Hemoglobin H (Hb H) disease is a hereditary hemolytic anemia characterized by the severe deficiency in a-chain synthesis due to a-globin gene deletions or mutations, leading to a relative excess of ß-chains. Due to the high incidence of Hb H disease, which affects the structure, quantity, and glycation capacity o...
Jing Liu, Tian-Qi Yuan, Jian-Gen Wan et al.· Clinical Chemistry· 0 citations
Glial fibrillary acidic protein (GFAP) is an intermediate filament protein predominantly expressed in astrocytes and certain neural stem/progenitor cells within the central nervous system. Growing evidence indicates that serum/plasma GFAP is associated with traumatic brain injury, neurodegenerative diseases (e.g....
E. Jian-fei, Kang Wang, Guo-Ping Wu et al.· Clinical Chemistry· 0 citations
Catecholamines (CAs) are neuroactive substances containing catechol and amino groups. Imbalances in their levels often indicate the development of various diseases, including pheochromocytoma, paraganglioma, neuroblastoma, and hypertension. Therefore, rapid and convenient monitoring of plasma CAs levels is crucia...
Ke-Qi Sun, Yue Zhao, Zhi-Ling An et al.· Clinical Chemistry· 0 citations
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