These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
24. Evidence for pore formation in host cell membranes by ESX-1-secreted ESAT-6 and its role in Mycobacterium marinum escape from the vacuole. Smith J; Manoranjan J; Pan M; Bohsali A; Xu J; Liu J; McDonald KL; Szyk A; LaRonde-LeBlanc N; Gao LY Infect Immun; 2008 Dec; 76(12):5478-87. PubMed ID: 18852239 [TBL] [Abstract][Full Text] [Related]
25. Shiga Toxins Activate the NLRP3 Inflammasome Pathway To Promote Both Production of the Proinflammatory Cytokine Interleukin-1β and Apoptotic Cell Death. Lee MS; Kwon H; Lee EY; Kim DJ; Park JH; Tesh VL; Oh TK; Kim MH Infect Immun; 2016 Jan; 84(1):172-86. PubMed ID: 26502906 [TBL] [Abstract][Full Text] [Related]
26. Pure Hemozoin is inflammatory in vivo and activates the NALP3 inflammasome via release of uric acid. Griffith JW; Sun T; McIntosh MT; Bucala R J Immunol; 2009 Oct; 183(8):5208-20. PubMed ID: 19783673 [TBL] [Abstract][Full Text] [Related]
27. The adaptor ASC has extracellular and 'prionoid' activities that propagate inflammation. Franklin BS; Bossaller L; De Nardo D; Ratter JM; Stutz A; Engels G; Brenker C; Nordhoff M; Mirandola SR; Al-Amoudi A; Mangan MS; Zimmer S; Monks BG; Fricke M; Schmidt RE; Espevik T; Jones B; Jarnicki AG; Hansbro PM; Busto P; Marshak-Rothstein A; Hornemann S; Aguzzi A; Kastenmüller W; Latz E Nat Immunol; 2014 Aug; 15(8):727-37. PubMed ID: 24952505 [TBL] [Abstract][Full Text] [Related]
28. The loss of the PDIM/PGL virulence lipids causes differential secretion of ESX-1 substrates in Jones BS; Hu DD; Nicholson KR; Cronin RM; Weaver SD; Champion MM; Champion PA mSphere; 2024 May; 9(5):e0000524. PubMed ID: 38661343 [TBL] [Abstract][Full Text] [Related]
29. Asc and Ipaf Inflammasomes direct distinct pathways for caspase-1 activation in response to Legionella pneumophila. Case CL; Shin S; Roy CR Infect Immun; 2009 May; 77(5):1981-91. PubMed ID: 19237518 [TBL] [Abstract][Full Text] [Related]
30. Activation of an NLRP3 inflammasome restricts Mycobacterium kansasii infection. Chen CC; Tsai SH; Lu CC; Hu ST; Wu TS; Huang TT; Saïd-Sadier N; Ojcius DM; Lai HC PLoS One; 2012; 7(4):e36292. PubMed ID: 22558425 [TBL] [Abstract][Full Text] [Related]
31. Neisseria gonorrhoeae activates the proteinase cathepsin B to mediate the signaling activities of the NLRP3 and ASC-containing inflammasome. Duncan JA; Gao X; Huang MT; O'Connor BP; Thomas CE; Willingham SB; Bergstralh DT; Jarvis GA; Sparling PF; Ting JP J Immunol; 2009 May; 182(10):6460-9. PubMed ID: 19414800 [TBL] [Abstract][Full Text] [Related]
32. The Lienard J; Nobs E; Lovins V; Movert E; Valfridsson C; Carlsson F Proc Natl Acad Sci U S A; 2020 Jan; 117(2):1160-1166. PubMed ID: 31879349 [TBL] [Abstract][Full Text] [Related]
33. Mycobacterium tuberculosis Toxin CpnT Is an ESX-5 Substrate and Requires Three Type VII Secretion Systems for Intracellular Secretion. Izquierdo Lafuente B; Ummels R; Kuijl C; Bitter W; Speer A mBio; 2021 Mar; 12(2):. PubMed ID: 33653883 [TBL] [Abstract][Full Text] [Related]
34. An NLRP7-containing inflammasome mediates recognition of microbial lipopeptides in human macrophages. Khare S; Dorfleutner A; Bryan NB; Yun C; Radian AD; de Almeida L; Rojanasakul Y; Stehlik C Immunity; 2012 Mar; 36(3):464-76. PubMed ID: 22361007 [TBL] [Abstract][Full Text] [Related]
35. Activation of the NLRP3 inflammasome by Mycobacterium tuberculosis is uncoupled from susceptibility to active tuberculosis. Dorhoi A; Nouailles G; Jörg S; Hagens K; Heinemann E; Pradl L; Oberbeck-Müller D; Duque-Correa MA; Reece ST; Ruland J; Brosch R; Tschopp J; Gross O; Kaufmann SH Eur J Immunol; 2012 Feb; 42(2):374-84. PubMed ID: 22101787 [TBL] [Abstract][Full Text] [Related]
36. A novel ESX-1 locus reveals that surface-associated ESX-1 substrates mediate virulence in Mycobacterium marinum. Kennedy GM; Hooley GC; Champion MM; Mba Medie F; Champion PA J Bacteriol; 2014 May; 196(10):1877-88. PubMed ID: 24610712 [TBL] [Abstract][Full Text] [Related]
37. The antagonistic transcription factors, EspM and EspN, regulate the ESX-1 secretion system in Nicholson KR; Cronin RM; Prest RJ; Menon AR; Yang Y; Jennisch MK; Champion MM; Tobin DM; Champion PA mBio; 2024 Apr; 15(4):e0335723. PubMed ID: 38445877 [TBL] [Abstract][Full Text] [Related]
38. The Type I IFN response to infection with Mycobacterium tuberculosis requires ESX-1-mediated secretion and contributes to pathogenesis. Stanley SA; Johndrow JE; Manzanillo P; Cox JS J Immunol; 2007 Mar; 178(5):3143-52. PubMed ID: 17312162 [TBL] [Abstract][Full Text] [Related]
39. NLRP3 (NALP3, Cryopyrin) facilitates in vivo caspase-1 activation, necrosis, and HMGB1 release via inflammasome-dependent and -independent pathways. Willingham SB; Allen IC; Bergstralh DT; Brickey WJ; Huang MT; Taxman DJ; Duncan JA; Ting JP J Immunol; 2009 Aug; 183(3):2008-15. PubMed ID: 19587006 [TBL] [Abstract][Full Text] [Related]
40. The NLRP3 inflammasome is released as a particulate danger signal that amplifies the inflammatory response. Baroja-Mazo A; Martín-Sánchez F; Gomez AI; Martínez CM; Amores-Iniesta J; Compan V; Barberà-Cremades M; Yagüe J; Ruiz-Ortiz E; Antón J; Buján S; Couillin I; Brough D; Arostegui JI; Pelegrín P Nat Immunol; 2014 Aug; 15(8):738-48. PubMed ID: 24952504 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]