يعرض 1 - 16 نتائج من 16 نتيجة بحث عن '"A. V. Gurshchenkov"', وقت الاستعلام: 0.42s تنقيح النتائج
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    المساهمون: The work was carried out with the financial support of the Russian Science Foundation (project No. 20-15-00271 P)., Работа выполнена при финансовой поддержке Российского научного фонда (проект № 20-15-00271П).

    المصدر: Translational Medicine; Том 11, № 2 (2024); 170-180 ; Трансляционная медицина; Том 11, № 2 (2024); 170-180 ; 2410-5155 ; 2311-4495

    وصف الملف: application/pdf

    Relation: https://transmed.almazovcentre.ru/jour/article/view/889/569; https://transmed.almazovcentre.ru/jour/article/downloadSuppFile/889/1986; https://transmed.almazovcentre.ru/jour/article/downloadSuppFile/889/2003; https://transmed.almazovcentre.ru/jour/article/downloadSuppFile/889/2004; Devi S, Kim JJ, Singh AP, et al. Proteotoxicity: A Fatal Consequence of Environmental Pollutants-Induced Impairments in Protein Clearance Machinery. J Pers Med. 2021;11(2):69. DOI:10.3390/jpm11020069.; Schreiber A, Peter M. Substrate recognition in selective autophagy and the ubiquitin-proteasome system. Biochim Biophys Acta. 2014;1843(1):163–81. DOI:10.1016/j.bbamcr.2013.03.019.; Castets P, Frank S, Sinnreich M, Ruegg MA. “Get the Balance Right”: Pathological Significance of Autophagy Perturbation in Neuromuscular Disorders. J Neuromuscul Dis. 2016;3(2):127–55. DOI:10.3233/JND-160153; Bonuccelli G, Sotgia F, Schubert W, et al. Proteasome inhibitor (MG-132) treatment of mdx mice rescues the expression and membrane localization of dystrophin and dystrophin-associated proteins. Am J Pathol. 2003;163(4):1663–75. DOI:10.1016/S0002-9440(10)63523-7.; Bodine SC, Baehr LM. Skeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx/atrogin-1. Am J Physiol Endocrinol Metab. 2014;307(6):E469–84. DOI:10.1152/ajpendo.00204.2014.; Tannous P, Zhu H, Johnstone JL, et al. Autophagy is an adaptive response in desmin-related cardiomyopathy. Proc Natl Acad Sci U S A. 2008;105(28):9745–9750. DOI:10.1073/pnas.0706802105.; Carmignac V, Svensson M, Korner Z, et al. Autophagy is increased in laminin alpha2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A. Hum Mol Genet. 2011;20(24):4891–902. DOI:10.1093/hmg/ddr427.; Gawlik KI, Durbeej M. Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies. Skelet Muscle. 2011;1(1):9. DOI:10.1186/2044-5040-1-9.; Malicdan MC, Nishino I. Autophagy in lysosomal myopathies. Brain Pathol. 2012;22(1):82–88. DOI:10.1111/j.1750-3639.2011.00543.x.; Al-Qusairi L, Prokic I, Amoasii L, et al. Lack of myotubularin (MTM1) leads to muscle hypotrophy through unbalanced regulation of the autophagy and ubiquitin-proteasome pathways. FASEB J. 2013;27(8):3384–94. DOI:10.1096/fj.12-220947.; Claeys KG, Fardeau M. Myofibrillar myopathies. Handb Clin Neurol. 2013;113:1337–42. DOI:10.1016/B978-0-444-59565-2.00005-8.; Fetalvero KM, Yu Y, Goetschkes M, et al. Defective autophagy and mTORC1 signaling in myotubularin null mice. Mol Cell Biol. 2013;33(1):98–110. DOI:10.1128/MCB.01075-12.; Zech ATL, Singh SR, Schlossarek S, Carrier L. Autophagy in cardiomyopathies. Biochim Biophys Acta Mol Cell Res. 2020;1867(3):118432. DOI:10.1016/j.bbamcr.2019.01.013.; Sandri M, Robbins J. Proteotoxicity: an underappreciated pathology in cardiac disease. J Mol Cell Cardiol. 2014;71:3–10. DOI:10.1016/j.yjmcc.2013.12.015.; Verdonschot JAJ, Vanhoutte EK, Claes GRF, et al. A mutation update for the FLNC gene in myopathies and cardiomyopathies. Hum Mutat. 2020;41(6):1091–1111. DOI:10.1002/humu.24004.; Cassandrini D, Merlini L, Pilla F, et al. Protein aggregates and autophagy involvement in a family with a mutation in Z-band alternatively spliced PDZ-motif protein. Neuromuscul Disord. 2021;31(1):44–51. DOI:10.1016/j.nmd.2020.11.008.; Bhuiyan MS, Pattison JS, Osinska H, et al. Enhanced autophagy ameliorates cardiac proteinopathy. J Clin Invest. 2013;123(12):5284–97. DOI:10.1172/JCI70877.; Pattison JS, Osinska H, Robbins J. Atg7 induces basal autophagy and rescues autophagic deficiency in CryABR120G cardiomyocytes. Circ Res. 2011;109(2):151– 60. DOI:10.1161/CIRCRESAHA.110.237339; Song L, Su M, Wang S, et al. MiR-451 is decreased in hypertrophic cardiomyopathy and regulates autophagy by targeting TSC1. J Cell Mol Med. 2014;18(11):2266–2274. DOI:10.1111/jcmm.12380.; Singh SR, Zech ATL, Geertz B, et al. Activation of Autophagy Ameliorates Cardiomyopathy in Mybpc3-Targeted Knockin Mice. Circ Heart Fail. 2017;10(10). DOI:10.1161/CIRCHEARTFAILURE.117.004140.; Iskratsch T, Lange S, Dwyer J, et al. Formin follows function: a muscle-specific isoform of FHOD3 is regulated by CK2 phosphorylation and promotes myofibril maintenance. Journal of Cell Biology. 2010;191(6):1159–72. DOI:10.1083/jcb.201005060.; Ruparelia AA, Oorschot V, Ramm G, Bryson-Richardson RJ. FLNC myofibrillar myopathy results from impaired autophagy and protein insufficiency. Hum Mol Genet. 2016;25(11):2131–2142. DOI:10.1093/hmg/ddw080.; McNamara JW, Parker BL, Voges HK, et al. Alpha kinase 3 signaling at the M-band maintains sarcomere integrity and proteostasis in striated muscle. Nature Cardiovascular Research. 2023;2(2):159–173. DOI: https://doi.org/10.1038/s44161-023-00219-9.; Kumar V, Kumar P, Chauhan L, et al. Novel combination of FLNC (c.5707G>A; p. Glu1903Lys) and BAG3 (c.610G>A; p.Gly204Arg) genetic variant expressing restrictive cardiomyopathy phenotype in an adolescent girl. J Genet. 2022;101:54.; Teixeira CA, Almeida Mdo R, Saraiva MJ. Impairment of autophagy by TTR V30M aggregates: in vivo reversal by TUDCA and curcumin. Clin Sci (Lond). 2016;130(18):1665–75. DOI:10.1042/CS20160075.; Yanagisawa H, Hossain MA, Miyajima T, et al. Dysregulated DNA methylation of GLA gene was associated with dysfunction of autophagy. Mol Genet Metab. 2019;126(4):460–465. DOI:10.1016/j.ymgme.2019.03.003.; https://transmed.almazovcentre.ru/jour/article/view/889

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    المصدر: Siberian Journal of Clinical and Experimental Medicine; Том 36, № 1 (2021); 134-140 ; Сибирский журнал клинической и экспериментальной медицины; Том 36, № 1 (2021); 134-140 ; 2713-265X ; 2713-2927

    وصف الملف: application/pdf

    Relation: https://www.sibjcem.ru/jour/article/view/1144/607; Hang D., Nguyen A., Schaff H. Surgical treatment for hypertrophic cardiomyopathy: A historical perspective. Ann. Cardiothorac. Surg. 2017;6(4):318–328. DOI:10.21037/acs.2017.04.03.; Kotkar K., Said S., Dearani J., Schaff H. Hypertrophic obstructive cardiomyopathy: The Mayo Clinic experience. Ann. Cardiothorac. Surg. 2017;6(4):329–336. DOI:10.21037/acs.2017.07.03.; Dearani J.A. Modified Konno instead of myectomy: Another tool in the box? J. Thorac. Cardiovasc. Surg. 2018;56(6):2295–2296. DOI:10.1016/j.jtcvs.2018.07.039.; Гурщенков А.В., Сухова И.В., Зайцев В.В., Майстренко А.Д., Дьяченко Я.А., Агаев Р.С. и др. Пятилетний опыт использования мобилизации сердца при септальной миоэктомии. Кардиология и сердечно-сосудистая хирургия. 2018;11(4):54–58. DOI:10.17116/kardio201811454.; Laredo M., Khraiche D., Raisky O., Gaudin R., Bajolle F., Maltret A. et al. Long-term results of the modified Konno procedure in high-risk children with obstructive hypertrophic cardiomyopathy. J. Thorac. Cardiovasc. Surg. 2018;156(6):2285–2294.e2. DOI:10.1016/j.jtcvs.2018.06.040.; Manouguian S., Seybold-Epting W. Patch enlargement of the aortic valve ring by extending the aortic incision into the anterior mitral leaflet: New operative technique. J. Thorac. Cardiovasc. Surg. 1979;78(3):402–412. DOI:10.1016/s0022-5223(19)38105-x.; Konno S., Imai Y., Iida Y., Nakajima M., Tatsuno K. A new method for prosthetic valve replacement in congenital aortic stenosis associated with hypoplasia of the aortic valve ring. J. Thorac. Cardiovasc. Surg. 1975;70(5):909–917. DOI:10.1016/s0022-5223(19)39673-4.; Murphy D., Poirier N. A technique of aortic valvuloplasty for aortic insufficiency associated with ventricular septal defect. J. Thorac. Cardiovasc. Surg. 1972;64(5):800–802.; Garamella J., Schmidt W., Jensen N., Lynch M. Clinical experiences with the bicuspid operation for aortic regurgitation. Ann. Surg. 1963;157(2):310–313. DOI:10.1097/00000658-196302000-00021.; Vouhè P., Poulain H., Bloch G., Loisance D., Gamain J., Lombaert M. et al. Aortoseptal approach for optimal resection of diffuse subvalvular aortic stenosis. J. Thorac. Cardiovasc. Surg. 1984;87(6):887–893. DOI:10.1016/s0022-5223(19)38418-1.; Reid K. The anatomy of the sinus of Valsalva. Thorax. 1970;25(1):79–85. DOI:10.1136/thx.25.1.79.; Gutermann H., Pettinari M., Van Kerrebroeck C., Vander Laenen M., Engelen K., Fret T. et al. Myectomy and mitral repair through the left atrium in hypertrophic obstructive cardiomyopathy: The preferred approach for contemporary surgical candidates? J. Thorac. Cardiovasc. Surg. 2014;147(6):1833–1836. DOI:10.1016/j.jtcvs.2013.07.024.; Borisov K. Right ventricle myectomy. Ann. Cardiothorac. Surg. 2017;6(4):402–409. DOI:10.21037/acs.2017.07.10.; Kotkar K., Said S., Schaff H. Transapical approach for myectomy in hypertrophic cardiomyopathy. Ann. Cardiothorac. Surg. 2017;6(4):419–422. DOI:10.21037/acs.2017.06.02.; Elmistekawy E., Lapierre H., Mesana T., Ruel M. Apico-aortic conduit for severe aortic stenosis: Technique, applications, and systematic review. J. Saudi Heart Assoc. 2010;22(4):187–194. DOI:10.1016/j.jsha.2010.06.003.; https://www.sibjcem.ru/jour/article/view/1144

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