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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.
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.
Kross-korrektsiya defitsita r-geksozaminidazy a v mutantnykh kletkakh patsienta s bolezn'yu Teya-Saksa s ispol'zovaniem geneticheski modifitsirovannykh stvolovykh kletok
Shaymardanova A.A., Chulpanova D.S., Solov'eva V.V., Issa S.S., Mullagulova A.I., Titova A.A., Mukhamedshina Y.O., Kostennikov A.A., Timofeeva A.V., Aymaletdinov A.M., Nigmetzyanov I.R., Rizvanov A.A.
Gene and cell therapy of retinal diseases
Maximov V.V., Lagarkova M.A., Kiselev S.L.
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.
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.
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.
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.
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.
Gene and stem-cell therapy for neurodegenerative diseases
Islamov R.R., Rizvanov А.А., Guseva D.S., Kiasov A.P.
Methods of gene delivery and perspectives of their application in the gene therapy
Apartsin E.K., Knauer N.Y.
Gene therapy approaches to the duchenne muscular dystrophy theatment
Zaynitdinova M.I., Smirnikhina S.A., Lavrov A.V., Eremin I.I., Pulin A.A.
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.
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.
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.
Autologichnyy obogashchennyy geneticheskim materialom leykokontsentrat dlya preventivnoy gennoy terapii ishemicheskogo insul'ta v modeli na mini-svin'yakh
Targachev S.S., Trofimov D.A., Kundakchyan G.G., Agaev A.M., Novichenkov L.A., Garifulin R.R., Izmaylov A.A., Sokolov M.E., Markosyan V.A., Safiullov Z.Z.
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.
Otsenka effektivnosti plazmidnykh konstruktsiy dlya razrabotki gennoy terapii poyasno-konechnostnykh myshechnykh distrofiy R1 i R9
Slesarenko Y.S., Yakovlev I.A., Deev R.V., Isaev A.A.
Tay-Sachs disease: diagnostic, modeling and treatment approaches
Solovyeva V.V., Shaimardanova A.A., Chulpanova D.S., Kitaeva K.V., 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.
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.
Izuchenie mekhanizmov farmakologicheskoy aktivnosti novogo bitsistronnogo genoterapevticheskogo preparata na osnove plazmidy s genami VEGF165 i HGF cheloveka
Radnaeva A.V., Makarevich P.I., Boldyreva M.A., Parfenova E.V.
Gene therapy in regenerative medicine: latest achievements and actual directions of development
Slobodkina E.A., Karagyaur M.N., Balabanyan V.Y., Makarevich P.I.
Dvukhvektornaya sistema na osnove adenoassotsiirovannogo virusa dlya gennoy terapii disferlinopatii
Yakovlev I.A., Emelin A.M., Limaev I.S., Chernova O.N., Mavlikeev M.O., Soldatov V.O., Deykin A.V., Korokin M.V., Pokrovskiy M.V., Rizvanov A.A., Deev R.V., Isaev A.A.
Vliyanie autologichnogo leykokontsentrata, obogashchennogo geneticheskim materialom, na remodelirovanie neyroglii v golovnom mozge mini-sviney s ishemicheskim insul'tom
Petrova V.P., Siraeva A.R., Gaynullin I.I., Akhmetov R.K., Minyazeva I.S., Yapparova K.R., Trofimov D.A., Markosyan V.A., Islamov R.R., Safiullov Z.Z.
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.
Opportunities of using gene therapy in patient with non-reconstructable critical limb ischemia in proximal reocclusion
Chervyakov Y.V., Ha H.N.
Preand posttranscriptional genetic information modification in muscular dystrophy treatment
Yakovlev I.A., Deev R.V., Solovyeva V.V., Rizvanov A.A., Isaev A.A.
Regulyatsiya ekspressii genov adipotsitov 3T3-L1 s pomoshch'yu sistemy CRISPRa/i
Yudaeva A.D., Michurina S.S., Stafeev Y.S., Men'shikov M.Y., Parfenova E.V.
Transplantatsiya adipotsitarnoy tkaneinzhenernoy konstruktsii s CRISPR-oposredovannoy aktivatsiey ekspressii UCP1
Michurina S.S., Stafeev Y.S., Truong V.A., Men'shikov M.Y., Khu Y.C., Parfenova E.V.
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.
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.
The natural and synthetic polymers of the non-lipid origin in gene delivery
Bogdanenko E.V., Zhdanov R.I.
Gennaya terapiya naosnove mikrornk dlya GNAO1-entsefalopatii s dominantnonegativnym variantom C.607 G>A
Lunev E.A., Klement'eva N.V., Savchenko I.M., Karan' A.A., Dzhenkova M.A., Egorova T.V., Bardina M.V.
Chromatographic purification of plasmid DNA for clinical applications (gene therapy)
Romanova J.J., Salafutdinov I.I., Zamalyutdinova N.M., 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.
Analiz effektivnosti gennoy terapii na osnove adenoassotsiirovannykh virusov posle formirovaniya vektornogo immuniteta
Shaymardanova A.A., Mullagulova A.I., Solov'eva V.V., Mukhamedshina Y.O., Kostennikov A.A., Rizvanov A.A.
Model'nye nanokorpuskulyarnye nositeli dlya vnutriyadernoy dostavki fiziologicheski aktivnykh veshchestv
Ivanovskaya E.V., Dyatlov V.A.
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.
Modern pathogenesis-based methods and development of new gene and cell-based methods for cystic fibrosis treatment
Smirnikhina S.A., Lavrov A.V.
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.
1 - 44 of 44 Items

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