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Ordinary and Activated Bone Grafts: Applied Classification and the Main Features

Deev R., Drobyshev A., Bozo I., Isaev A.

© 2015 R. V. Deev et al. Bone grafts are medical devices that are in high demand in clinical

Ordinary and Activated Bone Grafts: Applied Classification and the Main Features

Deev R., Drobyshev A., Bozo I., Isaev A.

© 2015 R. V. Deev et al. Bone grafts are medical devices that are in high demand in clinical

Serum trace element profiles, prolactin, and cortisol in transient ischemic attack patients

Klimenko L.L., Budanova M.N., Baskakov I.S., Deev A.I., Skalny A.V., Tinkov A.A., Turna A.A., Nikonorov A.A., Savostina M.S., Mazilina A.N.

Iron status in male patients with acute ischemic stroke is associated with brain damage markers

Klimenko L.L., Skalny A.V., Turna A.A., Tinkov A.A., Budanova M.N., Baskakov I.S., Savostina M.S., Mazilina A.N., Deev A.I., Nikonorov A.A.

Corrigendum: Twenty-year clinical progression of dysferlinopathy in patients from Dagestan [Front Neurol, 8, (2017) (77)] doi: 10.3389/fneur.2017.00077

Umakhanova Z., Bardakov S., Mavlikeev M., Chernova O., Magomedova R., Akhmedova P., Yakovlev I., Dalgatov G., Fedotov V., Isaev A., Deev R.

V. Deev. Theoretical part of this work was supported by Russian Scientific Foundation grant (14

Gene- and cell-based therapy of muscle system hereditary disorders: State-of-art

Deev R., Mavlikeev M., Bozo I., Pulin A., Eremin I.

RNA Editing for Muscular Dystrophy Therapy

Yakovlev I., Deev R., Rizvanov A., Isaev A.

dystrophies became a focus for gene therapy. Multiple pre-clinical studies have shown successful restoration

Formation of the recombinant adenovirus encoding codon-optimized dysferlin gene and analysis of the recombinant protein expression in cell culture in vitro

Starostina I., Solovyeva V., Shevchenko K., Deev R., Isaev A., Rizvanov A.

), adenoviral vectors are suitable for the creation of genetic constructs, which are capable of delivering a

Pre- and posttranscriptional genetic information modification in muscular dystrophy treatment

Yakovlev I., Deev R., Solovyeva V., Rizvanov A., Isaev A.

Nowadays, a whole range of genetherapeutic methods is being used to restore a lost protein function

Modeling and gene therapy of dysferlinopathy

Starostina I., Solovyeva V., Yuryeva K., Shevchenko K., Fedotov V., Rizvanov A., Deev R., Isaev A.

Dysferlinopathies is a group of autosomal-recessive inherited neuromuscular diseases, which

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