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Page 1
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: berul ci. Circ Res. 2001 Mar 2;88(4):383-9. doi: 10.1161/01.res.88.4.383. Circ Res. 2001. PMID: 11230104
Cardiomyopathy in Irx4-deficient mice is preceded by abnormal ventricular gene expression.
Bruneau BG, Bao ZZ, Fatkin D, Xavier-Neto J, Georgakopoulos D, Maguire CT, Berul CI, Kass DA, Kuroski-de Bold ML, de Bold AJ, Conner DA, Rosenthal N, Cepko CL, Seidman CE, Seidman JG. Bruneau BG, et al. Among authors: berul ci. Mol Cell Biol. 2001 Mar;21(5):1730-6. doi: 10.1128/MCB.21.5.1730-1736.2001. Mol Cell Biol. 2001. PMID: 11238910 Free PMC article.
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: berul ci. Circulation. 2003 Jun 10;107(22):2850-6. doi: 10.1161/01.CIR.0000075270.13497.2B. Epub 2003 Jun 2. Circulation. 2003. PMID: 12782567
A mouse model of congenital heart disease: cardiac arrhythmias and atrial septal defect caused by haploinsufficiency of the cardiac transcription factor Csx/Nkx2.5.
Tanaka M, Berul CI, Ishii M, Jay PY, Wakimoto H, Douglas P, Yamasaki N, Kawamoto T, Gehrmann J, Maguire CT, Schinke M, Seidman CE, Seidman JG, Kurachi Y, Izumo S. Tanaka M, et al. Among authors: berul ci. Cold Spring Harb Symp Quant Biol. 2002;67:317-25. doi: 10.1101/sqb.2002.67.317. Cold Spring Harb Symp Quant Biol. 2002. PMID: 12858555 No abstract available.
251 results