Microstructure and Mechanical Properties of β-Titanium Ti-15Mo Alloy Produced by Combined Processing including ECAP-Conform and Drawing

por Gatina, Svetlana A., Polyakova, Veronika V., Polyakov, Alexander V., Semenova, Irina P.
Publicado 2022

Microstructural Features and Microhardness of the Ti-6Al-4V Alloy Synthesized by Additive Plasma Wire Deposition Welding

por Semenova, Irina P., Shchitsyn, Yuri D., Trushnikov, Dmitriy N., Gareev, Alfiz I., Polyakov, Alexander V., Pesin, Mikhail V.
Publicado 2023

Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4-Related Retinal Dystrophy in an Eastern European Population

por Kadyshev, Vitaly V., Alekseeva, Ekaterina A., Strelnikov, Vladimir V., Stepanova, Anna A., Polyakov, Alexander V., Marakhonov, Andrey V., Kutsev, Sergey I., Zinchenko, Rena A.
Publicado 2023

Molybdenum Disulfide Surface Modification of Ultrafine-Grained Titanium for Enhanced Cellular Growth and Antibacterial Effect

por Shin, Myeong Hwan, Baek, Seung Mi, Polyakov, Alexander V., Semenova, Irina P., Valiev, Ruslan Z., Hwang, Woon-bong, Hahn, Sei Kwang, Kim, Hyoung Seop
Publicado 2018

Epidemiology of Rare Hereditary Diseases in the European Part of Russia: Point and Cumulative Prevalence

por Zinchenko, Rena A., Ginter, Eugeny K., Marakhonov, Andrey V., Petrova, Nika V., Kadyshev, Vitaly V., Vasilyeva, Tatyana P., Alexandrova, Oksana U., Polyakov, Alexander V., Kutsev, Sergey I.
Publicado 2021

Corrigendum: Epidemiology of rare hereditary diseases in the European part of Russia: Point and cumulative prevalence

por Zinchenko, Rena A., Ginter, Eugeny K., Marakhonov, Andrey V., Petrova, Nika V., Kadyshev, Vitaly V., Vasilyeva, Tatyana P., Alexandrova, Oksana U., Polyakov, Alexander V., Kutsev, Sergey I.
Publicado 2022

Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia

por Altamura, Concetta, Ivanova, Evgeniya A., Imbrici, Paola, Conte, Elena, Camerino, Giulia Maria, Dadali, Elena L., Polyakov, Alexander V., Kurbatov, Sergei Aleksandrovich, Girolamo, Francesco, Carratù, Maria Rosaria, Desaphy, Jean-François
Publicado 2020

Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletions

por Bliznetz, Elena A, Lalayants, Maria R, Markova, Tatiana G, Balanovsky, Oleg P, Balanovska, Elena V, Skhalyakho, Roza A, Pocheshkhova, Elvira A, Nikitina, Natalya V, Voronin, Sergey V, Kudryashova, Elena K, Glotov, Oleg S, Polyakov, Alexander V
Publicado 2017

Epidemiology of Hereditary Diseases in the Karachay-Cherkess Republic

por Zinchenko, Rena A., Makaov, Amin Kh., Marakhonov, Andrey V., Galkina, Varvara A., Kadyshev, Vitaly V., El’chinova, Galina I., Dadali, Elena L., Mikhailova, Lyudmila K., Petrova, Nika V., Petrina, Nina E., Vasilyeva, Tatyana A., Gundorova, Polina, Polyakov, Alexander V., Alexandrova, Oksana Y., Kutsev, Sergey I., Ginter, Eugeny K.
Publicado 2020