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  • 1-10 ل  20 نتائج ل ""Cardiomyopathy, Hypertrophic genetics""

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Echocardiography Guiding Percutaneous Treatment of Obstructive Hypertrophic Cardiomyopathy: Navigating (In Known Waters) Is Necessary

Subjects: Gradiente; Técnicas de Ablação/métodos; Cardiomiopatia Hipertrófica Obstrutiva/genética

  • Source: Arquivos Brasileiros de Cardiologia, Volume: 118, Issue: 5, Pages: 873-874, Published: 13 MAY 2022

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Single-cell transcriptomics provides insights into hypertrophic cardiomyopathy

Subjects: Heart Defects, Congenital; Sarcomeres; Hypertrophic/genetics

  • Source: Cell Reports, 39(6). Cell PressCell Reports, 39(6):110809. Cell PressWehrens, M, de Leeuw, A E, Wright-Clark, M, Eding, J E C, Boogerd, C J, Molenaar, B, van der Kraak, P H, Kuster, D W D,

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The «Amish» NM_000256.3:c.3330+2TG splice variant in MYBPC3 associated with hypertrophic cardiomyopathy is an ancient Swiss mutation

Subjects: Adult; Humans; Infant, Newborn

  • Source: European journal of medical genetics, vol. 65, no. 12, pp. 104627

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Myocyte-Specific Upregulation of ACE2 in Cardiovascular Disease

Subjects: Cardiomyopathy, Dilated/genetics; Myocardium/metabolism; Cathepsin L

  • Source: CirculationCirculation, American Heart Association, 2020, ⟨10.1161/CIRCULATIONAHA.120.047911⟩medRxivCirculation, 142(7), 708-710. LIPPINCOTT WILLIAMS & WILKINS

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Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Subjects: Linkage disequilibrium; Cardiomyopathy, Dilated/genetics; Left

  • Source: Nature genetics, 53(2), 128-134. Nature Publishing GroupNature geneticsTadros, R, Francis, C, Xu, X, Vermeer, A M C, Harper, A

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Proteomic and Functional Studies Reveal Detyrosinated Tubulin as Treatment Target in Sarcomere Mutation-Induced Hypertrophic Cardiomyopathy

Subjects: Male; Carrier Proteins/genetics; Heart disease

  • Source: Circulation. Heart failureCirculation. Heart failure, 2021, 14 (1), ⟨10.1161/CIRCHEARTFAILURE.120.007022⟩Circulation. Heart failure, 14(1):e007022. Lippincott Williams & Wilkins

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Hypertrophic Cardiomyopathy: A Review

Subjects: medicine.medical_specialty; Heart disease; Cardiomiopatia Hipertrófica/genética

  • Source: Arquivos Brasileiros de Cardiologia, Volume: 115, Issue: 5, Pages: 927-935, Published: 07 DEC 2020Arquivos Brasileiros de Cardiologia v.115 n.5 2020Arquivos Brasileiros de Cardiologia

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Inhibition of the Hypoxia-Inducible Factor 1α-Induced Cardiospecific HERNA1 Enhance-Templated RNA Protects From Heart Disease

Subjects: Male; RNA, Untranslated; heart failure

  • Source: Circulation, vol. 139, no. 24, pp. 2778-2792CirculationCirculation, 139 (24)

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Measurement of myofilament-localised calcium dynamics in adult cardiomyocytes and the effect of hypertrophic cardiomyopathy mutations

Subjects: cardiomyopathies; Adult; Male

  • Source: Sparrow, A J, Sievert, K, Patel, S, Chang, Y-F, Broyles, C N, Brook, F A, Watkins, H, Geeves, M A, Redwood, C S, Robinson, P & Daniels, M J 2019, ' Measurement of Myofilament-Localized Calcium

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Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?

Subjects: Electron Transport Complex I/metabolism; Male; Mitochondrial Diseases

  • Source: Orphanet Journal of Rare DiseasesOrphanet journal of rare diseases 13(1), 120 (2018). doi:10.1186/s13023-018-0784-8Orphanet Journal of Rare Diseases, Vol. 13, no. 1, p. 120 [1-10]

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  • 1-10 ل  20 نتائج ل ""Cardiomyopathy, Hypertrophic genetics""