Similar articles for PMID: 31430208

Year	Number of Results
1995	1
1998	2
1999	5
2000	2
2001	7
2002	1
2003	3
2004	1
2005	3
2006	4
2007	6
2008	6
2009	7
2010	10
2011	4
2012	9
2013	7
2014	11
2015	14
2016	13
2017	8
2018	11
2019	7
2020	14
2021	20
2022	13
2023	7
2024	0

1

Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy.

Frank D, Yusuf Rangrez A, Friedrich C, Dittmann S, Stallmeyer B, Yadav P, Bernt A, Schulze-Bahr E, Borlepawar A, Zimmermann WH, Peischard S, Seebohm G, Linke WA, Baba HA, Krüger M, Unger A, Usinger P, Frey N, Schulze-Bahr E. Frank D, et al. Circ Genom Precis Med. 2019 Aug;12(8):e002491. doi: 10.1161/CIRCGEN.119.002491. Epub 2019 Aug 20. Circ Genom Precis Med. 2019. PMID: 31430208 Free article.

2

A cardiac α-actin (ACTC1) p. Gly247Asp mutation inhibits SRF-signaling in vitro in neonatal rat cardiomyocytes.

Rangrez AY, Kilian L, Stiebeling K, Dittmann S, Schulze-Bahr E, Frey N, Frank D. Rangrez AY, et al. Biochem Biophys Res Commun. 2019 Oct 20;518(3):500-505. doi: 10.1016/j.bbrc.2019.08.081. Epub 2019 Aug 18. Biochem Biophys Res Commun. 2019. PMID: 31434612

3

Alpha-cardiac actin mutations produce atrial septal defects.

Matsson H, Eason J, Bookwalter CS, Klar J, Gustavsson P, Sunnegårdh J, Enell H, Jonzon A, Vikkula M, Gutierrez I, Granados-Riveron J, Pope M, Bu'Lock F, Cox J, Robinson TE, Song F, Brook DJ, Marston S, Trybus KM, Dahl N. Matsson H, et al. Hum Mol Genet. 2008 Jan 15;17(2):256-65. doi: 10.1093/hmg/ddm302. Epub 2007 Oct 18. Hum Mol Genet. 2008. PMID: 17947298

4

Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect.

Greenway SC, McLeod R, Hume S, Roslin NM, Alvarez N, Giuffre M, Zhan SH, Shen Y, Preuss C, Andelfinger G; FORGE Canada Consortium; Jones SJ, Gerull B. Greenway SC, et al. Can J Cardiol. 2014 Feb;30(2):181-7. doi: 10.1016/j.cjca.2013.12.003. Epub 2013 Dec 6. Can J Cardiol. 2014. PMID: 24461919

5

Data on the role of cardiac α-actin (ACTC1) gene mutations on SRF-signaling.

Rangrez AY, Kilian L, Stiebeling K, Dittmann S, Yadav P, Schulze-Bahr E, Frey N, Frank D. Rangrez AY, et al. Data Brief. 2020 Jan 2;28:105071. doi: 10.1016/j.dib.2019.105071. eCollection 2020 Feb. Data Brief. 2020. PMID: 31921954 Free PMC article.

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

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.

8

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.

Kamisago M, Sharma SD, DePalma SR, Solomon S, Sharma P, McDonough B, Smoot L, Mullen MP, Woolf PK, Wigle ED, Seidman JG, Seidman CE. Kamisago M, et al. N Engl J Med. 2000 Dec 7;343(23):1688-96. doi: 10.1056/NEJM200012073432304. N Engl J Med. 2000. PMID: 11106718 Free article.

9

A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defect.

Zhou YM, Dai XY, Huang RT, Xue S, Xu YJ, Qiu XB, Yang YQ. Zhou YM, et al. Mol Med Rep. 2016 Oct;14(4):3307-14. doi: 10.3892/mmr.2016.5609. Epub 2016 Aug 9. Mol Med Rep. 2016. PMID: 27510170

10

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

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