about
Zipper-like internalization of Dr-positive Escherichia coli by epithelial cells is preceded by an adhesin-induced mobilization of raft-associated molecules in the initial step of adhesion.Bacterial guanine nucleotide exchange factors SopE-like and WxxxE effectors.NleH effectors interact with Bax inhibitor-1 to block apoptosis during enteropathogenic Escherichia coli infection.pH-, Lactic acid-, and non-lactic acid-dependent activities of probiotic Lactobacilli against Salmonella enterica Serovar Typhimurium.Binding to Na(+) /H(+) exchanger regulatory factor 2 (NHERF2) affects trafficking and function of the enteropathogenic Escherichia coli type III secretion system effectors Map, EspI and NleH.The type III secretion effector NleF of enteropathogenic Escherichia coli activates NF-κB early during infection.Role of NleH, a type III secreted effector from attaching and effacing pathogens, in colonization of the bovine, ovine, and murine gut.The Type III Secretion System Effector SeoC of Salmonella enterica subsp. salamae and S. enterica subsp. arizonae ADP-Ribosylates Src and Inhibits Opsonophagocytosis.Bacterial virulence factor inhibits caspase-4/11 activation in intestinal epithelial cells.Fresh fruit and vegetables as vehicles for the transmission of human pathogens.Bax inhibitor 1 in apoptosis and disease.Enterohemorrhagic Escherichia coli exploits EspA filaments for attachment to salad leaves.The Enterohemorrhagic Escherichia coli Effector EspW Triggers Actin Remodeling in a Rac1-Dependent Manner.The mechanisms used by enteropathogenic Escherichia coli to control filopodia dynamics.The Type III Secretion System Effector SptP of Salmonella enterica Serovar Typhi.Differential recognition of members of the carcinoembryonic antigen family by Afa/Dr adhesins of diffusely adhering Escherichia coli (Afa/Dr DAEC).EspM2 is a RhoA guanine nucleotide exchange factor.Older leaves of lettuce (Lactuca spp.) support higher levels of Salmonella enterica ser. Senftenberg attachment and show greater variation between plant accessions than do younger leaves.EspZ of enteropathogenic and enterohemorrhagic Escherichia coli regulates type III secretion system protein translocation.The enteropathogenic Escherichia coli effector NleH inhibits apoptosis induced by Clostridium difficile toxin B.Subversion of actin dynamics by EspM effectors of attaching and effacing bacterial pathogens.Fresh produce as a potential vector for bacterial human pathogens.Citrobacter rodentium Subverts ATP Flux and Cholesterol Homeostasis in Intestinal Epithelial Cells In Vivo.hCEACAM1-4L downregulates hDAF-associated signalling after being recognized by the Dr adhesin of diffusely adhering Escherichia coli.Attaching and effacing (A/E) lesion formation by enteropathogenic E. coli on human intestinal mucosa is dependent on non-LEE effectors.Cellulose mediates attachment of Salmonella enterica Serovar Typhimurium to tomatoes.Salmonella enterica strains belonging to O serogroup 1,3,19 induce chlorosis and wilting of Arabidopsis thaliana leaves.Interaction of Salmonella enterica with basil and other salad leaves.Broad-Spectrum Regulation of Nonreceptor Tyrosine Kinases by the Bacterial ADP-Ribosyltransferase EspJ.Flagella mediate attachment of enterotoxigenic Escherichia coli to fresh salad leaves.Interaction of enteroaggregative Escherichia coli with salad leaves.The Citrobacter rodentium type III secretion system effector EspO affects mucosal damage repair and antimicrobial responsesAntimicrobial Potential of Probiotic or Potentially Probiotic Lactic Acid Bacteria, the First Results of the International European Research Project PROPATH of the PROEUHEALTH ClusterPutting the "A" into WaSH: a call for integrated management of water, animals, sanitation, and hygiene
P50
Q31080703-AB17C5D6-E036-4725-A11E-610235550A4BQ33528372-DCCC953E-8BE3-4BE0-8794-1CB3085C9DAAQ33733678-703700BA-EC2E-4E13-ADBF-F9EE5331DC0EQ34098013-C8C366A4-7813-4627-8E7E-0F3F4D8CE5A9Q34462401-448D447C-CBDF-4413-AFE9-5E8BDE68DBF9Q34596147-7C133082-ECEE-46BE-80F3-A2CD2B3CCCBEQ36950038-FB172C4D-A177-4B01-9CE7-B24153A259D1Q37425037-4BA29C69-D2D5-4BD9-A31C-18AAAB524196Q37507829-FC0BF534-8194-4C19-BBAF-054906D349C0Q37773384-AEC0B180-75FA-4476-9EE0-BE5865166B07Q37836378-5B47B456-C559-4434-9849-BC98AFC795A0Q38607160-0FDDD324-0D82-4A95-B08D-A8FC4874345FQ38718455-CDA317ED-FEC2-4178-BA50-392012F00660Q39910582-CE7D6C3A-13F2-408B-BFFB-69CDABACDA08Q40077659-E16149AC-BE8C-4DC2-8998-2D2D1AAC531CQ40558577-38C1A53F-903A-4043-9E0A-6D98AAED574FQ40593889-6848A600-8179-4A2B-9F8B-0B69D6F6FB64Q41249515-BFC8499A-6957-479F-A931-91656BFE1F82Q42103443-DDF5EA31-9926-4061-9741-273A183F3EB7Q42708074-9EE5BE51-AE1F-44C4-8BB1-1E2C24AEE752Q42815784-4551C777-9CA8-4D05-9F23-E9095D6031CEQ42924583-74379572-595F-4863-89E1-A7703DBC7F1EQ46291702-A452AB60-BA9F-41B8-96C8-2A901DEDFFB9Q46916819-D1286029-12A3-44FC-9F69-FC94EB137969Q47097262-34EA2217-C7E8-44DD-AB23-E41DD1E16EE8Q50035763-FA6593D6-9FA0-4064-9841-C15DEEFBB291Q50043437-ACFDFC70-E2FB-4ADD-B968-6BD307E5E4E2Q50058965-E9F36EDD-82C4-48C2-8BDC-659C3D469B83Q52595435-F6D1B75F-A89D-4CE8-AF3D-6F9B3BCA8195Q54369586-384FAE5C-A1BD-4166-92F7-DED0B95AF4CEQ54400992-A9640805-8E74-479A-A692-BAA36556B0E5Q58478613-102F3D80-8A1D-4AE5-A689-E52459554CB4Q63859690-5B4911AB-619A-40E5-8955-CAD97F226523Q92791982-14D423A0-517A-4510-A237-86C310141B45
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Cedric N Berger
@ast
Cedric N Berger
@en
Cedric N Berger
@es
Cedric N Berger
@nl
type
label
Cedric N Berger
@ast
Cedric N Berger
@en
Cedric N Berger
@es
Cedric N Berger
@nl
prefLabel
Cedric N Berger
@ast
Cedric N Berger
@en
Cedric N Berger
@es
Cedric N Berger
@nl
P106
P21
P31
P496
0000-0002-1316-5985