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.
278 related articles for article (PubMed ID: 21048787)
1. Skin commensals amplify the innate immune response to pathogens by activation of distinct signaling pathways. Wanke I; Steffen H; Christ C; Krismer B; Götz F; Peschel A; Schaller M; Schittek B J Invest Dermatol; 2011 Feb; 131(2):382-90. PubMed ID: 21048787 [TBL] [Abstract][Full Text] [Related]
2. Innate immune response of oral and foreskin keratinocytes: utilization of different signaling pathways by various bacterial species. Chung WO; Dale BA Infect Immun; 2004 Jan; 72(1):352-8. PubMed ID: 14688115 [TBL] [Abstract][Full Text] [Related]
3. Epidermal growth factor receptor inhibitors selectively inhibit the expressions of human β-defensins induced by Staphylococcus epidermidis. Park K; Ommori R; Imoto K; Asada H J Dermatol Sci; 2014 Aug; 75(2):94-9. PubMed ID: 24831548 [TBL] [Abstract][Full Text] [Related]
4. Keratinocytes as sensors and central players in the immune defense against Staphylococcus aureus in the skin. Bitschar K; Wolz C; Krismer B; Peschel A; Schittek B J Dermatol Sci; 2017 Sep; 87(3):215-220. PubMed ID: 28655473 [TBL] [Abstract][Full Text] [Related]
5. Differential innate immune responses of a living skin equivalent model colonized by Staphylococcus epidermidis or Staphylococcus aureus. Holland DB; Bojar RA; Farrar MD; Holland KT FEMS Microbiol Lett; 2009 Jan; 290(2):149-55. PubMed ID: 19054079 [TBL] [Abstract][Full Text] [Related]
6. Selective induction of antimicrobial peptides from keratinocytes by staphylococcal bacteria. Ommori R; Ouji N; Mizuno F; Kita E; Ikada Y; Asada H Microb Pathog; 2013 Mar; 56():35-9. PubMed ID: 23178253 [TBL] [Abstract][Full Text] [Related]
7. Signal transduction and nuclear responses in Staphylococcus aureus-induced expression of human beta-defensin 3 in skin keratinocytes. Menzies BE; Kenoyer A Infect Immun; 2006 Dec; 74(12):6847-54. PubMed ID: 16954397 [TBL] [Abstract][Full Text] [Related]
8. Differential utilization of nuclear factor-kappaB signaling pathways for gingival epithelial cell responses to oral commensal and pathogenic bacteria. Chung WO; Dale BA Oral Microbiol Immunol; 2008 Apr; 23(2):119-26. PubMed ID: 18279179 [TBL] [Abstract][Full Text] [Related]
9. Staphylococcus epidermidis-induced Interleukin-1 Beta and Human Beta-defensin-2 Expression in Human Keratinocytes is Regulated by the Host Molecule A20 (TNFAIP3). Simanski M; Erkens AS; Rademacher F; Harder J Acta Derm Venereol; 2019 Feb; 99(2):181-187. PubMed ID: 30328471 [TBL] [Abstract][Full Text] [Related]
10. Toll-like receptor expression in human keratinocytes: nuclear factor kappaB controlled gene activation by Staphylococcus aureus is toll-like receptor 2 but not toll-like receptor 4 or platelet activating factor receptor dependent. Mempel M; Voelcker V; Köllisch G; Plank C; Rad R; Gerhard M; Schnopp C; Fraunberger P; Walli AK; Ring J; Abeck D; Ollert M J Invest Dermatol; 2003 Dec; 121(6):1389-96. PubMed ID: 14675188 [TBL] [Abstract][Full Text] [Related]
11. The antimicrobial skin barrier in patients with atopic dermatitis. Schittek B Curr Probl Dermatol; 2011; 41():54-67. PubMed ID: 21576947 [TBL] [Abstract][Full Text] [Related]
12. New mechanisms of skin innate immunity: ASK1-mediated keratinocyte differentiation regulates the expression of beta-defensins, LL37, and TLR2. Sayama K; Komatsuzawa H; Yamasaki K; Shirakata Y; Hanakawa Y; Ouhara K; Tokumaru S; Dai X; Tohyama M; Ten Dijke P; Sugai M; Ichijo H; Hashimoto K Eur J Immunol; 2005 Jun; 35(6):1886-95. PubMed ID: 15864780 [TBL] [Abstract][Full Text] [Related]
13. Microbial symbiosis with the innate immune defense system of the skin. Gallo RL; Nakatsuji T J Invest Dermatol; 2011 Oct; 131(10):1974-80. PubMed ID: 21697881 [TBL] [Abstract][Full Text] [Related]
14. Bovine TLR2 and TLR4 properly transduce signals from Staphylococcus aureus and E. coli, but S. aureus fails to both activate NF-kappaB in mammary epithelial cells and to quickly induce TNFalpha and interleukin-8 (CXCL8) expression in the udder. Yang W; Zerbe H; Petzl W; Brunner RM; Günther J; Draing C; von Aulock S; Schuberth HJ; Seyfert HM Mol Immunol; 2008 Mar; 45(5):1385-97. PubMed ID: 17936907 [TBL] [Abstract][Full Text] [Related]
15. Salivary epithelial cells as model to study immune response against cutaneous pathogens. Negrini TC; Arthur RA; Waeiss RA; Carlosa IZ; Srinivasan M Clin Transl Sci; 2014 Feb; 7(1):48-51. PubMed ID: 24118988 [TBL] [Abstract][Full Text] [Related]
16. A novel lipopeptide from skin commensal activates TLR2/CD36-p38 MAPK signaling to increase antibacterial defense against bacterial infection. Li D; Lei H; Li Z; Li H; Wang Y; Lai Y PLoS One; 2013; 8(3):e58288. PubMed ID: 23472173 [TBL] [Abstract][Full Text] [Related]
18. Staphylococcus aureus and Escherichia coli elicit different innate immune responses from bovine mammary epithelial cells. Fu Y; Zhou E; Liu Z; Li F; Liang D; Liu B; Song X; Zhao F; Fen X; Li D; Cao Y; Zhang X; Zhang N; Yang Z Vet Immunol Immunopathol; 2013 Oct; 155(4):245-52. PubMed ID: 24018311 [TBL] [Abstract][Full Text] [Related]
19. Importance of phosphoinositide binding by human β-defensin 3 for Akt-dependent cytokine induction. Phan TK; Lay FT; Hulett MD Immunol Cell Biol; 2018 Jan; 96(1):54-67. PubMed ID: 29359392 [TBL] [Abstract][Full Text] [Related]