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Volumn 98, Issue 6, 1996, Pages 636-639

Absence of association between the Gly40→Ser mutation in the human glucagon receptor and Japanese patients with non-insulin-dependent diabetes mellitus or impaired glucose tolerance

Author keywords

[No Author keywords available]

Indexed keywords

GLUCAGON RECEPTOR; GLYCINE; SERINE;

EID: 0029658230     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050274     Document Type: Article
Times cited : (9)

References (10)
  • 3
    • 1842267323 scopus 로고
    • Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct DNA sequencing of in vitro amplified cDNA
    • Gibbs RA, Nguyen PN, McBride LJ, Koepf SM, Caskey CT (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    Koepf, S.M.4    Caskey, C.T.5
  • 5
    • 0029051799 scopus 로고
    • Lack of association between the Gly40ser polymorphism in the glucagon receptor gene and NIDDM in Finland
    • Huang X, Orho M, Lehto M, Groop L (1995) Lack of association between the Gly40ser polymorphism in the glucagon receptor gene and NIDDM in Finland. Diabetologia 38:1246-1248
    • (1995) Diabetologia , vol.38 , pp. 1246-1248
    • Huang, X.1    Orho, M.2    Lehto, M.3    Groop, L.4
  • 6
    • 0028024242 scopus 로고
    • Lack of association between mitochondrial gene mutation np 3243 and type 1 diabetes mellitus and autoimmune thyroid diseases
    • Odawara M, Sasaki K, Nagafuchi S, Tanae A, Yamashita K (1994) Lack of association between mitochondrial gene mutation np 3243 and type 1 diabetes mellitus and autoimmune thyroid diseases [letter]. Lancet 344:1086
    • (1994) Lancet , vol.344 , pp. 1086
    • Odawara, M.1    Sasaki, K.2    Nagafuchi, S.3    Tanae, A.4    Yamashita, K.5
  • 9
    • 0027369567 scopus 로고
    • Prevalence of mitochondrial gene mutations in families with diabetes mellitus
    • Vionnet N, Passa P, Froguel P (1993) Prevalence of mitochondrial gene mutations in families with diabetes mellitus [letter]. Lancet 342:1429-1430
    • (1993) Lancet , vol.342 , pp. 1429-1430
    • Vionnet, N.1    Passa, P.2    Froguel, P.3
  • 10
    • 0021776150 scopus 로고
    • Diabetes mellitus. Report of WHO study group
    • World Health Organization (1985) Diabetes mellitus. Report of WHO study group. World Health Organ Tech Rep Ser 727:1-113
    • (1985) World Health Organ Tech Rep Ser , vol.727 , pp. 1-113


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.