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Volumn 51, Issue 24, 2012, Pages 3351-3357

Taurine Ameliorates Impaired the Mitochondrial Function and Prevents Stroke-like Episodes in Patients with MELAS

Author keywords

MELAS; Post transcriptional modification; Stroke like episodes; Taurine

Indexed keywords

TAURINE;

EID: 84877157309     PISSN: 09182918     EISSN: 13497235     Source Type: Journal    
DOI: 10.2169/internalmedicine.51.7529     Document Type: Article
Times cited : (50)

References (14)
  • 1
    • 84867597592 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.