نتایج جستجو برای: tau proteins

تعداد نتایج: 574187  

Journal: :Journal of cell science 2001
H N Dawson A Ferreira M V Eyster N Ghoshal L I Binder M P Vitek

Conflicting evidence supports a role for tau as an essential neuronal cytoskeletal protein or as a redundant protein whose function can be fulfilled by other microtubule-associated proteins. To investigate the function of tau in axonogenesis, we created tau deficient mice by disrupting the TAU gene. The engineered mice do not express the tau protein, appear physically normal and are able to rep...

Journal: :Science 2008
Ram Dixit Jennifer L Ross Yale E Goldman Erika L F Holzbaur

Dynein and kinesin motor proteins transport cellular cargoes toward opposite ends of microtubule tracks. In neurons, microtubules are abundantly decorated with microtubule-associated proteins (MAPs) such as tau. Motor proteins thus encounter MAPs frequently along their path. To determine the effects of tau on dynein and kinesin motility, we conducted single-molecule studies of motor proteins mo...

Journal: :Trends in cell biology 2005
Peter W Baas Liang Qiang

Recent studies shed new light on a potential cascade of events by which neurological diseases such as Alzheimer's lead to axonal degeneration. In this model, the pathology starts with an elevation in microtubule-associated proteins (MAPs) such as tau. This renders the microtubules less accessible to motor proteins, which impairs their capacity to sustain anterograde axonal transport of proteins...

Journal: :Clinical chemistry 2015
Daniel R Beriault Eleftherios P Diamandis Erik Portelius Armand Perret-Liaudet Stephen Salloway

The initial pathophysiologic changes of AD are found in the hippocampus region of the brain, disrupting memory and the ability to learn. AD progression is linked to nerve cell dysfunction and cell death due to the accumulation of 2 protein aggregates: -amyloid (A ) and tau. In the cerebrospinal fluid (CSF), these proteins are biomarkers for AD. Cleavage of the amyloid precursor protein (APP) ge...

Journal: :Muscle & nerve 2009
Mohammad Salajegheh Jack L Pinkus Remedios Nazareno Anthony A Amato Kenneth C Parker Steven A Greenberg

Sarcoplasmic accumulation of phosphorylated-tau has been widely stated to occur in and contribute to the pathogenesis of muscle disease in inclusion body myositis. Twenty inflammatory myopathy and 10 normal muscle samples along with a range of other tissues were stained with anti-"tau" antibodies (tau-5, pS422, and SMI-31). Myonuclear and sarcoplasmic fractions were prepared using differential ...

Journal: :Journal of neurochemistry 1997
N Sergeant J P David M Goedert R Jakes P Vermersch L Buée D Lefranc A Wattez A Delacourte

PHF-tau proteins are the major components of the paired helical filament (PHF) from Alzheimer's disease (AD) neurofibrillary lesions. They differ both qualitatively and quantitatively in their degree of phosphorylation when compared with native tau proteins. However, little is known about the extent and heterogeneity of phosphorylated sites or the isoform composition and the isoelectric variant...

2016
Sacnicte Ramirez-Rios Eric Denarier Eléa Prezel Angélique Vinit Virginie Stoppin-Mellet François Devred Pascale Barbier Vincent Peyrot Carmen Laura Sayas Jesus Avila Leticia Peris Annie Andrieux Laurence Serre Anne Fourest-Lieuvin Isabelle Arnal

Proper regulation of microtubule dynamics is essential for cell functions and involves various microtubule-associated proteins (MAPs). Among them, end-binding proteins (EBs) accumulate at microtubule plus ends, whereas structural MAPs bind along the microtubule lattice. Recent data indicate that the structural MAP tau modulates EB subcellular localization in neurons. However, the molecular dete...

Journal: :International journal of molecular medicine 2015
Cao Chen Yan Lv Qi Shi Bao-Yun Zhang Li-Na Chen Kang Xiao Jing Sun Xiao-Ping Dong

The aggregations of tau protein in brain tissue have been described in a large number of neurodegenerative diseases; however, due to the lack of tau isoform- or exon-specific antibodies, the exact situations under which various brain tau isoforms can be found and their exact contributions during disease progression remain unknown. Therefore, in this study, we prepared tau exon-specific monoclon...

Journal: :Neuroscience letters 1998
M L Caillet-Boudin L Dupont-Wallois C Soulié A Delacourte

Phosphorylation is the major post-translational modification of Tau proteins and it plays an important role in Tau biological functions. Hyperphosphorylation of these proteins occurs during neurodegenerative disorders such as Alzheimer's disease. It was hypothesized that some variants of apolipoprotein E (apo E) may have a protective effect against the normal or pathological phosphorylation of ...

Journal: :Human molecular genetics 2008
Jose A Rodríguez-Navarro Ana Gómez Izaskun Rodal Juan Perucho Armando Martinez Vicente Furió Israel Ampuero María J Casarejos Rosa M Solano Justo García de Yébenes Maria A Mena

Deposition of proteins leading to amyloid takes place in some neurodegenerative diseases such as Alzheimer's disease and Huntington's disease. Mutations of tau and parkin proteins produce neurofibrillary abnormalities without deposition of amyloid. Here we report that mature, parkin null, over-expressing human mutated tau (PK(-/-)/Tau(VLW)) mice have altered behaviour and dopamine neurotransmis...

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