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Current approaches to the genetic modification of mesenchymal stromal cells to increase their therapeutic efficacy
Limareva L.V., Gribkova O.V., Iliasov P.V., Grischuk Y.К.
Effectiveness of cell and gene therapy in treatment of obliterating diseases of the arteries in the lower extremities: a review
Ha H.N., Chervyakov Y.V., Gavrilenko A.V.
Evaluation of in vitro functional activity of ANB4 drug for the treatment of spinal muscular atrophy
Rodenkov E.M., Kozhemyakina N.V., Zonis Y.A., Gershovich P.M., Lalaev B.Y.
Gene technologies in ischemic stroke preclinical studies
Safiullov Z.Z., Markosyan V.A., Chelyshev Y.A.
Adeno-associated viruses in gene therapy for spinal muscular atrophies: trend or triumph?
Slobodkina E.A., Akopyan Z.A., Makarevich P.I.
Prospects for the use of gene and cell therapy for the treatment of muscular dystrophy
Sukach A.N.
Autosomal recessive congenital ichthyosis: diagnosis, modeling and approaches to therapy
Ponomarev A.S., Chulpanova D.S., Shaimardanova A.A., Rizvanov A.A., Solovyeva V.V.
Methods of gene delivery and perspectives of their application in the gene therapy
Apartsin E.K., Knauer N.Y.
Artificial chromosomes for gene therapy and tissue replacement
Likovykh M., Kouprina N., Larionov V., Tomilin A.
The first clinical experience of direct gene therapy using VEGF and bFGF in treatmentpatients with critical lower limb ischemia
Plotnikov M.V., Rizvanov A.A., Masgutov R.F., Mavlikeev M.O., Salafutdinov I.I., Gazizov I.M., Romanova Y.D., Shamsutdinova I.I., Bogov A.A., Maksimov A.V.
Efficiency and mechanism of antitumor activity of cardiolipin-like lipid/thymidine kinase gene HSV-tklipoplexes in the presence of gancyclovir
Moskovtsev A.A., Sokolovskaya A.A., Ibragimova M.Y., Dojnikova A.N., Sebyakin U.L., Zhdanov R.I.
Geneand cell-based therapy of muscle system hereditary disorders: state-of-art
Deev R.V., Mavlikeev M.O., Bozo I.Y., Pulin A.A., Eremin I.I.
Gene and cell therapy of retinal diseases
Maximov V.V., Lagarkova M.A., Kiselev S.L.
Prospects of increasing the effectiveness of cardio-vascular gene and cell therapy: genetically modified cells
Shevchenko E.K., Talitskiy A.K., Parfenova E.V., Shevchenko E.K., Talitskiy A.K., Parfyonova Y.V.
The prospects of creating a pacemaker cardiac tissue using modern technologies
Bayramova S.A., Strelnikov A.G., Romanov A.B., Yakubov A.A., Losik D.V., Pavlova S.V., Agladze K.I., Pokushalov E.A.
Gene and stem-cell therapy for neurodegenerative diseases
Islamov R.R., Rizvanov А.А., Guseva D.S., Kiasov A.P.
Regenerative technologies in treatment of diabetic foot ulcers
Kalinin R.E., Suchkov I.A., Mzhavanadze N.D., Krylov A.A., Isaev A.A., Plaksa I.L., Deev R.V.
Modern approaches to peripheral nerve regeneration after injury: the prospects of gene and cell therapy
Karagyaur M.N., Makarevich P.I., Shevchenko E.K., Stambolsky D.V., Kalinina N.I., Parfyonova Y.V.
The natural and synthetic polymers of the non-lipid origin in gene delivery
Bogdanenko E.V., Zhdanov R.I.
Site-specific genome editing for hematopoetic stem cells transplantation-based gene therapy approaches
Lepik K.V., Popova M.O., Shakirova A.I., Sergeev V.S., Potter A.Y., Barkhatov I.M., Fehse B., Afanasyev B.V.
Opportunities of using gene therapy in patient with non-reconstructable critical limb ischemia in proximal reocclusion
Chervyakov Y.V., Ha H.N.
Combined use of plasmid drug pCMV-VEGFA and autodermoplasty for stimulation of skin defects healing in the experiment
Bilialov A.I., Abyzova M.S., Titova A.A., Mavlikeev M.O., Krilov A., Bozo I.Y., Deev R.V.
Gene therapy approaches to the duchenne muscular dystrophy theatment
Zaynitdinova M.I., Smirnikhina S.A., Lavrov A.V., Eremin I.I., Pulin A.A.
Morphological changes in myelinated fibers of the spinal cord and the sciatic nerve in mice after modeling of the hypogravity and the approach of their correction by preventive gene therapy
Lisyukov A.N., Kuznetsov M.S., Saitov V.R., Salnikova M.M., Bikmullina I.A., Koshpaeva E.S., Tyapkina O.V., Valiullin V.V., Islamov R.R.
Modern pathogenesis-based methods and development of new gene and cell-based methods for cystic fibrosis treatment
Smirnikhina S.A., Lavrov A.V.
Preand posttranscriptional genetic information modification in muscular dystrophy treatment
Yakovlev I.A., Deev R.V., Solovyeva V.V., Rizvanov A.A., Isaev A.A.
Generation of recombinant adenoviral vectors encoding neural cell adhesion molecules ncam1, ncam2 and l1cam
Fedotova V.Y., Cherenkova E.E., Islamov R.R., Rizvanov A.A.
Pathohistological assessment of skeletal muscle after direct gene therapy with vegf165 of patients with peripheral arterial diseases
Mavlikeev M.O., Plotnikov M.V., Maksimov A.V., Gafiyatullina G.R., Murtazin A.I., Teregulov U.E., Shamsutdinova I.I., Gumerova A.A., Rizvanov A.A., Kiassov A.P.
New therapeutic strategies for the treatment of metachromatic leukodystrophy
Shaimardanova A.A., Chulpanova D.S., Solovyeva V.V., Mullagulova A.I., Kitaeva K.V., Rizvanov A.A.
Chromatographic purification of plasmid DNA for clinical applications (gene therapy)
Romanova J.J., Salafutdinov I.I., Zamalyutdinova N.M., Rizvanov A.A.
Novel plasmid constructs with angiogenic growth factors genes - human VEGF, HGF and angiopoietin-1 for therapeutic angiogenesis
Makarevich P.I., Shevelev3 A.Y., Rybalkin I.N., Kashirina N.M., Lipatova L.N., Tsokolaeva Z.I., Shevchenko E.K., Beloglazova I.B., Boldyreva M.A., Rubina К.A., Vlasik T.N., Parfyonova Y.V.
Tay-Sachs disease: diagnostic, modeling and treatment approaches
Solovyeva V.V., Shaimardanova A.A., Chulpanova D.S., Kitaeva K.V., Rizvanov A.A.
Gene therapy in regenerative medicine: latest achievements and actual directions of development
Slobodkina E.A., Karagyaur M.N., Balabanyan V.Y., Makarevich P.I.
Uluchshenie dostavki kompleksov plazmidnoy DNKs polikationom v kletki chelovekav prisutstvii bloksopolimerov etilen-i propilenoksida
Martynova, A.D., Shevchenko, V.D., Bondar, O.V., Abdullin T.I.
Legislative regulation and use of genetic information in the Russian Federation and abroad
Vulf M.A., Yurova K.A., Skuratovskaia D.A., Litvinova L.S.
Formation of the recombinant adenovirus encoding codon-optimized dysferlin gene and analysisof the recombinant protein expression in cell culture in vitro
Starostina I.G., Solovyeva V.V., Shevchenko K.G., Deev R.V., Isaev A.A., Rizvanov A.A.
Efficacy of combined use of plasmid constructs containing HGF and angiopoietin-1 genes to restore blood flow in ischemic tissues
Rubina K.A., Semina E.V., Diykanov D.T., Boldyreva M.A., Makarevich P.I., Parfyonova Y.V., Akopyan Z.A., Tkachuk V.A.
Delivery of nerve growth factor (NGF) gene via recombinant plasmid vector induces angiogenesis in murine ischemic hind limb
Boldyreva M.A., Makarevich P.I., Rafieva L.M., Beloglazova I.B., Dergilev K.V., Kostrov S.V., Parfyonova Y.V.
1 - 38 of 38 Items

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