Tanno Y - Search Results

1

Quantitation of heteroplasmy of mitochondrial tRNA(Leu(UUR)) gene using PCR-SSCP.

Tanno Y, Yoneda M, Tanaka K, Tanaka H, Yamazaki M, Nishizawa M, Wakabayashi K, Ohama E, Tsuji S. Tanno Y, et al. Muscle Nerve. 1995 Dec;18(12):1390-7. doi: 10.1002/mus.880181208. Muscle Nerve. 1995. PMID: 7477061

2

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: tanno y. Neurology. 1991 Nov;41(11):1838-40. doi: 10.1212/wnl.41.11.1838. Neurology. 1991. PMID: 1682854

3

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. 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

4

[Molecular genetic analysis for myoclonus epilepsy associated with ragged-red fibers (MERRF)].

Tanno Y, Yoneda M, Tanaka K, Tsuji S. Tanno Y, et al. Nihon Rinsho. 1993 Sep;51(9):2379-85. Nihon Rinsho. 1993. PMID: 8411716 Review. Japanese.

5

[Molecular genetic analysis for Leber's hereditary optic neuropathy (LHON)].

Tanno Y, Yoneda M, Tanaka K, Tsuji S. Tanno Y, et al. Nihon Rinsho. 1993 Sep;51(9):2396-402. Nihon Rinsho. 1993. PMID: 8411719 Review. Japanese.

6

[Molecular genetic analysis of neurologic diseases].

Tsuji S, Tanno Y, Yoneda M. Tsuji S, et al. Among authors: tanno y. Hum Cell. 1990 Dec;3(4):318-22. Hum Cell. 1990. PMID: 1710491 Japanese.

7

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: tanno y. Biochem Int. 1990 Aug;21(5):789-96. Biochem Int. 1990. PMID: 2124116

8

Uniform tissue distribution of tRNA(Lys) mutation in mitochondrial DNA in MERRF patients.

Tanno Y, Yoneda M, Tanaka K, Kondo R, Hozumi I, Wakabayashi K, Yamada M, Fukuhara N, Ikuta F, Tsuji S. Tanno Y, et al. Neurology. 1993 Jun;43(6):1198-200. doi: 10.1212/wnl.43.6.1198. Neurology. 1993. PMID: 8170566

9

[Familial posterior cortical atrophy with visual agnosia and Bálint's syndrome].

Otsuki M, Soma Y, Tanaka M, Tanaka K, Tanno Y, Uesugi Y, Tsuji S. Otsuki M, et al. Among authors: tanno y. No To Shinkei. 1995 Dec;47(12):1185-90. No To Shinkei. 1995. PMID: 8534556 Japanese.

10

The 8,344 mutation in mitochondrial DNA: a comparison between the proportion of mutant DNA and clinico-pathologic findings.

Ozawa M, Goto Y, Sakuta R, Tanno Y, Tsuji S, Nonaka I. Ozawa M, et al. Among authors: tanno y. Neuromuscul Disord. 1995 Nov;5(6):483-8. doi: 10.1016/0960-8966(95)00009-c. Neuromuscul Disord. 1995. PMID: 8580730

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