Kostareva AA - Search Results

1

[Practical guidelines for the diagnosis and treatment of transthyretin amyloid cardiomyopathy (ATTR-CM or transthyretin cardiac amyloidosis)].

Tereshchenko SN, Zhirov IV, Moiseeva OM, Adasheva TV, Ansheles AA, Barbarash OL, Galyavich AS, Gudkova AI, Zateyshchikov DA, Kostareva AA, Nasonova SN, Nedogoda SV, Pecherina TB, Ryzhkova DV, Sergienko VB. Tereshchenko SN, et al. Among authors: kostareva aa. Ter Arkh. 2022 May 26;94(4):584-595. doi: 10.26442/00403660.2022.04.201465. Ter Arkh. 2022. PMID: 36286812 Russian.

2

Valve Interstitial Cells: The Key to Understanding the Pathophysiology of Heart Valve Calcification.

Rutkovskiy A, Malashicheva A, Sullivan G, Bogdanova M, Kostareva A, Stensløkken KO, Fiane A, Vaage J. Rutkovskiy A, et al. J Am Heart Assoc. 2017 Sep 14;6(9):e006339. doi: 10.1161/JAHA.117.006339. J Am Heart Assoc. 2017. PMID: 28912209 Free PMC article. Review. No abstract available.

3

Early changes of gene expression profiles in the rat model of arterial injury.

Fedorov A, Kostareva A, Raud J, Roy J, Hedin U, Razuvaev A. Fedorov A, et al. J Vasc Interv Radiol. 2014 May;25(5):789-796.e7. doi: 10.1016/j.jvir.2013.11.031. Epub 2014 Feb 6. J Vasc Interv Radiol. 2014. PMID: 24508346

4

Forced expression of desmin and desmin mutants in cultured cells: impact of myopathic missense mutations in the central coiled-coil domain on network formation.

Bär H, Kostareva A, Sjöberg G, Sejersen T, Katus HA, Herrmann H. Bär H, et al. Exp Cell Res. 2006 May 15;312(9):1554-65. doi: 10.1016/j.yexcr.2006.01.021. Epub 2006 Mar 7. Exp Cell Res. 2006. PMID: 16519886

5

Severe muscle disease-causing desmin mutations interfere with in vitro filament assembly at distinct stages.

Bär H, Mücke N, Kostareva A, Sjöberg G, Aebi U, Herrmann H. Bär H, et al. Proc Natl Acad Sci U S A. 2005 Oct 18;102(42):15099-104. doi: 10.1073/pnas.0504568102. Epub 2005 Oct 10. Proc Natl Acad Sci U S A. 2005. PMID: 16217025 Free PMC article.

6

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: kostareva aa. 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.

7

Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland.

Martin AR, Karczewski KJ, Kerminen S, Kurki MI, Sarin AP, Artomov M, Eriksson JG, Esko T, Genovese G, Havulinna AS, Kaprio J, Konradi A, Korányi L, Kostareva A, Männikkö M, Metspalu A, Perola M, Prasad RB, Raitakari O, Rotar O, Salomaa V, Groop L, Palotie A, Neale BM, Ripatti S, Pirinen M, Daly MJ. Martin AR, et al. Am J Hum Genet. 2018 May 3;102(5):760-775. doi: 10.1016/j.ajhg.2018.03.003. Epub 2018 Apr 26. Am J Hum Genet. 2018. PMID: 29706349 Free PMC article.

8

Inflammation and Mechanical Stress Stimulate Osteogenic Differentiation of Human Aortic Valve Interstitial Cells.

Bogdanova M, Kostina A, Zihlavnikova Enayati K, Zabirnyk A, Malashicheva A, Stensløkken KO, Sullivan GJ, Kaljusto ML, Kvitting JP, Kostareva A, Vaage J, Rutkovskiy A. Bogdanova M, et al. Front Physiol. 2018 Nov 20;9:1635. doi: 10.3389/fphys.2018.01635. eCollection 2018. Front Physiol. 2018. PMID: 30524301 Free PMC article.

9

Tissue-Specific Influence of Lamin A Mutations on Notch Signaling and Osteogenic Phenotype of Primary Human Mesenchymal Cells.

Perepelina K, Klauzen P, Kostareva A, Malashicheva A. Perepelina K, et al. Cells. 2019 Mar 21;8(3):266. doi: 10.3390/cells8030266. Cells. 2019. PMID: 30901896 Free PMC article.

10

[Hereditary cardiomyopathies: a review. Mutation of structural proteins a common cause of hereditary cardiomyopathy].

Sjöberg G, Kostareva A, Sejersen T. Sjöberg G, et al. Lakartidningen. 2005 Mar 14-20;102(11):845-7, 850-3. Lakartidningen. 2005. PMID: 15835520 Review. Swedish.

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