Takeda S - Search Results

1

Differential roles of MMP-9 in early and late stages of dystrophic muscles in a mouse model of Duchenne muscular dystrophy.

Shiba N, Miyazaki D, Yoshizawa T, Fukushima K, Shiba Y, Inaba Y, Imamura M, Takeda S, Koike K, Nakamura A. Shiba N, et al. Among authors: takeda s. Biochim Biophys Acta. 2015 Oct;1852(10 Pt A):2170-82. doi: 10.1016/j.bbadis.2015.07.008. Epub 2015 Jul 10. Biochim Biophys Acta. 2015. PMID: 26170062 Free article.

2

A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans.

Yoshida K, Furihata K, Takeda S, Nakamura A, Yamamoto K, Morita H, Hiyamuta S, Ikeda S, Shimizu N, Yanagisawa N. Yoshida K, et al. Among authors: takeda s. Nat Genet. 1995 Mar;9(3):267-72. doi: 10.1038/ng0395-267. Nat Genet. 1995. PMID: 7539672

3

Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy.

Yoshida K, Ikeda S, Nakamura A, Kagoshima M, Takeda S, Shoji S, Yanagisawa N. Yoshida K, et al. Among authors: takeda s. Muscle Nerve. 1993 Nov;16(11):1161-6. doi: 10.1002/mus.880161104. Muscle Nerve. 1993. PMID: 8413368

4

Reduction of serum IgG level and peripheral T-cell counts are correlated with CTG repeat lengths in myotonic dystrophy patients.

Nakamura A, Kojo T, Arahata K, Takeda S. Nakamura A, et al. Among authors: takeda s. Neuromuscul Disord. 1996 May;6(3):203-10. doi: 10.1016/0960-8966(96)00010-7. Neuromuscul Disord. 1996. PMID: 8784809

5

Insertional mutation by transposable element, L1, in the DMD gene results in X-linked dilated cardiomyopathy.

Yoshida K, Nakamura A, Yazaki M, Ikeda S, Takeda S. Yoshida K, et al. Among authors: takeda s. Hum Mol Genet. 1998 Jul;7(7):1129-32. doi: 10.1093/hmg/7.7.1129. Hum Mol Genet. 1998. PMID: 9618170

6

A novel Sac I RFLP in the 3' untranslated region of the myotonin protein kinase gene.

Nakamura A, Minami N, Kamitani T, Kamakura K, Arahata K, Takeda S. Nakamura A, et al. Among authors: takeda s. J Hum Genet. 1999;44(2):135-7. doi: 10.1007/s100380050128. J Hum Genet. 1999. PMID: 10083743

7

[Glycerol kinase deficiency with dystrophinopathy].

Nakamura A, Takeda S. Nakamura A, et al. Among authors: takeda s. Ryoikibetsu Shokogun Shirizu. 2001;(35):28-30. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11555931 Review. Japanese. No abstract available.

8

Progression of dystrophic features and activation of mitogen-activated protein kinases and calcineurin by physical exercise, in hearts of mdx mice.

Nakamura A, Yoshida K, Takeda S, Dohi N, Ikeda S. Nakamura A, et al. Among authors: takeda s. FEBS Lett. 2002 Jun 5;520(1-3):18-24. doi: 10.1016/s0014-5793(02)02739-4. FEBS Lett. 2002. PMID: 12044863 Free article.

9

Alpha1-syntrophin-deficient skeletal muscle exhibits hypertrophy and aberrant formation of neuromuscular junctions during regeneration.

Hosaka Y, Yokota T, Miyagoe-Suzuki Y, Yuasa K, Imamura M, Matsuda R, Ikemoto T, Kameya S, Takeda S. Hosaka Y, et al. Among authors: takeda s. J Cell Biol. 2002 Sep 16;158(6):1097-107. doi: 10.1083/jcb.200204076. Epub 2002 Sep 9. J Cell Biol. 2002. PMID: 12221071 Free PMC article.

10

Identification and characterization of epsilon-sarcoglycans in the central nervous system.

Nishiyama A, Endo T, Takeda S, Imamura M. Nishiyama A, et al. Among authors: takeda s. Brain Res Mol Brain Res. 2004 Jun 18;125(1-2):1-12. doi: 10.1016/j.molbrainres.2004.01.012. Brain Res Mol Brain Res. 2004. PMID: 15193417

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