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Volumn 34, Issue 1, 2007, Pages 133-137

β-cell function in individuals carrying the mitochondrial tRNA Leu (UUR) mutation

Author keywords

cell function; C peptide; Mitochondrial DNA mutation

Indexed keywords

C PEPTIDE; GLUCOSE; INSULIN; MITOCHONDRIAL DNA; SUSTACAL; TRANSFER RNA; UBIDECARENONE; UNCLASSIFIED DRUG; VINOCARD Q10;

EID: 33846005866     PISSN: 08853177     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.mpa.0000246659.38375.4d     Document Type: Article
Times cited : (16)

References (23)
  • 1
  • 2
    • 33645313021 scopus 로고
    • Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
    • Reardon W, Ross RJ, Sweeney MG, et al. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA. Lancet. 1993;341:1291-1292.
    • (1993) Lancet , vol.341 , pp. 1291-1292
    • Reardon, W.1    Ross, R.J.2    Sweeney, M.G.3
  • 3
    • 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;30:962-968.
    • (1994) N Engl J Med , vol.30 , pp. 962-968
    • Kadowaki, T.1    Kadowaki, H.2    Mori, Y.3
  • 5
    • 0029875834 scopus 로고
    • Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu (UUR) gene mutation
    • Velho G, Byrne MM, Clèment C, et al. Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu (UUR) gene mutation. Diabetes. 1995;45:478-487.
    • (1995) Diabetes , vol.45 , pp. 478-487
    • Velho, G.1    Byrne, M.M.2    Clèment, C.3
  • 6
    • 0029867177 scopus 로고    scopus 로고
    • Insulin resistance associated with maternally inherited diabetes and deafness
    • Gebhart SS, Shoffner JM, Koontz D, et al. Insulin resistance associated with maternally inherited diabetes and deafness. Metabolism. 1996;45:526-531.
    • (1996) Metabolism , vol.45 , pp. 526-531
    • Gebhart, S.S.1    Shoffner, J.M.2    Koontz, D.3
  • 8
    • 3042631694 scopus 로고    scopus 로고
    • Cesarini PR, Mendon0a E, Fernandes V, et al. Prevalence of immunologic markers (Anti-GAD and Anti-IA-2) in first-degree relatives of patients with type I diabetes in greater area of São Paulo. Rev Assoc Med Bras. 2003;49:395-400.
    • Cesarini PR, Mendon0a E, Fernandes V, et al. Prevalence of immunologic markers (Anti-GAD and Anti-IA-2) in first-degree relatives of patients with type I diabetes in greater area of São Paulo. Rev Assoc Med Bras. 2003;49:395-400.
  • 9
    • 0025742834 scopus 로고
    • Relationship between first-phase insulin secretion and age, HLA, islet cell antibody status, and development of type 1 diabetes in 220 juvenile first-degree relatives of diabetic patients
    • Robert JJ, Deschamps I, Chevenne D, et al. Relationship between first-phase insulin secretion and age, HLA, islet cell antibody status, and development of type 1 diabetes in 220 juvenile first-degree relatives of diabetic patients. Diabetes. 1991;14:718-723.
    • (1991) Diabetes , vol.14 , pp. 718-723
    • Robert, J.J.1    Deschamps, I.2    Chevenne, D.3
  • 10
    • 0028997729 scopus 로고
    • The b-cell and diabetes
    • Polonski KS. The b-cell and diabetes. Diabetes. 1995;45:705-717.
    • (1995) Diabetes , vol.45 , pp. 705-717
    • Polonski, K.S.1
  • 11
    • 0026941505 scopus 로고
    • C-peptide used in the estimation of islet b-cell function in diabetes
    • Gjessing HJ. C-peptide used in the estimation of islet b-cell function in diabetes. Dan Med Bull. 1992;39:438-452.
    • (1992) Dan Med Bull , vol.39 , pp. 438-452
    • Gjessing, H.J.1
  • 13
    • 0021278601 scopus 로고
    • Differential sensitivity to B-cell secretogogues in "early" type I diabetes mellitus
    • Ganda OP, Srikanta S, Brink SJ, et al. Differential sensitivity to B-cell secretogogues in "early" type I diabetes mellitus. Diabetes. 1984;33:516-521.
    • (1984) Diabetes , vol.33 , pp. 516-521
    • Ganda, O.P.1    Srikanta, S.2    Brink, S.J.3
  • 14
    • 0021224142 scopus 로고
    • Pre-type I diabetes. Linear loss of beta cell response to intravenous glucose
    • Srikanta S, Ganda OP, Gleason RE, et al. Pre-type I diabetes. Linear loss of beta cell response to intravenous glucose. Diabetes. 1984;33:717-720.
    • (1984) Diabetes , vol.33 , pp. 717-720
    • Srikanta, S.1    Ganda, O.P.2    Gleason, R.E.3
  • 15
    • 0017236889 scopus 로고
    • Relationships between fasting plasma glucose levels and insulin secretion during intravenous glucose tolerance tests
    • Brunzell JD, Robertson RP, Lerner RL, et al. Relationships between fasting plasma glucose levels and insulin secretion during intravenous glucose tolerance tests. J Clin Endocrinol Metab. 1976;42:222-229.
    • (1976) J Clin Endocrinol Metab , vol.42 , pp. 222-229
    • Brunzell, J.D.1    Robertson, R.P.2    Lerner, R.L.3
  • 16
    • 0020490209 scopus 로고
    • Characterization of the adenine nucleotide translocase of pancreatic islet mitochondria
    • Yousufzai SYK, Bradford MW, Shirago E, et al. Characterization of the adenine nucleotide translocase of pancreatic islet mitochondria. FEBS Lett. 1982;137:205-208.
    • (1982) FEBS Lett , vol.137 , pp. 205-208
    • Yousufzai, S.Y.K.1    Bradford, M.W.2    Shirago, E.3
  • 17
    • 0033569992 scopus 로고    scopus 로고
    • Leu(UUR) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate
    • Leu(UUR) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate. J Biol Chem. 1999;274:29744-29748.
    • (1999) J Biol Chem , vol.274 , pp. 29744-29748
    • Janssen, G.M.C.1    Maassen, J.A.2    van den Ouweland, J.M.W.3
  • 18
    • 0026457825 scopus 로고
    • Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy
    • Yoneda M, Chomyn A, Martinuzzi A, et al. Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy. Proc Natl Acad Sci U S A. 1992;89:11164-11168.
    • (1992) Proc Natl Acad Sci U S A , vol.89 , pp. 11164-11168
    • Yoneda, M.1    Chomyn, A.2    Martinuzzi, A.3
  • 19
    • 0029056559 scopus 로고
    • A case of diabetic amyotrophy associated with 3243 mitochondrial tRNA(leu; UUR) mutation and successful therapy with Coenzyme Q10
    • Suzuki S, Kadowaki H, Atsumi Y, et al. A case of diabetic amyotrophy associated with 3243 mitochondrial tRNA(leu; UUR) mutation and successful therapy with Coenzyme Q10. Endocr J. 1995;42:141-145.
    • (1995) Endocr J , vol.42 , pp. 141-145
    • Suzuki, S.1    Kadowaki, H.2    Atsumi, Y.3
  • 20
    • 0031596402 scopus 로고    scopus 로고
    • The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation
    • Suzuki S, Hinokio Y, Ohtomo M, et al. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation. Diabetologia. 1998;41:584-588.
    • (1998) Diabetologia , vol.41 , pp. 584-588
    • Suzuki, S.1    Hinokio, Y.2    Ohtomo, M.3
  • 21
    • 0030823104 scopus 로고    scopus 로고
    • Leu (UUR) mutation: Clinical features and coenzyme Q10 treatment
    • Leu (UUR) mutation: clinical features and coenzyme Q10 treatment. Mol Aspects Med. 1997;18(suppl 1):s181-s188.
    • (1997) Mol Aspects Med , vol.18 , Issue.SUPPL. 1
    • Suzuki, Y.1    Taniyama, M.2    Muramatsu, T.3
  • 22
    • 0028802967 scopus 로고
    • Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?
    • Silvestre-Aillaud P, BenDahan D, Pasquis-Fluckinger V, et al. Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA? Diabetes Care. 1995;38:1485-1486.
    • (1995) Diabetes Care , vol.38 , pp. 1485-1486
    • Silvestre-Aillaud, P.1    BenDahan, D.2    Pasquis-Fluckinger, V.3
  • 23
    • 0033970418 scopus 로고    scopus 로고
    • Correction of pancreatic B-cell dysfunction with coenzyme Q10 in a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome and diabetes mellitus
    • Liou CW, Huang CH, Lin TK, et al. Correction of pancreatic B-cell dysfunction with coenzyme Q10 in a patient with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome and diabetes mellitus. Eur Neurol. 2000;43:54-56.
    • (2000) Eur Neurol , vol.43 , pp. 54-56
    • Liou, C.W.1    Huang, C.H.2    Lin, T.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.