about
Host, pathogen and environment: a bacterial gbpA gene expression study in response to magnesium environment and presence of prawn carapace and commercial chitinRepair of a Bacterial Small β-Barrel Toxin Pore Depends on Channel WidthThe out-of-the-delta hypothesis: dense human populations in low-lying river deltas served as agents for the evolution of a deadly pathogenOrigins of pandemic Vibrio cholerae from environmental gene pools.Transcriptional characterization of Vibrio fischeri during colonization of juvenile Euprymna scolopes.Distinct stages during colonization of the mouse gastrointestinal tract by Candida albicansBiofilm Formation and Detachment in Gram-Negative Pathogens Is Modulated by Select Bile AcidsHigh-Resolution Crystal Structures Elucidate the Molecular Basis of Cholera Blood Group Dependence.OxyR-activated expression of Dps is important for Vibrio cholerae oxidative stress resistance and pathogenesis.Characterization of Vibrio cholerae isolates from 1976 to 2013 in Shandong Province, China.Small Molecules That Sabotage Bacterial Virulence.Biofilm Producing Salmonella Typhi: Chronic Colonization and Development of Gallbladder Cancer.Temporal dynamics of ovine airway epithelial cell differentiation at an air-liquid interface.Interactions of Intestinal Bacteria with Components of the Intestinal Mucus.Environmental vibrios represent a source of antagonistic compounds that inhibit pathogenic Vibrio cholerae and Vibrio parahaemolyticus strains.Modulating the Global Response Regulator, LuxO of V. cholerae Quorum Sensing System Using a Pyrazine Dicarboxylic Acid Derivative (PDCApy): An Antivirulence ApproachVibrio cholerae genomic diversity within and between patients.Cyclic-di-GMP regulation of virulence in bacterial pathogens.Emerging mechanisms of antimicrobial resistance in bacteria and fungi: advances in the era of genomics.The Global Acetylome of the Human Pathogen Vibrio cholerae V52 Reveals Lysine Acetylation of Major Transcriptional Regulators.Flagellar motility, extracellular proteases and Vibrio cholerae detachment from abiotic and biotic surfaces.The effect of bacterial chemotaxis on host infection and pathogenicity.Environmental role of pathogenic traits in Vibrio cholerae.The effects of inulin, dried Jerusalem artichoke tuber and a multispecies probiotic preparation on microbiota ecology and immune status of the large intestine in young pigs.A Periplasmic Polymer Curves Vibrio cholerae and Promotes Pathogenesis.Characterization of the gluconate utilization system of Vibrio cholerae with special reference to virulence modulation.The type VI secretion system can modulate host intestinal mechanics to displace gut bacterial symbiontsAnti-biofilm Properties of the Fecal Probiotic Lactobacilli Against Vibrio spp.Cell Propagation of Cholera Toxin CTA ADP-Ribosylating Factor by Exosome Mediated Transfer.Expression of Hemolysin Is Regulated Under the Collective Actions of HapR, Fur, and HlyU in Vibrio cholerae El Tor Serogroup O1.Catabolism of mucus components influences motility of Vibrio cholerae in the presence of environmental reservoirs
P2860
Q28833418-E713CFC8-1CD4-4653-935D-B7FE9F65EDD8Q30152663-2B747301-6D3E-4BDF-A68E-A2800E574097Q30381075-61710A8B-1003-4E39-9957-992718A7ED39Q30396614-01B15159-BBB9-473A-AD41-A1CBAD74B96EQ33617304-223C9CB8-F085-48B5-978C-E8EA44EF498CQ35918461-2C727023-B68C-4CAD-AA4A-C917391BB042Q35963091-4684EA01-24E2-49C2-87AE-F75413968555Q35991196-AB3615D7-54E5-4A41-9538-0025C386B81EQ36267396-999CB5D9-1324-4AD7-BD85-0A62C42DC70EQ37572623-D722FC2F-42CE-477F-8ED9-3B15D65FEB56Q39139601-97E82F95-B1CF-4C7F-BA9D-37AE41BE3C2DQ40041251-6CC26F30-D685-466A-A8A5-E53FE9A0323FQ40118808-48A611A0-C831-47B6-A4AB-0DBBB07DE6DCQ41450553-2E33CFFF-428A-4806-9CD0-5B1AF83E7558Q42374314-20BDD971-DA7A-4E80-98FB-563FFD710E08Q42655611-5B9E85F7-8974-425C-B901-22126C602A16Q47564692-F91E3298-F060-4670-92A7-DEC84770B7D6Q47679214-E59ABA56-94E5-41CF-8395-0681FEE198B4Q47741040-20ABA349-486D-4A9C-87FF-9DECB2643BA0Q49627247-37DDF998-76F1-4E45-B41F-B7BCC4BE13E3Q50076981-C9229867-6ED8-4A32-A23F-D6F89457A5C5Q50082618-B7C4AFCB-EF03-4021-8A76-9478EF3DEFCCQ51144560-F075D647-937D-4E59-A342-82FCFF8206E6Q51153073-68BBF798-022C-4959-A31D-AB6374D8285CQ51192303-38A44D0E-9A77-412D-9247-FCC2FFB9EBF4Q51482431-9069C3F4-AF2E-40E6-A986-4A9067F75883Q53585512-1FA927FF-293E-4FD4-AACE-BE5340F026DBQ53685610-2085E6A7-299D-4384-B8E0-D372DC054086Q54956421-4F96BA33-C95C-4B3E-860A-6586C434863AQ55423886-DFFDF790-CB5D-481F-8C05-A4F0F9503BF9Q57922508-5DDF6082-6410-473D-9B62-602DAD8A3B5E
P2860
description
2015 nî lūn-bûn
@nan
2015 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Intestinal Colonization Dynamics of Vibrio cholerae.
@ast
Intestinal Colonization Dynamics of Vibrio cholerae.
@en
Intestinal Colonization Dynamics of Vibrio cholerae.
@nl
type
label
Intestinal Colonization Dynamics of Vibrio cholerae.
@ast
Intestinal Colonization Dynamics of Vibrio cholerae.
@en
Intestinal Colonization Dynamics of Vibrio cholerae.
@nl
prefLabel
Intestinal Colonization Dynamics of Vibrio cholerae.
@ast
Intestinal Colonization Dynamics of Vibrio cholerae.
@en
Intestinal Colonization Dynamics of Vibrio cholerae.
@nl
P2860
P921
P1433
P1476
Intestinal Colonization Dynamics of Vibrio cholerae
@en
P2093
Kali Pruss
Ronald K Taylor
P2860
P304
P356
10.1371/JOURNAL.PPAT.1004787
P5008
P577
2015-05-21T00:00:00Z