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Molecular Microbiology|June 1, 1997
Identification of Pseudomonas aeruginosa genes required for epithelial cell injuryP J Kang, A R Hauser, G Apodaca, et al.Molecular Microbiology|May 5, 2016
A scaffold protein connects type IV pili with the Chp chemosensory system to mediate activation of virulence signaling in Pseudomonas aeruginosaYuki F Inclan, Alexandre Persat, Alexander Greninger, et al.Agents and Actions|November 1, 1994
Histamine as an autocrine growth factor in experimental mammary carcinomasG P Cricco, C A Davio, G Martin, et al.Journal of Cutaneous Pathology|September 2, 2022
Pilot study of fluorescence imitating brightfield imaging for rapid, slide-free dermatopathologyTess N Engel, Tanishq Mathew Abraham, Taryn Morningstar, et al.Cell Reports|August 18, 2024
The Chlamydia effector IncE employs two short linear motifs to reprogram host vesicle traffickingKhavong Pha, Kathleen Mirrashidi, Jessica Sherry, et al.Biorxiv : the Preprint Server for Biology|May 7, 2024
The Chlamydia effector IncE employs two short linear motifs to reprogram host vesicle traffickingKhavong Pha, Katherine Mirrashidi, Jessica Sherry, et al.Current Research in Toxicology|April 30, 2026
A mechanistic evaluation of the metabolism disrupting potential of methyl tert-butyl etherA N Buerger, M J Vincent, S Fitch, et al.Plos Pathogens|November 7, 2014
The Pseudomonas aeruginosa type III translocon is required for biofilm formation at the epithelial barrierCindy S Tran, Stephanie M Rangel, Henrik Almblad, et al.The EMBO Journal|February 16, 2023
Two antagonistic response regulators control Pseudomonas aeruginosa polarization during mechanotaxisMarco J Kühn, Henriette Macmillan, Lorenzo Talà, et al.Cellular Microbiology|March 14, 2013
Endosulfatases SULF1 and SULF2 limit Chlamydia muridarum infectionJ H Kim, C Chan, C Elwell, et al.Pageof 17