Site-specific AGE modifications in the extracellular matrix: A role for glyoxal in protein damage in diabetes

Clinical Chemistry and Laboratory Medicine

Volumn 52, Issue 1, 2014, Pages 39-45

  Voziyan, Paul ^a   Brown, Kyle L ^a   Chetyrkin, Sergei ^a   Hudson, Billy ^a,b  

^a VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

advanced glycation end products; collagen IV; diabetes; extracellular matrix; glyoxal; mass spectrometry; methylglyoxal; pyridoxamine

Indexed keywords

ADVANCED GLYCATION END PRODUCT; CARBONYL DERIVATIVE; GLYOXAL; METHYLGLYOXAL; REACTIVE CARBONYL SPECIES; UNCLASSIFIED DRUG;

CELL INTERACTION; CELL METABOLISM; DIABETES MELLITUS; EXPERIMENTAL DIABETES MELLITUS; EXTRACELLULAR MATRIX; HYPERGLYCEMIA; PRIORITY JOURNAL; PROFESSIONAL KNOWLEDGE; PROTEIN FUNCTION; PROTEIN MODIFICATION; PROTEIN STRUCTURE; REVIEW; TURNOVER TIME;

ALDEHYDES; DIABETES MELLITUS; EXTRACELLULAR MATRIX; EXTRACELLULAR MATRIX PROTEINS; GLYCOSYLATION END PRODUCTS, ADVANCED; GLYOXAL; HUMANS; KETONES;

EID: 84891409949     PISSN: 14346621     EISSN: 14374331     Source Type: Journal    
DOI: 10.1515/cclm-2012-0818     Document Type: Review

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