Another method of treating sickle cell anemia
A similar, but less effective technique for removing the defective version of HBB was presented by another group of scientists from the University of Berkeley just a month ago.
08.11.2016A similar, but less effective technique for removing the defective version of HBB was presented by another group of scientists from the University of Berkeley just a month ago.
08.11.2016Scientists from Washington State University have found a way to prevent the development of tumor cells – an infrequent but dangerous byproduct of gene therapy.
08.11.2016Researchers from Newcastle have turned E. coli into tiny living light bulbs that glow, effectively absorbing thermal energy from the environment.
02.11.2016Scientists used the CRISPR/Cas9 gene editing system to find mutations that make human immune cells resistant to HIV infection.
31.10.2016We are talking about a genetically modified variety of Aedes aegypti mosquitoes, which are carriers of dangerous Zika, dengue and chikungunya viruses.
27.10.2016American scientists have developed a method of genetic correction based on peptidonucleic acids, which effectively eliminated the symptoms of beta-thalassemia in mice.
27.10.2016The compact semi-automatic system is designed to produce individual genetically modified hematopoietic cells of patients in medical institutions.
24.10.2016It is possible to get rid of the immunodeficiency virus thanks to the revolutionary CRISPR/Cas9 system, which will allow cutting HIV genes from the DNA of the patient's cells.
19.10.2016Scientists from three American universities have tested a method of genetic therapy of sickle cell anemia using CRISPR/Cas9 technology on mice.
14.10.2016Molecular biologists have created and tested the first retroviral therapy for the treatment of Alzheimer's disease, relieving and protecting mice from the consequences of its development.
11.10.2016Why people are afraid of GMOs, how the GMO ban will affect science, how China is fighting GMOs and multinational companies, and how GMOs interact with nature.
29.09.2016Modified regulatory RNA molecules sent to the tumor in nanoparticles discourage cancer cells from traveling.
26.09.2016Restoration of severed nerve pathways is an important achievement in the search for treatment of glaucoma and other eye diseases associated with damage to the optic nerve.
23.09.2016Molecular biologists have successfully used the CRISPR/Cas9 genomic editor for the first time to suppress the growth of cancer cells and turn on their suicide program.
12.09.2016GM technologies open up prospects for the creation of fundamentally new drugs and, probably, will make it possible to transplant animal organs to humans.
09.09.2016An entry has been opened for free online courses on GMOs - one of the first available to a wide audience in the world and the first in Russian. And more – about biosensors, gemology…
07.09.2016The matter is rather in the historical component: the cabbage tasted had a genome edited using CRISPR-Cas9 technology.
07.09.2016According to the researchers, unlike other genome editing methods, Target-AID technology provides a greater variety and a high level of operations.
31.08.2016In the next phase of clinical trials of gene therapy for Parkinson's disease, patients will be injected with a triple dose of the drug VY-AADC01, delivered directly to the brain.
26.08.2016Removing some of the synonymous codons will create an "artificial" bacterium that is unable to reproduce outside the laboratory and at the same time resistant to all existing viruses.
26.08.2016You can write to the editor at:
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