128 related articles for article (PubMed ID: 21256114)
21. Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy.
Van Driest SL; Vasile VC; Ommen SR; Will ML; Tajik AJ; Gersh BJ; Ackerman MJ
J Am Coll Cardiol; 2004 Nov; 44(9):1903-10. PubMed ID: 15519027
[TBL] [Abstract][Full Text] [Related]
22. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.
Niimura H; Bachinski LL; Sangwatanaroj S; Watkins H; Chudley AE; McKenna W; Kristinsson A; Roberts R; Sole M; Maron BJ; Seidman JG; Seidman CE
N Engl J Med; 1998 Apr; 338(18):1248-57. PubMed ID: 9562578
[TBL] [Abstract][Full Text] [Related]
23. Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy.
Kabaeva ZT; Perrot A; Wolter B; Dietz R; Cardim N; Correia JM; Schulte HD; Aldashev AA; Mirrakhimov MM; Osterziel KJ
Eur J Hum Genet; 2002 Nov; 10(11):741-8. PubMed ID: 12404107
[TBL] [Abstract][Full Text] [Related]
24. Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy.
Geier C; Gehmlich K; Ehler E; Hassfeld S; Perrot A; Hayess K; Cardim N; Wenzel K; Erdmann B; Krackhardt F; Posch MG; Osterziel KJ; Bublak A; Nägele H; Scheffold T; Dietz R; Chien KR; Spuler S; Fürst DO; Nürnberg P; Ozcelik C
Hum Mol Genet; 2008 Sep; 17(18):2753-65. PubMed ID: 18505755
[TBL] [Abstract][Full Text] [Related]
25. Decreased interactions of mutant muscle LIM protein (MLP) with N-RAP and alpha-actinin and their implication for hypertrophic cardiomyopathy.
Gehmlich K; Geier C; Osterziel KJ; Van der Ven PF; Fürst DO
Cell Tissue Res; 2004 Aug; 317(2):129-36. PubMed ID: 15205937
[TBL] [Abstract][Full Text] [Related]
26. A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy.
Meurs KM; Sanchez X; David RM; Bowles NE; Towbin JA; Reiser PJ; Kittleson JA; Munro MJ; Dryburgh K; Macdonald KA; Kittleson MD
Hum Mol Genet; 2005 Dec; 14(23):3587-93. PubMed ID: 16236761
[TBL] [Abstract][Full Text] [Related]
27. Terminal assembly of sarcomeric filaments by intermolecular beta-sheet formation.
Pinotsis N; Abrusci P; Djinović-Carugo K; Wilmanns M
Trends Biochem Sci; 2009 Jan; 34(1):33-9. PubMed ID: 18996015
[TBL] [Abstract][Full Text] [Related]
28. Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation.
Knoblauch H; Geier C; Adams S; Budde B; Rudolph A; Zacharias U; Schulz-Menger J; Spuler A; Yaou RB; Nürnberg P; Voit T; Bonne G; Spuler S
Ann Neurol; 2010 Jan; 67(1):136-40. PubMed ID: 20186852
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. [A novel missense mutation, K124N, in the troponin T gene of Chinese populations with hypertrophic cardiomyopathy].
An FS; Zhang Y; Li DQ; Yang XS; Li L; Zhang C; Yan ML; Wang Y; An GP
Zhonghua Yi Xue Za Zhi; 2004 Aug; 84(16):1340-3. PubMed ID: 15387941
[TBL] [Abstract][Full Text] [Related]
31. Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein.
Rottbauer W; Gautel M; Zehelein J; Labeit S; Franz WM; Fischer C; Vollrath B; Mall G; Dietz R; Kübler W; Katus HA
J Clin Invest; 1997 Jul; 100(2):475-82. PubMed ID: 9218526
[TBL] [Abstract][Full Text] [Related]
32. Ubiquitin-proteasome system impairment caused by a missense cardiac myosin-binding protein C mutation and associated with cardiac dysfunction in hypertrophic cardiomyopathy.
Bahrudin U; Morisaki H; Morisaki T; Ninomiya H; Higaki K; Nanba E; Igawa O; Takashima S; Mizuta E; Miake J; Yamamoto Y; Shirayoshi Y; Kitakaze M; Carrier L; Hisatome I
J Mol Biol; 2008 Dec; 384(4):896-907. PubMed ID: 18929575
[TBL] [Abstract][Full Text] [Related]
33. [Hereditary cardiomyopathies: a review. Mutation of structural proteins a common cause of hereditary cardiomyopathy].
Sjöberg G; Kostareva A; Sejersen T
Lakartidningen; 2005 Mar 14-20; 102(11):845-7, 850-3. PubMed ID: 15835520
[TBL] [Abstract][Full Text] [Related]
34. Familial hypertrophic cardiomyopathy: a paradigm of the cardiac hypertrophic response to injury.
Marian AJ; Roberts R
Ann Med; 1998 Aug; 30 Suppl 1():24-32. PubMed ID: 9800880
[TBL] [Abstract][Full Text] [Related]
35. The role of the M-band myomesin proteins in muscle integrity and cardiac disease.
Lamber EP; Guicheney P; Pinotsis N
J Biomed Sci; 2022 Mar; 29(1):18. PubMed ID: 35255917
[TBL] [Abstract][Full Text] [Related]
36. Functional analysis of slow myosin heavy chain 1 and myomesin-3 in sarcomere organization in zebrafish embryonic slow muscles.
Xu J; Gao J; Li J; Xue L; Clark KJ; Ekker SC; Du SJ
J Genet Genomics; 2012 Feb; 39(2):69-80. PubMed ID: 22361506
[TBL] [Abstract][Full Text] [Related]
37. Perturbation of the titin/MURF1 signaling complex is associated with hypertrophic cardiomyopathy in a fish model and in human patients.
Higashikuse Y; Mittal N; Arimura T; Yoon SH; Oda M; Enomoto H; Kaneda R; Hattori F; Suzuki T; Kawakami A; Gasch A; Furukawa T; Labeit S; Fukuda K; Kimura A; Makino S
Dis Model Mech; 2019 Nov; 12(11):. PubMed ID: 31628103
[TBL] [Abstract][Full Text] [Related]
38. Purification and biochemical characterization of myomesin, a myosin-binding and titin-binding protein, from bovine skeletal muscle.
Obermann WM; Plessmann U; Weber K; Fürst DO
Eur J Biochem; 1995 Oct; 233(1):110-5. PubMed ID: 7588733
[TBL] [Abstract][Full Text] [Related]
39. Identification of novel interactions between domains of Myosin binding protein-C that are modulated by hypertrophic cardiomyopathy missense mutations.
Moolman-Smook J; Flashman E; de Lange W; Li Z; Corfield V; Redwood C; Watkins H
Circ Res; 2002 Oct; 91(8):704-11. PubMed ID: 12386147
[TBL] [Abstract][Full Text] [Related]
40. Fast-folding alpha-helices as reversible strain absorbers in the muscle protein myomesin.
Berkemeier F; Bertz M; Xiao S; Pinotsis N; Wilmanns M; Gräter F; Rief M
Proc Natl Acad Sci U S A; 2011 Aug; 108(34):14139-44. PubMed ID: 21825161
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]