-
1
-
-
84867597592
-
Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs
-
Suzuki T, Nagao A, Suzuki T. Human mitochondrial diseases caused by lack of taurine modification in mitochondrial tRNAs. WIREs RNA 2: 376–386, 2011.
-
(2011)
WIREs RNA
, vol.2
, pp. 376-386
-
-
Suzuki, T.1
Nagao, A.2
Suzuki, T.3
-
2
-
-
0013936167
-
Codon-anticodon pairing: The wobble hypothesis
-
Click FHC. Codon-anticodon pairing: The wobble hypothesis. J Mol Biol 19: 548–555, 1966.
-
(1966)
J Mol Biol
, vol.19
, pp. 548-555
-
-
Click, F.H.C.1
-
3
-
-
0002090634
-
Modified nucleosides in translation
-
Grosjean H, Benne R, Eds. ASM Press, Washington, D.C
-
Curran JF. Modified nucleosides in translation. In: Modification and Editing of RNA. Grosjean H, Benne R, Eds. ASM Press, Washington, D.C, 1998: 493–516.
-
(1998)
Modification and Editing of RNA.
, pp. 493-516
-
-
Curran, J.F.1
-
4
-
-
0033968067
-
Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA (Lys) with the MERRF encephalomyopathy pathogenic mutation
-
Yasukawa T, Suzuki T, Ishii N, Ueda T, Ohta S, Watanabe K. Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA (Lys) with the MERRF encephalomyopathy pathogenic mutation. FEBS Lett 467: 175–178, 2000.
-
(2000)
FEBS Lett
, vol.467
, pp. 175-178
-
-
Yasukawa, T.1
Suzuki, T.2
Ishii, N.3
Ueda, T.4
Ohta, S.5
Watanabe, K.6
-
5
-
-
0034635519
-
Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs (Leu) (UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
-
Yasukawa T, Suzuki T, Ueda T, Ohta S, Watanabe K. Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs (Leu) (UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. J Biol Chem 275: 4251–4257, 2000.
-
(2000)
J Biol Chem
, vol.275
, pp. 4251-4257
-
-
Yasukawa, T.1
Suzuki, T.2
Ueda, T.3
Ohta, S.4
Watanabe, K.5
-
6
-
-
0035801225
-
Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease
-
Yasukawa T, Suzuki T, Ishii N, Ohta S, Watanabe K. Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease. EMBO J 20: 4794–4802, 2001.
-
(2001)
EMBO J
, vol.20
, pp. 4794-4802
-
-
Yasukawa, T.1
Suzuki, T.2
Ishii, N.3
Ohta, S.4
Watanabe, K.5
-
7
-
-
80755169463
-
Human mitochondrial tRNAs: Biogenesis, function, structural aspects, and diseases
-
Suzuki T, Nagao A, Suzuki T. Human mitochondrial tRNAs: Biogenesis, function, structural aspects, and diseases. Annu Rev Genet 45: 299–329, 2011.
-
(2011)
Annu Rev Genet
, vol.45
, pp. 299-329
-
-
Suzuki, T.1
Nagao, A.2
Suzuki, T.3
-
8
-
-
18844430007
-
Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease
-
Kirino Y, Goto Y, Campos Y, et al. Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease. Proc Natl Acad Sci USA 102: 7127–7132, 2005.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 7127-7132
-
-
Kirino, Y.1
Goto, Y.2
Campos, Y.3
-
9
-
-
6344221310
-
Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease
-
Kirino Y, Yasukawa T, Ohta S, et al. Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease. Proc Natl Acad Sci USA 101: 15070–15075, 2004.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 15070-15075
-
-
Kirino, Y.1
Yasukawa, T.2
Ohta, S.3
-
10
-
-
0025836655
-
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
-
Hayashi J, Ohta S, Kikuchi A, et al. Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction. Proc Natl Acad Sci USA 88: 10614–10618, 1991.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 10614-10618
-
-
Hayashi, J.1
Ohta, S.2
Kikuchi, A.3
-
11
-
-
77951497956
-
Astaxanthin protects mitochondrial redox state and functional integrity against oxidative stress
-
Wolf AM, Asoh S, Hiranuma H, et al. Astaxanthin protects mitochondrial redox state and functional integrity against oxidative stress. J Nutr Biochem 21: 381–389, 2010.
-
(2010)
J Nutr Biochem
, vol.21
, pp. 381-389
-
-
Wolf, A.M.1
Asoh, S.2
Hiranuma, H.3
-
12
-
-
0032780959
-
Chloromethyl-X-rosamine (MitoTracker Red) photosensitizes mitochondria and induces apotosis in intact human cells
-
Minamikawa T, Sriratana A, Williams DA, et al. Chloromethyl-X-rosamine (MitoTracker Red) photosensitizes mitochondria and induces apotosis in intact human cells. J Cell Sci 112: 2419–2430, 1999.
-
(1999)
J Cell Sci
, vol.112
, pp. 2419-2430
-
-
Minamikawa, T.1
Sriratana, A.2
Williams, D.A.3
-
13
-
-
85024747407
-
Clinical evaluation by double-blind trial of taurine for acute hepatitis
-
(in Japanese)
-
Kamada T, Koizumi T, Tsujii M, et al. Clinical evaluation by double-blind trial of taurine for acute hepatitis. Sulfur-containing Amino Acid 3: 223–235, 1980 (in Japanese).
-
(1980)
Sulfur-containing Amino Acid
, vol.3
, pp. 223-235
-
-
Kamada, T.1
Koizumi, T.2
Tsujii, M.3
-
14
-
-
0023224703
-
Myocardial failure in cats associated with low plasma taurine: A reversible cardiomyopathy
-
Pion PD, Kittleson MD, Rogers QR, et al. Myocardial failure in cats associated with low plasma taurine: A reversible cardiomyopathy. Science 237: 764–768, 1987.
-
(1987)
Science
, vol.237
, pp. 764-768
-
-
Pion, P.D.1
Kittleson, M.D.2
Rogers, Q.R.3
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