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Notch-dependent EMT is attenuated in patients with aortic aneurysm and bicuspid aortic valve.
Kostina AS, Uspensky VЕ, Irtyuga OB, Ignatieva EV, Freylikhman O, Gavriliuk ND, Moiseeva OM, Zhuk S, Tomilin A, Kostareva АА, Malashicheva AB. Kostina AS, et al. Among authors: zhuk s. Biochim Biophys Acta. 2016 Apr;1862(4):733-740. doi: 10.1016/j.bbadis.2016.02.006. Epub 2016 Feb 10. Biochim Biophys Acta. 2016. PMID: 26876948 Free article.
Variants in the NOTCH1 gene in patients with aortic coarctation.
Freylikhman O, Tatarinova T, Smolina N, Zhuk S, Klyushina A, Kiselev A, Moiseeva O, Sjoberg G, Malashicheva A, Kostareva A. Freylikhman O, et al. Among authors: zhuk s. Congenit Heart Dis. 2014 Sep-Oct;9(5):391-6. doi: 10.1111/chd.12157. Epub 2014 Jan 12. Congenit Heart Dis. 2014. PMID: 24418111
Case Reports: Emery-Dreifuss Muscular Dystrophy Presenting as a Heart Rhythm Disorders in Children.
Kovalchuk T, Yakovleva E, Fetisova S, Vershinina T, Lebedeva V, Lyubimtseva T, Lebedev D, Mitrofanova L, Ryzhkov A, Sokolnikova P, Fomicheva Y, Kozyreva A, Zhuk S, Smolina N, Zlotina A, Pervunina T, Kostareva A, Vasichkina E. Kovalchuk T, et al. Among authors: zhuk s. Front Cardiovasc Med. 2021 May 7;8:668231. doi: 10.3389/fcvm.2021.668231. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34026875 Free PMC article.
Case Report: Two New Cases of Autosomal-Recessive Hypertrophic Cardiomyopathy Associated With TRIM63-Compound Heterozygous Variant.
Andreeva S, Chumakova O, Karelkina E, Lebedeva V, Lubimtseva T, Semenov A, Nikitin A, Speshilov G, Kozyreva A, Sokolnikova P, Zhuk S, Fomicheva Y, Moiseeva O, Kostareva A. Andreeva S, et al. Among authors: zhuk s. Front Genet. 2022 Feb 22;13:743472. doi: 10.3389/fgene.2022.743472. eCollection 2022. Front Genet. 2022. PMID: 35273634 Free PMC article.
Desmin mutations impact the autophagy flux in C2C12 cell in mutation-specific manner.
Sukhareva KS, Smolina NA, Churkina AI, Kalugina KK, Zhuk SV, Khudiakov AA, Khodot AA, Faggian G, Luciani GB, Sejersen T, Kostareva AA. Sukhareva KS, et al. Among authors: zhuk sv. Cell Tissue Res. 2023 Aug;393(2):357-375. doi: 10.1007/s00441-023-03790-6. Epub 2023 Jun 6. Cell Tissue Res. 2023. PMID: 37277577 Free PMC article.
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood.
Muravyev A, Vershinina T, Tesner P, Sjoberg G, Fomicheva Y, Čajbiková NN, Kozyreva A, Zhuk S, Mamaeva E, Tarnovskaya S, Jornholt J, Sokolnikova P, Pervunina T, Vasichkina E, Sejersen T, Kostareva A. Muravyev A, et al. Among authors: zhuk s. Orphanet J Rare Dis. 2022 Sep 14;17(1):358. doi: 10.1186/s13023-022-02477-5. Orphanet J Rare Dis. 2022. PMID: 36104822 Free PMC article.
46 results