Shiraishi T - Search Results

1

Inhibition of nonsense-mediated mRNA decay rescues the phenotype in Ullrich's disease.

Usuki F, Yamashita A, Higuchi I, Ohnishi T, Shiraishi T, Osame M, Ohno S. Usuki F, et al. Among authors: shiraishi t. Ann Neurol. 2004 May;55(5):740-4. doi: 10.1002/ana.20107. Ann Neurol. 2004. PMID: 15122717

2

Inhibition of SMG-8, a subunit of SMG-1 kinase, ameliorates nonsense-mediated mRNA decay-exacerbated mutant phenotypes without cytotoxicity.

Usuki F, Yamashita A, Shiraishi T, Shiga A, Onodera O, Higuchi I, Ohno S. Usuki F, et al. Among authors: shiraishi t. Proc Natl Acad Sci U S A. 2013 Sep 10;110(37):15037-42. doi: 10.1073/pnas.1300654110. Epub 2013 Aug 27. Proc Natl Acad Sci U S A. 2013. PMID: 23983263 Free PMC article.

3

Frameshift mutation in the collagen VI gene causes Ullrich's disease.

Higuchi I, Shiraishi T, Hashiguchi T, Suehara M, Niiyama T, Nakagawa M, Arimura K, Maruyama I, Osame M. Higuchi I, et al. Among authors: shiraishi t. Ann Neurol. 2001 Aug;50(2):261-5. doi: 10.1002/ana.1120. Ann Neurol. 2001. PMID: 11506412

4

Fibronectin receptor reduction in skin and fibroblasts of patients with Ullrich's disease.

Hu J, Higuchi I, Shiraishi T, Suehara M, Niiyama T, Horikiri T, Uchida Y, Saito A, Osame M. Hu J, et al. Among authors: shiraishi t. Muscle Nerve. 2002 Nov;26(5):696-701. doi: 10.1002/mus.10250. Muscle Nerve. 2002. PMID: 12402292

5

Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency.

Higashi K, Higuchi I, Niiyama T, Uchida Y, Shiraishi T, Hashiguchi A, Saito A, Horikiri T, Suehara M, Arimura K, Osame M. Higashi K, et al. Among authors: shiraishi t. Muscle Nerve. 2006 Jan;33(1):120-6. doi: 10.1002/mus.20449. Muscle Nerve. 2006. PMID: 16258947

6

Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease.

Niiyama T, Higuchi I, Suehara M, Hashiguchi T, Shiraishi T, Nakagawa M, Arimura K, Maruyama I, Osame M. Niiyama T, et al. Among authors: shiraishi t. Acta Neuropathol. 2002 Jul;104(1):67-71. doi: 10.1007/s00401-002-0522-z. Epub 2002 Apr 30. Acta Neuropathol. 2002. PMID: 12070666

7

Capillary changes in skeletal muscle of patients with Ullrich's disease with collagen VI deficiency.

Niiyama T, Higuchi I, Hashiguchi T, Suehara M, Uchida Y, Horikiri T, Shiraishi T, Saitou A, Hu J, Nakagawa M, Arimura K, Osame M. Niiyama T, et al. Among authors: shiraishi t. Acta Neuropathol. 2003 Aug;106(2):137-42. doi: 10.1007/s00401-003-0714-1. Epub 2003 May 8. Acta Neuropathol. 2003. PMID: 12736748

8

Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiency.

Higuchi I, Horikiri T, Niiyama T, Suehara M, Shiraishi T, Hu J, Uchida Y, Saito A, Nakagawa M, Arimura K, Osame M. Higuchi I, et al. Among authors: shiraishi t. Neuromuscul Disord. 2003 May;13(4):310-6. doi: 10.1016/s0960-8966(02)00282-1. Neuromuscul Disord. 2003. PMID: 12868500

9

Expression of midkine in regenerating skeletal muscle fibers and cultured myoblasts of human skeletal muscle.

Hu J, Higuchi I, Yoshida Y, Shiraishi T, Osame M. Hu J, et al. Among authors: shiraishi t. Eur Neurol. 2002;47(1):20-5. doi: 10.1159/000047942. Eur Neurol. 2002. PMID: 11803188

10

Different pattern of HSP47 expression in skeletal muscle of patients with neuromuscular diseases.

Higuchi I, Hashiguchi A, Matsuura E, Higashi K, Shiraishi T, Hirata N, Arimura K, Osame M. Higuchi I, et al. Among authors: shiraishi t. Neuromuscul Disord. 2007 Mar;17(3):221-6. doi: 10.1016/j.nmd.2006.11.008. Epub 2007 Feb 26. Neuromuscul Disord. 2007. PMID: 17324572

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