Genetic engineering in Chinese
Chinese scientists have something to brag about: crucian carp without small bones and dozens of varieties of genetically modified plants are ready for implementation.
15.02.2022Chinese scientists have something to brag about: crucian carp without small bones and dozens of varieties of genetically modified plants are ready for implementation.
15.02.2022Overexpression of just one gene in microglia cells caused them to actively destroy this dangerous protein.
11.02.2022Gene therapy has helped children with hereditary Tay—Sachs disease to get rid of seizures.
11.02.2022The neurons of genetically modified mice were activated by ultrasound.
10.02.2022Researchers from the University of Cambridge have demonstrated the work of innovative mitochondrial genome editing technology in live mice.
09.02.2022When editing embryos, CRISPR-Cas9 can generate unexpected mutations that are inherited by offspring.
08.02.2022German researchers will start breeding genetically modified pigs to transplant their hearts to humans.
04.02.2022Functional CAR-T cells were preserved in the blood of clinical trial participants who were cured of leukemia in 2010.
03.02.2022Governments around the world are considering how to regulate the use of plant genome editing technologies.
31.01.2022"Quiet" areas have been found in the genome, in which genes can be embedded without the risk of undesirable consequences.
26.01.2022Scientists plan to use the gene drive method to reduce insect pest resistance to insecticides.
24.01.2022Russian biotechnologists used an Australian relative of ordinary tobacco to produce a vaccine against coronavirus.
19.01.2022A calf born in Yekaterinburg is expected to be immune to leukemia, hornless and hypoallergenic milk.
18.01.2022Scientists from the USA have created virus-like particles carrying ribonucleoproteins for editing bases instead of DNA.
17.01.2022Retrons act as DNA factories, producing a large number of copies of template DNA inside cells.
11.01.2022Genetically modified killer T-lymphocytes synthesize the drug and deliver it to the tumor.
10.01.2022CRISPR-Cas9-editing of resting CD4+ T cells can be used in HIV therapy studies.
28.12.2021The antisense oligonucleotide suppressed the expression of the mutant gene leading to the development of amyotrophic lateral sclerosis.
27.12.2021The first of its kind method of dual gene therapy eliminates severe hearing loss in mice.
20.12.2021This is the name of the method of treatment of sickle cell anemia tested on a group of 36 patients.
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