Mutant insulin syndromes.

@article{Vinik1988MutantIS,
  title={Mutant insulin syndromes.},
  author={Aaron I Vinik and G. Bell},
  journal={Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme},
  year={1988},
  volume={20 1},
  pages={
          1-10
        }
}
  • A. Vinik, G. Bell
  • Published 1988
  • Medicine, Biology
  • Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
Highly sensitive procedures for the characterization of molecular species of insulin in the circulation and for the isolation of the gene encoding human insulin have recently been developed. Nine subjects with abnormal forms of insulin or proinsulin have been reported. These include: [Leu B25], [Ser B24], [Leu A3] insulin as well as others that have not yet been identified. The clinical syndrome associated with the secretion of an abnormal insulin or proinsulin molecule presents with apparent… 
INS-gene mutations: from genetics and beta cell biology to clinical disease.
A new case of familial hyperproinsulinemia.
TLDR
The data strongly suggest that this family is a new case of familial hyperproinsulinemia, and the defect resides in the proinsulin molecule, not in the converting enzymes.
Mutant INS-Gene Induced Diabetes of Youth: Proinsulin Cysteine Residues Impose Dominant-Negative Inhibition on Wild-Type Proinsulin Transport
TLDR
The molecular pathogenesis of MIDY is initiated by perturbation of the disulfide-coupled folding pathway of wild-type proinsulin, and the early events described herein precede cell death and loss of beta cell mass.
Proinsulin misfolding and diabetes: mutant INS gene-induced diabetes of youth
Evaluation of conformational changes in diabetes‐associated mutation in insulin a chain: A molecular dynamics study
TLDR
The analysis of molecular dynamics simulations in wild‐type and mutant (CysA7 to Tyr or C(A7)Y) insulin A chain in aqueous solutions suggests that MIDY mutant involves formation of a partially folded intermediate with conformational change in N‐terminal region in A chain that generates flexible N-terminal domain, which may lead to the abnormal interactions with other proinsulins in the aggregation process.
Prevalence of beta allele of the insulin gene in type II diabetes mellitus
TLDR
The more frequent occurrence of the alpha allele of the insulin gene within the control population as compared with a prevalence of the beta allele in the diabetic patients was observed and seems to be associated with the disease.
Molecular etiologies of mody and other early-onset forms of diabetes
TLDR
Biochemical and genetic studies have demonstrated that the MODY genes are functionally related and form an integrated transcriptional network that is important for many metabolic pathways.
Genetic determinants of type 2 diabetes mellitus
TLDR
To make sense of human type 2 diabetes in the post‐genomic era, it is essential to have well‐defined phenotypes in addition to sufficient numbers of individuals with the appropriate pedigree structure from families and/or communities.
“Register-shift” insulin analogs uncover constraints of proteotoxicity in protein evolution
TLDR
The results suggest that this binding mode is associated with toxic misfolding and so is disallowed in evolution, and the implicit threat of proteotoxicity limits sequence variation among vertebrate insulins and insulin-like growth factors.
Insulin Resistance, Diabetes and its Complications
  • D. Ng
  • Medicine, Biology
  • 2006
TLDR
The development of clinical diabetes is a result of combined genetic susceptibility and environmental stressors, and identification of candidate genes may provide a more refined framework for either better understanding of the pathophysiological processes and/or for identifying novel targets for pharmacological interventions.
...
1
2
3
...