메뉴 건너뛰기




Volumn 57, Issue 4, 2008, Pages 799-800

Insulin mutations in diabetes: The clinical spectrum

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIBODY; INSULIN;

EID: 42449143869     PISSN: 00121797     EISSN: 1939327X     Source Type: Journal    
DOI: 10.2337/db08-0116     Document Type: Note
Times cited : (15)

References (20)
  • 1
    • 33646074794 scopus 로고    scopus 로고
    • Genetic basis of maturity-onset diabetes of the young
    • Vaxillaire M, Froguel P: Genetic basis of maturity-onset diabetes of the young. Endocrinol Metab Clin North Am 35:371-384, 2006
    • (2006) Endocrinol Metab Clin North Am , vol.35 , pp. 371-384
    • Vaxillaire, M.1    Froguel, P.2
  • 2
    • 38449089658 scopus 로고    scopus 로고
    • Overview of neonatal diabetes
    • Hamilton-Shield JP: Overview of neonatal diabetes. Endocr Dev 12:12-23, 2007
    • (2007) Endocr Dev , vol.12 , pp. 12-23
    • Hamilton-Shield, J.P.1
  • 8
    • 42449127920 scopus 로고    scopus 로고
    • Nordb0 AM, Ræder H, St0y J, Lipkind GM, Steiner DF, Philipson LH, Bergmann I, Aarskog D, Undlien DE, G Joner, Søvik O, the Norwegian Childhood Diabetes Study Group, Bell GI, Njølstad PR: Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes
    • Molven A, Ringdal M, Nordb0 AM, Ræder H, St0y J, Lipkind GM, Steiner DF, Philipson LH, Bergmann I, Aarskog D, Undlien DE, G Joner, Søvik O, the Norwegian Childhood Diabetes Study Group, Bell GI, Njølstad PR: Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. Diabetes 57:1131-1135, 2008
    • (2008) Diabetes , vol.57 , pp. 1131-1135
    • Molven, A.1    Ringdal, M.2
  • 12
    • 0343853015 scopus 로고
    • A mutation in the B chain coding region is associated with impaired proinsulin conversion in a family with hyperproinsulinemia
    • Chan SJ, Seino S, Gruppuso PA, Schwartz R, Steiner DF: A mutation in the B chain coding region is associated with impaired proinsulin conversion in a family with hyperproinsulinemia. Proc Natl Acad Sci USA 84:2194-2197, 1987
    • (1987) Proc Natl Acad Sci USA , vol.84 , pp. 2194-2197
    • Chan, S.J.1    Seino, S.2    Gruppuso, P.A.3    Schwartz, R.4    Steiner, D.F.5
  • 14
    • 0022004535 scopus 로고
    • Posttrans-lational cleavage of proinsulin is blocked by a point mutation in familial hyperproinsulinemia
    • Shibasaki Y, Kawakami T, Kanazawa Y, Akanuma Y, Takaku F: Posttrans-lational cleavage of proinsulin is blocked by a point mutation in familial hyperproinsulinemia. J Clin Invest 76:378-380, 1985
    • (1985) J Clin Invest , vol.76 , pp. 378-380
    • Shibasaki, Y.1    Kawakami, T.2    Kanazawa, Y.3    Akanuma, Y.4    Takaku, F.5
  • 15
    • 0026688937 scopus 로고
    • A novel point mutation in the human insulin gene giving rise to hyperproinsulinemia (proinsulin Kyoto)
    • Yano H, Kitano N, Morimoto M, Polonsky KS, Imura H, Seino Y: A novel point mutation in the human insulin gene giving rise to hyperproinsulinemia (proinsulin Kyoto). J Clin Invest 89:1902-1907, 1992
    • (1992) J Clin Invest , vol.89 , pp. 1902-1907
    • Yano, H.1    Kitano, N.2    Morimoto, M.3    Polonsky, K.S.4    Imura, H.5    Seino, Y.6
  • 18
    • 0022549577 scopus 로고
    • Diabetes due to secretion of a structurally abnormal insulin (insulin Wakayama): Clinical and functional characteristics of [LeuA3] insulin
    • Nanjo K, Sanke T, Miyano M, Okai K, Sowa R, Kondo M, Nishimura S, Iwo K, Miyamura K, Given BD, et al: Diabetes due to secretion of a structurally abnormal insulin (insulin Wakayama): clinical and functional characteristics of [LeuA3] insulin. J Clin Invest 77:514-519, 1986
    • (1986) J Clin Invest , vol.77 , pp. 514-519
    • Nanjo, K.1    Sanke, T.2    Miyano, M.3    Okai, K.4    Sowa, R.5    Kondo, M.6    Nishimura, S.7    Iwo, K.8    Miyamura, K.9    Given, B.D.10
  • 20
    • 8744262895 scopus 로고    scopus 로고
    • Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2
    • Zung A, Glaser B, Nimri R, Zadik Z: Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2. J Clin Endocrinol Metab 89:5504-5507, 2004
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 5504-5507
    • Zung, A.1    Glaser, B.2    Nimri, R.3    Zadik, Z.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.