Sunada Y - Search Results

1

Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.

Takeda S, Kondo M, Sasaki J, Kurahashi H, Kano H, Arai K, Misaki K, Fukui T, Kobayashi K, Tachikawa M, Imamura M, Nakamura Y, Shimizu T, Murakami T, Sunada Y, Fujikado T, Matsumura K, Terashima T, Toda T. Takeda S, et al. Among authors: sunada y. Hum Mol Genet. 2003 Jun 15;12(12):1449-59. doi: 10.1093/hmg/ddg153. Hum Mol Genet. 2003. PMID: 12783852

2

Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy.

Toda T, Kobayashi K, Takeda S, Sasaki J, Kurahashi H, Kano H, Tachikawa M, Wang F, Nagai Y, Taniguchi K, Taniguchi M, Sunada Y, Terashima T, Endo T, Matsumura K. Toda T, et al. Among authors: sunada y. Congenit Anom (Kyoto). 2003 Jun;43(2):97-104. doi: 10.1111/j.1741-4520.2003.tb01033.x. Congenit Anom (Kyoto). 2003. PMID: 12893968 Review.

3

Deficiency of a 180-kDa extracellular matrix protein in Fukuyama type congenital muscular dystrophy skeletal muscle.

Sunada Y, Saito F, Higuchi I, Matsumura K, Shimizu T. Sunada Y, et al. Neuromuscul Disord. 2002 Feb;12(2):117-20. doi: 10.1016/s0960-8966(01)00251-6. Neuromuscul Disord. 2002. PMID: 11738352

4

The role of dystroglycan, a novel receptor of laminin and agrin, in cell differentiation.

Matsumura K, Yamada H, Saito F, Sunada Y, Shimizu T. Matsumura K, et al. Among authors: sunada y. Histol Histopathol. 1997 Jan;12(1):195-203. Histol Histopathol. 1997. PMID: 9046055 Review.

5

Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity.

Sunada Y, Ohi H, Hase A, Ohi H, Hosono T, Arata S, Higuchi S, Matsumura K, Shimizu T. Sunada Y, et al. Hum Mol Genet. 2001 Feb 1;10(3):173-8. doi: 10.1093/hmg/10.3.173. Hum Mol Genet. 2001. PMID: 11159934

6

Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin.

Kobayashi K, Sasaki J, Kondo-Iida E, Fukuda Y, Kinoshita M, Sunada Y, Nakamura Y, Toda T. Kobayashi K, et al. Among authors: sunada y. FEBS Lett. 2001 Feb 2;489(2-3):192-6. doi: 10.1016/s0014-5793(01)02088-9. FEBS Lett. 2001. PMID: 11165248 Free article.

7

Three-dimensional MR imaging of brain surface anomalies in Fukuyama-type congenital muscular dystrophy.

Toda T, Watanabe T, Matsumura K, Sunada Y, Yamada H, Nakano I, Mannen T, Kanazawa I, Shimizu T. Toda T, et al. Among authors: sunada y. Muscle Nerve. 1995 May;18(5):508-17. doi: 10.1002/mus.880180506. Muscle Nerve. 1995. PMID: 7739638

8

Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse.

Matsumura K, Yamada H, Saito F, Sunada Y, Shimizu T. Matsumura K, et al. Among authors: sunada y. Neuromuscul Disord. 1997 Jan;7(1):7-12. doi: 10.1016/s0960-8966(96)00402-6. Neuromuscul Disord. 1997. PMID: 9132144 Review.

9

Overexpression of P104L mutant caveolin-3 in mice develops hypertrophic cardiomyopathy with enhanced contractility in association with increased endothelial nitric oxide synthase activity.

Ohsawa Y, Toko H, Katsura M, Morimoto K, Yamada H, Ichikawa Y, Murakami T, Ohkuma S, Komuro I, Sunada Y. Ohsawa Y, et al. Among authors: sunada y. Hum Mol Genet. 2004 Jan 15;13(2):151-7. doi: 10.1093/hmg/ddh014. Epub 2003 Nov 25. Hum Mol Genet. 2004. PMID: 14645200

10

Endoplasmic reticulum stress response in P104L mutant caveolin-3 transgenic mice.

Kuga A, Ohsawa Y, Okada T, Kanda F, Kanagawa M, Toda T, Sunada Y. Kuga A, et al. Among authors: sunada y. Hum Mol Genet. 2011 Aug 1;20(15):2975-83. doi: 10.1093/hmg/ddr201. Epub 2011 May 24. Hum Mol Genet. 2011. PMID: 21610159

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