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Author Correction: Tbx5 maintains atrial identity in postnatal cardiomyocytes by regulating an atrial-specific enhancer network.
Sweat ME, Cao Y, Zhang X, Burnicka-Turek O, Perez-Cervantes C, Kulandaisamy A, Lu F, Keating EM, Akerberg BN, Ma Q, Wakimoto H, Gorham JM, Hill LD, Song MK, Trembley MA, Wang P, Gianeselli M, Prondzynski M, Bortolin RH, Bezzerides VJ, Chen K, Seidman JG, Seidman CE, Moskowitz IP, Pu WT. Sweat ME, et al. Among authors: moskowitz ip. Nat Cardiovasc Res. 2023 Nov;2(11):1095. doi: 10.1038/s44161-023-00373-0. Nat Cardiovasc Res. 2023. PMID: 39196102 No abstract available.
Defective sumoylation pathway directs congenital heart disease.
Wang J, Chen L, Wen S, Zhu H, Yu W, Moskowitz IP, Shaw GM, Finnell RH, Schwartz RJ. Wang J, et al. Among authors: moskowitz ip. Birth Defects Res A Clin Mol Teratol. 2011 Jun;91(6):468-76. doi: 10.1002/bdra.20816. Epub 2011 May 11. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21563299 Free PMC article.
Comparison of two murine models of familial hypertrophic cardiomyopathy.
McConnell BK, Fatkin D, Semsarian C, Jones KA, Georgakopoulos D, Maguire CT, Healey MJ, Mudd JO, Moskowitz IP, Conner DA, Giewat M, Wakimoto H, Berul CI, Schoen FJ, Kass DA, Seidman CE, Seidman JG. McConnell BK, et al. Among authors: moskowitz ip. Circ Res. 2001 Mar 2;88(4):383-9. doi: 10.1161/01.res.88.4.383. Circ Res. 2001. PMID: 11230104
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.
Arad M, Moskowitz IP, Patel VV, Ahmad F, Perez-Atayde AR, Sawyer DB, Walter M, Li GH, Burgon PG, Maguire CT, Stapleton D, Schmitt JP, Guo XX, Pizard A, Kupershmidt S, Roden DM, Berul CI, Seidman CE, Seidman JG. Arad M, et al. Among authors: moskowitz ip. Circulation. 2003 Jun 10;107(22):2850-6. doi: 10.1161/01.CIR.0000075270.13497.2B. Epub 2003 Jun 2. Circulation. 2003. PMID: 12782567
85 results