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Mukhamadiyarov R.A.

Research Institute of Complex Problems of Cardiovascular Diseases

Koshelev V.A.

Research Institute for Complex Issues of Cardiovascular Diseases

Frolov A.V.

Research Institute for Complex Issues of Cardiovascular Diseases

Mironov A.V.

Academician Barbarash Kemerovo Regional Clinical Cardiology Dispensary

Shabaev A.R.

Research Institute for Complex Problems of Cardiovascular Diseases;
Barbarash Kuzbass Clinical Cardiology Dispensary

Evtushenko A.V.

Research Institute for Complex Issues of Cardiovascular Diseases

Lyapin A.A.

Research Institute for Complex Issues of Cardiovascular Diseases

Kutikhin A.G.

Research Institute of Complex Problems of Cardiovascular Diseases

Ultrastructure of neointima of native and artificial elements of the blood circulatory system

Authors:

Mukhamadiyarov R.A., Koshelev V.A., Frolov A.V., Mironov A.V., Shabaev A.R., Evtushenko A.V., Lyapin A.A., Kutikhin A.G.

More about the authors

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To cite this article:

Mukhamadiyarov RA, Koshelev VA, Frolov AV, et al. . Ultrastructure of neointima of native and artificial elements of the blood circulatory system. Russian Journal of Archive of Pathology. 2022;84(3):14‑23. (In Russ.)
https://doi.org/10.17116/patol20228403114

References:

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  5. Williams H, Slater S, George SJ. Suppression of neointima formation by targeting β-catenin/TCF pathway. Biosci Rep. 2016; 36(6):e00427. https://doi.org/10.1042/BSR20160229
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  9. He Y, Jiao D, Chen P, Li N, Jin C. The relationship of lumen diameter and neointimal hyperplasia with inflation pressure. Technol Health Care. 2019;27(4):407-415.  https://doi.org/10.3233/THC-181184
  10. De Meyer GR, Bult H. Mechanisms of neointima formation--lessons from experimental models. Vasc Med. 1997;2(3):179-189.  https://doi.org/10.1177/1358863X9700200304
  11. Lijnen HR, Van Hoef B, Umans K, Collen D. Neointima formation and thrombosis after vascular injury in transgenic mice overexpressing plasminogen activator inhibitor-1 (PAI-1). J Thromb Haemost. 2004;2(1):16-22.  https://doi.org/10.1111/j.1538-7836.2003.00533.x
  12. Dobaczewski M, Gonzalez-Quesada C, Frangogiannis NG. The extracellular matrix as a modulator of the inflammatory and reparative response following myocardial infarction. J Mol Cell Cardiol. 2010;48(3):504-511.  https://doi.org/10.1016/j.yjmcc.2009.07.015
  13. Ebert MLA, Schmidt VF, Pfaff L, von Thaden A, Kimm MA, Wildgruber M. Animal models of neointimal hyperplasia and restenosis: species-specific differences and implications for translational research. JACC Basic Transl Sci. 2021;6(11):900-917.  https://doi.org/10.1016/j.jacbts.2021.06.006
  14. Mukhamadiyarov RA, Bogdanov LA, Glushkova TV, Shishkova DK, Kostyunin AE, Koshelev VA, Shabaev AR, Frolov AV, Stasev AN, Lyapin AA, Kutikhin AG. EMbedding and backscattered scanning electron microscopy: a detailed protocol for the whole-specimen, high-resolution analysis of cardiovascular tissues. Front Cardiovasc Med. 2021;8:739549. https://doi.org/10.3389/fcvm.2021.739549
  15. Mukhamadiyarov RA, Kutikhin AG. Backscattered scanning electron microscopy approach for assessment of microvessels under conditions of normal microanatomy and pathological neovascularization. Bull Exp Biol Med. 2020;169(4):525-530.  https://doi.org/10.1007/s10517-020-04927-1
  16. Nokhrin AV, Tarasov RS, Mukhamadiyarov RA, Shishkova DK, Kutikhin AG, Dzyuman AN, Khlusov IA, Barbarash LS. Two-stage approach for surgical treatment of tetralogy of Fallot in underweight children: Clinical and morphological outcomes. J Card Surg. 2019;34(5):293-299.  https://doi.org/10.1111/jocs.14031
  17. van Hinsbergh VW, Koolwijk P, Hanemaaijer R. Role of fibrin and plasminogen activators in repair-associated angiogenesis: in vitro studies with human endothelial cells. EXS. 1997;79:391-411.  https://doi.org/10.1007/978-3-0348-9006-9_16

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