Deciphering a Molecular Mechanism of Neonatal Diabetes Mellitus by the Chemical Synthesis of a Protein Diastereomer, [d-AlaB8]Human Proinsulin-Reference-Cited by-同舟云学术

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Deciphering a Molecular Mechanism of Neonatal Diabetes Mellitus by the Chemical Synthesis of a Protein Diastereomer, [d-AlaB8]Human Proinsulin

Published:2014-08 Issue:34 Volume:289 Page:23683-23692
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Avital-Shmilovici Michal,Whittaker Jonathan,Weiss Michael A.,Kent Stephen B.H.

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference58 articles.

1. Aetiopathology and genetic basis of neonatal diabetes;Shield;Arch. Dis. Child. Fetal Neonatal Ed,1997

2. Insulin gene mutations as a cause of permanent neonatal diabetes;Støy;Proc. Natl. Acad. Sci. U.S.A,2007

3. Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus;Colombo;J. Clin. Investig,2008

4. Mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood;Edghill;Diabetes,2008

5. Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes;Molven;Diabetes,2008

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1. A Review of the Biosynthesis and Structural Implications of Insulin Gene Mutations Linked to Human Disease;Cells;2023-03-25

2. Diabetes-Associated Mutations in Proinsulin Provide a “Molecular Rheostat” of Nascent Foldability;Current Diabetes Reports;2022-02

3. The rippled β-sheet layer configuration—a novel supramolecular architecture based on predictions by Pauling and Corey;Chemical Science;2022

4. A viral insulin-like peptide is a natural competitive antagonist of the human IGF-1 receptor;Molecular Metabolism;2021-11

5. Structural Lessons From the Mutant Proinsulin Syndrome;Frontiers in Endocrinology;2021-09-30

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