메뉴 건너뛰기




Volumn 15, Issue 3, 2000, Pages 385-388

Prevalence of Japanese dialysis patients with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene

Author keywords

3243 point mutation; Deafness; Diabetes mellitus; End stage renal disease; Mitochondrial DNA

Indexed keywords

ARGININE; GUANINE; MITOCHONDRIAL RNA; TRANSFER RNA;

EID: 17744419840     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/15.3.385     Document Type: Article
Times cited : (18)

References (21)
  • 1
    • 0031869732 scopus 로고    scopus 로고
    • Incidence and Prevalence of ESRD; USRDS 1998 Annual Data Report
    • Incidence and Prevalence of ESRD; USRDS 1998 Annual Data Report. Am J Kidney Dis 1998; 32 [Suppl. 1]: S38-S49
    • (1998) Am J Kidney Dis , vol.32 , Issue.SUPPL. 1
  • 2
    • 0343898370 scopus 로고    scopus 로고
    • An overview of regular dialysis treatment in Japan (as of Dec. 31, 1998)
    • An overview of regular dialysis treatment in Japan (as of Dec. 31, 1998). Jpn Soc Dial Ther 1999; 64
    • (1999) Jpn Soc Dial Ther , pp. 64
  • 4
    • 0028328317 scopus 로고
    • A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA
    • Kadowaki T, Kadowaki H, Mori Y et al. A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA. N Engl J Med 1994; 330: 962-968
    • (1994) N Engl J Med , vol.330 , pp. 962-968
    • Kadowaki, T.1    Kadowaki, H.2    Mori, Y.3
  • 5
    • 0028966152 scopus 로고
    • Mitochondrial mutation in diabetic patient with gastrointestinal symptoms
    • Letter
    • Kishimoto M, Hashiramoto M, Kanda F, Tanaka M, Kasuga M. Mitochondrial mutation in diabetic patient with gastrointestinal symptoms. Lancet 1995; 345: 452 (Letter)
    • (1995) Lancet , vol.345 , pp. 452
    • Kishimoto, M.1    Hashiramoto, M.2    Kanda, F.3    Tanaka, M.4    Kasuga, M.5
  • 6
    • 0027968580 scopus 로고
    • The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan
    • Otabe S, Sakura H, Shimokawa K et al. The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in Japan. J Clin Endocrinol Metab 1994; 79: 768-771
    • (1994) J Clin Endocrinol Metab , vol.79 , pp. 768-771
    • Otabe, S.1    Sakura, H.2    Shimokawa, K.3
  • 9
    • 0019423856 scopus 로고
    • Sequence and organization of the human mitochondrial genome
    • Anderson S, Bankier AT, Barrell BG et al. Sequence and organization of the human mitochondrial genome. Nature 1981; 290: 457-465
    • (1981) Nature , vol.290 , pp. 457-465
    • Anderson, S.1    Bankier, A.T.2    Barrell, B.G.3
  • 10
    • 0025666322 scopus 로고
    • LEU(UUR) gene associated with the MELAS subgroup in mitochondrial encephalomyopathies
    • LEU(UUR) gene associated with the MELAS subgroup in mitochondrial encephalomyopathies. Nature 1990; 348: 651-653
    • (1990) Nature , vol.348 , pp. 651-653
    • Goto, Y.1    Nonaka, I.2    Horai, S.3
  • 14
    • 0028818655 scopus 로고
    • Clinical spectrum of the MELAS mutation in a large pedigree
    • Damian MS, Seibel P, Reichmann H et al. Clinical spectrum of the MELAS mutation in a large pedigree. Acta Neurol Scand 1995; 92: 409-415
    • (1995) Acta Neurol Scand , vol.92 , pp. 409-415
    • Damian, M.S.1    Seibel, P.2    Reichmann, H.3
  • 17
    • 0343461873 scopus 로고
    • An autopsy case of mitochondrial encepharlopathy (MELAS) with special reference to extra-neuromuscular abnormalities
    • Ban S, Mori N, Saito K, Mizukami K, Suzuki T, Shiraishi H. An autopsy case of mitochondrial encepharlopathy (MELAS) with special reference to extra-neuromuscular abnormalities. J Neurol Sci 1992; 92: 818-825
    • (1992) J Neurol Sci , vol.92 , pp. 818-825
    • Ban, S.1    Mori, N.2    Saito, K.3    Mizukami, K.4    Suzuki, T.5    Shiraishi, H.6
  • 18
    • 0006288487 scopus 로고    scopus 로고
    • An autopsy case of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) undergoing long-term hemodialysis
    • Tomonari H, Yoshida H, Omura K et al. An autopsy case of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) undergoing long-term hemodialysis. J Jpn Soc Dial Ther 1996; 29: 1097-1102
    • (1996) J Jpn Soc Dial Ther , vol.29 , pp. 1097-1102
    • Tomonari, H.1    Yoshida, H.2    Omura, K.3
  • 19
    • 0027996170 scopus 로고
    • Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands
    • 't Hart LM, Lemkes HH, Heine RJ et al. Prevalence of maternally inherited diabetes and deafness in diabetic populations in The Netherlands. Diabetologia 1994; 37: 1169-1170
    • (1994) Diabetologia , vol.37 , pp. 1169-1170
    • 'T Hart, L.M.1    Lemkes, H.H.2    Heine, R.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.