Horai S - Search Results

1

Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy.

Yoneda M, Tsuji S, Yamauchi T, Inuzuka T, Miyatake T, Horai S, Ozawa T. Yoneda M, et al. Among authors: horai s. Lancet. 1989 May 13;1(8646):1076-7. doi: 10.1016/s0140-6736(89)92470-7. Lancet. 1989. PMID: 2566021 No abstract available.

2

A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibers.

Yoneda M, Tanno Y, Horai S, Ozawa T, Miyatake T, Tsuji S. Yoneda M, et al. Among authors: horai s. Biochem Int. 1990 Aug;21(5):789-96. Biochem Int. 1990. PMID: 2124116

3

Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy.

Ozawa T, Yoneda M, Tanaka M, Ohno K, Sato W, Suzuki H, Nishikimi M, Yamamoto M, Nonaka I, Horai S. Ozawa T, et al. Among authors: horai s. Biochem Biophys Res Commun. 1988 Aug 15;154(3):1240-7. doi: 10.1016/0006-291x(88)90272-0. Biochem Biophys Res Commun. 1988. PMID: 2841928

4

Differently deleted mitochondrial genomes in maternally inherited chronic progressive external ophthalmoplegia.

Tanaka M, Yoneda M, Ohno K, Sato W, Yamamoto M, Nonaka I, Horai S, Ozawa T. Tanaka M, et al. Among authors: horai s. J Inherit Metab Dis. 1989;12(3):359-62. doi: 10.1007/BF01799242. J Inherit Metab Dis. 1989. PMID: 2515390 No abstract available.

5

Specific amplification of deleted mitochondrial DNA from a myopathic patient and analysis of deleted region with S1 nuclease.

Tanaka-Yamamoto T, Tanaka M, Ohno K, Sato W, Horai S, Ozawa T. Tanaka-Yamamoto T, et al. Among authors: horai s. Biochim Biophys Acta. 1989 Nov 2;1009(2):151-5. doi: 10.1016/0167-4781(89)90094-8. Biochim Biophys Acta. 1989. PMID: 2804078

6

Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS).

Yoneda M, Tanaka M, Nishikimi M, Suzuki H, Tanaka K, Nishizawa M, Atsumi T, Ohama E, Horai S, Ikuta F, et al. Yoneda M, et al. Among authors: horai s. J Neurol Sci. 1989 Sep;92(2-3):143-58. doi: 10.1016/0022-510x(89)90132-9. J Neurol Sci. 1989. PMID: 2809615

7

Enzymatic and genetic adaptation of soleus muscle mitochondria to physical training in rats.

Murakami T, Shimomura Y, Fujitsuka N, Nakai N, Sugiyama S, Ozawa T, Sokabe M, Horai S, Tokuyama K, Suzuki M. Murakami T, et al. Among authors: horai s. Am J Physiol. 1994 Sep;267(3 Pt 1):E388-95. doi: 10.1152/ajpendo.1994.267.3.E388. Am J Physiol. 1994. PMID: 7943219

8

Mitochondrial DNA mutation and Leigh's syndrome.

Sakuta R, Goto Y, Horai S, Ogino T, Yoshinaga H, Ohtahara S, Nonaka I. Sakuta R, et al. Among authors: horai s. Ann Neurol. 1992 Oct;32(4):597-8. doi: 10.1002/ana.410320428. Ann Neurol. 1992. PMID: 1456751 No abstract available.

9

The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).

Nishino I, Komatsu M, Kodama S, Horai S, Nonaka I, Goto Y. Nishino I, et al. Among authors: horai s. Muscle Nerve. 1996 Dec;19(12):1603-4. doi: 10.1002/(SICI)1097-4598(199612)19:12<1603::AID-MUS10>3.0.CO;2-S. Muscle Nerve. 1996. PMID: 8941275 No abstract available.

10

A Caucasian family with the 3271 mutation in mitochondrial DNA.

Marie SK, Goto Y, Passos-Bueno MR, Zatz M, Carvalho AA, Carvalho M, Levy JA, Palou VB, Campiotto S, Horai S, et al. Marie SK, et al. Among authors: horai s. Biochem Med Metab Biol. 1994 Aug;52(2):136-9. doi: 10.1006/bmmb.1994.1045. Biochem Med Metab Biol. 1994. PMID: 7993661

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