review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Jessica A Sexton | |
Joseph P Vogel | |||
P2860 | cites work | The genome sequence of Rickettsia prowazekii and the origin of mitochondria | Q22122428 |
Bacteria in the leaf ecosystem with emphasis on Pseudomonas syringae-a pathogen, ice nucleus, and epiphyte | Q24548485 | ||
Coxiella burnetii exhibits morphological change and delays phagolysosomal fusion after internalization by J774A.1 cells | Q28138558 | ||
Turning on ARF: the Sec7 family of guanine-nucleotide-exchange factors | Q28143666 | ||
Structural mimicry in bacterial virulence | Q28212980 | ||
Type IV secretion: intercellular transfer of macromolecules by systems ancestrally related to conjugation machines | Q28213223 | ||
Altered states: involvement of phosphorylated CagA in the induction of host cellular growth changes by Helicobacter pylori | Q28776428 | ||
Identification of Brucella spp. genes involved in intracellular trafficking. | Q30686264 | ||
The gene encoding the 17-kDa antigen of Bartonella henselae is located within a cluster of genes homologous to the virB virulence operon | Q30883995 | ||
Biochemistry of type IV secretion | Q33536554 | ||
Cell biology of Legionella pneumophila | Q33536575 | ||
Identification of genes required for chronic persistence of Brucella abortus in mice | Q33597577 | ||
Helicobacter pylori virulence and genetic geography | Q33639332 | ||
The Yersinia deadly kiss. | Q33738622 | ||
Virulent Brucella abortus prevents lysosome fusion and is distributed within autophagosome-like compartments | Q33754151 | ||
A homologue of an operon required for DNA transfer in Agrobacterium is required in Brucella abortus for virulence and intracellular multiplication | Q33791293 | ||
Q fever epidemiology and pathogenesis | Q33922199 | ||
Bacterial type IV secretion: conjugation systems adapted to deliver effector molecules to host cells | Q33987714 | ||
The T-pilus of Agrobacterium tumefaciens | Q33987720 | ||
Pseudomonas syringae Hrp type III secretion system and effector proteins. | Q33988466 | ||
Involvement of a plasmid in virulence of Campylobacter jejuni 81-176. | Q34007504 | ||
The role of the T-pilus in horizontal gene transfer and tumorigenesis | Q34106667 | ||
Brucellosis: a worldwide zoonosis | Q34137725 | ||
Interaction of Legionella pneumophila with Acanthamoeba castellanii: uptake by coiling phagocytosis and inhibition of phagosome-lysosome fusion | Q34731994 | ||
Tyrosine phosphorylation of the Helicobacter pylori CagA antigen after cag-driven host cell translocation | Q35015052 | ||
Host cell killing and bacterial conjugation require overlapping sets of genes within a 22-kb region of the Legionella pneumophila genome. | Q35880737 | ||
Protein synthesis by intact Coxiella burnetii cells | Q36293685 | ||
pH dependence of the Coxiella burnetii glutamate transport system | Q36328141 | ||
The Legionnaires' disease bacterium (Legionella pneumophila) inhibits phagosome-lysosome fusion in human monocytes | Q36348251 | ||
Lysosomal response of a murine macrophage-like cell line persistently infected with Coxiella burnetii. | Q36348953 | ||
Formation of a novel phagosome by the Legionnaires' disease bacterium (Legionella pneumophila) in human monocytes | Q36349063 | ||
Legionella pneumophila replication vacuoles mature into acidic, endocytic organelles | Q36369087 | ||
Agrobacterium tumefaciens T-complex transport apparatus: a paradigm for a new family of multifunctional transporters in eubacteria | Q36860645 | ||
Identification of a Legionella pneumophila locus required for intracellular multiplication in human macrophages | Q37246061 | ||
Pathogenesis of Brucella | Q37871945 | ||
Genes for the type IV secretion system in an intracellular symbiont, Wolbachia, a causative agent of various sexual alterations in arthropods | Q39501418 | ||
Adaptation of a conjugal transfer system for the export of pathogenic macromolecules | Q40721209 | ||
A homologue of the Agrobacterium tumefaciens VirB and Bordetella pertussis Ptl type IV secretion systems is essential for intracellular survival of Brucella suis | Q40925092 | ||
An overview of human brucellosis | Q40946012 | ||
Legionella pneumophila DotA protein is required for early phagosome trafficking decisions that occur within minutes of bacterial uptake | Q41033239 | ||
The molecular ecology of legionellae | Q41129990 | ||
Altered intracellular targeting properties associated with mutations in the Legionella pneumophila dotA gene | Q41432231 | ||
Cloning, sequencing, and expression of three Bartonella henselae genes homologous to the Agrobacterium tumefaciens VirB region | Q42623245 | ||
The transfer region of IncI1 plasmid R64: similarities between R64 tra and legionella icm/dot genes | Q42623822 | ||
Isolated Coxiella burnetii synthesizes DNA during acid activation in the absence of host cells | Q44984008 | ||
The Legionella pneumophila IcmR protein exhibits chaperone activity for IcmQ by preventing its participation in high-molecular-weight complexes | Q47208585 | ||
Relationships between a new type IV secretion system and the icm/dot virulence system of Legionella pneumophila | Q47910965 | ||
Conjugative transfer by the virulence system of Legionella pneumophila | Q48040136 | ||
Evidence that Dot-dependent and -independent factors isolate the Legionella pneumophila phagosome from the endocytic network in mouse macrophages. | Q54021239 | ||
Possible origin of the Legionella pneumophila virulence genes and their relation to Coxiella burnetii | Q62673792 | ||
Two distinct defects in intracellular growth complemented by a single genetic locus in Legionella pneumophila | Q72951041 | ||
Identification of Icm protein complexes that play distinct roles in the biogenesis of an organelle permissive for Legionella pneumophila intracellular growth | Q73293325 | ||
P433 | issue | 3 | |
P304 | page(s) | 178-185 | |
P577 | publication date | 2002-03-01 | |
P1433 | published in | Traffic | Q1572846 |
P1476 | title | Type IVB secretion by intracellular pathogens | |
P478 | volume | 3 |
Q50739945 | A C-terminal translocation signal is necessary, but not sufficient for type IV secretion of the Helicobacter pylori CagA protein. |
Q33315560 | A functional genomic yeast screen to identify pathogenic bacterial proteins |
Q34557138 | A microbial strategy to multiply in macrophages: the pregnant pause |
Q37190720 | Aggravating genetic interactions allow a solution to redundancy in a bacterial pathogen |
Q33417268 | An anomalous type IV secretion system in Rickettsia is evolutionarily conserved |
Q35060259 | Autophagy and inflammatory cell death, partners of innate immunity |
Q92526712 | Bacteria-Killing Type IV Secretion Systems |
Q27027905 | Bacterial Type IV secretion systems: versatile virulence machines |
Q37445142 | Bacterial type IV secretion systems in human disease |
Q55099790 | Biological Diversity and Evolution of Type IV Secretion Systems. |
Q35697536 | Cellular autophagy: surrender, avoidance and subversion by microorganisms |
Q35098243 | Cluster of type IV secretion genes in Helicobacter pylori's plasticity zone |
Q34796849 | Comparative Genomics Reveal That Host-Innate Immune Responses Influence the Clinical Prevalence of Legionella pneumophila Serogroups. |
Q37075501 | Comparative genomics reveal extensive transposon-mediated genomic plasticity and diversity among potential effector proteins within the genus Coxiella |
Q24673132 | Conjugative plasmid transfer in gram-positive bacteria |
Q46936695 | Coxiella burnetii inhabits a cholesterol-rich vacuole and influences cellular cholesterol metabolism |
Q35947318 | Coxiella burnetii inhibits apoptosis in human THP-1 cells and monkey primary alveolar macrophages |
Q40378276 | Coxiella burnetii modulates Beclin 1 and Bcl-2, preventing host cell apoptosis to generate a persistent bacterial infection |
Q34283480 | Coxiella burnetii type IVB secretion system region I genes are expressed early during the infection of host cells |
Q27665064 | Crystal Structure of Legionella DotD: Insights into the Relationship between Type IVB and Type II/III Secretion Systems |
Q35060264 | Cytosolic recognition of flagellin by mouse macrophages restricts Legionella pneumophila infection |
Q96431854 | Dual-Seq reveals genome and transcriptome of Caedibacter taeniospiralis, obligate endosymbiont of Paramecium |
Q35689293 | Environmental mimics and the Lvh type IVA secretion system contribute to virulence-related phenotypes of Legionella pneumophila |
Q57291163 | Evolution of the Arsenal of Legionella pneumophila Effectors To Modulate Protist Hosts |
Q37644958 | Functional diversity of ankyrin repeats in microbial proteins |
Q39776740 | Functional similarities between the icm/dot pathogenesis systems of Coxiella burnetii and Legionella pneumophila |
Q36747848 | Genetic and functional characterization of the type IV secretion system in Wolbachia |
Q33328314 | Genome-wide screen for temperature-regulated genes of the obligate intracellular bacterium, Rickettsia typhi |
Q41195589 | Icm/dot-independent entry of Legionella pneumophila into amoeba and macrophage hosts |
Q37523328 | IcmF and DotU are required for optimal effector translocation and trafficking of the Legionella pneumophila vacuole |
Q27679067 | IcmQ in the Type 4b Secretion System Contains an NAD+ Binding Domain |
Q35220590 | Identification of non-dot/icm suppressors of the Legionella pneumophila DeltadotL lethality phenotype |
Q52579481 | Impact of Three Different Mutations in Ehrlichia chaffeensis in Altering the Global Gene Expression Patterns |
Q46318305 | In situ structure of the Legionella Dot/Icm type IV secretion system by electron cryotomography. |
Q37523824 | Legionella pneumophila DotU and IcmF are required for stability of the Dot/Icm complex. |
Q34632057 | Legionella pneumophila adaptation to intracellular life and the host response: clues from genomics and transcriptomics |
Q35165499 | Legionella pneumophila catalase-peroxidases are required for proper trafficking and growth in primary macrophages |
Q44482825 | Maturation of the Coxiella burnetii parasitophorous vacuole requires bacterial protein synthesis but not replication |
Q37036006 | Mechanism and Function of Type IV Secretion During Infection of the Human Host |
Q34049976 | Molecular pathogenesis of the obligate intracellular bacterium Coxiella burnetii |
Q53944716 | Naip5 affects host susceptibility to the intracellular pathogen Legionella pneumophila. |
Q34714115 | Nitric oxide partially controls Coxiella burnetii phase II infection in mouse primary macrophages |
Q34038979 | Peptide linkage mapping of the Agrobacterium tumefaciens vir-encoded type IV secretion system reveals protein subassemblies |
Q37237972 | Phosphatidylcholine synthesis is required for optimal function of Legionella pneumophila virulence determinants |
Q21563646 | Phylogenomics of the reproductive parasite Wolbachia pipientis wMel: a streamlined genome overrun by mobile genetic elements |
Q34271469 | Plasma Membrane Disruption: Repair, Prevention, Adaptation |
Q21092256 | Plasmids and rickettsial evolution: insight from Rickettsia felis |
Q34012244 | Polar localization of the Coxiella burnetii type IVB secretion system |
Q33818331 | Predicted hexameric structure of the Agrobacterium VirB4 C terminus suggests VirB4 acts as a docking site during type IV secretion |
Q37910755 | Protein Secretion Systems in Pseudomonas aeruginosa: An Essay on Diversity, Evolution, and Function |
Q37864610 | Protein coadaptation and the design of novel approaches to identify protein-protein interactions. |
Q30354618 | Proteinaceous determinants of surface colonization in bacteria: bacterial adhesion and biofilm formation from a protein secretion perspective. |
Q33269800 | Reductive genome evolution from the mother of Rickettsia |
Q40902149 | Regulation of hypercompetence in Legionella pneumophila |
Q35142697 | Show me the substrates: modulation of host cell function by type IV secretion systems. |
Q33946571 | Specificity of Legionella pneumophila and Coxiella burnetii vacuoles and versatility of Legionella pneumophila revealed by coinfection |
Q24649157 | Structure and function of interacting IcmR-IcmQ domains from a type IVb secretion system in Legionella pneumophila |
Q37583353 | Temporal analysis of Coxiella burnetii morphological differentiation |
Q41773449 | The DotL protein, a member of the TraG-coupling protein family, is essential for Viability of Legionella pneumophila strain Lp02. |
Q40262478 | The Legionella pneumophila IcmS-LvgA protein complex is important for Dot/Icm-dependent intracellular growth |
Q40634202 | The Legionella pneumophila PilT homologue DotB exhibits ATPase activity that is critical for intracellular growth |
Q39927528 | The PmrA/PmrB two-component system of Legionella pneumophila is a global regulator required for intracellular replication within macrophages and protozoa |
Q21563623 | The Wolbachia genome of Brugia malayi: endosymbiont evolution within a human pathogenic nematode |
Q33296886 | The complete genome sequence of Yersinia pseudotuberculosis IP31758, the causative agent of Far East scarlet-like fever |
Q33640294 | The conserved Tarp actin binding domain is important for chlamydial invasion |
Q24548624 | The genome of the obligately intracellular bacterium Ehrlichia canis reveals themes of complex membrane structure and immune evasion strategies |
Q38665269 | The novel Pseudomonas putida plasmid p12969-2 harbors an In127-carrying multidrug-resistant region |
Q90076937 | The opportunistic pathogen Stenotrophomonas maltophilia utilizes a type IV secretion system for interbacterial killing |
Q35579496 | The outs and ins of bacterial type IV secretion substrates |
Q57340328 | The pGRT1 plasmid of Pseudomonas putida DOT-T1E encodes functions relevant for survival under harsh conditions in the environment |
Q37189773 | Type IV secretion systems: tools of bacterial horizontal gene transfer and virulence |
Q37899756 | Type IVB Secretion Systems of Legionella and Other Gram-Negative Bacteria. |
Q33559645 | Type V protein secretion pathway: the autotransporter story |
Q34441405 | Type-IVC secretion system: a novel subclass of type IV secretion system (T4SS) common existing in gram-positive genus Streptococcus |
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