메뉴 건너뛰기




Volumn 12, Issue 1, 1999, Pages 27-30

The prevalence of mitochondrial gene mutations in childhood diabetes in Japan

Author keywords

[No Author keywords available]

Indexed keywords

LEUCINE TRANSFER RNA; MITOCHONDRIAL DNA;

EID: 0032936226     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPEM.1999.12.1.27     Document Type: Article
Times cited : (12)

References (16)
  • 2
    • 0028910844 scopus 로고
    • Prevalence and clinical characterization of Japanese diabetes mellitus with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNAleu(UUR) gene
    • Odawara M, Sasaki K, Yamashita K, Prevalence and clinical characterization of Japanese diabetes mellitus with an A-to-G mutation at nucleotide 3243 of the mitochondrial tRNAleu(UUR) gene. J Clin Endocrinol Metab 1995; 80: 1290-1294.
    • (1995) J Clin Endocrinol Metab , vol.80 , pp. 1290-1294
    • Odawara, M.1    Sasaki, K.2    Yamashita, K.3
  • 4
    • 0029914927 scopus 로고    scopus 로고
    • Maternally inherited diabetes and deafness: A new diabetes subtype
    • Maassen JA, Kadowaki T. Maternally inherited diabetes and deafness: a new diabetes subtype. Diabetologia 1996; 39: 375-382.
    • (1996) Diabetologia , vol.39 , pp. 375-382
    • Maassen, J.A.1    Kadowaki, T.2
  • 6
    • 0027268052 scopus 로고
    • Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetes
    • Oka Y, Katagiri H, Yazaki Y, Murase T, Kobayashi T. Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetes. Lancet 1993; 342: 527-528.
    • (1993) Lancet , vol.342 , pp. 527-528
    • Oka, Y.1    Katagiri, H.2    Yazaki, Y.3    Murase, T.4    Kobayashi, T.5
  • 7
    • 0024359710 scopus 로고
    • Type 1 (insulin-dependent) diabetes in Japanese children is not a uniform disease
    • Urakami T, Miyamoto Y, Fujita H, Kitagawa T. Type 1 (insulin-dependent) diabetes in Japanese children is not a uniform disease. Diabetologia 1989; 32: 312-315.
    • (1989) Diabetologia , vol.32 , pp. 312-315
    • Urakami, T.1    Miyamoto, Y.2    Fujita, H.3    Kitagawa, T.4
  • 8
    • 0031688082 scopus 로고    scopus 로고
    • The descriptive epidemiology of type I (insulin-dependent) diabetes mellitus in Hokkaido, Japan: Childhood IDDM Hokkaido Registry
    • Matsuura N, Fukuda K, Okuno A, Harada S, Fukushima N, Koike A, Ito Y, Hotsubo T. The descriptive epidemiology of type I (insulin-dependent) diabetes mellitus in Hokkaido, Japan: Childhood IDDM Hokkaido Registry. Diabetes Care 1998; 21: 1632-1636.
    • (1998) Diabetes Care , vol.21 , pp. 1632-1636
    • Matsuura, N.1    Fukuda, K.2    Okuno, A.3    Harada, S.4    Fukushima, N.5    Koike, A.6    Ito, Y.7    Hotsubo, T.8
  • 9
    • 0030483329 scopus 로고    scopus 로고
    • Molecular epidemiology of IDDM in the Western Pacific rim region
    • Matsuura N, Ko KW, Park YS, Elliott R, WHO DIAMOND Molecular Epidemiology Sub-Project Group. Molecular epidemiology of IDDM in the Western Pacific rim region. Diab Res Clin Pract 1996; 34 (Suppl): s117-s123.
    • (1996) Diab Res Clin Pract , vol.34 , Issue.SUPPL.
    • Matsuura, N.1    Ko, K.W.2    Park, Y.S.3    Elliott, R.4
  • 11
    • 0028574053 scopus 로고
    • Mitochondrial DNA sequence variation in human evolution and disease
    • Wallace DC. Mitochondrial DNA sequence variation in human evolution and disease. Proc Natl Acad Sci USA 1994; 91: 8739-8745.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 8739-8745
    • Wallace, D.C.1
  • 12
    • 0030046495 scopus 로고    scopus 로고
    • Mitochondria and diabetes. Genetic, biochemical, and clinical implications of the cellular energy circuit
    • Gerbitz KD, Gempel K, Brdiczka D. Mitochondria and diabetes. Genetic, biochemical, and clinical implications of the cellular energy circuit. Diabetes 1996; 45: 113-126.
    • (1996) Diabetes , vol.45 , pp. 113-126
    • Gerbitz, K.D.1    Gempel, K.2    Brdiczka, D.3
  • 16
    • 6844259878 scopus 로고    scopus 로고
    • A new point mutation (3426, A to G) in mitochondrial NADH dehydrogenase gene in Korean diabetic patients which mimics 3243 mutation by restriction fragment length polymorphism pattern
    • Shin CS, Kim SK, Park KS, Kim WB Kim SY, Cho BY, Lee HK, Koh CS, Shin CH, Lee JB. A new point mutation (3426, A to G) in mitochondrial NADH dehydrogenase gene in Korean diabetic patients which mimics 3243 mutation by restriction fragment length polymorphism pattern. Endocr J 1998; 45: 105-110.
    • (1998) Endocr J , vol.45 , pp. 105-110
    • Shin, C.S.1    Kim, S.K.2    Park, K.S.3    Kim, W.B.4    Kim, S.Y.5    Cho, B.Y.6    Lee, H.K.7    Koh, C.S.8    Shin, C.H.9    Lee, J.B.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.