about
Differential Role of the T6SS in Acinetobacter baumannii VirulenceBrucella control of dendritic cell maturation is dependent on the TIR-containing protein Btp1.The glyceraldehyde-3-phosphate dehydrogenase and the small GTPase Rab 2 are crucial for Brucella replication.Coxiella burnetii, the agent of Q fever, replicates within trophoblasts and induces a unique transcriptional response.Brucella coopts the small GTPase Sar1 for intracellular replicationThe Brucella abortus phosphoglycerate kinase mutant is highly attenuated and induces protection superior to that of vaccine strain 19 in immunocompromised and immunocompetent miceA Pseudomonas aeruginosa TIR effector mediates immune evasion by targeting UBAP1 and TLR adaptors.Brucella β 1,2 cyclic glucan is an activator of human and mouse dendritic cells.In search of Brucella abortus type IV secretion substrates: screening and identification of four proteins translocated into host cells through VirB system.Bacterial interactions with the eukaryotic secretory pathway.The TIR Homologue Lies near Resistance Genes in Staphylococcus aureus, Coupling Modulation of Virulence and Antimicrobial Susceptibility.Pathogen-endoplasmic-reticulum interactions: in through the out door.BtpB, a novel Brucella TIR-containing effector protein with immune modulatory functions.Internal affairs: investigating the Brucella intracellular lifestyle.Brucella T4SS: the VIP pass inside host cells.Microscopy-based Assays for High-throughput Screening of Host Factors Involved in Brucella Infection of Hela Cells.Identification of a Brucella spp. secreted effector specifically interacting with human small GTPase Rab2.SseG, a virulence protein that targets Salmonella to the Golgi network.Functional Characterization of Pseudomonas Contact Dependent Growth Inhibition (CDI) Systems.The translocated Salmonella effector proteins SseF and SseG interact and are required to establish an intracellular replication niche.The Environmental Acinetobacter baumannii Isolate DSM30011 Reveals Clues into the Preantibiotic Era Genome Diversity, Virulence Potential, and Niche Range of a Predominant Nosocomial PathogenRelatedness of wildlife and livestock avian isolates of the nosocomial pathogen Acinetobacter baumannii to lineages spread in hospitals worldwide.Pathogenic brucellae replicate in human trophoblasts.Unsaturated Fatty Acids Affect Quorum Sensing Communication System and Inhibit Motility and Biofilm Formation of Acinetobacter baumannii.Intracellular replication of Salmonella typhimurium strains in specific subsets of splenic macrophages in vivo.The influence of two-partner secretion systems on the virulence of Acinetobacter baumannii.Protein-Protein Interactions: Pull-Down Assays.Inactivation of formyltransferase (wbkC) gene generates a Brucella abortus rough strain that is attenuated in macrophages and in mice.Synthesis of phosphatidylcholine, a typical eukaryotic phospholipid, is necessary for full virulence of the intracellular bacterial parasite Brucella abortusCyclic β-1,2-glucan is a brucella virulence factor required for intracellular survivalContrasting roles of macrophages and dendritic cells in controlling initial pulmonary Brucella infectionInvestigating TLR signaling responses in murine dendritic cells upon bacterial infectionNontypable Haemophilus influenzae: an intracellular phase within epithelial cells might contribute to persistenceIdentification of a Contact-Dependent Growth Inhibition (CDI) System That Reduces Biofilm Formation and Host Cell Adhesion of Acinetobacter baumannii DSM30011 StrainBioinformatic Analysis of the Type VI Secretion System and Its Potential Toxins in the Acinetobacter GenusThe TIR-domain containing effectors BtpA and BtpB from Brucella abortus impact NAD metabolism
P50
Q28548409-8F283EC0-5BCA-43F2-8D7B-33FB2E6E9246Q33319274-255B9761-857B-4E5A-AD93-C21AF6CDDD2BQ33474813-37B87566-ACA9-4EBF-8E53-E2DFB50999C4Q33778585-ADAD8E6E-8E33-433D-A50D-978304E211F2Q33817784-107C61B2-786F-4089-A508-53265C8C29EBQ33826026-E37FD150-626A-43B8-A3AE-6036D84C5F5FQ33863431-6E197742-534F-40C0-985F-62EDD0A52940Q34481835-CCAB9DD0-F486-4B7A-85C1-107E415B75D1Q35113343-CFBA2A36-1700-4183-85EF-BA94E879B3D6Q36032390-2E793BC7-5312-417A-B1D7-C1E2B2BE7909Q36242810-622F9934-9181-4422-BDB9-5B590C638331Q36402241-60FC90C5-4B47-4BBA-BF06-6A7AEB197CB3Q36989053-CDE6895B-2738-4A8A-BEA3-CC9E8BCAE26FQ37988968-D7295E8A-143F-4F86-B332-80C9DB059827Q38073982-E0AB80DA-C933-43B1-A559-05106AA1B3E4Q38933720-FDF62F26-F6B7-427E-9F32-2C1D27D2E831Q39557059-4C99609E-32FC-4277-8477-1E7CA35A22C8Q39927890-4909CCD7-A550-41CB-B5CE-0783166BB242Q40063938-5DCC34BB-B21D-4E19-A02A-AF522E1F9510Q40468478-EAF7E37E-0270-462B-9961-C01DE84430F4Q41692213-33137517-E747-4D98-8755-5B8F73677FD5Q43168703-8BD04202-8629-4895-B8E8-93720150760EQ45928570-7A741198-9FC4-4A3A-87F3-9A687729670DQ49321181-D5109D7C-81F8-4F90-A673-B530A057F6E8Q50113387-A50D2B29-4753-47C2-9D7C-79F132EA45A9Q50243106-7E9C78CF-051C-477A-91D5-1EFC59ED42DBQ50913373-DE4A1504-1599-4B6F-A50C-6C32F474C15DQ52601690-18B58473-BD30-4A38-B8E5-7FE6C6451ED5Q57040915-393580C4-A75D-42D0-BD00-DFCC67CE8FB6Q57040921-7C8E5A19-F152-4631-9F52-8C255B244C8FQ57041981-A46F8562-7C84-49CD-BB3C-B93C6EB2B208Q59276493-02E8FC89-1CA1-4274-A247-1109A50661E3Q59892475-02166576-E54D-48F1-BC92-6772EAB5B932Q91316601-83E334B4-CD5F-4A39-82DF-28D0CEA9F932Q91316710-428B4BFB-4E30-4AE6-8104-11F0C207559EQ91987560-5F8A66C5-75CC-4142-8E63-09F397BC4529
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Suzana P Salcedo
@ast
Suzana P Salcedo
@en
Suzana P Salcedo
@es
Suzana P Salcedo
@nl
Suzana P Salcedo
@sl
type
label
Suzana P Salcedo
@ast
Suzana P Salcedo
@en
Suzana P Salcedo
@es
Suzana P Salcedo
@nl
Suzana P Salcedo
@sl
altLabel
Suzana Pinto Salcedo
@en
Twitter account: @SSalcedoLab
@en
prefLabel
Suzana P Salcedo
@ast
Suzana P Salcedo
@en
Suzana P Salcedo
@es
Suzana P Salcedo
@nl
Suzana P Salcedo
@sl
P1053
C-2853-2014
P106
P21
P2798
P31
P3829
P496
0000-0001-5149-7756
P569
2000-01-01T00:00:00Z