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Aldose Reductase–Mediated Phosphorylation of p53 Leads to Mitochondrial Dysfunction and Damage in Diabetic Platelets
Author(s) -
Wai Ho Tang,
Jeremiah Stitham,
Jin Yu,
Renjing Liu,
Seung Hee Lee,
Jing Du,
Gourg Atteya,
Scott Gleim,
Geralyn Spollett,
Kathleen A. Martin,
John Hwa
Publication year - 2014
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.113.005224
Subject(s) - aldose reductase , mitochondrion , reactive oxygen species , platelet , medicine , diabetes mellitus , hyperactivation , endocrinology , apoptosis , platelet activation , microbiology and biotechnology , biology , biochemistry
Platelet abnormalities are well-recognized complications of diabetes mellitus. Mitochondria play a central role in platelet metabolism and activation. Mitochondrial dysfunction is evident in diabetes mellitus. The molecular pathway for hyperglycemia-induced mitochondrial dysfunction in platelets in diabetes mellitus is unknown.

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