Chen SN - Search Results

1

Echocardiographic Strain Abnormalities Precede Left Ventricular Hypertrophy Development in Hypertrophic Cardiomyopathy Mutation Carriers.

Canciello G, Lombardi R, Borrelli F, Ordine L, Chen SN, Santoro C, Frisso G, di Napoli S, Polizzi R, Cristiano S, Esposito G, Losi MA. Canciello G, et al. Among authors: chen sn. Int J Mol Sci. 2024 Jul 25;25(15):8128. doi: 10.3390/ijms25158128. Int J Mol Sci. 2024. PMID: 39125703 Free PMC article.

2

Editorial of Special Issue "Genetics and Molecular Pathogenesis of Non-Ischemic Cardiomyopathies".

Lombardi R, Chen SN. Lombardi R, et al. Among authors: chen sn. Int J Mol Sci. 2020 Dec 10;21(24):9398. doi: 10.3390/ijms21249398. Int J Mol Sci. 2020. PMID: 33321793 Free PMC article.

3

Established and Emerging Mechanisms in the Pathogenesis of Arrhythmogenic Cardiomyopathy: A Multifaceted Disease.

Gao S, Puthenvedu D, Lombardi R, Chen SN. Gao S, et al. Among authors: chen sn. Int J Mol Sci. 2020 Aug 31;21(17):6320. doi: 10.3390/ijms21176320. Int J Mol Sci. 2020. PMID: 32878278 Free PMC article. Review.

4

A polygenic risk score after corrective surgery for transposition of the great arteries: Can genetics add value to clinical predictors of outcome?

Lombardi R, Chen SN. Lombardi R, et al. Among authors: chen sn. Int J Cardiol. 2023 Feb 15;373:55-56. doi: 10.1016/j.ijcard.2022.11.044. Epub 2022 Nov 25. Int J Cardiol. 2023. PMID: 36442671 No abstract available.

5

Arrhythmogenic Cardiomyopathy and Skeletal Muscle Dystrophies: Shared Histopathological Features and Pathogenic Mechanisms.

Gao S, Chen SN, Di Nardo C, Lombardi R. Gao S, et al. Among authors: chen sn. Front Physiol. 2020 Jul 30;11:834. doi: 10.3389/fphys.2020.00834. eCollection 2020. Front Physiol. 2020. PMID: 32848821 Free PMC article. Review.

6

Antifibrotic effects of antioxidant N-acetylcysteine in a mouse model of human hypertrophic cardiomyopathy mutation.

Marian AJ, Senthil V, Chen SN, Lombardi R. Marian AJ, et al. Among authors: chen sn. J Am Coll Cardiol. 2006 Feb 21;47(4):827-34. doi: 10.1016/j.jacc.2005.10.041. Epub 2006 Jan 26. J Am Coll Cardiol. 2006. PMID: 16487852 Free PMC article.

7

Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy.

Daw EW, Chen SN, Czernuszewicz G, Lombardi R, Lu Y, Ma J, Roberts R, Shete S, Marian AJ. Daw EW, et al. Among authors: chen sn. Hum Mol Genet. 2007 Oct 15;16(20):2463-71. doi: 10.1093/hmg/ddm202. Epub 2007 Jul 25. Hum Mol Genet. 2007. PMID: 17652099 Free PMC article.

8

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy.

Osio A, Tan L, Chen SN, Lombardi R, Nagueh SF, Shete S, Roberts R, Willerson JT, Marian AJ. Osio A, et al. Among authors: chen sn. Circ Res. 2007 Mar 30;100(6):766-8. doi: 10.1161/01.RES.0000263008.66799.aa. Epub 2007 Mar 8. Circ Res. 2007. PMID: 17347475 Free PMC article.

9

Pathogenesis of hypertrophic cardiomyopathy caused by myozenin 2 mutations is independent of calcineurin activity.

Ruggiero A, Chen SN, Lombardi R, Rodriguez G, Marian AJ. Ruggiero A, et al. Among authors: chen sn. Cardiovasc Res. 2013 Jan 1;97(1):44-54. doi: 10.1093/cvr/cvs294. Epub 2012 Sep 17. Cardiovasc Res. 2013. PMID: 22987565 Free PMC article.

10

DNA Damage Response/TP53 Pathway Is Activated and Contributes to the Pathogenesis of Dilated Cardiomyopathy Associated With LMNA (Lamin A/C) Mutations.

Chen SN, Lombardi R, Karmouch J, Tsai JY, Czernuszewicz G, Taylor MRG, Mestroni L, Coarfa C, Gurha P, Marian AJ. Chen SN, et al. Circ Res. 2019 Mar 15;124(6):856-873. doi: 10.1161/CIRCRESAHA.118.314238. Circ Res. 2019. PMID: 30696354 Free PMC article.

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