Gene therapy for "children in a bubble"
The UK National Health Service will pay for genetic therapy of hereditary immunodeficiency.
26.10.2017The UK National Health Service will pay for genetic therapy of hereditary immunodeficiency.
26.10.2017Biologists from Moscow, Kazan and the UK have created an experimental gene therapy and cured a horse of lameness with its help.
20.10.2017The term "genetically modified organism" implies that the genome of an object has been changed. How and why is it changed?
17.10.2017Arctic Apples, which do not change color in the air, will be available to buy in 400 supermarkets in the United States in November 2017.
17.10.2017The FDA Advisory Committee recommended approving a method of gene therapy for a disease that inevitably leads to complete blindness.
16.10.2017The CRISPR/Cas9 system was used to correct the mutation that causes glaucoma in mice, as well as in the culture of human retinal tissue cells.
12.10.2017Scientists believe that their experiment opens up new prospects for the creation of a male "genetic contraceptive."
12.10.2017With the help of the "base editor" developed on the basis of the CRISPR/Cas9 system, the single-nucleotide substitution was corrected in a quarter of cases.
10.10.2017MIT scientists have shown that using CRISPR/Cas13 it is possible to effectively destroy the mRNA of selected genes.
09.10.2017Chinese geneticists have eliminated the congenital disease beta-thalassemia in a human embryo by correcting an error in one "letter" of the beta-globin gene.
03.10.2017The CRISPR-Cas9 system was improved by mutating one of the domains of its enzymatic component.
27.09.2017American geneticists have disabled one of the genes responsible for the development of the human embryo to understand what role it plays in this process.
21.09.2017Genetically modified mice have all the symptoms of MDP: depression in response to stress and manic behavior.
20.09.2017Japanese scientists by changing one gene with the help of the genome editor – the CRISPR-Cas9 system – turned purple ipomoea flowers into white.
20.09.2017The experimental drug golodirsen in phase I/II clinical trials coped with one of the forms of Duchenne muscular dystrophy.
08.09.2017Novartis wins the race – last week the regulator approved the company's gene therapy for the treatment of acute lymphoblastic leukemia.
07.09.2017Treatment of progressive blindness involves virus-vector delivery of recombinant DNA developed for the synthesis of a functioning REP-1 gene.
07.09.2017The appearance of the world's first T-cell CAR therapy heralds the beginning of a new era in the biotechnology industry and the management of oncological diseases.
06.09.2017The newly released new version of the game offers its participants to create a new RNA molecule using CRISPR/Cas9 genome editing technology.
04.09.2017Scientists used the new method to treat RNA-associated diseases, for example, type I and II myotonic dystrophy and Huntington's disease.
04.09.2017You can write to the editor at:
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