Similar articles for PMID: 9218526

Year	Number of Results
1990	1
1991	2
1992	4
1993	8
1994	7
1995	4
1996	5
1997	4
1998	13
1999	10
2000	6
2001	5
2002	8
2003	2
2004	4
2005	6
2006	1
2007	4
2008	4
2009	1
2010	5
2011	4
2012	6
2013	3
2014	2
2015	5
2016	3
2017	4
2018	3
2019	2
2020	3
2021	7
2022	1
2023	1
2024	0

1

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. Rottbauer W, et al. J Clin Invest. 1997 Jul 15;100(2):475-82. doi: 10.1172/JCI119555. J Clin Invest. 1997. PMID: 9218526 Free PMC article.

2

COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytes.

Flavigny J, Souchet M, Sébillon P, Berrebi-Bertrand I, Hainque B, Mallet A, Bril A, Schwartz K, Carrier L. Flavigny J, et al. J Mol Biol. 1999 Nov 26;294(2):443-56. doi: 10.1006/jmbi.1999.3276. J Mol Biol. 1999. PMID: 10610770

3

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. Niimura H, et al. N Engl J Med. 1998 Apr 30;338(18):1248-57. doi: 10.1056/NEJM199804303381802. N Engl J Med. 1998. PMID: 9562578 Free article.

4

Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy.

Richard P, Isnard R, Carrier L, Dubourg O, Donatien Y, Mathieu B, Bonne G, Gary F, Charron P, Hagege M, Komajda M, Schwartz K, Hainque B. Richard P, et al. J Med Genet. 1999 Jul;36(7):542-5. J Med Genet. 1999. PMID: 10424815 Free PMC article.

5

Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy.

Carrier L, Bonne G, Bährend E, Yu B, Richard P, Niel F, Hainque B, Cruaud C, Gary F, Labeit S, Bouhour JB, Dubourg O, Desnos M, Hagège AA, Trent RJ, Komajda M, Fiszman M, Schwartz K. Carrier L, et al. Circ Res. 1997 Mar;80(3):427-34. Circ Res. 1997. PMID: 9048664

6

[High-risk hypertrophic cardiomyopathy associated with a novel mutation in cardiac Myosin-binding protein C].

García-Pavía P, Segovia J, Molano J, Mora R, Kontny F, Erik Berge K, Leren TP, Alonso-Pulpón L. García-Pavía P, et al. Rev Esp Cardiol. 2007 Mar;60(3):311-4. Rev Esp Cardiol. 2007. PMID: 17394878 Free article. Spanish.

7

Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations.

Frank-Hansen R, Page SP, Syrris P, McKenna WJ, Christiansen M, Andersen PS. Frank-Hansen R, et al. Eur J Hum Genet. 2008 Sep;16(9):1062-9. doi: 10.1038/ejhg.2008.52. Epub 2008 Mar 12. Eur J Hum Genet. 2008. PMID: 18337725

8

Functional and spectroscopic studies of a familial hypertrophic cardiomyopathy mutation in Motif X of cardiac myosin binding protein-C.

Brown LJ, Singh L, Sale KL, Yu B, Trent R, Fajer PG, Hambly BD. Brown LJ, et al. Eur Biophys J. 2002 Sep;31(5):400-8. doi: 10.1007/s00249-002-0236-0. Epub 2002 Jun 25. Eur Biophys J. 2002. PMID: 12202917

9

Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C.

Gruen M, Gautel M. Gruen M, et al. J Mol Biol. 1999 Feb 26;286(3):933-49. doi: 10.1006/jmbi.1998.2522. J Mol Biol. 1999. PMID: 10024460

10

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. Jääskeläinen P, et al. J Mol Med (Berl). 2002 Jul;80(7):412-22. doi: 10.1007/s00109-002-0323-9. Epub 2002 Apr 11. J Mol Med (Berl). 2002. PMID: 12110947

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