A New Variant of Charcot-Marie-Tooth Disease Type 2 Is Probably the Result of a Mutation in the Neurofilament-Light Gene by Mersiyanova, Irina V., Perepelov, Alexander V., Polyakov, Alexander V., Sitnikov, Vladimir F., Dadali, Elena L., Oparin, Roman B., Petrin, Alexander N., Evgrafov, Oleg V.

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The role of the reduction of extracellular calcium ion concentrations in activation of human peripheral blood T cells by Litvinov, I. S., Mersiyanova, I. V.

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Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients by Mersiyanova, Irina V., Ismailov, Sookhrat M., Polyakov, Alexandr V., Dadali, Elena L., Fedotov, Valeriy P., Nelis, Eva, Löfgren, Ann, Timmerman, Vincent, Van Broeckhoven, Christine, Evgrafov, Oleg V.

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Screening for Mutations in the Peripheral Myelin Genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth Neuropathy Patients by Mersiyanova, I V, Ismailov, S M, Polyakov, A V, Dadali, EL, Fedotov, V P, Nelis, E, Loefgren, A, Timmerman, V, Van Broeckhoven, C, Evgrafov, O V

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High frequency of HLA DQA10301 in Yakuts: no correlation with IDDM incidence by Mersiyanova, I V, Osakovsky, V L, Knyazev YuA, Eugrafov, O V

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Update on the genetic landscape of Diamond‐Blackfan anemia in the Russian Federation by Pavlova, Anna V., Ovsyannikova, Galina S., Kurnikova, Maria A., Mersiyanova, Irina V., Yasko, Lyudmila A., Raykina, Elena V., Maschan, Alexey A., Smetanina, Natalia S.

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Probing Peptide Sequences on Their Ability to Generate Affinity Sites in Molecularly Imprinted Polymers by Piletska, Elena V, Guerreiro, Antonio, Mersiyanova, Margarita, Cowen, Todd, Canfarotta, Francesco, Piletsky, Stanislav, Karim, Kal, Piletsky, Sergey

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Clinical and genomic heterogeneity of Diamond Blackfan anemia in the Russian Federation by Smetanina, Natalia S., Mersiyanova, Irina V., Kurnikova, Maria A., Ovsyannikova, Galina S., Hachatryan, Lili A., Bobrynina, Vlasta O., Maschan, Michael A., Novichkova, Galina. A., Lipton, Jeffrey M., Maschan, Alexey A.

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The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries by Sharapova, Svetlana O, Skomska-Pawliszak, Małgorzata, Rodina, Yulia A, Wolska-Kuśnierz, Beata, Dabrowska-Leonik, Nel, Mikołuć, Bozena, Pashchenko, Olga E, Pasic, Srdjan, Freiberger, Tomáš, Milota, Tomáš, Formánková, Renata, Szaflarska, Anna, Siedlar, Maciej, Avčin, Tadej, Markelj, Gašper, Ciznar, Peter, Kalwak, Krzysztof, Kołtan, Sylwia, Jackowska, Teresa, Drabko, Katarzyna, Gagro, Alenka, Pac, Małgorzata, Naumova, Elissaveta, Kandilarova, Snezhina, Babol-Pokora, Katarzyna, Varabyou, Dzmitry S, Barendregt, Barbara H, Raykina, Elena V, Varlamova, Tatiana V, Pavlova, Anna V, Grombirikova, Hana, Debeljak, Maruša, Mersiyanova, Irina V, Bondarenko, Anastasiia V, Chernyshova, Liudmyla I, Kostyuchenko, Larysa V, Guseva, Marina N, Rascon, Jelena, Muleviciene, Audrone, Preiksaitiene, Egle, Geier, Christoph B, Leiss-Piller, Alexander, Yamazaki, Yasuhiro, Kawai, Tomoki, Walter, Jolan E, Kondratenko, Irina V, Šedivá, Anna, van der Burg, Mirjam, Kuzmenko, Natalia B, Notarangelo, Luigi D, Bernatowska, Ewa, Aleinikova, Olga V

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Screening for mutations in the peripheral myelin genesPMP22,MPZ andCx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients by Mersiyanova, Irina V., Ismailov, Sookhrat M., Polyakov, Alexandr V., Dadali, Elena L., Fedotov, Valeriy P., Nelis, Eva, L fgren, Ann, Timmerman, Vincent, Van Broeckhoven, Christine, Evgrafov, Oleg V.

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Screening For Mutations In The Peripheral Myelin Genes PMP22, MPZ AND CX32 (GJB1) in Russian Charcot‐Marie‐Tooth Neuropathy Patients by Mersiyanova, I.V., Ismailov, S.M., Polyakov, A.V., Dadali, E.L., Fedotov, V.P., Nelis, E., Lofgren, A., Timmerman, V., Van Broeckhoven, C., Evgrafov, O.V.

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