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2002 1
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Page 1
Special Issue "Cardiovascular Genetics".
Brodehl A, Milting H, Gerull B. Brodehl A, et al. Among authors: gerull b. Genes (Basel). 2021 Mar 26;12(4):479. doi: 10.3390/genes12040479. Genes (Basel). 2021. PMID: 33810227 Free PMC article.
RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing.
Guo W, Schafer S, Greaser ML, Radke MH, Liss M, Govindarajan T, Maatz H, Schulz H, Li S, Parrish AM, Dauksaite V, Vakeel P, Klaassen S, Gerull B, Thierfelder L, Regitz-Zagrosek V, Hacker TA, Saupe KW, Dec GW, Ellinor PT, MacRae CA, Spallek B, Fischer R, Perrot A, Özcelik C, Saar K, Hubner N, Gotthardt M. Guo W, et al. Among authors: gerull b. Nat Med. 2012 May;18(5):766-73. doi: 10.1038/nm.2693. Nat Med. 2012. PMID: 22466703 Free PMC article.
Have we found the genetic signature for vasovagal syncope?
Sheldon RS, Gerull B. Sheldon RS, et al. Among authors: gerull b. Eur Heart J. 2023 Mar 21;44(12):1081-1083. doi: 10.1093/eurheartj/ehac821. Eur Heart J. 2023. PMID: 36734005 No abstract available.
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy.
Gerull B, Heuser A, Wichter T, Paul M, Basson CT, McDermott DA, Lerman BB, Markowitz SM, Ellinor PT, MacRae CA, Peters S, Grossmann KS, Drenckhahn J, Michely B, Sasse-Klaassen S, Birchmeier W, Dietz R, Breithardt G, Schulze-Bahr E, Thierfelder L. Gerull B, et al. Nat Genet. 2004 Nov;36(11):1162-4. doi: 10.1038/ng1461. Epub 2004 Oct 17. Nat Genet. 2004. PMID: 15489853
Immuno-metabolic interfaces in cardiac disease and failure.
Bertero E, Dudek J, Cochain C, Delgobo M, Ramos G, Gerull B, Higuchi T, Vaeth M, Zernecke A, Frantz S, Hofmann U, Maack C. Bertero E, et al. Among authors: gerull b. Cardiovasc Res. 2022 Jan 7;118(1):37-52. doi: 10.1093/cvr/cvab036. Cardiovasc Res. 2022. PMID: 33537710 Review.
71 results