Miyabayashi S - Search Results

1

Gene therapy for mitochondrial disease by delivering restriction endonuclease SmaI into mitochondria.

Tanaka M, Borgeld HJ, Zhang J, Muramatsu S, Gong JS, Yoneda M, Maruyama W, Naoi M, Ibi T, Sahashi K, Shamoto M, Fuku N, Kurata M, Yamada Y, Nishizawa K, Akao Y, Ohishi N, Miyabayashi S, Umemoto H, Muramatsu T, Furukawa K, Kikuchi A, Nakano I, Ozawa K, Yagi K. Tanaka M, et al. Among authors: miyabayashi s. J Biomed Sci. 2002;9(6 Pt 1):534-41. doi: 10.1159/000064726. J Biomed Sci. 2002. PMID: 12372991

2

Extensive defects of mitochondrial electron-transfer chain in muscular cytochrome c oxidase deficiency.

Tanaka M, Miyabayashi S, Nishikimi M, Suzuki H, Shimomura Y, Ito K, Narisawa K, Tada K, Ozawa T. Tanaka M, et al. Among authors: miyabayashi s. Pediatr Res. 1988 Oct;24(4):447-54. doi: 10.1203/00006450-198810000-00006. Pediatr Res. 1988. PMID: 2845344

3

Defects in muscle fiber growth in fatal infantile cytochrome c oxidase deficiency.

Nonaka I, Koga Y, Okino E, Kikuchi A, Fujisawa K, Miyabayashi S. Nonaka I, et al. Among authors: miyabayashi s. Brain Dev. 1988;10(4):223-30. doi: 10.1016/s0387-7604(88)80002-0. Brain Dev. 1988. PMID: 2851269

4

Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy.

Miyabayashi S, Ito T, Abukawa D, Narisawa K, Tada K, Tanaka M, Ozawa T, Droste M, Kadenbach B. Miyabayashi S, et al. J Inherit Metab Dis. 1987;10(3):289-92. doi: 10.1007/BF01800084. J Inherit Metab Dis. 1987. PMID: 2828763 No abstract available.

5

Cytochrome C oxidase-deficient mitochondria in mitochondrial myopathy.

Haginoya K, Miyabayashi S, Iinuma K, Okino E, Maesaka H, Tada K. Haginoya K, et al. Among authors: miyabayashi s. Pediatr Neurol. 1992 Jan-Feb;8(1):13-8. doi: 10.1016/0887-8994(92)90046-2. Pediatr Neurol. 1992. PMID: 1313674

6

Influence of ageing on onset of mitochondrial disease.

Miyabayashi S, Hayashi JI, Tada K. Miyabayashi S, et al. J Inherit Metab Dis. 1994;17(5):606-10. doi: 10.1007/BF00711599. J Inherit Metab Dis. 1994. PMID: 7837768 No abstract available.

7

A new type of mitochondrial DNA deletion in patients with encephalomyopathy.

Miyabayashi S, Hanamizu H, Endo H, Tada K, Horai S. Miyabayashi S, et al. J Inherit Metab Dis. 1991;14(5):805-12. doi: 10.1007/BF01799954. J Inherit Metab Dis. 1991. PMID: 1779627 No abstract available.

8

Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation.

Hotta O, Inoue CN, Miyabayashi S, Furuta T, Takeuchi A, Taguma Y. Hotta O, et al. Among authors: miyabayashi s. Kidney Int. 2001 Apr;59(4):1236-43. doi: 10.1046/j.1523-1755.2001.0590041236.x. Kidney Int. 2001. PMID: 11260383 Free article.

9

Functional and morphological abnormalities of mitochondria in human cells containing mitochondrial DNA with pathogenic point mutations in tRNA genes.

Hayashi J, Ohta S, Kagawa Y, Takai D, Miyabayashi S, Tada K, Fukushima H, Inui K, Okada S, Goto Y, et al. Hayashi J, et al. Among authors: miyabayashi s. J Biol Chem. 1994 Jul 22;269(29):19060-6. J Biol Chem. 1994. PMID: 7518448 Free article.

10

Accumulation of mtDNA with a mutation at position 3271 in tRNA(Leu)(UUR) gene introduced from a MELAS patient to HeLa cells lacking mtDNA results in progressive inhibition of mitochondrial respiratory function.

Hayashi J, Ohta S, Takai D, Miyabayashi S, Sakuta R, Goto Y, Nonaka I. Hayashi J, et al. Among authors: miyabayashi s. Biochem Biophys Res Commun. 1993 Dec 30;197(3):1049-55. doi: 10.1006/bbrc.1993.2584. Biochem Biophys Res Commun. 1993. PMID: 8280119

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

81 results

Search Page

Filters