one of the major causes of blindness in humans. The study, to be published March 17 in the Journal of Experimental Medicine, uses ...
Mar 17, 2023
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DNA sequences between mitochondria within a single cell are vastly different, found researchers in the Perelman School of Medicine at the University of Pennsylvania. This knowledge will help to better illuminate the underlying ...
Dec 6, 2017
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New research led by the Murdoch Children's Research Institute (MCRI), has combined gene editing technology with stem cell kidney regeneration to correct a patient's gene mutation.
May 4, 2018
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A particular mutation in one strain of the new SARS-CoV-2 coronavirus may have helped it infect more human cells and turn it into the dominant strain worldwide, new laboratory research shows.
Jun 15, 2020
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An international team of researchers led by the University of British Columbia has made a scientific advance they hope will lead to the development of preventative treatments for multiple sclerosis (MS).
Jun 6, 2019
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(Medical Xpress)—Perhaps the boldest attempt to date at a single unified explanation of cancer is that offered by Albert Szent-Gyorgi in his classic book, The Living State. That was over 40 years ago. His insights on the ...
A new study led by University of California, Irvine (UCI) researchers identifies two ways in which APOBEC3A— a vital enzyme that is responsible for genetic changes resulting in a variety of cancers while protecting our ...
Aug 13, 2021
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A woman's bone marrow may determine her ability to start and sustain a pregnancy, report Yale researchers in PLOS Biology. The study shows that when an egg is fertilized, stem cells leave the bone marrow and travel via the ...
Sep 12, 2019
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Mutations in a subunit of a receptor that binds the major inhibitory neurotransmitter GABAA in the brain have been linked, through a common mechanism, to epilepsy, autism and intellectual disability, researchers at Vanderbilt ...
Oct 4, 2019
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A genetic mutation that leads to a rare, but devastating blindness-causing syndrome has been discovered in monkeys for the first time. The finding offers a promising way to develop gene and cell therapies that could treat ...
Oct 25, 2019
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