Wakimoto H - Search Results

1

Mouse Model of Human Congenital Heart Disease: Progressive Atrioventricular Block Induced by a Heterozygous Nkx2-5 Homeodomain Missense Mutation.

Chowdhury R, Ashraf H, Melanson M, Tanada Y, Nguyen M, Silberbach M, Wakimoto H, Benson DW, Anderson RH, Kasahara H. Chowdhury R, et al. Among authors: wakimoto h. Circ Arrhythm Electrophysiol. 2015 Oct;8(5):1255-64. doi: 10.1161/CIRCEP.115.002720. Epub 2015 Jul 30. Circ Arrhythm Electrophysiol. 2015. PMID: 26226998 Free PMC article.

2

Maturational atrioventricular nodal physiology in the mouse.

Maguire CT, Bevilacqua LM, Wakimoto H, Gehrmann J, Berul CI. Maguire CT, et al. Among authors: wakimoto h. J Cardiovasc Electrophysiol. 2000 May;11(5):557-64. doi: 10.1111/j.1540-8167.2000.tb00009.x. J Cardiovasc Electrophysiol. 2000. PMID: 10826935

3

Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein.

Kasahara H, Wakimoto H, Liu M, Maguire CT, Converso KL, Shioi T, Huang WY, Manning WJ, Paul D, Lawitts J, Berul CI, Izumo S. Kasahara H, et al. Among authors: wakimoto h. J Clin Invest. 2001 Jul;108(2):189-201. doi: 10.1172/JCI12694. J Clin Invest. 2001. PMID: 11457872 Free PMC article.

4

Developmentally modulated cardiac conduction failure in transgenic mice with fetal or postnatal overexpression of DNA nonbinding mutant Nkx2.5.

Wakimoto H, Kasahara H, Maguire CT, Izumo S, Berul CI. Wakimoto H, et al. J Cardiovasc Electrophysiol. 2002 Jul;13(7):682-8. doi: 10.1046/j.1540-8167.2002.00682.x. J Cardiovasc Electrophysiol. 2002. PMID: 12139292

5

Nkx2.5 homeoprotein regulates expression of gap junction protein connexin 43 and sarcomere organization in postnatal cardiomyocytes.

Kasahara H, Ueyama T, Wakimoto H, Liu MK, Maguire CT, Converso KL, Kang PM, Manning WJ, Lawitts J, Paul DL, Berul CI, Izumo S. Kasahara H, et al. Among authors: wakimoto h. J Mol Cell Cardiol. 2003 Mar;35(3):243-56. doi: 10.1016/s0022-2828(03)00002-6. J Mol Cell Cardiol. 2003. PMID: 12676539

6

Cardiac electrophysiological phenotypes in postnatal expression of Nkx2.5 transgenic mice.

Wakimoto H, Kasahara H, Maguire CT, Moskowitz IP, Izumo S, Berul CI. Wakimoto H, et al. Genesis. 2003 Nov;37(3):144-50. doi: 10.1002/gene.10236. Genesis. 2003. PMID: 14595838

7

Absence of Msx2 does not affect cardiac conduction or rescue conduction defects associated with Nkx2-5 mutation.

Jay PY, Maguire CT, Wakimoto H, Izumo S, Berul CI. Jay PY, et al. Among authors: wakimoto h. J Cardiovasc Electrophysiol. 2005 Jan;16(1):82-5. doi: 10.1046/j.1540-8167.2005.04365.x. J Cardiovasc Electrophysiol. 2005. PMID: 15673394

8

Perinatal loss of Nkx2-5 results in rapid conduction and contraction defects.

Briggs LE, Takeda M, Cuadra AE, Wakimoto H, Marks MH, Walker AJ, Seki T, Oh SP, Lu JT, Sumners C, Raizada MK, Horikoshi N, Weinberg EO, Yasui K, Ikeda Y, Chien KR, Kasahara H. Briggs LE, et al. Among authors: wakimoto h. Circ Res. 2008 Sep 12;103(6):580-90. doi: 10.1161/CIRCRESAHA.108.171835. Epub 2008 Aug 8. Circ Res. 2008. PMID: 18689573 Free PMC article.

9

Slow progressive conduction and contraction defects in loss of Nkx2-5 mice after cardiomyocyte terminal differentiation.

Takeda M, Briggs LE, Wakimoto H, Marks MH, Warren SA, Lu JT, Weinberg EO, Robertson KD, Chien KR, Kasahara H. Takeda M, et al. Among authors: wakimoto h. Lab Invest. 2009 Sep;89(9):983-93. doi: 10.1038/labinvest.2009.59. Epub 2009 Jun 22. Lab Invest. 2009. PMID: 19546853 Free PMC article.

10

A targeted disruption in connexin40 leads to distinct atrioventricular conduction defects.

Bevilacqua LM, Simon AM, Maguire CT, Gehrmann J, Wakimoto H, Paul DL, Berul CI. Bevilacqua LM, et al. Among authors: wakimoto h. J Interv Card Electrophysiol. 2000 Oct;4(3):459-67. doi: 10.1023/a:1009800328836. J Interv Card Electrophysiol. 2000. PMID: 11046183

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