Komuro I - Search Results

1

Deficiency of Myo18B in mice results in embryonic lethality with cardiac myofibrillar aberrations.

Ajima R, Akazawa H, Kodama M, Takeshita F, Otsuka A, Kohno T, Komuro I, Ochiya T, Yokota J. Ajima R, et al. Among authors: komuro i. Genes Cells. 2008 Oct;13(10):987-99. doi: 10.1111/j.1365-2443.2008.01226.x. Epub 2008 Aug 29. Genes Cells. 2008. PMID: 18761673 Free article.

2

Molecular mechanism of cardiac cellular hypertrophy by mechanical stress.

Yamazaki T, Komuro I, Yazaki Y. Yamazaki T, et al. Among authors: komuro i. J Mol Cell Cardiol. 1995 Jan;27(1):133-40. doi: 10.1016/s0022-2828(08)80013-2. J Mol Cell Cardiol. 1995. PMID: 7760338 Review.

3

Molecular cloning and characterization of human cardiac homeobox gene CSX1.

Shiojima I, Komuro I, Mizuno T, Aikawa R, Akazawa H, Oka T, Yamazaki T, Yazaki Y. Shiojima I, et al. Among authors: komuro i. Circ Res. 1996 Nov;79(5):920-9. doi: 10.1161/01.res.79.5.920. Circ Res. 1996. PMID: 8888684

4

Downregulation of polo-like kinase correlates with loss of proliferative ability of cardiac myocytes.

Georgescu SP, Komuro I, Hiroi Y, Mizuno T, Kudoh S, Yamazaki T, Yazaki Y. Georgescu SP, et al. Among authors: komuro i. J Mol Cell Cardiol. 1997 Mar;29(3):929-37. doi: 10.1006/jmcc.1996.0334. J Mol Cell Cardiol. 1997. PMID: 9152854

5

Autoregulation of human cardiac homeobox gene CSX1: mediation by the enhancer element in the first intron.

Oka T, Komuro I, Shiojima I, Hiroi Y, Mizuno T, Aikawa R, Akazawa H, Yamazaki T, Yazaki Y. Oka T, et al. Among authors: komuro i. Heart Vessels. 1997;Suppl 12:10-4. Heart Vessels. 1997. PMID: 9476533 Review.

6

Context-dependent transcriptional cooperation mediated by cardiac transcription factors Csx/Nkx-2.5 and GATA-4.

Shiojima I, Komuro I, Oka T, Hiroi Y, Mizuno T, Takimoto E, Monzen K, Aikawa R, Akazawa H, Yamazaki T, Kudoh S, Yazaki Y. Shiojima I, et al. Among authors: komuro i. J Biol Chem. 1999 Mar 19;274(12):8231-9. doi: 10.1074/jbc.274.12.8231. J Biol Chem. 1999. PMID: 10075728 Free article.

7

Targeted disruption of the homeobox transcription factor Bapx1 results in lethal skeletal dysplasia with asplenia and gastroduodenal malformation.

Akazawa H, Komuro I, Sugitani Y, Yazaki Y, Nagai R, Noda T. Akazawa H, et al. Among authors: komuro i. Genes Cells. 2000 Jun;5(6):499-513. doi: 10.1046/j.1365-2443.2000.00339.x. Genes Cells. 2000. PMID: 10886375 Free article.

8

Functional analyses of three Csx/Nkx-2.5 mutations that cause human congenital heart disease.

Zhu W, Shiojima I, Hiroi Y, Zou Y, Akazawa H, Mizukami M, Toko H, Yazaki Y, Nagai R, Komuro I. Zhu W, et al. Among authors: komuro i. J Biol Chem. 2000 Nov 10;275(45):35291-6. doi: 10.1074/jbc.M000525200. J Biol Chem. 2000. PMID: 10948187 Free article.

9

Rho plays an important role in angiotensin II-induced hypertrophic responses in cardiac myocytes.

Aikawa R, Komuro I, Nagai R, Yazaki Y. Aikawa R, et al. Among authors: komuro i. Mol Cell Biochem. 2000 Sep;212(1-2):177-82. Mol Cell Biochem. 2000. PMID: 11108149

10

Smads, TAK1, and their common target ATF-2 play a critical role in cardiomyocyte differentiation.

Monzen K, Hiroi Y, Kudoh S, Akazawa H, Oka T, Takimoto E, Hayashi D, Hosoda T, Kawabata M, Miyazono K, Ishii S, Yazaki Y, Nagai R, Komuro I. Monzen K, et al. Among authors: komuro i. J Cell Biol. 2001 May 14;153(4):687-98. doi: 10.1083/jcb.153.4.687. J Cell Biol. 2001. PMID: 11352931 Free PMC article.

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