Nonaka I - Search Results

1

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: nonaka i. 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

2

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: nonaka i. Ann Neurol. 1992 Oct;32(4):597-8. doi: 10.1002/ana.410320428. Ann Neurol. 1992. PMID: 1456751 No abstract available.

3

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy.

Goto Y, Tojo M, Tohyama J, Horai S, Nonaka I. Goto Y, et al. Among authors: nonaka i. Ann Neurol. 1992 Jun;31(6):672-5. doi: 10.1002/ana.410310617. Ann Neurol. 1992. PMID: 1514779

4

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation.

Goto Y, Horai S, Matsuoka T, Koga Y, Nihei K, Kobayashi M, Nonaka I. Goto Y, et al. Among authors: nonaka i. Neurology. 1992 Mar;42(3 Pt 1):545-50. doi: 10.1212/wnl.42.3.545. Neurology. 1992. PMID: 1549215

5

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.

Chomyn A, Martinuzzi A, Yoneda M, Daga A, Hurko O, Johns D, Lai ST, Nonaka I, Angelini C, Attardi G. Chomyn A, et al. Among authors: nonaka i. Proc Natl Acad Sci U S A. 1992 May 15;89(10):4221-5. doi: 10.1073/pnas.89.10.4221. Proc Natl Acad Sci U S A. 1992. PMID: 1584755 Free PMC article.

6

Muscle histopathology in myoclonus epilepsy with ragged-red fibers (MERRF).

Matsuoka T, Goto Y, Yoneda M, Nonaka I. Matsuoka T, et al. Among authors: nonaka i. J Neurol Sci. 1991 Dec;106(2):193-8. doi: 10.1016/0022-510x(91)90257-8. J Neurol Sci. 1991. PMID: 1666407

7

Simple detection of tRNA(Lys) mutation in myoclonus epilepsy associated with ragged-red fibers (MERRF) by polymerase chain reaction with a mismatched primer.

Yoneda M, Tanno Y, Nonaka I, Miyatake T, Tsuji S. Yoneda M, et al. Among authors: nonaka i. Neurology. 1991 Nov;41(11):1838-40. doi: 10.1212/wnl.41.11.1838. Neurology. 1991. PMID: 1682854

8

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction.

Hayashi J, Ohta S, Kikuchi A, Takemitsu M, Goto Y, Nonaka I. Hayashi J, et al. Among authors: nonaka i. Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10614-8. doi: 10.1073/pnas.88.23.10614. Proc Natl Acad Sci U S A. 1991. PMID: 1720544 Free PMC article.

9

[A case of facioscapulohumeral muscular dystrophy with infantile spasms, sensorineural deafness and retinal vessel abnormality].

Akiyama C, Suzuki H, Nonaka I. Akiyama C, et al. Among authors: nonaka i. No To Hattatsu. 1991 Jul;23(4):395-9. No To Hattatsu. 1991. PMID: 1908258 Review. Japanese.

10

Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patients.

Tanno Y, Yoneda M, Nonaka I, Tanaka K, Miyatake T, Tsuji S. Tanno Y, et al. Among authors: nonaka i. Biochem Biophys Res Commun. 1991 Sep 16;179(2):880-5. doi: 10.1016/0006-291x(91)91900-w. Biochem Biophys Res Commun. 1991. PMID: 1910341

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