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15篇 您的检索式:作者名="Argent G"
    题名 作者 年代 出处 被引量
1Predicting freshwater fish distributions using landscape-level variables 显示文摘Argent D G Bishop J A Stauffer J R Jr 2003Fisheries Research2003,60,1:1
2TGF-βsignaling is activated in patients with chronic HBV infection and repressed by SMAD7 overexpression after successful antiviral treatment显示文摘Argentou N Germanidis G Hytiroglou P 2016Inflamm Res2016,65,5:1
3The wild bananas of Papua New Guinea 显示文摘Argent G C G 1976Notes from the Royal Botanic Garden Edinburgh1976,35,:1
4Two interesting wild Musa species (Musaceae) from Sabah, Malaysia 显示文摘Argent G 2000Gardens'' bulletin Singapore2000,52,:1
5A successful,sustainable and low cost control-programme for bovine hypodermosis in France显示文摘BOULARD C ALVINERIE M ARGENTE G 2008Vet Parasitol2008,158,12:1
6The diversity of 15 ha of lowland mixed dipterocarp forest, Central Kalimantan 显示文摘Wilkie P Argent G Cambell E 2004Biodiversity and Conservation2004,13,:1
7Chromosome number of some tropical Rhododendrons (section Vireya)显示文摘Atkinson R Jong K Argent G 2000 2000EDBG J Bot2000,57,1:1
8Proton Conduction in aPhosphonate-Based Metal-Organic Framework Mediated by Intrinsic “FreeDiffusion inside a Sphere”显示文摘PiliS Argent S P Morris C G 2016+J Am Chem Soc2016,138,20:1
9Liver Foxp3 and PD1/PDL1 expression is down - regulated in chronic HBV hepatitis on maintained remission related to the degree of inflammation 显示文摘Germanidis G Argentou N Hytiroglou P 2013Front Immunol2013,,4:1
10Does adherence to treat- ment targets in children with severe traumatic brain injury avoid brain hypoxia A brain tissue oxygenation study显示文摘Figaji A A Fieggen A G Argent A C et aI 2008Neurosurgery2008,63,1:1
11Assessment of the validity of the section in Musa (Musaceae) using AFLP显示文摘Wong C Kiew R Argent G 2002Ann Bot2002,,90:1
12Pediatric intensive care in South Africa: an account of making optimum use of limited resources at the Red Cross War Memorial Children's Hospital显示文摘Andrew C Argent Johann Ahrens Brenda M Morrow Louis G Reynolds Mark Hatherill Shamiel Salie Solomon R Benatar 2014Pediatric critical care medicine:a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies2014,15,1:1
13Stream fish community response to a gradient of specific conductance 显示文摘KIMMEL W G ARGENT D G 2009Water Air & Soil Pollution2009,206,:1
14Rapid detection of MYD88-L265P mutation by PCR-RFLP in B-cell lymphoproliferative disorders显示文摘Argentou N Vassilopoulos G Ioannou M 2014Leukemia2014,28,2:1
15Effect of herpesvirus infection on pancreatic duct cell secretion显示文摘AIM: To examine the effect of acute infection caused by herpesvirus (pseudorabies virus, PRV) on pancreatic ductal secretion.METHODS: The virulent Ba-DupGreen (BDG) and nonvirulent Ka-RREpOlacgfp (KEG) genetically modified strains of PRV were used in this study and both of them contain the gene for green fluorescent protein (GFP). Small intra/interlobular ducts were infected with BDG virus (107 PFU/mL for 6 h) or with KEG virus (1010 PFU/mL for 6 h), while non-infected ducts were incubated only with the culture media. The ducts were then cultured for a further 18 h.The rate of HCO3- secretion [base efflux -J(B-)] was determined from the buffering capacity of the cells and the initial rate of intracellular acidification (1) after sudden blockage of basolateral base loaders with dihydro-4,4,-diisothiocyanatostilbene-2,2,-disulfonic acid (500 μmol/L)and amiloride (200 μmol/L), and (2) after alkali loading the ducts by exposure to NH4Cl. All the experiments were performed in HCO3--buffered Ringer solution at 37 ℃ (n = 5ducts for each experimental condition). Viral structural proteins were visualized by immunohistochemistry. Virallyencoded GFP and immunofluorescence signals were recorded by a confocal laser scanning microscope.RESULTS: The BDG virus infected the majority of accessible cells of the duct as judged by the appearance of GFP and viral antigens in the ductal cells. KEG virus caused a similarly high efficiency of infection. After blockage of basolateral base loaders, BDG infection significantly elevated -J(B-) 24 h after the infection, compared to the non-infected group. However, KEG infection did not modify -J(B-). After alkali loading the ducts, -J(B-) was significantly elevated in the BDG group compared to the control group 24 h after the infection. As we found with the inhibitor stop method, no change was observed in the group KEG compared to the non-infected group.CONCLUSION: Incubation with the BDG or KEG strains of PRV results in an effective infection of ductal epithelial cells. The BDG strain of PRV, which is able to initiate a lytic viral cycle, stimulates HcO3- secretion in guinea pig pancreatic duct by about four- to fivefold, 24 h after the infection. However, the KEG strain of PRV, which can infect,but fails to replicate, has no effect on HCO3- secretion.We suggest that this response of pancreatic ducts to virulent PRV infection may represent a defense mechanism against invasive pathogens to avoid pancreatic injury.Péter Hegyi Balázs rdg Zoltán Rakonczai Jr Tamás Takács János Lonovics Annamária Szabolcs Réka Sári András Tóth Julius G Papp András Varró Mária K Kovács Mike A Gray Barry E Argent Zsolt Boldogki 2005World Journal of Gastroenterology2005,11,38:0
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