361 related articles for article (PubMed ID: 17097032)
41. Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
Blair E; Redwood C; de Jesus Oliveira M; Moolman-Smook JC; Brink P; Corfield VA; Ostman-Smith I; Watkins H
Circ Res; 2002 Feb; 90(3):263-9. PubMed ID: 11861413
[TBL] [Abstract][Full Text] [Related]
42. Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects.
Monserrat L; Hermida-Prieto M; Fernandez X; Rodríguez I; Dumont C; Cazón L; Cuesta MG; Gonzalez-Juanatey C; Peteiro J; Alvarez N; Penas-Lado M; Castro-Beiras A
Eur Heart J; 2007 Aug; 28(16):1953-61. PubMed ID: 17611253
[TBL] [Abstract][Full Text] [Related]
43. [The genotype-phenotype correlation of MYH7 gene G15391A mutation and MYBPC3 gene G12101A mutation in familial hypertrophic cardiomyopathy].
WANG H; ZOU YB; WANG JZ; SONG L; SUN K; SONG XD; WANG XJ; ZHANG CN; HUI RT
Zhonghua Xin Xue Guan Bing Za Zhi; 2008 Dec; 36(12):1059-62. PubMed ID: 19134269
[TBL] [Abstract][Full Text] [Related]
44. Cardiac and skeletal muscle expression of mutant β-myosin heavy chains, degree of functional impairment and phenotypic heterogeneity in hypertrophic cardiomyopathy.
Di Domenico M; Casadonte R; Ricci P; Santini M; Frati G; Rizzo A; Carratelli CR; Lamberti M; Parrotta E; Quaresima B; Faniello CM; Costanzo F; Cuda G
J Cell Physiol; 2012 Oct; 227(10):3471-6. PubMed ID: 22213221
[TBL] [Abstract][Full Text] [Related]
45. The left and right ventricle of a patient with a R723G mutation of the beta-myosin heavy chain and severe hypertrophic cardiomyopathy show no differences in the expression of myosin mRNA.
Borchert B; Tripathi S; Francino A; Navarro-Lopez F; Kraft T
Cardiol J; 2010; 17(5):518-22. PubMed ID: 20865685
[TBL] [Abstract][Full Text] [Related]
46. Pediatric restrictive cardiomyopathy associated with a mutation in beta-myosin heavy chain.
Ware SM; Quinn ME; Ballard ET; Miller E; Uzark K; Spicer RL
Clin Genet; 2008 Feb; 73(2):165-70. PubMed ID: 18076673
[TBL] [Abstract][Full Text] [Related]
47. A PCR-based integrated protocol for the structural analysis of the 13th exon of the human beta-myosin heavy chain gene (MYH7): development of a diagnostic tool for HCM disease.
Stravopodis DJ; Zapheiropoulos AZ; Voutsinas G; Margaritis LH; Papassideri IS
Exp Mol Pathol; 2008 Jun; 84(3):245-50. PubMed ID: 18499102
[TBL] [Abstract][Full Text] [Related]
48. Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland.
Jääskeläinen P; Kuusisto J; Miettinen R; Kärkkäinen P; Kärkkäinen S; Heikkinen S; Peltola P; Pihlajamäki J; Vauhkonen I; Laakso M
J Mol Med (Berl); 2002 Jul; 80(7):412-22. PubMed ID: 12110947
[TBL] [Abstract][Full Text] [Related]
49. Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy.
Perkins MJ; Van Driest SL; Ellsworth EG; Will ML; Gersh BJ; Ommen SR; Ackerman MJ
Eur Heart J; 2005 Nov; 26(22):2457-62. PubMed ID: 16087648
[TBL] [Abstract][Full Text] [Related]
50. Identification of a novel missense mutation in the cardiac beta-myosin heavy chain gene in a Chinese patient with sporadic hypertrophic cardiomyopathy.
Kuang SQ; Yu JD; Lu L; He LM; Gong LS; Chen SJ; Chen Z
J Mol Cell Cardiol; 1996 Sep; 28(9):1879-83. PubMed ID: 8899546
[TBL] [Abstract][Full Text] [Related]
51. A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy.
Jääskeläinen P; Heliö T; Aalto-Setälä K; Kaartinen M; Ilveskoski E; Hämäläinen L; Melin J; Kärkkäinen S; Peuhkurinen K; Nieminen MS; Laakso M; ; Kuusisto J
Ann Med; 2014 Sep; 46(6):424-9. PubMed ID: 24888384
[TBL] [Abstract][Full Text] [Related]
52. Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy.
Kaski JP; Syrris P; Esteban MT; Jenkins S; Pantazis A; Deanfield JE; McKenna WJ; Elliott PM
Circ Cardiovasc Genet; 2009 Oct; 2(5):436-41. PubMed ID: 20031618
[TBL] [Abstract][Full Text] [Related]
53. β-Myosin heavy chain variant Val606Met causes very mild hypertrophic cardiomyopathy in mice, but exacerbates HCM phenotypes in mice carrying other HCM mutations.
Blankenburg R; Hackert K; Wurster S; Deenen R; Seidman JG; Seidman CE; Lohse MJ; Schmitt JP
Circ Res; 2014 Jul; 115(2):227-37. PubMed ID: 24829265
[TBL] [Abstract][Full Text] [Related]
54. Lifelong left ventricular remodeling of hypertrophic cardiomyopathy caused by a founder frameshift deletion mutation in the cardiac Myosin-binding protein C gene among Japanese.
Kubo T; Kitaoka H; Okawa M; Matsumura Y; Hitomi N; Yamasaki N; Furuno T; Takata J; Nishinaga M; Kimura A; Doi YL
J Am Coll Cardiol; 2005 Nov; 46(9):1737-43. PubMed ID: 16256878
[TBL] [Abstract][Full Text] [Related]
55. Microsatellite marker analysis in the treatment and diagnosis of familial hypertrophic cardiomyopathy.
Smolik S; Domal-Kwiatkowska D; Kapral M; Weglarz L
Acta Pol Pharm; 2010; 67(6):669-72. PubMed ID: 21229884
[TBL] [Abstract][Full Text] [Related]
56. Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.
Doolan A; Tebo M; Ingles J; Nguyen L; Tsoutsman T; Lam L; Chiu C; Chung J; Weintraub RG; Semsarian C
J Mol Cell Cardiol; 2005 Feb; 38(2):387-93. PubMed ID: 15698845
[TBL] [Abstract][Full Text] [Related]
57. Mutations profile in Chinese patients with hypertrophic cardiomyopathy.
Song L; Zou Y; Wang J; Wang Z; Zhen Y; Lou K; Zhang Q; Wang X; Wang H; Li J; Hui R
Clin Chim Acta; 2005 Jan; 351(1-2):209-16. PubMed ID: 15563892
[TBL] [Abstract][Full Text] [Related]
58. A missense mutation of cardiac beta-myosin heavy chain gene linked to familial hypertrophic cardiomyopathy in affected Japanese families.
Harada H; Kimura A; Nishi H; Sasazuki T; Toshima H
Biochem Biophys Res Commun; 1993 Jul; 194(2):791-8. PubMed ID: 8343162
[TBL] [Abstract][Full Text] [Related]
59. [The genotype-phenotype correlation of the MYH7 gene c.1273G > a mutation in familial hypertrophic cardiomyopathy].
Wang H; Zou YB; Song L; Wang JZ; Sun K; Song XD; Gao S; Zhang CN; Hui RT
Yi Chuan; 2009 May; 31(5):485-8. PubMed ID: 19586842
[TBL] [Abstract][Full Text] [Related]
60. Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy.
Waldmüller S; Sakthivel S; Saadi AV; Selignow C; Rakesh PG; Golubenko M; Joseph PK; Padmakumar R; Richard P; Schwartz K; Tharakan JM; Rajamanickam C; Vosberg HP
J Mol Cell Cardiol; 2003 Jun; 35(6):623-36. PubMed ID: 12788380
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]