Similar articles for PMID: 10528865

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

1

Cardiac and skeletal actin gene mutations are not a common cause of dilated cardiomyopathy.

Mayosi BM, Khogali S, Zhang B, Watkins H. Mayosi BM, et al. J Med Genet. 1999 Oct;36(10):796-7. doi: 10.1136/jmg.36.10.796. J Med Genet. 1999. PMID: 10528865 Free PMC article. No abstract available.

2

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure.

Olson TM, Michels VV, Thibodeau SN, Tai YS, Keating MT. Olson TM, et al. Science. 1998 May 1;280(5364):750-2. doi: 10.1126/science.280.5364.750. Science. 1998. PMID: 9563954

3

[Detection of cardiac actin and desman gene mutations in children with dilated cardiomyopathy].

Liu F, Ning SB, Lu Y. Liu F, et al. Zhonghua Er Ke Za Zhi. 2007 Jan;45(1):75-7. Zhonghua Er Ke Za Zhi. 2007. PMID: 17349161 Chinese. No abstract available.

4

Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.

Zhao Y, Cao H, Song Y, Feng Y, Ding X, Pang M, Zhang Y, Zhang H, Ding J, Xia X. Zhao Y, et al. Int J Mol Med. 2016 Jun;37(6):1511-20. doi: 10.3892/ijmm.2016.2565. Epub 2016 Apr 14. Int J Mol Med. 2016. PMID: 27082122 Free PMC article.

5

Epidemiology of desmin and cardiac actin gene mutations in a european population of dilated cardiomyopathy.

Tesson F, Sylvius N, Pilotto A, Dubosq-Bidot L, Peuchmaurd M, Bouchier C, Benaiche A, Mangin L, Charron P, Gavazzi A, Tavazzi L, Arbustini E, Komajda M. Tesson F, et al. Eur Heart J. 2000 Nov;21(22):1872-6. doi: 10.1053/euhj.2000.2245. Eur Heart J. 2000. PMID: 11052860

6

A novel alpha-tropomyosin mutation associates with dilated and non-compaction cardiomyopathy and diminishes actin binding.

van de Meerakker JB, Christiaans I, Barnett P, Lekanne Deprez RH, Ilgun A, Mook OR, Mannens MM, Lam J, Wilde AA, Moorman AF, Postma AV. van de Meerakker JB, et al. Biochim Biophys Acta. 2013 Apr;1833(4):833-9. doi: 10.1016/j.bbamcr.2012.11.003. Epub 2012 Nov 9. Biochim Biophys Acta. 2013. PMID: 23147248 Free article.

7

Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes.

Kaski JP, Syrris P, Burch M, Tomé-Esteban MT, Fenton M, Christiansen M, Andersen PS, Sebire N, Ashworth M, Deanfield JE, McKenna WJ, Elliott PM. Kaski JP, et al. Heart. 2008 Nov;94(11):1478-84. doi: 10.1136/hrt.2007.134684. Epub 2008 May 8. Heart. 2008. PMID: 18467357

8

Mutational analysis of the cardiac actin gene in familial and sporadic dilated cardiomyopathy.

Takai E, Akita H, Shiga N, Kanazawa K, Yamada S, Terashima M, Matsuda Y, Iwai C, Kawai K, Yokota Y, Yokoyama M. Takai E, et al. Am J Med Genet. 1999 Oct 8;86(4):325-7. doi: 10.1002/(sici)1096-8628(19991008)86:4<325::aid-ajmg5>3.0.co;2-u. Am J Med Genet. 1999. PMID: 10494087

9

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.

Nowak KJ, Wattanasirichaigoon D, Goebel HH, Wilce M, Pelin K, Donner K, Jacob RL, Hübner C, Oexle K, Anderson JR, Verity CM, North KN, Iannaccone ST, Müller CR, Nürnberg P, Muntoni F, Sewry C, Hughes I, Sutphen R, Lacson AG, Swoboda KJ, Vigneron J, Wallgren-Pettersson C, Beggs AH, Laing NG. Nowak KJ, et al. Nat Genet. 1999 Oct;23(2):208-12. doi: 10.1038/13837. Nat Genet. 1999. PMID: 10508519

10

A missense variant in desmoglein-2 predisposes to dilated cardiomyopathy.

Posch MG, Posch MJ, Geier C, Erdmann B, Mueller W, Richter A, Ruppert V, Pankuweit S, Maisch B, Perrot A, Buttgereit J, Dietz R, Haverkamp W, Ozcelik C. Posch MG, et al. Mol Genet Metab. 2008 Sep-Oct;95(1-2):74-80. doi: 10.1016/j.ymgme.2008.06.005. Epub 2008 Aug 3. Mol Genet Metab. 2008. PMID: 18678517

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