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Vol 17, No 2 (2022)
Molecular and genetic features of calpainopathy
Mkrtchyan L.A., Slesarenko Y.S., Yakovlev I.A., Bardakov S.N., Deev R.V.
PDF
(Rus)
Vol 17, No 3 (2022)
Kletochnaya model' dlya izucheniya molekulyarnogeneticheskikh mekhanizmov bolezni parkinsona, assotsiirovannoy s mutatsiey v gene GBA
Drozdova E.S., Grigor'eva E.V., Pavlova S.V., Medvedev S.P., Sorogina D.A., Kopytova A.E., Baydakova G.V., Zakharova E.Y., Pchelina S.N., Zakayan S.M.
PDF
(Rus)
Vol 14, No 4 (2019)
Mutation lanscape of acute myeloid leukemia in elderly patients
Vinogradov A.V., Rezaykin A.V., Sazonov S.V., Sergeev A.G., Kapitonova M.Y.
PDF
(Rus)
Vol 15, No 3 (2020)
Genetic analysis of patients with hypertrophic cardiomyopathy
Dementyeva E.V., Vyatkin Y.V., Kretov E.I., Elisaphenko E.A., Medvedev S.P., Zakian S.M.
PDF
(Rus)
Vol 13, No 4 (2018)
Long QT syndrome: genetic analysis of patients
Dementyeva E.V., Medvedev S.P., Elisaphenko E.A., Bayramova S.A., Pokushalov E.A., Agladze K.I., Zakian S.M.
PDF
(Rus)
Vol 13, No 3 (2018)
Clinical and pathological features DNMT3A, FLT3, KIT, NPM1, NRAS, TP53 and wT1 genes mutations detection in acute myeloid leukemia patients aged 15-45 years old
Vinogradov A.V., Rezaykin A.V., Sazonov S.V., Sergeev A.G.
PDF
(Rus)
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