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Volumn 786, Issue , 1996, Pages 72-81

Involvement of mitochondrial gene abnormalities in the pathogenesis of diabetes mellitus

Author keywords

[No Author keywords available]

Indexed keywords

INSULIN; MITOCHONDRIAL DNA;

EID: 0029742667     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1996.tb39053.x     Document Type: Conference Paper
Times cited : (5)

References (25)
  • 1
    • 0027474253 scopus 로고
    • Mitochondrial gene mutation and insulin-deficient type of diabetes mellitus
    • KADOWAKI, H., K. TOBE, Y. MORI et al. 1993. Mitochondrial gene mutation and insulin-deficient type of diabetes mellitus. Lancet 341: 893-894.
    • (1993) Lancet , vol.341 , pp. 893-894
    • Kadowaki, H.1    Tobe, K.2    Mori, Y.3
  • 2
    • 0026906885 scopus 로고
    • Leu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
    • Leu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat. Genet. 1: 368-371.
    • (1992) Nat. Genet. , vol.1 , pp. 368-371
    • Van Den Ouweland, J.M.W.1    Lemkes, H.H.P.J.2    Ruitenbeek, W.3
  • 3
    • 0025285086 scopus 로고
    • Lessons learned from molecular biology of insulin-gene mutations
    • STEINER, D. F., H. S. TAGER, S. J. CHAN et al. 1990. Lessons learned from molecular biology of insulin-gene mutations. Diabetes Care 13: 600-609.
    • (1990) Diabetes Care , vol.13 , pp. 600-609
    • Steiner, D.F.1    Tager, H.S.2    Chan, S.J.3
  • 4
    • 0023886838 scopus 로고
    • Insulin-resistant diabetes due to a point mutation that prevents insulin proreceptor processing
    • YOSHIMASA, Y., S. SEINO, J. WHITTAKER et al. 1988. Insulin-resistant diabetes due to a point mutation that prevents insulin proreceptor processing. Science 240: 784-787.
    • (1988) Science , vol.240 , pp. 784-787
    • Yoshimasa, Y.1    Seino, S.2    Whittaker, J.3
  • 5
    • 0023896248 scopus 로고
    • Two mutant alleles of the insulin receptor gene in a patient with extreme insulin resistance
    • KADOWAKI, T., C. L. BEVINS, A. CAMA et al. 1988. Two mutant alleles of the insulin receptor gene in a patient with extreme insulin resistance. Science 240: 787-790.
    • (1988) Science , vol.240 , pp. 787-790
    • Kadowaki, T.1    Bevins, C.L.2    Cama, A.3
  • 6
    • 0024323165 scopus 로고
    • Human diabetes associated with a mutation in the tyrosine kinase domain of the insulin receptor
    • ODAWARA, M., T. KADOWAKI, R. YAMAMOTO-HONDA et al. 1989. Human diabetes associated with a mutation in the tyrosine kinase domain of the insulin receptor. Science 245: 66-68.
    • (1989) Science , vol.245 , pp. 66-68
    • Odawara, M.1    Kadowaki, T.2    Yamamoto-Honda, R.3
  • 7
    • 0024348797 scopus 로고
    • Human diabetes associated with a deletion of the tyrosine kinase domain of the insulin receptor
    • TAIRA, M., M. TAIRA, N. HASHIMOTO et al. 1989. Human diabetes associated with a deletion of the tyrosine kinase domain of the insulin receptor. Science 245: 63-66.
    • (1989) Science , vol.245 , pp. 63-66
    • Taira, M.1    Taira, M.2    Hashimoto, N.3
  • 8
    • 0026761432 scopus 로고
    • Mutations in the insulin receptor gene
    • TAYLOR, S. I., A. CAMA, D. ACCILI et al. 1992. Mutations in the insulin receptor gene. Endocr. Rev. 13: 566-595.
    • (1992) Endocr. Rev. , vol.13 , pp. 566-595
    • Taylor, S.I.1    Cama, A.2    Accili, D.3
  • 9
    • 0026562918 scopus 로고
    • Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus
    • VIONNET, N., M. STOFFEL, J. TAKEDA et al. 1992. Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus. Nature 356: 721-722.
    • (1992) Nature , vol.356 , pp. 721-722
    • Vionnet, N.1    Stoffel, M.2    Takeda, J.3
  • 10
    • 0027472126 scopus 로고
    • Familial hyperglycemia due to mutations in glucokinase: Definition of a new subtype of non-insulin-dependent (type 2) diabetes mellitus
    • FROGUEL, P., H. ZOUALI, N. VIONNET et al. 1993. Familial hyperglycemia due to mutations in glucokinase: definition of a new subtype of non-insulin-dependent (type 2) diabetes mellitus. N. Engl. J. Med. 328: 697-702.
    • (1993) N. Engl. J. Med. , vol.328 , pp. 697-702
    • Froguel, P.1    Zouali, H.2    Vionnet, N.3
  • 11
    • 0027312093 scopus 로고
    • Mutations of the human glucokinase gene and diabetes mellitus
    • BELL, G. I., P. FROGUEL, S. HISHI et al. 1993. Mutations of the human glucokinase gene and diabetes mellitus. Trends Endocr. Metab. 4: 86-90.
    • (1993) Trends Endocr. Metab. , vol.4 , pp. 86-90
    • Bell, G.I.1    Froguel, P.2    Hishi, S.3
  • 13
    • 0026793446 scopus 로고
    • Role of glucose and insulin resistance in development of type 2 diabetes mellitus: Results of a 25-year follow-up study
    • MARTIN, B. C., J. H. WARRAM, A. S. KROLEWSKI, R. N. BERGMAN, J. S. SOELDNER & C. R. KAHN. 1992. Role of glucose and insulin resistance in development of type 2 diabetes mellitus: results of a 25-year follow-up study. Lancet 340: 925-929.
    • (1992) Lancet , vol.340 , pp. 925-929
    • Martin, B.C.1    Warram, J.H.2    Krolewski, A.S.3    Bergman, R.N.4    Soeldner, J.S.5    Kahn, C.R.6
  • 14
    • 0028229508 scopus 로고
    • Insulin resistance or insulin deficiency. Which is the primary cause of NIDDM?
    • TAYLOR, S. I., D. ACCILI & Y. IMAI. 1994. Insulin resistance or insulin deficiency. Which is the primary cause of NIDDM? Diabetes 43: 735-740.
    • (1994) Diabetes , vol.43 , pp. 735-740
    • Taylor, S.I.1    Accili, D.2    Imai, Y.3
  • 15
    • 0025854490 scopus 로고
    • Importance of maternal history of non-insulin dependent diabetes patients
    • ALCOLADO, J. C. & R. ALCOLADO. 1991. Importance of maternal history of non-insulin dependent diabetes patients. Br. Med. J. 302: 1178-1180.
    • (1991) Br. Med. J. , vol.302 , pp. 1178-1180
    • Alcolado, J.C.1    Alcolado, R.2
  • 16
    • 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 348: 651-653.
    • (1990) Nature , vol.348 , pp. 651-653
    • Goto, Y.1    Nonaka, I.2    Horai, S.3
  • 17
    • 0028328317 scopus 로고
    • A subtype of diabetes mellitus associated with mutation of mitochondrial DNA
    • KADOWAKI, T., H. KADOWAKI, Y. MORI et al. 1994. A subtype of diabetes mellitus associated with mutation of mitochondrial DNA. N. Engl. J. Med. 330: 962-968.
    • (1994) N. Engl. J. Med. , vol.330 , pp. 962-968
    • Kadowaki, T.1    Kadowaki, H.2    Mori, Y.3
  • 18
    • 0025992003 scopus 로고
    • Respiration-deficient cells are caused by a single point mutations in the mitochondrial tRNA-Leu(UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
    • KOBAYASHI, Y., M. Y. MOMOI, K. TOMINAGA et al. 1991. Respiration-deficient cells are caused by a single point mutations in the mitochondrial tRNA-Leu(UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Am. J. Hum. Genet. 49: 590-599.
    • (1991) Am. J. Hum. Genet. , vol.49 , pp. 590-599
    • Kobayashi, Y.1    Momoi, M.Y.2    Tominaga, K.3
  • 19
    • 0021776150 scopus 로고
    • Diabetes mellitus. Report of WHO study group
    • World Health Organization. 1985. Diabetes mellitus. Report of WHO study group. Tech. Rep. Ser. 727: 1-113.
    • (1985) Tech. Rep. Ser. , vol.727 , pp. 1-113
  • 21
    • 0019423856 scopus 로고
    • Sequence and organization of the human mitochondrial genome
    • ANDERSON, S., A. T. BANKIER, B. G. BARRELL et al. 1981. Sequence and organization of the human mitochondrial genome. Nature 290: 457-465.
    • (1981) Nature , vol.290 , pp. 457-465
    • Anderson, S.1    Bankier, A.T.2    Barrell, B.G.3
  • 22
    • 0023850178 scopus 로고
    • Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
    • SAIKI, R. K., D. H. GELFAND, S. STOFFEL et al. 1988. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science 239: 487-491.
    • (1988) Science , vol.239 , pp. 487-491
    • Saiki, R.K.1    Gelfand, D.H.2    Stoffel, S.3
  • 23
    • 1842267323 scopus 로고
    • Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA
    • GIBBS, R. A., P. N. NGUYEN, L. J. MCBRIDE et al. 1989. Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA. Proc. Natl. Acad. Sci. USA 86: 1919-1923.
    • (1989) Proc. Natl. Acad. Sci. USA , vol.86 , pp. 1919-1923
    • Gibbs, R.A.1    Nguyen, P.N.2    Mcbride, L.J.3
  • 25
    • 0028024242 scopus 로고
    • Lack of association between mitochondrial gene mutation np 3243 and type 1 diabetes mellitus and autoimmune thyroid diseases
    • ODAWARA, M., K. SASAKI & K. YAMASHITA. 1994. Lack of association between mitochondrial gene mutation np 3243 and type 1 diabetes mellitus and autoimmune thyroid diseases. Lancet 344: 1086.
    • (1994) Lancet , vol.344 , pp. 1086
    • Odawara, M.1    Sasaki, K.2    Yamashita, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.