PubMed (GeneRIF) for id: 282996

Year	Number of Results
2009	2
2010	2
2011	1
2012	2
2013	2
2014	2
2015	1
2016	4
2017	1
2018	5
2019	3
2020	4
2021	5
2022	3
2023	2
2024	0

1

[Research progress on the expression of the RBM20 gene in dilated cardiomyopathy].

Lin X. Lin X. Zhongguo Dang Dai Er Ke Za Zhi. 2023 Oct 15;25(10):1084-1088. doi: 10.7499/j.issn.1008-8830.2306087. Zhongguo Dang Dai Er Ke Za Zhi. 2023. PMID: 37905768 Free PMC article. Review. Chinese.

2

Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants.

Cannie DE, Protonotarios A, Bakalakos A, Syrris P, Lorenzini M, De Stavola B, Bjerregaard L, Dybro AM, Hey TM, Hansen FG, Navarro Peñalver M, Crespo-Leiro MG, Larrañaga-Moreira JM, de Frutos F, Johnson R, Slater TA, Monserrat L, Sengupta A, Mestroni L, Taylor MRG, Sinagra G, Bilinska Z, Solla-Ruiz I, Arana Achaga X, Barriales-Villa R, Garcia-Pavia P, Gimeno JR, Dal Ferro M, Merlo M, Wahbi K, Fatkin D, Mogensen J, Rasmussen TB, Elliott PM. Cannie DE, et al. Circ Genom Precis Med. 2023 Oct;16(5):434-441. doi: 10.1161/CIRCGEN.123.004059. Epub 2023 Aug 18. Circ Genom Precis Med. 2023. PMID: 37593875 Free PMC article.

3

I536T variant of RBM20 affects splicing of cardiac structural proteins that are causative for developing dilated cardiomyopathy.

Yamamoto T, Sano R, Miura A, Imasaka M, Naito Y, Nishiguchi M, Ihara K, Otani N, Kominato Y, Ohmuraya M, Kuroyanagi H, Nishio H. Yamamoto T, et al. J Mol Med (Berl). 2022 Dec;100(12):1741-1754. doi: 10.1007/s00109-022-02262-8. Epub 2022 Oct 5. J Mol Med (Berl). 2022. PMID: 36198914 Free PMC article.

4

SR Protein Kinases Regulate the Splicing of Cardiomyopathy-Relevant Genes via Phosphorylation of the RSRSP Stretch in RBM20.

Sun M, Jin Y, Zhang Y, Gregorich ZR, Ren J, Ge Y, Guo W. Sun M, et al. Genes (Basel). 2022 Aug 25;13(9):1526. doi: 10.3390/genes13091526. Genes (Basel). 2022. PMID: 36140694 Free PMC article.

5

RBM20^S639G mutation is a high genetic risk factor for premature death through RNA-protein condensates.

Wang C, Zhang Y, Methawasin M, Braz CU, Gao-Hu J, Yang B, Strom J, Gohlke J, Hacker T, Khatib H, Granzier H, Guo W. Wang C, et al. J Mol Cell Cardiol. 2022 Apr;165:115-129. doi: 10.1016/j.yjmcc.2022.01.004. Epub 2022 Jan 15. J Mol Cell Cardiol. 2022. PMID: 35041844 Free PMC article.

6

Gain-of-function cardiomyopathic mutations in RBM20 rewire splicing regulation and re-distribute ribonucleoprotein granules within processing bodies.

Fenix AM, Miyaoka Y, Bertero A, Blue SM, Spindler MJ, Tan KKB, Perez-Bermejo JA, Chan AH, Mayerl SJ, Nguyen TD, Russell CR, Lizarraga PP, Truong A, So PL, Kulkarni A, Chetal K, Sathe S, Sniadecki NJ, Yeo GW, Murry CE, Conklin BR, Salomonis N. Fenix AM, et al. Nat Commun. 2021 Nov 3;12(1):6324. doi: 10.1038/s41467-021-26623-y. Nat Commun. 2021. PMID: 34732726 Free PMC article.

7

RBM20 Is a Candidate Gene for Hypertrophic Cardiomyopathy.

Dai J, Li Z, Huang W, Chen P, Sun Y, Wang H, Wu D, Chen Y, Li C, Xiao L, Liu H, Wei H, Li R, Duan Q, Peng L, Song X, Yu T, Wang Y, Wang DW. Dai J, et al. Can J Cardiol. 2021 Nov;37(11):1751-1759. doi: 10.1016/j.cjca.2021.07.014. Epub 2021 Jul 29. Can J Cardiol. 2021. PMID: 34333030 Free article.

8

The Combined Human Genotype of Truncating TTN and RBM20 Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy.

Gaertner A, Bloebaum J, Brodehl A, Klauke B, Sielemann K, Kassner A, Fox H, Morshuis M, Tiesmeier J, Schulz U, Knoell R, Gummert J, Milting H. Gaertner A, et al. Genes (Basel). 2021 Jun 8;12(6):883. doi: 10.3390/genes12060883. Genes (Basel). 2021. PMID: 34201072 Free PMC article.

9

Phenotype and progression among patients with dilated cardiomyopathy and RBM20 mutations.

Robles-Mezcua A, Rodríguez-Miranda L, Morcillo-Hidalgo L, Jiménez-Navarro M, García-Pinilla JM. Robles-Mezcua A, et al. Eur J Med Genet. 2021 Sep;64(9):104278. doi: 10.1016/j.ejmg.2021.104278. Epub 2021 Jun 24. Eur J Med Genet. 2021. PMID: 34174465

10

RBM20-Associated Ventricular Arrhythmias in a Patient with Structurally Normal Heart.

Vakhrushev Y, Kozyreva A, Semenov A, Sokolnikova P, Lubimtseva T, Lebedev D, Smolina N, Zhuk S, Mitrofanova L, Vasichkina E, Kostareva A. Vakhrushev Y, et al. Genes (Basel). 2021 Jan 13;12(1):94. doi: 10.3390/genes12010094. Genes (Basel). 2021. PMID: 33450993 Free PMC article.

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