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Clinical Response to Personalized Exercise Therapy in Heart Failure Patients with Reduced Ejection Fraction is Accompanied by Skeletal Muscle Histological Alterations.
Lelyavina TA, Galenko VL, Ivanova OA, Komarova MY, Ignatieva EV, Bortsova MA, Yukina GY, Khromova NV, Sitnikova MY, Kostareva AA, Sergushichev A, Dmitrieva RI. Lelyavina TA, et al. Among authors: sergushichev a. Int J Mol Sci. 2019 Nov 5;20(21):5514. doi: 10.3390/ijms20215514. Int J Mol Sci. 2019. PMID: 31694310 Free PMC article.
De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy.
Kiselev A, Vaz R, Knyazeva A, Khudiakov A, Tarnovskaya S, Liu J, Sergushichev A, Kazakov S, Frishman D, Smolina N, Pervunina T, Jorholt J, Sjoberg G, Vershinina T, Rudenko D, Arner A, Sejersen T, Lindstrand A, Kostareva A. Kiselev A, et al. Among authors: sergushichev a. Hum Mutat. 2018 Sep;39(9):1161-1172. doi: 10.1002/humu.23559. Epub 2018 Jun 17. Hum Mutat. 2018. PMID: 29858533
Skeletal Muscle Resident Progenitor Cells Coexpress Mesenchymal and Myogenic Markers and Are Not Affected by Chronic Heart Failure-Induced Dysregulations.
Dmitrieva RI, Lelyavina TA, Komarova MY, Galenko VL, Ivanova OA, Tikanova PA, Khromova NV, Golovkin AS, Bortsova MA, Sergushichev A, Sitnikova MY, Kostareva AA. Dmitrieva RI, et al. Among authors: sergushichev a. Stem Cells Int. 2019 Jan 3;2019:5690345. doi: 10.1155/2019/5690345. eCollection 2019. Stem Cells Int. 2019. PMID: 30719048 Free PMC article.
Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and Cardiomyopathy.
Kiselev A, Vaz R, Knyazeva A, Sergushichev A, Dmitrieva R, Khudiakov A, Jorholt J, Smolina N, Sukhareva K, Fomicheva Y, Mikhaylov E, Mitrofanova L, Predeus A, Sjoberg G, Rudenko D, Sejersen T, Lindstrand A, Kostareva A. Kiselev A, et al. Among authors: sergushichev a. Front Genet. 2019 Jun 26;10:608. doi: 10.3389/fgene.2019.00608. eCollection 2019. Front Genet. 2019. PMID: 31297131 Free PMC article.
Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro.
Perepelina K, Klauzen P, Khudiakov A, Zlotina A, Fomicheva Y, Rudenko D, Gordeev M, Sergushichev A, Malashicheva A, Kostareva A. Perepelina K, et al. Among authors: sergushichev a. Stem Cell Res. 2020 Mar;43:101714. doi: 10.1016/j.scr.2020.101714. Epub 2020 Jan 31. Stem Cell Res. 2020. PMID: 32059175 Free article.
Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln.
Perepelina K, Kostina A, Klauzen P, Khudiakov A, Rabino M, Crasto S, Zlotina A, Fomicheva Y, Sergushichev A, Oganesian M, Dmitriev A, Kostareva A, Di Pasquale E, Malashicheva A. Perepelina K, et al. Among authors: sergushichev a. Stem Cell Res. 2020 Jun 29;47:101895. doi: 10.1016/j.scr.2020.101895. Online ahead of print. Stem Cell Res. 2020. PMID: 32659731 Free article.
44 results