scholarly article | Q13442814 |
review article | Q7318358 |
P356 | DOI | 10.1016/J.SEMCDB.2009.03.015 |
P698 | PubMed publication ID | 19508853 |
P50 | author | Rebecca Roberts | Q41169574 |
P2093 | author name string | Thomas Wileman | |
Eleanor Cottam | |||
Roberto Pierini | |||
P2860 | cites work | Hepatitis C virus RNA polymerase and NS5A complex with a SNARE-like protein | Q22010735 |
The intracellular fate of Salmonella depends on the recruitment of kinesin | Q24302564 | ||
A Rab-GAP TBC domain protein binds hepatitis C virus NS5A and mediates viral replication | Q24337008 | ||
Human VAP-B is involved in hepatitis C virus replication through interaction with NS5A and NS5B | Q24338324 | ||
Subversion of cellular autophagosomal machinery by RNA viruses | Q24522711 | ||
Hijacking components of the cellular secretory pathway for replication of poliovirus RNA | Q24675864 | ||
SARS-coronavirus replication is supported by a reticulovesicular network of modified endoplasmic reticulum | Q27332392 | ||
Cellular COPII proteins are involved in production of the vesicles that form the poliovirus replication complex. | Q27469873 | ||
Participation of Rab5, an Early Endosome Protein, in Hepatitis C Virus RNA Replication Machinery | Q27480343 | ||
Localization and Membrane Topology of Coronavirus Nonstructural Protein 4: Involvement of the Early Secretory Pathway in Replication | Q27485022 | ||
Mouse Hepatitis Coronavirus RNA Replication Depends on GBF1-Mediated ARF1 Activation | Q27486170 | ||
Rab GTPases Are Recruited to Chlamydial Inclusions in Both a Species-Dependent and Species-Independent Manner | Q28203990 | ||
Aggresomes and autophagy generate sites for virus replication | Q28239704 | ||
Chlamydia pneumoniae inclusion membrane protein Cpn0585 interacts with multiple Rab GTPases | Q28251473 | ||
A bifunctional bacterial protein links GDI displacement to Rab1 activation | Q28253847 | ||
Rabs and their effectors: achieving specificity in membrane traffic | Q29619989 | ||
A network of Rab GTPases controls phagosome maturation and is modulated by Salmonella enterica serovar Typhimurium | Q30444185 | ||
The SPI-2 type III secretion system restricts motility of Salmonella-containing vacuoles | Q30480339 | ||
Salmonella trafficking is defined by continuous dynamic interactions with the endolysosomal system. | Q30480354 | ||
Cytoplasmic lipid droplets are translocated into the lumen of the Chlamydia trachomatis parasitophorous vacuole | Q30482674 | ||
Biogenesis of cytoplasmic membranous vesicles for plant potyvirus replication occurs at endoplasmic reticulum exit sites in a COPI- and COPII-dependent manner | Q30484853 | ||
RNA interference analysis of Legionella in Drosophila cells: exploitation of early secretory apparatus dynamics | Q33241705 | ||
COPI activity coupled with fatty acid biosynthesis is required for viral replication | Q33260346 | ||
Chlamydia causes fragmentation of the Golgi compartment to ensure reproduction. | Q37856042 | ||
Trafficking from CD63-positive late endocytic multivesicular bodies is essential for intracellular development of Chlamydia trachomatis | Q37863154 | ||
Chlamydia trachomatis uses host cell dynein to traffic to the microtubule-organizing center in a p50 dynamitin-independent process. | Q37868852 | ||
African swine fever virus causes microtubule-dependent dispersal of the trans-golgi network and slows delivery of membrane protein to the plasma membrane | Q39305357 | ||
Fowlpox virus encodes nonessential homologs of cellular alpha-SNAP, PC-1, and an orphan human homolog of a secreted nematode protein | Q39579796 | ||
Differential requirements for COPI coats in formation of replication complexes among three genera of Picornaviridae | Q39685149 | ||
SseG, a virulence protein that targets Salmonella to the Golgi network | Q39927890 | ||
Dynamic remodeling of the endosomal system during formation of Salmonella-induced filaments by intracellular Salmonella enterica | Q39935792 | ||
The unique architecture of Bunyamwera virus factories around the Golgi complex | Q39973171 | ||
Norwalk virus nonstructural protein p48 forms a complex with the SNARE regulator VAP-A and prevents cell surface expression of vesicular stomatitis virus G protein | Q40011733 | ||
Legionella pneumophila proteins that regulate Rab1 membrane cycling | Q40064228 | ||
TBC1D20 is a Rab1 GTPase-activating protein that mediates hepatitis C virus replication | Q40075069 | ||
A viral protein that blocks Arf1-mediated COP-I assembly by inhibiting the guanine nucleotide exchange factor GBF1. | Q40247187 | ||
Targeting of host Rab GTPase function by the intravacuolar pathogen Legionella pneumophila. | Q40258153 | ||
Intracellular Salmonella enterica redirect exocytic transport processes in a Salmonella pathogenicity island 2-dependent manner | Q40287796 | ||
Attachment and fusion of endoplasmic reticulum with vacuoles containing Legionella pneumophila | Q40293289 | ||
Poliovirus protein 3A binds and inactivates LIS1, causing block of membrane protein trafficking and deregulation of cell division. | Q40378746 | ||
A bacterial guanine nucleotide exchange factor activates ARF on Legionella phagosomes | Q40754890 | ||
Legionella pneumophila replication vacuole formation involves rapid recruitment of proteins of the early secretory system | Q40764000 | ||
Legionella pneumophila DotA protein is required for early phagosome trafficking decisions that occur within minutes of bacterial uptake | Q41033239 | ||
Salmonella SPI1 effector SipA persists after entry and cooperates with a SPI2 effector to regulate phagosome maturation and intracellular replication | Q42756733 | ||
Identification of essential host factors affecting tombusvirus RNA replication based on the yeast Tet promoters Hughes Collection | Q43155068 | ||
Intracellular location and translocation of silent and active poliovirus replication complexes | Q45275887 | ||
Poliovirus infection blocks ERGIC-to-Golgi trafficking and induces microtubule-dependent disruption of the Golgi complex. | Q46000819 | ||
Sorting nexin-1 defines an early phase of Salmonella-containing vacuole-remodeling during Salmonella infection | Q50061635 | ||
Functional dissection of SseF, a type III effector protein involved in positioning the salmonella-containing vacuole. | Q50079368 | ||
Brucella Intracellular Replication Requires Trafficking Through the Late Endosomal/Lysosomal Compartment | Q57662407 | ||
Reticulon 3 Binds the 2C Protein of Enterovirus 71 and Is Required for Viral Replication | Q57871120 | ||
The Legionella pneumophila effector protein DrrA is a Rab1 guanine nucleotide-exchange factor | Q60648871 | ||
Legionella phagosomes intercept vesicular traffic from endoplasmic reticulum exit sites | Q78559396 | ||
Inhibition of cellular protein secretion by picornaviral 3A proteins | Q81781504 | ||
SNARE protein mimicry by an intracellular bacterium | Q33325919 | ||
A critical role of a cellular membrane traffic protein in poliovirus RNA replication | Q33386005 | ||
Effects of foot-and-mouth disease virus nonstructural proteins on the structure and function of the early secretory pathway: 2BC but not 3A blocks endoplasmic reticulum-to-Golgi transport | Q33707361 | ||
Poliovirus proteins induce membrane association of GTPase ADP-ribosylation factor | Q33788730 | ||
Inhibition of poliovirus RNA synthesis by brefeldin A | Q33930647 | ||
A guide to viral inclusions, membrane rearrangements, factories, and viroplasm produced during virus replication | Q34006244 | ||
The chlamydial inclusion preferentially intercepts basolaterally directed sphingomyelin-containing exocytic vacuoles. | Q34180608 | ||
Lipid metabolism in Chlamydia trachomatis-infected cells: directed trafficking of Golgi-derived sphingolipids to the chlamydial inclusion | Q34271444 | ||
Restricted fusion of Chlamydia trachomatis vesicles with endocytic compartments during the initial stages of infection. | Q34581951 | ||
Lounging in a lysosome: the intracellular lifestyle of Coxiella burnetii | Q34611714 | ||
Inhibition of protein trafficking by coxsackievirus b3: multiple viral proteins target a single organelle | Q34716944 | ||
The chlamydial inclusion: escape from the endocytic pathway. | Q34762497 | ||
The Salmonella effector protein PipB2 is a linker for kinesin-1 | Q35037325 | ||
The GTPase Rab4 interacts with Chlamydia trachomatis inclusion membrane protein CT229. | Q35073695 | ||
Effects of picornavirus 3A Proteins on Protein Transport and GBF1-dependent COP-I recruitment. | Q35140000 | ||
Golgi-dependent transport of cholesterol to the Chlamydia trachomatis inclusion. | Q35144239 | ||
Inhibition of the secretory pathway by foot-and-mouth disease virus 2BC protein is reproduced by coexpression of 2B with 2C, and the site of inhibition is determined by the subcellular location of 2C. | Q35635282 | ||
Cellular autophagy: surrender, avoidance and subversion by microorganisms | Q35697536 | ||
Molecular determinants of the interaction between coxsackievirus protein 3A and guanine nucleotide exchange factor GBF1 | Q35857493 | ||
Salmonella impairs RILP recruitment to Rab7 during maturation of invasion vacuoles | Q35918621 | ||
Wrapping things up about virus RNA replication | Q36271058 | ||
Legionella subvert the functions of Rab1 and Sec22b to create a replicative organelle. | Q36399499 | ||
Parallels among positive-strand RNA viruses, reverse-transcribing viruses and double-stranded RNA viruses | Q36438773 | ||
Role for myosin II in regulating positioning of Salmonella-containing vacuoles and intracellular replication. | Q36710758 | ||
Involvement of cellular membrane traffic proteins in poliovirus replication | Q36716351 | ||
Coats, tethers, Rabs, and SNAREs work together to mediate the intracellular destination of a transport vesicle | Q36815404 | ||
The Salmonella-containing vacuole: moving with the times | Q36961170 | ||
Membrane dynamics and spatial distribution of Salmonella-containing vacuoles. | Q36993548 | ||
The subcellular distribution of multigene family 110 proteins of African swine fever virus is determined by differences in C-terminal KDEL endoplasmic reticulum retention motifs | Q37009261 | ||
Chlamydia effector proteins and new insights into chlamydial cellular microbiology | Q37094438 | ||
Modification of intracellular membrane structures for virus replication | Q37139313 | ||
Dynamic behavior of Salmonella-induced membrane tubules in epithelial cells | Q37193557 | ||
Salmonella-containing vacuoles: directing traffic and nesting to grow. | Q37263303 | ||
Inhibition of cellular protein secretion by poliovirus proteins 2B and 3A | Q37694671 | ||
P433 | issue | 7 | |
P921 | main subject | endoplasmic reticulum | Q79927 |
P304 | page(s) | 828-833 | |
P577 | publication date | 2009-09-01 | |
P1433 | published in | Seminars in Cell & Developmental Biology | Q14330411 |
P1476 | title | Modulation of membrane traffic between endoplasmic reticulum, ERGIC and Golgi to generate compartments for the replication of bacteria and viruses | |
P478 | volume | 20 |
Q33731298 | An inside job: subversion of the host secretory pathway by intestinal pathogens |
Q38144290 | Autophagy as a defence against intracellular pathogens |
Q27026776 | Bacterial pathogens commandeer Rab GTPases to establish intracellular niches |
Q34367380 | Foot-and-mouth disease virus 3C protease induces fragmentation of the Golgi compartment and blocks intra-Golgi transport |
Q30499676 | HIV-1 requires Arf6-mediated membrane dynamics to efficiently enter and infect T lymphocytes. |
Q43159984 | Host endoplasmic reticulum COPII proteins control cell-to-cell spread of the bacterial pathogen Listeria monocytogenes |
Q36581683 | Loss of a membrane trafficking protein αSNAP induces non-canonical autophagy in human epithelia |
Q42324739 | Orf virus interferes with MHC class I surface expression by targeting vesicular transport and Golgi |
Q27343029 | Phosphorylation of Golgi Peripheral Membrane Protein Grasp65 Is an Integral Step in the Formation of the Human Cytomegalovirus Cytoplasmic Assembly Compartment |
Q30537017 | Polymeric nucleic acid vehicles exploit active interorganelle trafficking mechanisms |
Q29616548 | Role of Rab GTPases in membrane traffic and cell physiology |
Q24306634 | Valosin-containing protein (VCP/p97) is required for poliovirus replication and is involved in cellular protein secretion pathway in poliovirus infection |
Q37941707 | Viral infection: Moving through complex and dynamic cell-membrane structures. |
Q34031231 | Virus factories, double membrane vesicles and viroplasm generated in animal cells |
Q38043543 | Virus factories: biogenesis and structural design |
Q34757858 | Virus morphogenesis in the cell: methods and observations |
Q35753330 | Yeast Surface Display of Two Proteins Previously Shown to Be Protective Against White Spot Syndrome Virus (WSSV) in Shrimp |
Search more.