|1.||Cho, Goang-Won: 1 article (10/2011)|
|2.||Park, Jiseon: 1 article (10/2011)|
|3.||Hong, Yoon-Ho: 1 article (10/2011)|
|4.||Kim, Seung Hyun: 1 article (10/2011)|
|5.||Kim, Myung-Hwa: 1 article (10/2011)|
|6.||Noh, Min-Young: 1 article (10/2011)|
|7.||Ku, Il-Whea: 1 article (10/2011)|
|8.||Kang, Byung Yong: 1 article (10/2011)|
|9.||Medina, Miguel: 1 article (01/2010)|
|10.||Avila, Jesús: 1 article (01/2010)|
|1.||Alzheimer Disease (Alzheimer's Disease)
10/01/2011 - "Glycogen synthase kinase-3β (GSK-3β), a serine/threonine kinase also known as tau protein kinase I, has been implicated in the pathogenic conditions of Alzheimer's disease. "
10/21/1996 - "Colocalization of these epitopes suggests that tau protein kinase I/glycogen synthase kinase-3 beta abnormally phosphorylates tau and is in a position to disrupt neuronal metabolism in anatomical areas vulnerable to Alzheimer's disease."
04/02/1996 - "In rat hippocampal culture, betaA exposure activates tau protein kinase I/glycogen synthase kinase 3beta (TPKI/GSK-3beta), which phosphorylates tau protein into Alzheimer disease-like forms, resulting in neuronal death. "
02/01/1995 - "Previously, tau protein kinase I/glycogen synthase kinase-3 beta/kinase FA(TPKI/GSK-3 beta/FA) was identified as a brain microtubule-associated tau kinase possibly involved in the Alzheimer disease-like phosphorylation of tau. "
02/01/1995 - "Tau protein kinase I/GSK-3 beta/kinase FA in heparin phosphorylates tau on Ser199, Thr231, Ser235, Ser262, Ser369, and Ser400 sites phosphorylated in Alzheimer disease brain."
10/21/1996 - "Here we present immunocytochemistry from Alzheimer's disease brains showing that focal subpopulations of hippocampal CA1 pyramidal neurons and neuritic plaques are strongly reactive for tau protein kinase I/glycogen synthase kinase-3 beta and tau phosphoserine 413 in early stages of pathology. "
01/01/2010 - "Besides having been identified as the major tau protein kinase, GSK-3 mediates Aβ neurotoxicity, plays an essential role in synaptic plasticity and memory, might be involved in Aβ formation, and it has an important role in inflammation and neuronal survival, all key features of AD neuropathology. "
|1.||Glycogen Synthase (Synthase I)
|3.||glycogen synthase kinase 3 beta
|4.||Cyclin-Dependent Kinase 5
|5.||Glycogen Synthase Kinase 3
|6.||Glycogen Synthase Kinases
|7.||Protein-Serine-Threonine Kinases (Protein-Serine-Threonine Kinase)
|8.||tau Proteins (tau Protein)