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Contract number
Time span of the project

As of 30.01.2020

Number of staff members
scientific publications
General information

Name of the project: Targeted stem cell genome modification as a platform for searching for new pharmaceuticals

Strategy for Scientific and Technological Development Priority Level: в

Goals and objectives

Research directions: Producing new knockout mouse lines immune to atherosclerosis, methods of stem cell genome modification and in vivo investigation of processes occurring in vessel walls, methods of of two-photon laser scanning microscopy; creating «cosmetics» containing hyaluronan for vessels

Project objective:

  • Research of possible ways for correction of atherosclerosis
  • Search for new targets for medications using targeted genome modification

The practical value of the study

  • We have created a bank of E.Coli strains and plasma vectors carrying genetic structures necessary for targeted genome modification.
  • Our researchers have prepared lines of the 129Ola embryo stem cells and tested methods of their modification and cloning.
  • Optical methods for research of glycocalyx. Data has been obtained on the key role of vessel endothelium glycocalyx in development of atherosclerosis.
  • We have refined the method of implanting telemetric sensors for ECG.
  • We have refined the method of hypertrophy of vessel walls in response to mechanical damage of endothelium.
  • We have created in vitro and in vivo models that allow us to analyze drugs and search for new targets for treatment of the Alzheimer's disease.
  • Our researchers have refined a method of immunoferment detection of syndekane in mouse blood plasma. A comparison of a commercial set for determining human syndekane with antibodies to syndekane-1 of mice produced at our Laboratory. We have shown high specificity of the method that allows to determine amount of syndekane diluted in plasma. We have also shown that in the process of development of atherosclerosis in mice of the ApoE line concentration of syndekane increases. We have drawn blood samples from mice with different stages of atheroma development.

Education and career development: 6 masters dissertations have been defended


University of Edinburgh (United Kingdom), A. Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences (Russia): joint research

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Kirkby N.S., Duthie K.M., Miller E., Kotelevtsev Y.V., Bagnall A.J., Webb D.J. and Hadoke P. W.F.
Non-endothelial Cell Endothelin-B Receptors Limit Neointima Formation Following Vascular Injury. Cardiovascular Research 95(1): 19–28 (2012).
Deuchar G.A., Patrick M.D., Hadoke W.F., Brownstein D.G., Webb D.J., Mullins J.J., K. Chapman, Seckl J. R. and Kotelevtsev Y.V.
11-Hydroxysteroid Dehydrogenase Type 2 Deficiency Accelerates Atherogenesis and Causes Proinflammatory Changes in the Endothelium in Apoe / Mice. Endocrinology 152(1): 236–246 (2011).
Other laboratories and scientists
Hosting organization
Field of studies
Invited researcher
Time span of the project
Laboratory for Super-elastic Bio-interfaces

Tomsk State University - (TSU)

Medical biotechnologies


Volinsky Alexei Aleksandrovich

USA, Russia


Laboratory for Omics Technologies and big data for Personalized Medicine and Health

Skolkovo Institute of Science and Technology - (Skoltech)

Medical biotechnologies


Borchers Christoph Hermann


Laboratory for Molecular Imaging

Federal State Institution «Federal Research Centre «Fundamentals of Biotechnology» of the RAS» - (Research Center of Biotechnology RAS)

Medical biotechnologies


Bogdanov Alexey Alexeyevich

United States, Russia

Zherdeva Vitoriya Vyacheslavovna