Similar articles for PMID: 19151713

Year	Number of Results
1994	1
1997	1
1998	3
2000	1
2001	2
2002	1
2003	3
2004	1
2006	1
2007	2
2008	4
2009	4
2010	4
2011	4
2012	3
2013	2
2014	5
2015	5
2016	6
2017	10
2018	8
2019	5
2020	6
2021	2
2022	1
2024	0

1

A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia.

Dhandapany PS, Sadayappan S, Xue Y, Powell GT, Rani DS, Nallari P, Rai TS, Khullar M, Soares P, Bahl A, Tharkan JM, Vaideeswar P, Rathinavel A, Narasimhan C, Ayapati DR, Ayub Q, Mehdi SQ, Oppenheimer S, Richards MB, Price AL, Patterson N, Reich D, Singh L, Tyler-Smith C, Thangaraj K. Dhandapany PS, et al. Nat Genet. 2009 Feb;41(2):187-91. doi: 10.1038/ng.309. Epub 2009 Jan 18. Nat Genet. 2009. PMID: 19151713 Free PMC article.

2

Limited distribution of a cardiomyopathy-associated variant in India.

Simonson TS, Zhang Y, Huff CD, Xing J, Watkins WS, Witherspoon DJ, Woodward SR, Jorde LB. Simonson TS, et al. Ann Hum Genet. 2010 Mar;74(2):184-8. doi: 10.1111/j.1469-1809.2010.00561.x. Epub 2010 Feb 18. Ann Hum Genet. 2010. PMID: 20201939 Free PMC article.

3

Role of common sarcomeric gene polymorphisms in genetic susceptibility to left ventricular dysfunction.

Kumar S, Mishra A, Srivastava A, Bhatt M, Garg N, Agarwal SK, Pande S, Mittal B. Kumar S, et al. J Genet. 2016 Jun;95(2):263-72. doi: 10.1007/s12041-016-0623-4. J Genet. 2016. PMID: 27350668 Free article.

4

Unexpected myopathy associated with a mutation in MYBPC3 and misplacement of the cardiac myosin binding protein C.

Tajsharghi H, Leren TP, Abdul-Hussein S, Tulinius M, Brunvand L, Dahl HM, Oldfors A. Tajsharghi H, et al. J Med Genet. 2010 Aug;47(8):575-7. doi: 10.1136/jmg.2009.072710. Epub 2009 Oct 26. J Med Genet. 2010. PMID: 19858127

5

Generation of a new human induced pluripotent stem cell (hiPSC) line from a South Asian Indian with a MYBPC3^Δ^25bp variant.

Chimata P, Kashyap DK, Sairam T, Ganesh A, Thangaraj K, Purushottam M, Viswanath B, Jain S, Dhandapany PS. Chimata P, et al. Stem Cell Res. 2022 Dec;65:102978. doi: 10.1016/j.scr.2022.102978. Epub 2022 Nov 15. Stem Cell Res. 2022. PMID: 36403549 Free article.

6

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. Waldmüller S, et al. J Mol Cell Cardiol. 2003 Jun;35(6):623-36. doi: 10.1016/s0022-2828(03)00050-6. J Mol Cell Cardiol. 2003. PMID: 12788380

7

Cardiac myosin-binding protein C (MYBPC3) in cardiac pathophysiology.

Carrier L, Mearini G, Stathopoulou K, Cuello F. Carrier L, et al. Gene. 2015 Dec 1;573(2):188-97. doi: 10.1016/j.gene.2015.09.008. Epub 2015 Sep 8. Gene. 2015. PMID: 26358504 Free PMC article. Review.

8

Genetic, clinical, molecular, and pathogenic aspects of the South Asian-specific polymorphic MYBPC3^Δ25bp variant.

Arif M, Nabavizadeh P, Song T, Desai D, Singh R, Bazrafshan S, Kumar M, Wang Y, Gilbert RJ, Dhandapany PS, Becker RC, Kranias EG, Sadayappan S. Arif M, et al. Biophys Rev. 2020 Aug;12(4):1065-1084. doi: 10.1007/s12551-020-00725-1. Epub 2020 Jul 12. Biophys Rev. 2020. PMID: 32656747 Free PMC article. Review.

9

Detection of a large duplication mutation in the myosin-binding protein C3 gene in a case of hypertrophic cardiomyopathy.

Meyer T, Pankuweit S, Richter A, Maisch B, Ruppert V. Meyer T, et al. Gene. 2013 Sep 15;527(1):416-20. doi: 10.1016/j.gene.2013.06.025. Epub 2013 Jun 29. Gene. 2013. PMID: 23816408

10

Association of 25 bp deletion in MYBPC3 gene with left ventricle dysfunction in coronary artery disease patients.

Srivastava A, Garg N, Mittal T, Khanna R, Gupta S, Seth PK, Mittal B. Srivastava A, et al. PLoS One. 2011;6(9):e24123. doi: 10.1371/journal.pone.0024123. Epub 2011 Sep 7. PLoS One. 2011. PMID: 21915287 Free PMC article.

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