نتایج جستجو برای: روش شبهطیفی tau

تعداد نتایج: 390439  

Journal: :PLoS genetics 2016
Kanae Ando Akiko Maruko-Otake Yosuke Ohtake Motoki Hayashishita Michiko Sekiya Koichi M Iijima

Abnormal accumulation of the microtubule-interacting protein tau is associated with neurodegenerative diseases including Alzheimer's disease (AD). β-amyloid (Aβ) lies upstream of abnormal tau behavior, including detachment from microtubules, phosphorylation at several disease-specific sites, and self-aggregation into toxic tau species in AD brains. To prevent the cascade of events leading to ne...

Journal: :Physical review letters 2003
R A Briere G P Chen T Ferguson G Tatishvili H Vogel N E Adam J P Alexander K Berkelman V Boisvert D G Cassel P S Drell J E Duboscq K M Ecklund R Ehrlich R S Galik L Gibbons B Gittelman S W Gray D L Hartill B K Heltsley L Hsu C D Jones J Kandaswamy D L Kreinick A Magerkurth H Mahlke-Krüger T O Meyer N B Mistry J R Patterson D Peterson J Pivarski S J Richichi D Riley A J Sadoff H Schwarthoff M R Shepherd J G Thayer D Urner T Wilksen A Warburton M Weinberger S B Athar P Avery L Breva-Newell V Potlia H Stoeck J Yelton K Benslama B I Eisenstein G D Gollin I Karliner N Lowrey C Plager C Sedlack M Selen J J Thaler J Williams K W Edwards D Besson X Zhao S Anderson V V Frolov D T Gong Y Kubota S Z Li R Poling A Smith C J Stepaniak J Urheim Z Metreveli K K Seth A Tomaradze P Zweber S Ahmed M S Alam J Ernst L Jian M Saleem F Wappler K Arms E Eckhart K K Gan C Gwon K Honscheid D Hufnagel H Kagan R Kass T K Pedlar E von Toerne M M Zoeller H Severini P Skubic S A Dytman J A Mueller S Nam V Savinov J W Hinson J Lee D H Miller V Pavlunin B Sanghi E I Shibata I P J Shipsey D Cronin-Hennessy A L Lyon C S Park W Park J B Thayer E H Thorndike T E Coan Y S Gao F Liu Y Maravin R Stroynowski M Artuso C Boulahouache S Blusk K Bukin E Dambasuren R Mountain H Muramatsu R Nandakumar T Skwarnicki S Stone J C Wang A H Mahmood S E Csorna I Danko G Bonvicini D Cinabro M Dubrovin S McGee A Bornheim E Lipeles S P Pappas A Shapiro W M Sun A J Weinstein

From electron-positron collision data collected with the CLEO detector operating at Cornell Electron Storage Ring near sqrt[s]=10.6 GeV, improved measurements of the branching fractions for tau decays into three explicitly identified hadrons and a neutrino are presented as B(tau(-)-->pi(-)pi(+)pi(-)nu(tau))=(9.13+/-0.05+/-0.46)%, B(tau(-)-->K-pi(+)pi(-)nu(tau))=(3.84+/-0.14+/-0.38) x 10(-3), B(...

2014
Nguyen-Vi Mohamed Vanessa Plouffe Gaudeline Rémillard-Labrosse Emmanuel Planel Nicole Leclerc

Recent studies have demonstrated that human tau can be secreted by neurons and non-neuronal cells, an event linked to the propagation of tau pathology in the brain. In the present study, we confirmed that under physiological conditions, one tau-positive band was detected in the culture medium with an anti-tau antibody recognizing total tau and the Tau-1 antibody directed against unphosphorylate...

2011
Wei Qian Hongwei Liang Jianhua Shi Nana Jin Inge Grundke-Iqbal Khalid Iqbal Cheng-Xin Gong Fei Liu

Abnormal alternative splicing of tau exon 10 results in imbalance of 3R-tau and 4R-tau expression, which is sufficient to cause neurofibrillary degeneration. Splicing factor SC35, a member of the superfamily of the serine/arginine-rich (SR) proteins, promotes tau exon 10 inclusion. The molecular mechanism by which SC35 participates in tau exon 10 splicing remains elusive. In the present study, ...

Journal: :Advances in experimental medicine and biology 2015
Akihiko Takashima

The pathological hallmarks of Alzheimer’s disease (AD) are extracellular β-amyloid deposition and intracellular tau inclusions. While β-amyloid deposition does not correlate with clinical progression of AD, the diffusion of neurofibrillary tangles (NFTs) from the entorhinal cortex to the neocortex, followed by neuronal and synapse loss, matches well with the clinical progression of AD symptomat...

Journal: :Journal of neurochemistry 2012
Connie Luk Yaroslau Compta Nadia Magdalinou Maria José Martí Geshanthi Hondhamuni Henrik Zetterberg Kaj Blennow Radu Constantinescu Yolande Pijnenburg Brit Mollenhauer Claudia Trenkwalder John Van Swieten Wan Zheng Chiu Barbara Borroni Ana Cámara Perdita Cheshire David R Williams Andrew J Lees Rohan de Silva

Characteristic tau isoform composition of the insoluble fibrillar tau inclusions define tauopathies, including Alzheimer's disease (AD), progressive supranuclear palsy (PSP) and frontotemporal dementia with parkinsonism linked to chromosome 17/frontotemporal lobar degeneration-tau (FTDP-17/FTLD-tau). Exon 10 splicing mutations in the tau gene, MAPT, in familial FTDP-17 cause elevation of tau is...

Journal: :The Journal of biological chemistry 2012
Xiaomin Yin Nana Jin Jianlan Gu Jianhua Shi Jianhua Zhou Cheng-Xin Gong Khalid Iqbal Inge Grundke-Iqbal Fei Liu

Tau exon 10, which encodes the second microtubule-binding repeat, is regulated by alternative splicing. Its alternative splicing generates Tau isoforms with three- or four-microtubule-binding repeats, named 3R-tau and 4R-tau. Adult human brain expresses equal levels of 3R-tau and 4R-tau. Imbalance of 3R-tau and 4R-tau causes Tau aggregation and neurofibrillary degeneration. In the present study...

2017
Ivan Koychev Roger N. Gunn Azadeh Firouzian Jennifer Lawson Giovanna Zamboni Basil Ridha Barbara J. Sahakian James B. Rowe Alan Thomas Lynn Rochester Dominic Ffytche Robert Howard Henrik Zetterberg Clare MacKay Simon Lovestone

BACKGROUND Combining PET amyloid-β (Aβ) and tau imaging may be critical for tracking disease progression in Alzheimer's disease (AD). OBJECTIVE We sought to characterize the relationship between Aβ and tau ligands as well as with other measures of pathology. METHODS We conducted a multi-center observational study in early AD (MMSE >20) participants aged 50 to 85 y. The schedule included cog...

Journal: :Brain : a journal of neurology 2003
Prudence M Stanford Claire E Shepherd Glenda M Halliday William S Brooks Peter W Schofield Henry Brodaty Ralph N Martins John B J Kwok Peter R Schofield

The majority of cases with frontotemporal dementia (FTD) have no tau deposition in the brain, yet mutations in the tau gene lead to a similar clinical phenotype with insoluble tau depositing in neuropathological lesions. We report two tau gene mutations at positions +19 and +29, in the intronic sequences immediately following the stem loop structure in exon 10, which segregate with FTD. Exon-tr...

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