A subdivided molecular architecture with separate features and stepwise emergence among proinsulin C-peptides
Author:
Funder
Swedish Research Council
Karolinska Institutet
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference35 articles.
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2. Acidic residues on the N-terminus of proinsulin C-Peptide are important for the folding of insulin precursor;Chen;J. Biochem.,2002
3. In vitro refolding of human proinsulin. Kinetic intermediates, putative disulfide-forming pathway folding initiation site, and potential role of C-peptide in folding process;Qiao;J. Biol. Chem.,2003
4. Proinsulin C-peptide elicits disaggregation of insulin resulting in enhanced physiological insulin effects;Shafqat;Cell Mol. Life Sci.,2006
5. C-peptide: a molecule balancing insulin states in secretion and diabetes-associated depository conditions;Landreh;Horm. Metab. Res.,2013
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2. C‐peptide prevents NF‐κB from recruiting p300 and binding to the inos promoter in diabetic nephropathy;The FASEB Journal;2018-01-05
3. Unraveling the aggregation propensity of human insulin C‐peptide;Peptide Science;2017-03
4. Alcohol dehydrogenase, SDR and MDR structural stages, present update and altered era;Chemico-Biological Interactions;2015-06
5. C-peptide: New findings and therapeutic possibilities;Diabetes Research and Clinical Practice;2015-03
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