Tanaka M - Search Results

1

Mitochondrial DNA deletions in inherited recurrent myoglobinuria.

Ohno K, Tanaka M, Sahashi K, Ibi T, Sato W, Yamamoto T, Takahashi A, Ozawa T. Ohno K, et al. Among authors: tanaka m. Ann Neurol. 1991 Apr;29(4):364-9. doi: 10.1002/ana.410290406. Ann Neurol. 1991. PMID: 1929207

2

Deficiency of subunits of Complex I and mitochondrial encephalomyopathy.

Ichiki T, Tanaka M, Nishikimi M, Suzuki H, Ozawa T, Kobayashi M, Wada Y. Ichiki T, et al. Among authors: tanaka m. Ann Neurol. 1988 Mar;23(3):287-94. doi: 10.1002/ana.410230312. Ann Neurol. 1988. PMID: 3132077

3

Strand asymmetry in human mitochondrial DNA mutations.

Tanaka M, Ozawa T. Tanaka M, et al. Genomics. 1994 Jul 15;22(2):327-35. doi: 10.1006/geno.1994.1391. Genomics. 1994. PMID: 7806218

4

Immunohistochemical studies on complexes I, II, III, and IV of mitochondria in Parkinson's disease.

Hattori N, Tanaka M, Ozawa T, Mizuno Y. Hattori N, et al. Among authors: tanaka m. Ann Neurol. 1991 Oct;30(4):563-71. doi: 10.1002/ana.410300409. Ann Neurol. 1991. PMID: 1665052

5

Mitochondrial DNA mutations and disturbances of energy metabolism in myocardium.

Ozawa T, Sugiyama S, Tanaka M, Hattori K. Ozawa T, et al. Among authors: tanaka m. Jpn Circ J. 1991 Nov;55(11):1158-64. doi: 10.1253/jcj.55.1158. Jpn Circ J. 1991. PMID: 1749073

6

Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genome.

Ohno K, Tanaka M, Ino H, Suzuki H, Tashiro M, Ibi T, Sahashi K, Takahashi A, Ozawa T. Ohno K, et al. Among authors: tanaka m. Biochim Biophys Acta. 1991 Aug 27;1090(1):9-16. doi: 10.1016/0167-4781(91)90030-p. Biochim Biophys Acta. 1991. PMID: 1832017

7

Detection of platelet mitochondrial DNA deletions in Kearns-Sayre syndrome.

Ota Y, Tanaka M, Sato W, Ohno K, Yamamoto T, Maehara M, Negoro T, Watanabe K, Awaya S, Ozawa T. Ota Y, et al. Among authors: tanaka m. Invest Ophthalmol Vis Sci. 1991 Sep;32(10):2667-75. Invest Ophthalmol Vis Sci. 1991. PMID: 1894466

8

[Detection of deletions in platelet mitochondrial DNA in Kearns-Sayre syndrome using polymerase chain reaction].

Ota Y, Awaya S, Tanaka M, Sato W, Ohno K, Yamamoto T, Ozawa T, Ota I. Ota Y, et al. Among authors: tanaka m. Nippon Ganka Gakkai Zasshi. 1991 Aug;95(8):776-82. Nippon Ganka Gakkai Zasshi. 1991. PMID: 1950835 Japanese.

9

Cytoplasmic body and mitochondrial DNA deletion.

Sahashi K, Ohno K, Tanaka M, Ibi T, Yamamoto T, Tashiro M, Sato W, Takahashi A, Ozawa T. Sahashi K, et al. Among authors: tanaka m. J Neurol Sci. 1990 Nov;99(2-3):291-300. doi: 10.1016/0022-510x(90)90163-h. J Neurol Sci. 1990. PMID: 1964959

10

[Mitochondrial DNA mutations and cardiomyopathy].

Ozawa T, Sugiyama S, Tanaka M. Ozawa T, et al. Among authors: tanaka m. Nihon Rinsho. 1991 Jan;49(1):204-10. Nihon Rinsho. 1991. PMID: 2002603 Japanese. No abstract available.

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