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61篇 您的检索式:作者名="Inger S"
    题名 作者 年代 出处 被引量
1Trace element modeling of pelite- derived gTanites 显示文摘HARRIS N B W INGER S 1992Contributions to Mineralogy and Petrology1992,110,:1
2Geochemical constraints on leucogranitemagmatism in the Langtang Valley, Nepal Himalaya显示文摘Inger S Harris N 1993Journal ofPetrology1993,34,:1
3Flocculation of colloidal silica with hydrolyzed aluminum:an Al solid state NMR investigation显示文摘 BOTTERO J Y D REN INGER L S 1997Langmuir1997,13,:1
4Source partitioning using stable isotopes: coping with too muchvariation 显示文摘Parnell A C Inger R Bearhop S 2010PLoS ONE2010,5,3:1
5A pilot study of sail and water restriction in patients with chronic heart failure 显示文摘Henriette P Inger E Karl S 2010Scand Cardiov J2010,44,4:1
6Carbon and nitrogen in forest floor and mineral soil under six common European tree species 显示文摘Lars V Inger K S Ingeborg C 2008Forest Ecology and Management2008,255,:1
7Source partitioning using stable isotopes: coping with too much variation显示文摘Parnell A C Inger R Bearhop S 2010PLoS One2010,5,3:1
8Are B lymphocytes of importance in severe Staphylococcus aureus infections? 显示文摘INGER G OLOF H MARTIN S 2000Infection and Immunity2000,68,5:1
9Stress and birefringence measurements during the uniaxial elongation of polystyrene melts 显示文摘VENERUS D C ZHU S H OTI'INGER H C 1999J Rheol1999,43,:1
10Source Partitioning Using Stable Isotopes: Coping with Too Much Variation显示文摘Parnell A C Inger R Bearhop S Jackson AL 2010PLoS ONE2010,5,3:1
11Targeting γ-secretase triggers the selective enrichment of oligomeric APP-CTFs in brain extracellular vesicles from Alzheimer cell and mouse models显示文摘Background:We recently demonstrated an endolysosomal accumulation of theβ-secretase-derived APP C-terminal fragment(CTF)C99 in brains of Alzheimer disease(AD)mouse models.Moreover,we showed that the treatment with theγ-secretase inhibitor(D6)led to further increased endolysosomal APP-CTF levels,but also revealed extracellular APP-CTF-associated immunostaining.We here hypothesized that this latter staining could reflect extracellular vesicle(EV)-associated APP-CTFs and aimed to characterize theseγ-secretase inhibitor-induced APPCTFs.Methods:EVs were purified from cell media or mouse brains from vehicle-or D6-treated C99 or APPswedish expressing cells/mice and analyzed for APP-CTFs by immunoblot.Combined pharmacological,immunological and genetic approaches(presenilin invalidation and C99 dimerization mutants(GXXXG))were used to characterize vesicle-containing APP-CTFs.Subcellular APP-CTF localization was determined by immunocytochemistry.Results:Purified EVs from both AD cell or mouse models were enriched in APP-CTFs as compared to EVs from control cells/brains.Surprisingly,EVs from D6-treated cells not only displayed increased C99 and C99-derived C83 levels but also higher molecular weight(HMW)APP-CTF-immunoreactivities that were hardly detectable in whole cell extracts.Accordingly,the intracellular levels of HMW APP-CTFs were amplified by the exosomal inhibitor GW4869.By combined pharmacological,immunological and genetic approaches,we established that these HMW APP-CTFs correspond to oligomeric APP-CTFs composed of C99 and/or C83.Immunocytochemical analysis showed that monomers were localized mainly to the trans-Golgi network,whereas oligomers were confined to endosomes and lysosomes,thus providing an anatomical support for the selective recovery of HMW APP-CTFs in EVs.The D6-induced APP-CTF oligomerization and subcellular mislocalization was indeed due toγ-secretase blockade,since it similarly occurred in presenilin-deficient fibroblasts.Further,our data proposed that besides favoring APP-CTF oligomerization by preventing C99 proteolysis,γ-secretase inhibiton also led to a defective SorLA-mediated retrograde transport of HMW APP-CTFs from endosomal compartments to the TGN.Conclusions:This is the first study to demonstrate the presence of oligomeric APP-CTFs in AD mouse models,the levels of which are selectively enriched in endolysosomal compartments including exosomes and amplified byγ-secretase inhibition.Future studies should evaluate the putative contribution of these exosome-associated APP-CTFs in AD onset,progression and spreading.Inger Lauritzen Anaïs Bécot Alexandre Bourgeois Raphaëlle Pardossi-Piquard Maria-Grazia Biferi Martine Barkats Fréderic Checler 2019Translational Neurodegeneration2019,8,1:1
12Effect of feeding different levels of foliage of Moringa oleifera to creole dairy cows on intake,digestibility, milk production and composition显示文摘NADIR R S EVA S INGER L 2006Livestock Science2006,10,1:1
13Specific T-Cell Epitopes for Immunoassay-Based Diagnosis of Mycobacterium tuberculosis Infection显示文摘Inger Brock Karin Weldingh Eliane M S Leyten 2004Journal of Clinical Microbiology2004,42,:1
14A human colon cancer cel capable of initiating tumour growth in immunodeficient mice显示文摘O'Brien CA Pol ett A Gal inger S Dick JE 0,,7123:1
15Multidiseiplinary management of lung cancer显示文摘SPIRA A ETI'INGER D S 2004N Engl J Med2004,350,4:1
16Trace element modelling of pelite-derived granites显示文摘Harris N Inger S 1992Contributions to Mineralogy and Petrology1992,110,:1
17Geochemical constraints on leucogranite magmatism in the Langtang Valley, Nepal Himalaya 显示文摘Inger S Harris N 1993Journal of Petrology1993,34,:1
18Effects of workplace incivility and empowerment on newly-graduated nur- ses organizational commitment显示文摘Smith L M Andrusyszyn M A and Lasch- inger H K S 2010Journal of Nursing Management2010,,18:1
19Source parti- tioning using stable isotopes:Coping with too much variation 显示文摘PARNELL A C INGER R BEARHOP S 2010PLOS ONE2010,5,3:1
20Urban tree effects on soil organic carbon 显示文摘Edmondson J L O' sullivan 0 S Inger R 2014PLoS One2014,9,10:1
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