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Retinal abnormalities in transgenic mice overexpressing aberrant human FUS[1-359] gene
Soldatov, V. O., Kukharsky, M. S., Puchenkova, O. A., Deykin, A. V., Pokrovskiy, M. V.
was carried out on 12 transgenic and 13 wild-type mice of 2.5-3 months of age. The study revealed
The tissue distribution of SARS-CoV-2 in transgenic mice with inducible ubiquitous expression of hACE2
Dolskiy, A. A., Gudymo, A. S., Taranov, O. S., Soldatov, V. O., Deykin, A. V.
is laboratory animals sensitive to the virus. Herein, we report SARSCoV- 2 infection in novel transgenic mice
Transgenic mice Cre-dependently expressing mutant polymerase-gamma: novel test-system for pharmacological study of mitoprotective drugs
Kubekina, M. V., Silaeva, Yu. Yu., Bruter, A. V., Kolesnik, I. M., Korokin, M. V.
Transgenic mice Cre-dependently expressing mutant polymerase-gamma: novel test
Intravenous Transplantation of Human Umbilical Cord Blood Mononuclear Cells Overexpressing Nerve Growth Factor Improves Spatial Memory in APP/PS1 Transgenic Mice with a Model of Alzheimer’s Disease
Kaligin M., Mukhamedshina Y., Rizvanov A., Zefirov A., Islamov R.
factor (NGF) for the treatment of Alzheimer’s disease in an APP/PS1 transgenic mice model
APPswe/PS1dE9/Blg Transgenic Mouse Line for Modeling Cerebral Amyloid Angiopathy Associated with Alzheimer’s Disease
Lysikova, E. A., Kuzubova, E. V., Radchenko, A. I., Patrakhanov, E. A., Chaprov, K. D., Korokin, M. V., Deykin, A. V., Gudyrev, O. S., Pokrovskii, M. V.
APPswe/PS1dE9 mice with a CH3 genetic background with C57Bl6/Chg mice. No difference was found
Investigation of the pharmacological activity of the tetrapeptide HAEЕ, zinc, and human serum albumin in a transgenic mouse model with tau protein overexpression (P301S)
Shmigerova, V.S., Stepenko, Yu.V., Kurbatova, A.A., Zhunusov, N.S., Lyapkalov, N.S.
composition HAEE-Zn-HSA at a dosage of 75 mg/kg, using a model of homozygous mice from a transgenic line
Analysis of the efficiency of gene-cell therapy in transgenic mice with amyotrophic lateral sclerosis phenotype
Mukhamedyarov M., Rizvanov A., Safiullov Z., Izmailov A., Sharifullina G., Solovieva V., Fedotova V., Salafutdinov I., Cherenkova E., Bashirov F., Kaligin M., Abdulkhakov S., Shmarov M., Logunov D., Naroditsky B., Kiyasov A., Zefirov A., Islamov R.
in SOD1 G93A transgenic mice receiving xenotransplantation of human umbilical cord blood mononuclear
A bioisostere of Dimebon/Latrepirdine delays the onset and slows the progression of pathology in FUS transgenic mice
Chaprov, K., Rezvykh, A., Funikov, S., Ivanova, T. A., Deykin, A. V.
transgenic mice and the effect of DF402 on their gait already at early pre-symptomatic stage. At this stage
Analysis of the efficiency of gene-cell therapy in transgenic mice with amyotrophic lateral sclerosis phenotype
Mukhamedyarov M., Rizvanov A., Safiullov Z., Izmailov A., Sharifullina G., Solovieva V., Fedotova V., Salafutdinov I., Cherenkova E., Bashirov F., Kaligin M., Abdulkhakov S., Shmarov M., Logunov D., Naroditsky B., Kiyasov A., Zefirov A., Islamov R.
in SOD1 G93A transgenic mice receiving xenotransplantation of human umbilical cord blood mononuclear
New personalized genetic mouse model of Lesch-Nyhan syndrome for pharmacology and gene therapy
Kalmykov., V. A., Kusov, P. A., Yablonskaia, M. I., Korshunov, E. N., Korshunova, D. S.
strain carrying a deletion in the HPRT1 gene. These mice can be effectively used for the preclinical

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