Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Hypertrophy and TPM1[original query] |
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Hypertrophic cardiomyopathy caused by a novel alpha-tropomyosin mutation (V95A) is associated with mild cardiac phenotype, abnormal calcium binding to troponin, abnormal myosin cycling, and poor prognosis. Circulation 2001 1 103 (1): 65-71. Karibe A, Tobacman L S, Strand J, Butters C, Back N, Bachinski L L, Arai A E, Ortiz A, Roberts R, Homsher E, Fananapazir |
Inducibility of life-threatening ventricular arrhythmias is related to maximum left ventricular thickness and clinical markers of sudden cardiac death in patients with hypertrophic cardiomyopathy attributable to the Asp175Asn mutation in the alpha-tropomyosin gene. Journal of molecular and cellular cardiology 2004 1 36 (1): 91-9. Hedman A, Hartikainen J, Vanninen E, Laitinen T, Jääskeläinen P, Laakso M, Peuhkurinen K, Kuusisto |
Shared genetic causes of cardiac hypertrophy in children and adults. The New England journal of medicine 2008 May 358 (18): 1899-908. Morita Hiroyuki, Rehm Heidi L, Menesses Andres, McDonough Barbara, Roberts Amy E, Kucherlapati Raju, Towbin Jeffrey A, Seidman J G, Seidman Christine |
[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy]. Revista española de cardiología 2009 Jan 62 (1): 48-56. García-Castro Mónica, Coto Eliecer, Reguero Julián R, Berrazueta José R, Alvarez Victoria, Alonso Belén, Sainz Rocío, Martín María, Morís Ces |
Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy. Circulation journal : official journal of the Japanese Circulation Society 2013 77 (9): 2358-65. Núñez Lucía, Gimeno-Blanes Juan Ramón, Rodríguez-García María Isabel, Monserrat Lorenzo, Zorio Esther, Coats Caroline, McGregor Christopher G, Hernandez del Rincón Juan Pedro, Castro-Beiras Alfonso, Hermida-Prieto Manu |
Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM. DNA and cell biology 2015 May 34 (5): 350-9. Selvi Rani Deepa, Nallari Pratibha, Dhandapany Perundurai S, Rani Jhansi, Meraj Khunza, Ganesan Mala, Narasimhan Calambur, Thangaraj Kumarasa |
Novel electrocardiographic features in carriers of hypertrophic cardiomyopathy causing sarcomeric mutations. Journal of electrocardiology 2018 12 51 (6): 983-989. Jalanko Mikko, Heliö Tiina, Mustonen Pirjo, Kokkonen Jorma, Huhtala Heini, Laine Mika, Jääskeläinen Pertti, Tarkiainen Mika, Lauerma Kirsi, Sipola Petri, Laakso Markku, Kuusisto Johanna, Nikus Kje |
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