Miyabayashi S - Search Results

1

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.

2

Nuclear but not mitochondrial genome involvement in human age-related mitochondrial dysfunction. Functional integrity of mitochondrial DNA from aged subjects.

Hayashi J, Ohta S, Kagawa Y, Kondo H, Kaneda H, Yonekawa H, Takai D, Miyabayashi S. Hayashi J, et al. Among authors: miyabayashi s. J Biol Chem. 1994 Mar 4;269(9):6878-83. J Biol Chem. 1994. PMID: 8120050 Free article.

3

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

4

Identification of inheritance modes of mitochondrial diseases by introduction of pure nuclei from mtDNA-less HeLa cells to patient-derived fibroblasts.

Isobe K, Kishino S, Inoue K, Takai D, Hirawake H, Kita K, Miyabayashi S, Hayashi JI. Isobe K, et al. Among authors: miyabayashi s. J Biol Chem. 1997 May 9;272(19):12606-10. doi: 10.1074/jbc.272.19.12606. J Biol Chem. 1997. PMID: 9139714 Free article.

5

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.

6

Complete repopulation of mouse mitochondrial DNA-less cells with rat mitochondrial DNA restores mitochondrial translation but not mitochondrial respiratory function.

Yamaoka M, Isobe K, Shitara H, Yonekawa H, Miyabayashi S, Hayashi JI. Yamaoka M, et al. Among authors: miyabayashi s. Genetics. 2000 May;155(1):301-7. doi: 10.1093/genetics/155.1.301. Genetics. 2000. PMID: 10790404 Free PMC article.

7

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

8

Mosaicism of mitochondria in mitochondrial myopathy: an electronmicroscopic analysis of cytochrome c oxidase.

Haginoya K, Miyabayashi S, Iinuma K, Tada K. Haginoya K, et al. Among authors: miyabayashi s. Acta Neuropathol. 1990;80(6):642-8. doi: 10.1007/BF00307633. Acta Neuropathol. 1990. PMID: 2177307

9

Clinical and biochemical phenotype of the MELAS mutation.

Miyabayashi S, Hanamizu H, Nakamura R, Hayashi JI, Tada K. Miyabayashi S, et al. J Inherit Metab Dis. 1993;16(5):886-92. doi: 10.1007/BF00714284. J Inherit Metab Dis. 1993. PMID: 8295406 No abstract available.

10

Quantitative evaluation of electron transport system proteins in mitochondrial encephalomyopathy.

Haginoya K, Miyabayashi S, Iinuma K, Tada K. Haginoya K, et al. Among authors: miyabayashi s. Acta Neuropathol. 1993;85(4):370-7. doi: 10.1007/BF00334446. Acta Neuropathol. 1993. PMID: 8386896

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