溶血素 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "溶血素" in Japanese language version.

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doi.org

“Di-rhamnolipid from Pseudomonas aeruginosa displays differential effects on human keratinocyte and fibroblast cultures”. J. Dermatol. Sci. 40 (2): 141–3. (November 2005). doi:10.1016/j.jdermsci.2005.08.005. PMC 1592130. PMID 16199139.
“Possible role of fungal hemolysins in sick building syndrome”. Adv. Appl. Microbiol. 55: 191–213. (2004). doi:10.1016/S0065-2164(04)55007-4. PMID 15350795.
“α-Hemolysin pore formation into a supported phospholipid bilayer using cell-free expression”. Biochim. Biophys. Acta 1808 (1): 271–8. (January 2011). doi:10.1016/j.bbamem.2010.07.027. PMID 20692229.
“The hemolysin of Escherichia coli”. Eur. J. Epidemiol. 4 (2): 135–43. (June 1988). doi:10.1007/BF00144740. PMID 3042445.
“Rapid assembly of a multimeric membrane protein pore”. Biophys. J. 101 (11): 2679–83. (December 2011). doi:10.1016/j.bpj.2011.09.054. PMC 3297801. PMID 22261056.
Duncan J. McGillivray, Gintaras Valincius, Frank Heinrich, Joseph W.F. Robertson, David J. Vanderah, Wilma Febo-Ayala, Ilja Ignatjev, Mathias Lösche, & John J. Kasianowicz (2009 Feb 18). “Structure of Functional Staphylococcus aureus α-Hemolysin Channels in Tethered Bilayer Lipid Membranes”. Biophysical Journal 96 (4): 1547–1553. doi:10.1016/j.bpj.2008.11.020. PMC 2717257. PMID 19217871.
“Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components”. J Chem Inf Model 45 (6): 1539–45. (2005). doi:10.1021/ci050175y. PMID 16309251.
“Structure of staphylococcal alpha-hemolysin, a heptameric transmembrane pore”. Science 274 (5294): 1859–66. (December 1996). doi:10.1126/science.274.5294.1859. PMID 8943190.
PDB: 3o44; “Crystal structure of the Vibrio cholerae cytolysin heptamer reveals common features among disparate pore-forming toxins”. Proc. Natl. Acad. Sci. U.S.A. 108 (18): 7385–90. (May 2011). doi:10.1073/pnas.1017442108. PMC 3088620. PMID 21502531.
PDB: 3b07; “Crystal structure of the octameric pore of staphylococcal γ-hemolysin reveals the β-barrel pore formation mechanism by two components”. Proc. Natl. Acad. Sci. U.S.A. 108 (42): 17314–9. (October 2011). doi:10.1073/pnas.1110402108. PMC 3198349. PMID 21969538.
Gouaux E (1998). “α-Hemolysin from Staphylococcus aureus: an archetype of β-barrel, channel-forming toxins”. J. Struct. Biol. 121 (2): 110–22. doi:10.1006/jsbi.1998.3959. PMID 9615434.
“Staphylococcus aureus α-hemolysin mediates virulence in a murine model of severe pneumonia through activation of the NLRP3 inflammasome”. J. Infect. Dis. 205 (5): 807–17. (March 2012). doi:10.1093/infdis/jir846. PMC 3274379. PMID 22279123.
“Apigenin alleviates the symptoms of Staphylococcus aureus pneumonia by inhibiting the production of alpha-hemolysin”. FEMS Microbiol. Lett. 338 (2): 124–31. (October 2012). doi:10.1111/1574-6968.12040. PMID 23113475.
“Staphylococcus aureus promotes autophagy by decreasing intracellular cAMP levels”. Autophagy 8 (12): 1865–7. (October 2012). doi:10.4161/auto.22161. PMC 3541307. PMID 23047465.
“The role of iron in the growth and hemolysin (Streptolysin S) production in Streptococcus pyogenes”. J. Basic Microbiol. 28 (7): 427–36. (1988). doi:10.1002/jobm.3620280703. PMID 3065477.
“Regulation of hemolysin expression and virulence of Staphylococcus aureus by a serine/threonine kinase and phosphatase”. PLoS ONE 5 (6): e11071. (2010). doi:10.1371/journal.pone.0011071. PMC 2884019. PMID 20552019.
“Anti-alpha-hemolysin monoclonal antibodies mediate protection against Staphylococcus aureus pneumonia”. Infect. Immun. 77 (7): 2712–8. (July 2009). doi:10.1128/IAI.00115-09. PMC 2708543. PMID 19380475.
“Thermostable direct hemolysin diminishes tyrosine phosphorylation of epidermal growth factor receptor through protein kinase C dependent mechanism”. Biochim. Biophys. Acta 1820 (7): 1073–80. (July 2012). doi:10.1016/j.bbagen.2012.04.011. PMID 22543197.
Kou Qin; Chunmin Dong; Guangyu Wu; Nevin A Lambert (August 2011). “Inactive-state preassembly of Gq-coupled receptors and Gq heterotrimers”. Nature Chemical Biology 7 (11): 740–747. doi:10.1038/nchembio.642. PMC 3177959. PMID 21873996.
Kou Qin; Pooja R. Sethi; Nevin A. Lambert (August 2008). “Abundance and stability of complexes containing inactive G protein-coupled receptors and G proteins”. The FASEB Journal 22 (8): 2920–2927. doi:10.1096/fj.08-105775. PMC 2493464. PMID 18434433.

fasebj.org

Kou Qin; Pooja R. Sethi; Nevin A. Lambert (August 2008). “Abundance and stability of complexes containing inactive G protein-coupled receptors and G proteins”. The FASEB Journal 22 (8): 2920–2927. doi:10.1096/fj.08-105775. PMC 2493464. PMID 18434433.

ijmm.org

Sritharan M (July 2006). “Iron and bacterial virulence”. Indian J Med Microbiol 24 (3): 163–4. PMID 16912433.

nih.gov

pubmed.ncbi.nlm.nih.gov

“Di-rhamnolipid from Pseudomonas aeruginosa displays differential effects on human keratinocyte and fibroblast cultures”. J. Dermatol. Sci. 40 (2): 141–3. (November 2005). doi:10.1016/j.jdermsci.2005.08.005. PMC 1592130. PMID 16199139.
“Possible role of fungal hemolysins in sick building syndrome”. Adv. Appl. Microbiol. 55: 191–213. (2004). doi:10.1016/S0065-2164(04)55007-4. PMID 15350795.
“α-Hemolysin pore formation into a supported phospholipid bilayer using cell-free expression”. Biochim. Biophys. Acta 1808 (1): 271–8. (January 2011). doi:10.1016/j.bbamem.2010.07.027. PMID 20692229.
“The hemolysin of Escherichia coli”. Eur. J. Epidemiol. 4 (2): 135–43. (June 1988). doi:10.1007/BF00144740. PMID 3042445.
“Rapid assembly of a multimeric membrane protein pore”. Biophys. J. 101 (11): 2679–83. (December 2011). doi:10.1016/j.bpj.2011.09.054. PMC 3297801. PMID 22261056.
Duncan J. McGillivray, Gintaras Valincius, Frank Heinrich, Joseph W.F. Robertson, David J. Vanderah, Wilma Febo-Ayala, Ilja Ignatjev, Mathias Lösche, & John J. Kasianowicz (2009 Feb 18). “Structure of Functional Staphylococcus aureus α-Hemolysin Channels in Tethered Bilayer Lipid Membranes”. Biophysical Journal 96 (4): 1547–1553. doi:10.1016/j.bpj.2008.11.020. PMC 2717257. PMID 19217871.
“Staphylococcal beta-hemolysin. II. Phospholipase C activity of purified beta-hemolysin”. J. Bacteriol. 94 (5): 1313–9. (November 1967). PMC 276826. PMID 4964474.
“Staphylococcus aureus bicomponent gamma-hemolysins, HlgA, HlgB, and HlgC, can form mixed pores containing all components”. J Chem Inf Model 45 (6): 1539–45. (2005). doi:10.1021/ci050175y. PMID 16309251.
“Structure of staphylococcal alpha-hemolysin, a heptameric transmembrane pore”. Science 274 (5294): 1859–66. (December 1996). doi:10.1126/science.274.5294.1859. PMID 8943190.
PDB: 3o44; “Crystal structure of the Vibrio cholerae cytolysin heptamer reveals common features among disparate pore-forming toxins”. Proc. Natl. Acad. Sci. U.S.A. 108 (18): 7385–90. (May 2011). doi:10.1073/pnas.1017442108. PMC 3088620. PMID 21502531.
PDB: 3b07; “Crystal structure of the octameric pore of staphylococcal γ-hemolysin reveals the β-barrel pore formation mechanism by two components”. Proc. Natl. Acad. Sci. U.S.A. 108 (42): 17314–9. (October 2011). doi:10.1073/pnas.1110402108. PMC 3198349. PMID 21969538.
Gouaux E (1998). “α-Hemolysin from Staphylococcus aureus: an archetype of β-barrel, channel-forming toxins”. J. Struct. Biol. 121 (2): 110–22. doi:10.1006/jsbi.1998.3959. PMID 9615434.
Sritharan M (July 2006). “Iron and bacterial virulence”. Indian J Med Microbiol 24 (3): 163–4. PMID 16912433.
“Staphylococcus aureus α-hemolysin mediates virulence in a murine model of severe pneumonia through activation of the NLRP3 inflammasome”. J. Infect. Dis. 205 (5): 807–17. (March 2012). doi:10.1093/infdis/jir846. PMC 3274379. PMID 22279123.
“Apigenin alleviates the symptoms of Staphylococcus aureus pneumonia by inhibiting the production of alpha-hemolysin”. FEMS Microbiol. Lett. 338 (2): 124–31. (October 2012). doi:10.1111/1574-6968.12040. PMID 23113475.
“Staphylococcus aureus promotes autophagy by decreasing intracellular cAMP levels”. Autophagy 8 (12): 1865–7. (October 2012). doi:10.4161/auto.22161. PMC 3541307. PMID 23047465.
“Effect of Escherichia coli alpha-hemolysin on human peripheral leukocyte function in vitro”. Infect. Immun. 37 (3): 966–74. (September 1982). PMC 347633. PMID 6752033.
“The role of iron in the growth and hemolysin (Streptolysin S) production in Streptococcus pyogenes”. J. Basic Microbiol. 28 (7): 427–36. (1988). doi:10.1002/jobm.3620280703. PMID 3065477.
“Regulation of hemolysin expression and virulence of Staphylococcus aureus by a serine/threonine kinase and phosphatase”. PLoS ONE 5 (6): e11071. (2010). doi:10.1371/journal.pone.0011071. PMC 2884019. PMID 20552019.
“Anti-alpha-hemolysin monoclonal antibodies mediate protection against Staphylococcus aureus pneumonia”. Infect. Immun. 77 (7): 2712–8. (July 2009). doi:10.1128/IAI.00115-09. PMC 2708543. PMID 19380475.
“Thermostable direct hemolysin diminishes tyrosine phosphorylation of epidermal growth factor receptor through protein kinase C dependent mechanism”. Biochim. Biophys. Acta 1820 (7): 1073–80. (July 2012). doi:10.1016/j.bbagen.2012.04.011. PMID 22543197.
Kou Qin; Chunmin Dong; Guangyu Wu; Nevin A Lambert (August 2011). “Inactive-state preassembly of Gq-coupled receptors and Gq heterotrimers”. Nature Chemical Biology 7 (11): 740–747. doi:10.1038/nchembio.642. PMC 3177959. PMID 21873996.
Kou Qin; Pooja R. Sethi; Nevin A. Lambert (August 2008). “Abundance and stability of complexes containing inactive G protein-coupled receptors and G proteins”. The FASEB Journal 22 (8): 2920–2927. doi:10.1096/fj.08-105775. PMC 2493464. PMID 18434433.

pmc.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

nhlbi.nih.gov

“What Is Hemolytic Anemia? - NHLBI, NIH”. United States National Institutes of Health (2011年4月1日). 2012年11月24日閲覧。

rcsb.org