Ikezawa M - Search Results

1

The role of receptors in the maturation-dependent adenoviral transduction of myofibers.

Cao B, Pruchnic R, Ikezawa M, Xiao X, Li J, Wickham TJ, Kovesdi I, Rudert WA, Huard J. Cao B, et al. Among authors: ikezawa m. Gene Ther. 2001 Apr;8(8):627-37. doi: 10.1038/sj.gt.3301425. Gene Ther. 2001. PMID: 11320409

2

Dystrophin delivery in dystrophin-deficient DMDmdx skeletal muscle by isogenic muscle-derived stem cell transplantation.

Ikezawa M, Cao B, Qu Z, Peng H, Xiao X, Pruchnic R, Kimura S, Miike T, Huard J. Ikezawa M, et al. Hum Gene Ther. 2003 Nov 1;14(16):1535-46. doi: 10.1089/104303403322495043. Hum Gene Ther. 2003. PMID: 14577915

3

Ex vivo gene transfer to mature skeletal muscle by using adenovirus helper cells.

Kimura S, Ikezawa M, Cao B, Kanda Y, Pruchnic R, Cummins J, Huard J, Miike T, Suzuki S. Kimura S, et al. Among authors: ikezawa m. J Gene Med. 2004 Feb;6(2):155-65. doi: 10.1002/jgm.480. J Gene Med. 2004. PMID: 14978769

4

Muscle stem cells differentiate into haematopoietic lineages but retain myogenic potential.

Cao B, Zheng B, Jankowski RJ, Kimura S, Ikezawa M, Deasy B, Cummins J, Epperly M, Qu-Petersen Z, Huard J. Cao B, et al. Among authors: ikezawa m. Nat Cell Biol. 2003 Jul;5(7):640-6. doi: 10.1038/ncb1008. Nat Cell Biol. 2003. PMID: 12792651

5

Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy.

Kimura S, Sugino S, Ohtani Y, Matsukura M, Nishino I, Ikezawa M, Sakata A, Kondo Y, Yoshioka K, Huard J, Nonaka I, Miike T. Kimura S, et al. Among authors: ikezawa m. Ann Neurol. 1998 Dec;44(6):967-71. doi: 10.1002/ana.410440618. Ann Neurol. 1998. PMID: 9851444

6

Immobility reduces muscle fiber necrosis in dystrophin deficient muscular dystrophy.

Kimura S, Ikezawa M, Nomura K, Ito K, Ozasa S, Ueno H, Yoshioka K, Yano S, Yamashita T, Matuskura M, Miike T. Kimura S, et al. Among authors: ikezawa m. Brain Dev. 2006 Aug;28(7):473-6. doi: 10.1016/j.braindev.2006.01.007. Epub 2006 Mar 3. Brain Dev. 2006. PMID: 16516424

7

Novel mutation in splicing donor of dystrophin gene first exon in a patient with dilated cardiomyopathy but no clinical signs of skeletal myopathy.

Kimura S, Ikezawa M, Ozasa S, Ito K, Ueno H, Yoshioka K, Ijiri S, Nomura K, Nakamura K, Matuskura M, Miike T. Kimura S, et al. Among authors: ikezawa m. J Child Neurol. 2007 Jul;22(7):901-6. doi: 10.1177/0883073807304705. J Child Neurol. 2007. PMID: 17715288

8

Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online.

Ikezawa M, Nishino I, Goto Y, Miike T, Nonaka I. Ikezawa M, et al. Hum Mutat. 1999;13(2):170. doi: 10.1002/(SICI)1098-1004(1999)13:2<170::AID-HUMU12>3.0.CO;2-7. Hum Mutat. 1999. PMID: 10094556

9

Adenoviral mediated MyoD gene transfer into fibroblasts: myogenic disease diagnosis.

Fujii I, Matsukura M, Ikezawa M, Suzuki S, Shimada T, Miike T. Fujii I, et al. Among authors: ikezawa m. Brain Dev. 2006 Aug;28(7):420-5. doi: 10.1016/j.braindev.2005.12.007. Epub 2006 Apr 3. Brain Dev. 2006. PMID: 16584859

10

Dystrophin gene analysis on 130 patients with Duchenne muscular dystrophy with a special reference to muscle mRNA analysis.

Ikezawa M, Minami N, Takahashi M, Goto Y, Miike T, Nonaka I. Ikezawa M, et al. Brain Dev. 1998 Apr;20(3):165-8. doi: 10.1016/s0387-7604(98)00012-6. Brain Dev. 1998. PMID: 9628192

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