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Delivery of cord blood cells modified with adenoviral vectors expressing GDNF into the area of spinal cord injury stimulates recovery of motor function and supports a population of glial cells
Mukhamedshina Y., Shaymardanova G., Salafutdinov I., Rizvanov A., Povysheva T., Masgutova G., Nigmetzyanova M., Chelyshev Y.
Delivery of cord blood cells modified with adenoviral vectors expressing GDNF into the area
Delivery of cord blood cells modified with adenoviral vectors expressing GDNF into the area of spinal cord injury stimulates recovery of motor function and supports a population of glial cells
Mukhamedshina Y., Shaymardanova G., Salafutdinov I., Rizvanov A., Povysheva T., Masgutova G., Nigmetzyanova M., Chelyshev Y.
Delivery of cord blood cells modified with adenoviral vectors expressing GDNF into the area
Triple-gene therapy for stroke: A proof-of-concept in vivo study in rats
-nuclear cells (UCB-MC) transduced with adenoviral vectors carrying genes encoding vascular endothelial growth
Development of vaccines based on adenoviral vectors: A review of foreign clinical studies (Part 1)
Cherenova L.V.
dissemination. Recent promising developments include genetically engineered vaccines based on adenoviral vectors
Influence of adenoviral transduction with Adv5-optHGF-RFP on phenotype of hepatic stellate cells
Shafigullina Aygul Kasyjmovna, Zaikina Elvira Ildarovna, Garanina Ekaterina Evgenevna, Titova Angelina Andreevna, Mavlikeev Mihail Olegovich, Rizvanov Albert Anatolevich, Gumerova Anisa Azatovna, Kiyasov Andrey Pavlovich
Adenoviral transduction of hepatic stellate cells is applicable for short time stimulation of genes
Adenoviral vector carrying glial cell-derived neurotrophic factor for direct gene therapy in comparison with human umbilical cord blood cell-mediated therapy of spinal cord injury in rat
Mukhamedshina Y., Shaymardanova G., Garanina, Salafutdinov I., Rizvanov, Islamov R., Chelyshev Y.
an adenoviral vector (AdV-GDNF group) in comparison with treatment performed using human umbilical cord blood
Adenoviral vector carrying glial cell-derived neurotrophic factor for direct gene therapy in comparison with human umbilical cord blood cell-mediated therapy of spinal cord injury in rat
Mukhamedshina Y., Shaymardanova G., Garanina, Salafutdinov I., Rizvanov, Islamov R., Chelyshev Y.
an adenoviral vector (AdV-GDNF group) in comparison with treatment performed using human umbilical cord blood
Preventive triple gene therapy reduces the negative consequences of ischemia-induced brain injury after modelling stroke in a rat
Markosyan V., Safiullov Z., Izmailov A., Fadeev F., Sokolov M., Kuznetsov M., Trofimov D., Kim E., Kundakchyan G., Gibadullin A., Salafutdinov I., Nurullin L., Bashirov F., Islamov R.
therapy for stroke. Adenoviral vectors carrying genes encoding vascular endothelial growth factor (VEGF
Effect of Adenoviral Transduction of Hepatic Stellate Cells with Adv5-optHGF-RFP on their Phenotype
Shafigullina A., Zaikina E., Garanina E., Sakhapov D., Titova A., Mavlikeev M., Rizvanov A., Gumerova A., Kiassov A.
) with adenoviral vector containing genes of hepatocytes growth factor (HGF) and red fluorescent protein (RFP) as a
Tandem Delivery of Multiple Therapeutic Genes Using Umbilical Cord Blood Cells Improves Symptomatic Outcomes in ALS
Islamov R., Rizvanov A., Fedotova V., Izmailov A., Safiullov Z., Garanina E., Salafutdinov I., Sokolov M., Mukhamedyarov M., Palotás A.
of human umbilical cord blood mononuclear cell (hUCBMC) cotransduced with adenoviral vectors expressing

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