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  1. The identification of wadB, a new glycosyltransferase gene, confirms the branched structure and the role in virulence of the lipopolysaccharide core of Brucella abortus
  2. Brucellosis as an Emerging Threat in Developing Economies: Lessons from Nigeria
  3. Mutants in the lipopolysaccharide of Brucella ovis are attenuated and protect against B. ovis infection in mice
  4. Brucella abortus Depends on Pyruvate Phosphate Dikinase and Malic Enzyme but Not on Fbp and GlpX Fructose-1,6-Bisphosphatases for Full Virulence in Laboratory Models
  5. Mutants in the lipopolysaccharide of
  6. Performance of skin tests with allergens from B. melitensis B115 and rough B. abortus mutants for diagnosing swine brucellosis
  7. Deletion of the GI-2 integrase and the wbkA flanking transposase improves the stability of Brucella melitensis Rev 1 vaccine
  8. Interactions of lipopolysaccharide with lipid membranes, raft models — A solid state NMR study
  9. Lipopolysaccharide as a target for brucellosis vaccine design
  10. Lipopolysaccharides with Acylation Defects Potentiate TLR4 Signaling and Shape T Cell Responses
  11. The Epitopic and Structural Characterization of Brucella suis Biovar 2 O-Polysaccharide Demonstrates the Existence of a New M-Negative C-Negative Smooth Brucella Serovar
  12. Brucella β 1,2 Cyclic Glucan Is an Activator of Human and Mouse Dendritic Cells
  13. Comparative Genomics of Early-Diverging Brucella Strains Reveals a Novel Lipopolysaccharide Biosynthesis Pathway
  14. Comparative Genomics of Early-Diverging Brucella Strains Reveals a Novel Lipopolysaccharide Biosynthesis Pathway
  15. The Lipopolysaccharide Core of Brucella abortus Acts as a Shield Against Innate Immunity Recognition
  16. What have we learned from brucellosis in the mouse model?
  17. Spontaneous Excision of the O-Polysaccharide wbkA Glycosyltranferase Gene Is a Cause of Dissociation of Smooth to Rough Brucella Colonies
  18. Identification and functional analysis of the cyclopropane fatty acid synthase of Brucella abortus
  19. Brucellosis at the animal/ecosystem/human interface at the beginning of the 21st century
  20. Identification of new IS711 insertion sites in Brucella abortus field isolates
  21. The Rose Bengal Test in Human Brucellosis: A Neglected Test for the Diagnosis of a Neglected Disease
  22. Brucella abortus Ornithine Lipids Are Dispensable Outer Membrane Components Devoid of a Marked Pathogen-Associated Molecular Pattern
  23. Chapter 7 Brucellosis
  24. Brucellosis seroprevalence in livestock in Uganda from 1998 to 2008: a retrospective study
  25. Structural Features Governing the Activity of Lactoferricin-Derived Peptides That Act in Synergy with Antibiotics againstPseudomonas aeruginosa In VitroandIn Vivo
  26. Genomic Island 2 Is an Unstable Genetic Element Contributing to Brucella Lipopolysaccharide Spontaneous Smooth-to-Rough Dissociation
  27. New Antiseptic Peptides To Protect against Endotoxin-Mediated Shock
  28. Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome
  29. Eradication of bovine brucellosis in the Azores, Portugal—Outcome of a 5-year programme (2002–2007) based on test-and-slaughter and RB51 vaccination
  30. Effective Antimicrobial and Anti-Endotoxin Activity of Cationic Peptides Based on Lactoferricin: A Biophysical and Microbiological Study
  31. Structural prerequisites for endotoxic activity in the Limulus test as compared to cytokine production in mononuclear cells
  32. The Differential Interaction of Brucella and Ochrobactrum with Innate Immunity Reveals Traits Related to the Evolution of Stealthy Pathogens
  33. Rough mutants defective in core and O-polysaccharide synthesis and export induce antibodies reacting in an indirect ELISA with smooth lipopolysaccharide and are less effective than Rev 1 vaccine against Brucella melitensis infection of sheep
  34. Is Brucella an enteric pathogen?
  35. DNA polymorphism analysis of Brucella lipopolysaccharide genes reveals marked differences in O-polysaccharide biosynthetic genes between smooth and rough Brucella species and novel species-specific markers
  36. Comparative analysis of selected methods for the assessment of antimicrobial and membrane-permeabilizing activity: a case study for lactoferricin derived peptides
  37. Brucellosis Vaccines: Assessment of Brucella melitensis Lipopolysaccharide Rough Mutants Defective in Core and O-Polysaccharide Synthesis and Export
  38. Mechanism of interaction of optimized Limulus -derived cyclic peptides with endotoxins: thermodynamic, biophysical and microbiological analysis
  39. BvrR/BvrS-Controlled Outer Membrane Proteins Omp3a and Omp3b Are Not Essential for Brucella abortus Virulence
  40. Brucella abortus Uses a Stealthy Strategy to Avoid Activation of the Innate Immune System during the Onset of Infection
  41. Thermodynamic Analysis of the Lipopolysaccharide-Dependent Resistance of Gram-Negative Bacteria against Polymyxin B
  42. Rationale for the Design of Shortened Derivatives of the NK-lysin-derived Antimicrobial Peptide NK-2 with Improved Activity against Gram-negative Pathogens
  43. Extensive Cell Envelope Modulation Is Associated with Virulence in Brucella abortus
  44. The Acyl Group as the Central Element of the Structural Organization of Antimicrobial Lipopeptide
  45. Synthesis of phosphatidylcholine, a typical eukaryotic phospholipid, is necessary for full virulence of the intracellular bacterial parasite Brucella abortus
  46. Increases of efficacy as vaccine against Brucella abortus infection in mice by simultaneous inoculation with avirulent smooth bvrS/bvrR and rough wbkA mutants
  47. Differential inductions of TNF-alpha and IGTP, IIGP by structurally diverse classic and non-classic lipopolysaccharides
  48. Brucella: Molecular and Cellular Biology Edited by Ignacio Lopez-Goni and Ignacio Moriyon Wymondham, UK: Horizon Bioscience, 2004. 432 pp., illustrated. $200.00 (cloth)
  49. Characterization of Brucella abortus lipopolysaccharide macrodomains as mega rafts
  50. The Genus Brucella
  51. Comparing Antimicrobial and Membrane Permeabilizing Activity of Peptides Derived from Human Cationic Proteins
  52. The Lipopolysaccharide of Brucella abortus BvrS/BvrR Mutants Contains Lipid A Modifications and Has Higher Affinity for Bactericidal Cationic Peptides
  53. Cyclic β-1,2-glucan is a brucella virulence factor required for intracellular survival
  54. Brucella lipopolysaccharide acts as a virulence factor
  55. Enhancement of endotoxin neutralization by coupling of a C12-alkyl chain to a lactoferricin-derived peptide
  56. Efficacy of Several Serological Tests and Antigens for Diagnosis of Bovine Brucellosis in the Presence of False-Positive Serological Results Due to Yersinia enterocolitica O:9
  57. Characterization of Brucella abortus O-Polysaccharide and Core Lipopolysaccharide Mutants and Demonstration that a Complete Core Is Required for Rough Vaccines To Be Efficient against Brucella abortus and Brucella ovis in the Mouse Model
  58. Pathogenic Yersinia enterocolitica Strains Increase the Outer Membrane Permeability in Response to Environmental Stimuli by Modulating Lipopolysaccharide Fluidity and Lipid A Structure
  59. Brucella evolution and taxonomy
  60. Regulation of Brucella virulence by the two-component system BvrR/BvrS
  61. The interaction of rough and smooth form lipopolysaccharides with polymyxins as studied by titration calorimetry
  62. The two-component system BvrR/BvrS essential for Brucella abortus virulence regulates the expression of outer membrane proteins with counterparts in members of the Rhizobiaceae
  63. Brucella melitensis : A nasty bug with hidden credentials for virulence
  64. Biophysical investigations into the interaction of lipopolysaccharide with polymyxins
  65. Brucella abortus and Its Closest Phylogenetic Relative, Ochrobactrum spp., Differ in Outer Membrane Permeability and Cationic Peptide Resistance
  66. The lipopolysaccharide outer core of Yersinia enterocolitica serotype O:3 is required for virulence and plays a role in outer membrane integrity
  67. Comparison of polyclonal, monoclonal and protein G peroxidase conjugates in an enzyme‐linked immunosorbent assay for the diagnosis of Brucella ovis in sheep
  68. A two‐component regulatory system playing a critical role in plant pathogens and endosymbionts is present in Brucella abortus and controls cell invasion and virulence
  69. Evaluation of the relatedness of Brucella spp. and Ochrobactrum anthropi and description of Ochrobactrum intermedium sp. nov., a new species with a closer relationship to Brucella spp.
  70. Yersinia pseudotuberculosis and Yersinia pestis show increased outer membrane permeability to hydrophobic agents which correlates with lipopolysaccharide acyl-chain fluidity
  71. Diagnosis and epidemiology of Brucella ovis infection in rams
  72. Structural studies on the lipopolysaccharide from a rough strain of Ochrobactrum anthropi containing a 2,3-diamino-2,3-dideoxy-d-glucose disaccharide lipid A backbone
  73. Determination of the O-specific polysaccharide structure in the lipopolysaccharide of Ochrobactrum anthropi LMG 3331
  74. Diagnosis of Brucella ovis infection of rams with an ELISA using protein G as conjugate
  75. Evaluation of whole cell and subcellular vaccines against Brucella ovis in rams
  76. An ELISA with Brucella lipopolysaccharide antigen for the diagnosis of B. melitensis infection in sheep and for the evaluation of serological responses following subcutaneous or conjunctival B. melitensis strain Rev 1 vaccination
  77. Comparison of three serological tests for Brucella ovis infection of rams using different antigenic extracts
  78. Immunization with Brucella melitensis Rev 1 against Brucella ovis infection of rams
  79. Properties of the outer membrane of Brucella
  80. In vitro interactions between lipopolysaccharides and heterologous outer membrane porin proteins
  81. Torulopsis navarrensis sp. nov. A new species of yeast isolated from an acid washed brown soil in the province of Navarra, Spain