نتایج جستجو برای: kendalls tau

تعداد نتایج: 20931  

Journal: :Journal of neurochemistry 2004
Tianbing Liu George Perry Hsien W Chan Giuseppe Verdile Ralph N Martins Mark A Smith Craig S Atwood

It has previously been reported that amyloid-beta (Abeta) peptide is neurotrophic to undifferentiated but neurotoxic to differentiated primary neurons. The underlying reasons for this differential effect is not understood. Recently, the toxicity of Abeta to neurons was shown to be dependent upon the activation of cyclin-dependent kinase 5 (Cdk5), thought to promote tau phosphorylation that lead...

Journal: :Sheng li xue bao : [Acta physiologica Sinica] 2005
Xiao-Chuan Wang Jing Zhang Xian Yu Liu Han Zhen-Tao Zhou Yao Zhang Jian-Zhi Wang

Hyperphosphorylated microtubule-associated protein tau is the major protein component of neurofibrillary tangles in the brain of patients with Alzheimer's disease (AD). Until now, there is no effective cure to arrest this hyperphosphorylation. The present study was designed to explore the in vivo preventive effect of melatonin on Alzheimer-like tau hyperphosphorylation. Isoproterenol, a beta-re...

Journal: :Human molecular genetics 2010
Kanae Iijima-Ando LiJuan Zhao Anthony Gatt Christopher Shenton Koichi Iijima

Hyperphosphorylation of the microtubule associated protein tau is detected in the brains of individuals with a range of neurodegenerative diseases including Alzheimer's disease (AD). An imbalance in phosphorylation and/or dephosphorylation of tau at disease-related sites has been suggested to initiate the abnormal metabolism and toxicity of tau in disease pathogenesis. However, the mechanisms u...

Journal: :Biochemical Society transactions 2010
Amy M Pooler Diane P Hanger

Tau is an abundant microtubule-associated protein which regulates the stability of the cytoskeleton. Tau binds microtubules directly through microtubule-binding domains in its C-terminus. However, tau is not only located in the cytosol of cells, but also associated with other intracellular domains, including the plasma membrane, suggesting that tau may have additional functions other than stabi...

Journal: :Cell reports 2016
Tara Vanderweyde Daniel J Apicco Katherine Youmans-Kidder Peter E A Ash Casey Cook Edroaldo Lummertz da Rocha Karen Jansen-West Alissa A Frame Allison Citro John D Leszyk Pavel Ivanov Jose F Abisambra Martin Steffen Hu Li Leonard Petrucelli Benjamin Wolozin

Dendritic mislocalization of microtubule associated protein tau is a hallmark of tauopathies, but the role of dendritic tau is unknown. We now report that tau interacts with the RNA-binding protein (RBP) TIA1 in brain tissue, and we present the brain-protein interactome network for TIA1. Analysis of the TIA1 interactome in brain tissue from wild-type (WT) and tau knockout mice demonstrates that...

Journal: :The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology 2011
Song-In Kim Won-Ki Lee Sang-Soo Kang Sue-Young Lee Myeong-Ja Jeong Hee Jae Lee Sung-Soo Kim Gall V W Johnson Wanjoo Chun

Neurofibrillary tangle (NFT) is a characteristic hallmark of Alzheimer's disease. GSK3β has been reported to play a major role in the NFT formation of tau. Dysfunction of autophagy might facilitate the aggregate formation of tau. The present study examined the role of GSK3β-mediated phosphorylation of tau species on their autophagic degradation. We transfected wild type tau (T4), caspase-3-clea...

2012
Cristian A. Lasagna-Reeves Diana L. Castillo-Carranza Urmi Sengupta Marcos J. Guerrero-Munoz Takaki Kiritoshi Volker Neugebauer George R. Jackson Rakez Kayed

Intracerebral injection of brain extracts containing amyloid or tau aggregates in transgenic animals can induce cerebral amyloidosis and tau pathology. We extracted pure populations of tau oligomers directly from the cerebral cortex of Alzheimer disease (AD) brain. These oligomers are potent inhibitors of long term potentiation (LTP) in hippocampal brain slices and disrupt memory in wild type m...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Dulal Panda Jonathan C Samuel Michelle Massie Stuart C Feinstein Leslie Wilson

The microtubule (MT)-associated protein tau is important in neuronal development and in Alzheimer's and other neurodegenerative diseases. Genetic analyses have established a cause-and-effect relationship between tau dysfunction/misregulation and neuronal cell death and dementia in frontotemporal dementia and parkinsonism associated with chromosome 17; several mutations causing this dementia lea...

Journal: :Biophysical journal 2014
Elka R Georgieva Shifeng Xiao Peter P Borbat Jack H Freed David Eliezer

Tau is a microtubule-associated protein that is genetically linked to dementia and linked to Alzheimer's disease via its presence in intraneuronal neurofibrillary tangle deposits, where it takes the form of aggregated paired helical and straight filaments. Although the precise mechanisms by which tau contributes to neurodegeneration remain unclear, tau aggregation is commonly considered to be a...

Journal: :Neuron 2016
Kathleen M. Schoch Sarah L. DeVos Rebecca L. Miller Seung J. Chun Michaela Norrbom David F. Wozniak Hana N. Dawson C. Frank Bennett Frank Rigo Timothy M. Miller

Pathological evidence for selective four-repeat (4R) tau deposition in certain dementias and exon 10-positioned MAPT mutations together suggest a 4R-specific role in causing disease. However, direct assessments of 4R toxicity have not yet been accomplished in vivo. Increasing 4R-tau expression without change to total tau in human tau-expressing mice induced more severe seizures and nesting beha...

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