A gene that cured a man of HIV a decade ago has been successfully added to developing monkey embryos in an effort to study more potential treatments for the disease.
Nov 17, 2020
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Use of thyroid hormone to boost hepatocyte proliferation enhanced the efficiency of CRISPR/Cas9-mediated gene correction in the mouse liver. This dietary induction of hepatocyte regeneration may be a viable clinical strategy ...
Nov 10, 2020
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5
Many of the diseases caused by point mutations have no established therapeutic approaches. Prof. Tsukahara and colleagues (Japan Advanced Institute of Science and Technology) are studying a therapeutic method using artificial ...
Jul 9, 2020
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When Wei Hsi (Ariel) Yeh was a young undergraduate student, one of her close friends went from normal hearing to complete deafness in the span of one month. He was 29 years old. No one knew why he lost his hearing; doctors ...
Jun 3, 2020
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A baby with incandescent green eyes, a baby stamped with a bar code, another with a glowing gold brain: these are some of the images illustrating stories about the gene-edited twin girls born last November after the world ...
May 30, 2019
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A second woman is said to be pregnant with a gene-edited baby in China, according to reports this year. It follows revelations last November that gene-edited twins had been born, which caused much debate.
Feb 19, 2019
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The media is buzzing with the surprise news that a Chinese researcher, Jainkui He, has created the world's first genome-edited twins. He did this, ostensibly, to provide resistance to HIV, the virus that causes AIDS.
Nov 28, 2018
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15
For the first time scientists have identified how to halt kidney disease in a life-limiting genetic condition, which may pave the way for personalised treatment in the future.
Nov 16, 2018
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An Oregon State University environmental ethicist and scientists from nine other universities say an international oversight panel is needed to guide decisions about whether and when to employ gene-editing technology to solve ...
Nov 5, 2018
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Scientists for the first time have used CRISPR gene editing to halt the progression of Duchenne muscular dystrophy (DMD) in a large mammal, according to a study by UT Southwestern that provides a strong indication that a ...
Aug 30, 2018
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