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2. Hyperproinsulinemia in a three-generation Caucasian family due to mutant proinsulin (Arg65-His) not associated with imparied glucose tolerance: the contribution of mutant proinsulin to insulin bioactivity. Röder ME, Vissing H, Nauck MA. J Clin Endocrinol Metab; 1996 Apr; 81(4):1634-40. PubMed ID: 8636380 [Abstract] [Full Text] [Related]
4. Posttranslational cleavage of proinsulin is blocked by a point mutation in familial hyperproinsulinemia. Shibasaki Y, Kawakami T, Kanazawa Y, Akanuma Y, Takaku F. J Clin Invest; 1985 Jul; 76(1):378-80. PubMed ID: 4019786 [Abstract] [Full Text] [Related]
11. Hyperproinsulinemia in a family with a proposed defect in conversion is linked to the insulin gene. Elbein SC, Gruppuso P, Schwartz R, Skolnick M, Permutt MA. Diabetes; 1985 Aug; 34(8):821-4. PubMed ID: 2991050 [Abstract] [Full Text] [Related]
14. 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. Proc Natl Acad Sci U S A; 1987 Apr; 84(8):2194-7. PubMed ID: 3470784 [Abstract] [Full Text] [Related]
16. Two novel mutations in the vasopressin V2 receptor gene in unrelated Japanese kindreds with nephrogenic diabetes insipidus. Tsukaguchi H, Matsubara H, Aritaki S, Kimura T, Abe S, Inada M. Biochem Biophys Res Commun; 1993 Dec 15; 197(2):1000-10. PubMed ID: 8267567 [Abstract] [Full Text] [Related]
19. Hyperproinsulinemia in Japan. Kanazawa Y, Kuzuya N, Takeuchi Y, Kubo F, Yamamoto W, Noda M. Diabetes Res Clin Pract; 1994 Oct 15; 24 Suppl():S143-4. PubMed ID: 7859596 [Abstract] [Full Text] [Related]
20. Cloning and analysis of the gene encoding hummingbird proinsulin. Fan L, Gardner P, Chan SJ, Steiner DF. Gen Comp Endocrinol; 1993 Jul 15; 91(1):25-30. PubMed ID: 8405887 [Abstract] [Full Text] [Related] Page: [Next] [New Search]