BÁO CÁO Y HỌC: " ANALYSIS OF PROTOTYPE FOAMY VIRUS PARTICLE-HOST CELL INTERACTION WITH AUTOFLUORESCENT RETROVIRAL PARTICLES" PPT
Tìm thấy 10,000 tài liệu liên quan tới tiêu đề "Báo cáo y học: " Analysis of Prototype Foamy Virus particle-host cell interaction with autofluoresce...":
, Petra Schwille2, Helmut Hanenberg3, Hanswalter Zentgraf4 and Dirk Lindemann*1AbstractBackground: The foamy virus (FV) replication cycle displays several unique features, which set them apart from orthoretroviruses. First, like other B/D type orthoretroviruses, FV capsids preassemble[r]
Appendix ................................................................................................................87viSummaryThere is substantial lack in the understanding of the role of host lipids in virusinfections, and this project aimed to identify possible lipid can[r]
down regulated. The other two IAPs, NIAP and suvivin, remain unchanged. The results suggest that the long time stimulation of HBV viral proteins indeed changes the expression of apoptosis profile of host cells, which probably results in the carcinogenesis of liver[r]
superheating followed by leaching out of the active constituents.Cell bursting phenomenon probably facilitates entry of theextracting solvent to solubilize out the target compound, thuslead to faster and efficient extraction. As compared to otherconventional techniques like Soxhl[r]
disseminating the results of biomedical research in our lifetime."Sir Paul Nurse, Cancer Research UKYour research papers will be:available free of charge to the entire biomedical communitypeer reviewed and published immediately upon acceptancecited in PubMed and archived on PubMed Cent[r]
Hindawi Publishing CorporationEURASIP Journal on Advances in Signal ProcessingVolume 2009, Article ID 692861, 13 pagesdoi:10.1155/2009/692861Research ArticleA Novel Approach to the Design of Oversampling Low-DelayComplex-Modulated Filter Bank PairsThomas Kurbiel (EURASIP Member), Heinz G. G¨o[r]
Site-directed mutagenesis and deletion studies showedthat the carboxy-terminal region of L2 somehow asso-ciates with the dynein motor [82]. This observation isin agreement with previous experiments that hadshown that bovine PV binds to microtubules andbecomes transported along t[r]
was used to clone the 5¢-end of agn13.2 mRNA usingSMART-PCR system (Clontech, Palo Alto, CA USA) andAGN4 [5¢-GCAGATCGTCTTGTCTTTTG-3¢] was used toclone the 3¢-end of agn13.2 mRNA using RACE-PCR system(Roche Diagnostics, Barcelona, Spain). RNA was extractedfrom mycelia grown for 8 h w[r]
2. Hirst GK: Genetic recombination with Newcastle diseasevirus, polioviruses and influenza virus. Cold Spring Harbor SympQuant Biol 1962, 27:303-309.3. Ledinko N: Genetic recombination with poliovirus type 1:studies of crosses between a normal horse serum-resistantmutant[r]
BioMed CentralPage 1 of 5(page number not for citation purposes)Virology JournalOpen AccessResearchRecombinant Tula hantavirus shows reduced fitness but is able to survive in the presence of a parental virus: analysis of consecutive passages in a cell cultur[r]
HA crosstalk with epithelium CD44v. This minireview high-lights recent findings in tumor–stromal interactions andtheir possible roles in HA–CD44v-induced tumor growthand invasion, together with fresh insights into the enigmaticnature of CD44 splice variants, and how the suppressi[r]
teins, we used the recombinant baculovirus expressionmethod described for determination of the H5 HA struc-ture, where the transmembrane domain had beenreplaced by the 'foldon' trimerization sequence, allowingfor expression of soluble HA trimers which could be puri-fied by virtue of[r]
50. Pownall, H.J. & Gotto, A.M. Jr (1999) Structure and dynamics ofhuman plasma lipoproteins. In Lipoproteins in Health and Disease(Betteridge, D.J., Illingworth, D.R. & Shepherd, J., eds), pp. 3–15.Arnold/Oxford University Press, New York.51. Ginsburg, G.S., Small, D.M. & At[r]
Chapter 065. Gene Therapy in Clinical Medicine (Part 1) Harrison's Internal Medicine > Chapter 65. Gene Therapy in Clinical Medicine Gene Therapy in Clinical Medicine: Introduction Gene transfer is a novel area of therapeutics in which the active agent is a nucleic acid sequence rathe[r]
against various strains including the recent pandemic H1N1-2009 influenza virus. KAA-2 inhibited infection of various influenza strains with EC50s of low nanomolar levels. Immunofluorescence microscopy using an anti-influenza antibody demonstrated that the antiviral activ[r]
particles only composed by SHBs can bind the human hepatocyte plasma membrane and this binding resulted in the internalization of the gold labeled sub viral particles [25]. However, despite the literature about HBV surface proteins, determination of which of the pr[r]
VirusesVirusesLiving or NotLiving or Not?????????????? Characteristics of VirusesCharacteristics of VirusesAmong the smallest Among the smallest biological particles biological particles that are capable of that are capable of causing diseases in causing d[r]
inhibits the down regulation of receptor-mediated endo-cytosis and macropinocytosis following exposure to a sol-uble immunogen [25]. In addition, IL-10 reduces theproduction of IL-2, IFN and TNF by murine Th1 cells [14]as well as the IL-12 production by APC [18]. IL-10 mayalso, interve[r]
ence is accompanied by a persistent state of oxidativesiege, and the survival of a given cell is determined by itsbalance of reactive oxygen intermediates and antioxi-dants. Disturbance of this balance can lead to disease [17].Further, since oxidative stress can in[r]