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Molecular Microbiology|September 3, 2004
A mycobacterial virulence gene cluster extending RD1 is required for cytolysis, bacterial spreading and ESAT-6 secretionLian-Yong Gao, Su Guo, Bryant McLaughlin, et al.Nano Letters|March 18, 2024
Strain Solitons in an Epitaxially Strained van der Waals-like MaterialJason T Dong, Hadass S Inbar, Connor P Dempsey, et al.Cellular Microbiology|April 12, 2001
Pseudomonas aeruginosa ExoT inhibits in vitro lung epithelial wound repairT K Geiser, B I Kazmierczak, L K Garrity-Ryan, et al.Cellular Microbiology|February 24, 2001
Host cell-derived sphingolipids are required for the intracellular growth of Chlamydia trachomatisC van Ooij, L Kalman, van Ijzendoorn, et al.Critical Care Medicine|May 7, 2002
Type III protein secretion is associated with poor clinical outcomes in patients with ventilator-associated pneumonia caused by Pseudomonas aeruginosaAlan R Hauser, Enesha Cobb, Maria Bodi, et al.Cell Reports|April 9, 2025
Antagonistic response regulators spatially regulate receptor methylation in the Pseudomonas aeruginosa Pil-Chp surface sensing systemRamiro Patino, Marco J Kühn, Henriette Macmillan, et al.Infection and Immunity|June 22, 1999
Pseudomonas aeruginosa gene products PilT and PilU are required for cytotoxicity in vitro and virulence in a mouse model of acute pneumoniaJ C Comolli, A R Hauser, L Waite, et al.The Biochemical Journal|December 1, 1996
Experimental evidence for structure-activity features in common between mammalian histidine decarboxylase and ornithine decarboxylaseN Engel, M T Olmo, C S Coleman, et al.American Journal of Veterinary Research|June 1, 1980
Clinical approach to determine the contribution of the palmar and palmar metacarpal nerves to the innervation of the equine fetlock jointB W Gray, H N Engel, P F Rumph, et al.Journal of the American Veterinary Medical Association|March 1, 1994
Orotracheal and nasotracheal intubation in llamasT W Riebold, H N Engel, T L Grubb, et al.Pageof 12