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	Mycobacterium tuberculosis H37Ra and H37Rv differential growth and cytokine/chemokine induction in murine macrophages in vitro. [My Copy] J Interferon Cytokine Res, Vol. 26, No. 1. (January 2006), pp. 27-33. by S. Freeman, F. A. Post, L. G. Bekker, et al.R. Harbacheuski, L. M. Steyn, B. Ryffel, N. D. Connell, B. N. Kreiswirth, G. Kaplan posted to chemokine cytokine murine_macrophage mycobacterium_tuberculosis tnf by jjray on 2007-08-02 18:30:38 as
	Virulent clinical isolates of Mycobacterium tuberculosis grow rapidly and induce cellular necrosis but minimal apoptosis in murine macrophages. [My Copy] J Leukoc Biol, Vol. 79, No. 1. (January 2006), pp. 80-86. by J. S. Park, M. H. Tamayo, M. Gonzalez-Juarrero, I. M. Orme, D. J. Ordway posted to apoptosis murine_macrophage mycobacterium_tuberculosis necrosis by jjray on 2007-07-09 02:13:32 as
	Survival of virulent Mycobacterium tuberculosis involves preventing apoptosis induced by Bcl-2 upregulation and release resulting from necrosis in J774 macrophages. [My Copy] Microbiol Immunol, Vol. 49, No. 9. (2005), pp. 845-852. by J. Zhang, R. Jiang, H. Takayama, Y. Tanaka posted to apoptosis macrophage murine_macrophage mycobacterium_tuberculosis necrosis by jjray on 2007-07-09 02:12:27 as
	Involvement of Caspase-9 in the Inhibition of Necrosis of RAW 264 Cells Infected with Mycobacterium tuberculosis [My Copy] Infect. Immun., Vol. 75, No. 6. (1 June 2007), pp. 2894-2902. by Ryosuke Uchiyama, Ikuo Kawamura, Takao Fujimura, et al.Michiko Kawanishi, Kohsuke Tsuchiya, Takanari Tominaga, Taijin Kaku, Yutaka Fukasawa, Shunsuke Sakai, Takamasa Nomura, Masao Mitsuyama posted to murine_macrophage mycobacterium_tuberculosis necrosis tnf by jjray on 2007-05-22 15:31:17 as
	TNF influences chemokine expression of macrophages in vitro and that of CD11b+ cells in vivo during Mycobacterium tuberculosis infection. [My Copy] J Immunol, Vol. 172, No. 11. (1 June 2004), pp. 6846-6857. by H. M. Algood, P. L. Lin, D. Yankura, A. Jones, J. Chan, J. L. Flynn posted to chemokine mouse murine_macrophage mycobacterium_tuberculosis tnf by jjray on 2007-05-08 14:57:30 as along with 1 person tkershaw
	Interaction with extracellular matrix proteins influences Lsh/Ity/Bcg (candidate Nramp) gene regulation of macrophage priming/activation for tumour necrosis factor-alpha and nitrite release. [My Copy] Immunology, Vol. 82, No. 1. (May 1994), pp. 42-50. by S. Formica, T. I. Roach, J. M. Blackwell posted to immune_activation lam macrophage_activation murine_macrophage tnf by jjray on 2007-04-16 16:38:20 as
	Distinct and Nonredundant In Vivo Functions of TNF Produced by T Cells and Macrophages/Neutrophils: Protective and Deleterious Effects [My Copy] Immunity, Vol. 22, No. 1. (January 2005), pp. 93-104. by Sergei I. Grivennikov, Alexei V. Tumanov, Dmitry J. Liepinsh, et al.Andrei A. Kruglov, Boris I. Marakusha, Alexander N. Shakhov, Takaya Murakami, Ludmila N. Drutskaya, Irmgard Forster, Bjorn E. Clausen, Lino Tessarollo, Bernhard Ryffel, Dmitry V. Kuprash, Sergei A. Nedospasov posted to murine_macrophage t_cell tnf by jjray on 2007-04-10 16:15:18 as
	TNF-alpha and IL-10 Modulate the Induction of Apoptosis by Virulent Mycobacterium tuberculosis in Murine Macrophages [My Copy] J Immunol, Vol. 162, No. 10. (15 May 1999), pp. 6122-6131. by Mauricio Rojas, Martin Olivier, Philippe Gros, Luis F. Barrera, Luis F. Garcia posted to murine_macrophage mycobacterium_tuberculosis tnf by jjray on 2007-04-05 19:04:08 as
	Effect of Mycobacterium tuberculosis-Specific 10-Kilodalton Antigen on Macrophage Release of Tumor Necrosis Factor Alpha and Nitric Oxide [My Copy] Infect. Immun., Vol. 70, No. 12. (1 December 2002), pp. 6558-6566. by Vladimir Trajkovic, Gyanesh Singh, Balwan Singh, Sarman Singh, Pawan Sharma posted to ifn-gamma mtsa-10 murine_macrophage mycobacterium_tuberculosis nitric_oxide synergistic_signals tnf by jjray on 2007-04-05 17:05:46 as
	Mycobacterium tuberculosis H37Ra and H37Rv Differential Growth and Cytokine/Chemokine Induction in Murine Macrophages In Vitro [My Copy] Journal of Interferon & Cytokine Research, Vol. 26, No. 1. (January 2006), pp. 27-33. by Sherry Freeman, Frank A. Post, Linda-Gail Bekker, et al.Ryhor Harbacheuski, Lafras M. Steyn, Bernhard Ryffel, Nancy D. Connell, Barry N. Kreiswirth, Gilla Kaplan posted to growth_rate host-pathogen_interaction murine_macrophage mycobacterium_tuberculosis tnf by jjray on 2007-04-05 17:01:48 as
	TLR2 but not TLR4 Signalling is Critically Involved in the Inhibition of IFN--induced Killing of Mycobacteria by Murine Macrophages [My Copy] Scandinavian Journal of Immunology, Vol. 65, No. 2. (February 2007), pp. 148-157. by Arko-Mensah, J., Julian, et al. E., Singh, M., Fernandez, C. posted to ifn-gamma inos macrophage_activation murine_macrophage mycobacterium_tuberculosis nitric_oxide tnf toll-like_receptor by jjray on 2007-04-05 16:54:43 as
	Mycobacterium tuberculosis Inhibits Macrophage Responses to IFN-gamma through Myeloid Differentiation Factor 88-Dependent and -Independent Mechanisms [My Copy] J Immunol, Vol. 172, No. 10. (15 May 2004), pp. 6272-6280. by Sarah M. Fortune, Alejandra Solache, Alejandra Jaeger, et al.Preston J. Hill, John T. Belisle, Barry R. Bloom, Eric J. Rubin, Joel D. Ernst posted to antagonist host-pathogen_interaction ifn-gamma macrophage_activation murine_macrophage mycobacterium_tuberculosis toll-like_receptor by jjray on 2007-03-30 21:12:58 as
	Host defense mechanisms triggered by microbial lipoproteins through toll-like receptors. [My Copy] Science (New York, N.Y.), Vol. 285, No. 5428. (30 July 1999), pp. 732-736. by H. D. Brightbill, D. H. Libraty, S. R. Krutzik, et al.R. B. Yang, J. T. Belisle, J. R. Bleharski, M. Maitland, M. V. Norgard, S. E. Plevy, S. T. Smale, P. J. Brennan, B. R. Bloom, P. J. Godowski, R. L. Modlin posted to human_monocyte macrophage_activation murine_macrophage mycobacterium_tuberculosis toll-like_receptor by jjray on 2007-03-30 20:23:26 as along with 2 people tomhebbron mtagaya
	TNF-alpha Gene Expression in Macrophages: Regulation by NF-kappaB Is Independent of c-Jun or C/EBPbeta [My Copy] J Immunol, Vol. 164, No. 8. (15 April 2000), pp. 4277-4285. by Hongtao Liu, Prodromos Sidiropoulos, Guobin Song, et al.Lisa J. Pagliari, Michael J. Birrer, Bernd Stein, Josef Anrather, Richard M. Pope posted to murine_macrophage nf-kappab tnf by jjray on 2007-03-28 22:39:04 as
	Tumor Necrosis Factor Alpha Transcription in Macrophages Is Attenuated by an Autocrine Factor That Preferentially Induces NF-kappa B p50 [My Copy] Mol. Cell. Biol., Vol. 18, No. 10. (1 October 1998), pp. 5678-5689. by Mark Baer, Allan Dillner, Richard C. Schwartz, Constance Sedon, Sergei Nedospasov, Peter F. Johnson posted to autocrine_paracrine murine_macrophage nf-kappab tnf by jjray on 2007-03-28 22:37:52 as
	Transcriptional noise and cellular heterogeneity in mammalian macrophages [My Copy] Philos Trans R Soc Lond B Biol Sci, Vol. 361, No. 1467. (29 March 2006), pp. 495-506. by S. Ramsey, A. Ozinsky, A. Clark, et al.K. D. Smith, P. de Atauri, V. Thorsson, D. Orrell, H. Bolouri posted to toll-like_receptor systems_approach stochastic signaling noise nf-kappab network_motifs murine_macrophage mathematical_model mammalian macrophage_activation immune_activation gene_regulation feedforward by jjray on 2007-01-30 16:48:47 as
	Absence of complement receptor 3 results in reduced binding and ingestion of Mycobacterium tuberculosis but has no significant effect on the induction of reactive oxygen and nitrogen intermediates or on the survival of the bacteria in resident and interferon-gamma activated macrophages [My Copy] Microbial Pathogenesis, Vol. 39, No. 3. (September 2005), pp. 57-67. by Amanda W. Rooyakkers, Richard W. Stokes posted to phagocytosis mycobacterium_tuberculosis murine_macrophage macrophage_activation immune_activation host-pathogen_interaction by jjray on 2007-01-17 18:06:20 as
	Killing of virulent Mycobacterium tuberculosis by reactive nitrogen intermediates produced by activated murine macrophages. [My Copy] J Exp Med, Vol. 175, No. 4. (1 April 1992), pp. 1111-1122. by J. Chan, Y. Xing, R. S. Magliozzo, B. R. Bloom posted to gene_regulation host-pathogen_interaction ifn-gamma immune_activation lam lps murine_macrophage mycobacterium_tuberculosis nitric_oxide pathogen_killing by jjray on 2006-12-20 18:56:30 as
	Lipoarabinomannans derived from different strains of Mycobacterium tuberculosis differentially stimulate the activation of NF-kappa B and KBF1 in murine macrophages. [My Copy] Infect Immun, Vol. 63, No. 5. (May 1995), pp. 1960-1968. by M. C. Brown, S. M. Taffet posted to immune_activation lam murine_macrophage mycobacterium_tuberculosis nf-kappab by jjray on 2006-12-20 17:55:05 as
	Induction of Inducible Nitric Oxide Synthase-NOmiddle dot by Lipoarabinomannan of Mycobacterium tuberculosis Is Mediated by MEK1-ERK, MKK7-JNK, and NF-kappaB Signaling Pathways [My Copy] Infect. Immun., Vol. 69, No. 4. (1 April 2001), pp. 2001-2010. by Edward D. Chan, Kristin R. Morris, John T. Belisle, et al.Preston Hill, Linda K. Remigio, Patrick J. Brennan, David W. Riches posted to immune_activation inos lam murine_macrophage nitric_oxide by jjray on 2006-12-20 17:49:05 as
	The SecA2 Secretion Factor of Mycobacterium tuberculosis Promotes Growth in Macrophages and Inhibits the Host Immune Response [My Copy] Infect. Immun., Vol. 74, No. 12. (1 December 2006), pp. 6855-6864. by Sherry Kurtz, Karen P. Mckinnon, Marschall S. Runge, Jenny P. Ting, Miriam Braunstein posted to early_immunity gene_regulation growth_rate host-pathogen_interaction ifn-gamma immune_activation inos intracellular murine_macrophage mycobacterium_tuberculosis nitric_oxide by jjray on 2006-11-21 19:47:34 as
	Requirement for multiple activation signals by anti-inflammatory feedback in macrophages. [My Copy] J Theor Biol, Vol. 241, No. 2. (21 July 2006), pp. 276-294. by J. C. Ray, D. E. Kirschner posted to biochemical_systems_theory evolution feedback gene_regulation ifn-gamma immune_activation inos iron lps mathematical_model mathematically_controlled_comparison murine_macrophage network network_motifs nf-kappab nitric_oxide piecewise_power-law power_law response_time robustness sensitivity_analysis signaling stat1 synergistic_signals systems_approach by jjray on 2006-09-28 21:24:15 as
	Release of reactive nitrogen intermediates and reactive oxygen intermediates from mouse peritoneal macrophages. Comparison of activating cytokines and evidence for independent production [My Copy] J Immunol, Vol. 141, No. 7. (1 October 1988), pp. 2407-2412. by Ah Ding, Cf Nathan, Dj Stuehr posted to cytokine immune_activation murine_macrophage nitric_oxide by jjray on 2006-09-28 21:06:38 as along with 2 people and 4 groups HEIRS devender HEIRS Immunology and Autoimmune Diseases HEIRS H2O2 and Other Oxidative Mediators HEIRS - Environmental Illness Research HEIRS Cellular Biology
	Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 97, No. 16. (2000), pp. 8841-8848. by C. Nathan, M. U. Shiloh posted to gene_regulation host-pathogen_interaction human_macrophage ifn-gamma immune_activation inos lung murine_macrophage mycobacterium_tuberculosis nadph_phagocyte_oxidase nitric_oxide pathogen_killing review by jjray on 2006-09-20 16:24:43 as
	The role of Toll-like receptors in immunity against mycobacterial infection. [My Copy] Microbes Infect, Vol. 4, No. 9. (July 2002), pp. 937-944. by K. A. Heldwein, M. J. Fenton posted to early_immunity gene_regulation host-pathogen_interaction immune_activation inos intracellular lam murine_macrophage mycobacterium_tuberculosis review synergistic_signals toll-like_receptor transcriptional_reprogramming by jjray on 2006-09-19 17:38:48 as
	Expression profiling of host pathogen interactions: how Mycobacterium tuberculosis and the macrophage adapt to one another [My Copy] Microbes and Infection, Vol. 8, No. 4. (April 2006), pp. 1132-1140. by Dirk Schnappinger, Gary K. Schoolnik, Sabine Ehrt posted to gene_regulation host-pathogen_interaction ider immune_activation inos intracellular lam mrna murine_macrophage mycobacterium_tuberculosis reciprocal_adaptation transcriptional_reprogramming by jjray on 2006-09-19 16:46:48 as
	Expression of Many Immunologically Important Genes in Mycobacterium tuberculosis-Infected Macrophages Is Independent of Both TLR2 and TLR4 but Dependent on IFN-alphabeta Receptor and STAT1 [My Copy] J Immunol, Vol. 175, No. 5. (1 September 2005), pp. 3318-3328. by Shuangping Shi, Antje Blumenthal, Christopher M. Hickey, Sheetal Gandotra, David Levy, Sabine Ehrt posted to cytokine gene_regulation ifn-gamma immune_activation murine_macrophage mycobacterium_tuberculosis myd88 toll-like_receptor by jjray on 2006-09-19 16:26:36 as
	Re-examination of the role of suppressor of cytokine signaling 1 (SOCS1) in the regulation of toll-like receptor signaling. [My Copy] J Biol Chem, Vol. 279, No. 52. (24 December 2004), pp. 54702-54707. by S. Gingras, E. Parganas, A. de Pauw, J. N. Ihle, P. J. Murray posted to feedback immune_activation lps murine_macrophage network_motifs nf-kappab signaling socs1 toll-like_receptor type-1_ifn by jjray on 2006-08-03 17:32:50 as
	Suppressor of cytokine signaling (SOCS) proteins indirectly regulate toll-like receptor signaling in innate immune cells. [My Copy] J Biol Chem, Vol. 279, No. 52. (24 December 2004), pp. 54708-54715. by A. Baetz, M. Frey, K. Heeg, A. H. Dalpke posted to feedback immune_activation lps murine_macrophage network_motifs nf-kappab signaling socs1 toll-like_receptor type-1_ifn by jjray on 2006-08-03 17:31:03 as
	SOCS-1 participates in negative regulation of LPS responses. [My Copy] Immunity, Vol. 17, No. 5. (November 2002), pp. 677-687. by R. Nakagawa, T. Naka, H. Tsutsui, et al.M. Fujimoto, A. Kimura, T. Abe, E. Seki, S. Sato, O. Takeuchi, K. Takeda, S. Akira, K. Yamanishi, I. Kawase, K. Nakanishi, T. Kishimoto posted to feedback immune_activation lps murine_macrophage network_motifs nf-kappab signaling socs1 toll-like_receptor by jjray on 2006-08-03 17:29:00 as
	SOCS1/JAB is a negative regulator of LPS-induced macrophage activation. [My Copy] Immunity, Vol. 17, No. 5. (November 2002), pp. 583-591. by I. Kinjyo, T. Hanada, K. Inagaki-Ohara, et al.H. Mori, D. Aki, M. Ohishi, H. Yoshida, M. Kubo, A. Yoshimura posted to feedback immune_activation lps murine_macrophage network_motifs nf-kappab signaling socs1 toll-like_receptor by jjray on 2006-08-03 17:27:07 as
	Induction of a homeostatic circuit in lung tissue by microbial compounds. [My Copy] Immunity, Vol. 24, No. 4. (April 2006), pp. 475-487. by K. Takabayshi, M. Corr, T. Hayashi, et al.V. Redecke, L. Beck, D. Guiney, D. Sheppard, E. Raz posted to homeostatic_circuit immune_activation immune_cell_kinetics lung murine_macrophage tgfbeta by jjray on 2006-08-03 16:22:06 as along with 1 person madhadron
	Toll-like receptor-2 mediates mycobacteria-induced proinflammatory signaling in macrophages. [My Copy] Proc Natl Acad Sci U S A, Vol. 96, No. 25. (7 December 1999), pp. 14459-14463. by D. M. Underhill, A. Ozinsky, K. D. Smith, A. Aderem posted to human_macrophage immune_activation murine_macrophage mycobacterium_tuberculosis nf-kappab signaling toll-like_receptor by jjray on 2005-11-08 18:56:51 as
	Mycobacterial growth inhibition by interferon-gamma-activated bone marrow macrophages and differential susceptibility among strains of Mycobacterium tuberculosis. [My Copy] J Immunol, Vol. 138, No. 12. (15 June 1987), pp. 4408-4413. by I. Flesch, S. H. Kaufmann posted to ifn-gamma immune_activation murine_macrophage mycobacterium_tuberculosis by jjray on 2005-11-04 16:33:32 as
	Activation of macrophages to inhibit proliferation of Mycobacterium tuberculosis: comparison of the effects of recombinant gamma-interferon on human monocytes and murine peritoneal macrophages. [My Copy] Immunology, Vol. 59, No. 3. (November 1986), pp. 333-338. by G. A. Rook, J. Steele, M. Ainsworth, B. R. Champion posted to human_monocyte ifn-gamma immune_activation murine_macrophage mycobacterium_tuberculosis by jjray on 2005-11-04 16:32:18 as
	Response of cultured macrophages to Mycobacterium tuberculosis, with observations on fusion of lysosomes with phagosomes. [My Copy] J Exp Med, Vol. 134, No. 3 Pt 1. (1 September 1971), pp. 713-740. by J. A. Armstrong, P. D. Hart posted to human_macrophage murine_macrophage mycobacterium_tuberculosis phagocytosis phagosome by jjray on 2005-10-31 21:04:17 as
	Identification of interferon-gamma as the lymphokine that activates human macrophage oxidative metabolism and antimicrobial activity. [My Copy] J Exp Med, Vol. 158, No. 3. (1 September 1983), pp. 670-689. by C. F. Nathan, H. W. Murray, M. E. Wiebe, B. Y. Rubin posted to human_macrophage ifn-gamma immune_activation murine_macrophage by jjray on 2005-10-31 21:00:22 as
	Cell biology of mycobacterium tuberculosis phagosome. [My Copy] Annu Rev Cell Dev Biol, Vol. 20 (2004), pp. 367-394. by I. Vergne, J. Chua, S. B. Singh, V. Deretic posted to human_macrophage murine_macrophage mycobacterium_tuberculosis phagocytosis phagosome review by jjray on 2005-10-31 20:47:19 as
	On the expression of nitric oxide synthase by human macrophages. Why no NO? [My Copy] J Leukoc Biol, Vol. 58, No. 6. (December 1995), pp. 643-649. by J. E. Albina posted to human_macrophage human_monocyte ifn-gamma immune_activation inos murine_macrophage nitric_oxide by jjray on 2005-10-14 20:52:04 as
	Molecular mechanisms of macrophage activation and deactivation by lipopolysaccharide: roles of the receptor complex. [My Copy] Pharmacol Ther, Vol. 100, No. 2. (November 2003), pp. 171-194. by M. Fujihara, M. Muroi, K. Tanamoto, T. Suzuki, H. Azuma, H. Ikeda posted to human_macrophage lps macrophage_deactivation murine_macrophage nf-kappab stat1 toll-like_receptor by jjray on 2005-10-05 20:26:00 as
	Deactivation of murine alveolar macrophages by peroxisome proliferator-activated receptor-gamma ligands. [My Copy] Am J Physiol Lung Cell Mol Physiol, Vol. 286, No. 3. (March 2004) by R. C. Reddy, V. G. Keshamouni, S. H. Jaigirdar, et al.X. Zeng, T. Leff, V. J. Thannickal, T. J. Standiford posted to macrophage_deactivation murine_macrophage nitric_oxide ppar-gamma by jjray on 2005-10-05 20:24:05 as
	Regulation of macrophage activation. [My Copy] Cell Mol Life Sci, Vol. 60, No. 11. (November 2003), pp. 2334-2346. by J. Ma, T. Chen, J. Mandelin, et al.A. Ceponis, N. E. Miller, M. Hukkanen, G. F. Ma, Y. T. Konttinen posted to cytokine human_macrophage ifn-gamma immune_activation irf-1 macrophage_deactivation murine_macrophage nf-kappab nitric_oxide stat1 tnf toll-like_receptor by jjray on 2005-10-05 20:22:21 as along with 1 person Zephyrus
	Macrophage deactivation by interleukin 10. [My Copy] J Exp Med, Vol. 174, No. 6. (1 December 1991), pp. 1549-1555. by C. Bogdan, Y. Vodovotz, C. Nathan posted to dose_response ifn-gamma immune_activation macrophage_deactivation murine_macrophage nitric_oxide quantitative_data by jjray on 2005-10-05 20:10:29 as
	Kinetic studies of the production of nitric oxide (NO) and tumour necrosis factor-alpha (TNF-alpha) in macrophages stimulated with Burkholderia pseudomallei endotoxin. [My Copy] Clin Exp Immunol, Vol. 122, No. 3. (December 2000), pp. 324-329. by P. Utaisincharoen, N. Tangthawornchaikul, W. Kespichayawattana, N. Anuntagool, P. Chaisuriya, S. Sirisinha posted to biochemistry co-culture dose_response gene_regulation immune_activation lps murine_macrophage nitric_oxide quantitative_data response_time tnf by jjray on 2005-09-16 21:56:45 as
	Autocrine/paracrine IFN-alphabeta mediates the lipopolysaccharide-induced activation of transcription factor Stat1alpha in mouse macrophages: pivotal role of Stat1alpha in induction of the inducible nitric oxide synthase gene. [My Copy] J Immunol, Vol. 161, No. 9. (1 November 1998), pp. 4803-4810. by J. J. Gao, M. B. Filla, M. J. Fultz, S. N. Vogel, S. W. Russell, W. J. Murphy posted to autocrine_paracrine biochemistry cytokine gene_regulation ifn-gamma immune_activation murine_macrophage network_motifs nitric_oxide stat1 transcription by jjray on 2005-09-16 21:19:31 as
	Induction of in vitro human macrophage anti-Mycobacterium tuberculosis activity: requirement for IFN-gamma and primed lymphocytes. [My Copy] J Immunol, Vol. 160, No. 9. (1 May 1998), pp. 4490-4499. by M. G. Bonecini-Almeida, S. Chitale, I. Boutsikakis, et al.J. Geng, H. Doo, S. He, J. L. Ho posted to co-culture growth_rate ifn-gamma immune_activation murine_macrophage mycobacterium_tuberculosis nitric_oxide by jjray on 2005-09-02 19:49:20 as
	Differential potentiation of anti-mycobacterial activity and reactive nitrogen intermediate-producing ability of murine peritoneal macrophages activated by interferon-gamma (IFN-gamma) and tumour necrosis factor-alpha (TNF-alpha). [My Copy] Clin Exp Immunol, Vol. 112, No. 1. (April 1998), pp. 63-68. by K. Sato, T. Akaki, H. Tomioka posted to co-culture growth_rate ifn-gamma immune_activation murine_macrophage mycobacterium_tuberculosis nitric_oxide quantitative_data tnf by jjray on 2005-09-02 19:41:14 as
	Human toll-like receptors mediate cellular activation by Mycobacterium tuberculosis. [My Copy] J Immunol, Vol. 163, No. 7. (1 October 1999), pp. 3920-3927. by T. K. Means, S. Wang, E. Lien, A. Yoshimura, D. T. Golenbock, M. J. Fenton posted to human_macrophage immune_activation murine_macrophage mycobacterium_tuberculosis nf-kappab signaling toll-like_receptor by jjray on 2005-08-31 19:28:43 as
	Iron down-regulates macrophage anti-tumour activity by blocking nitric oxide production. [My Copy] Clin Exp Immunol, Vol. 137, No. 1. (July 2004), pp. 109-116. by L. Harhaji, O. Vuckovic, D. Miljkovic, S. Stosic-Grujicic, V. Trajkovic posted to biochemistry immune_activation iron murine_macrophage nitric_oxide rat_macrophage by jjray on 2005-08-30 21:38:27 as
	The effect of iron on the expression of cytokines in macrophages infected with Mycobacterium tuberculosis. [My Copy] Scand J Immunol, Vol. 60, No. 4. (October 2004), pp. 329-337. by J. Serafín-López, R. Chacón-Salinas, S. Muñoz-Cruz, J. A. Enciso-Moreno, S. A. Estrada-Parra, I. Estrada-García posted to cytokine ifn-gamma immune_activation intracellular iron murine_macrophage mycobacterium_tuberculosis by jjray on 2005-08-30 21:36:12 as

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bacteria	259
mathematical_model	255
gene_regulation	251
stochastic	198
signaling	153
evolution	141
mycobacterium_tuberculosis	139
noise	131
network	129
feedback	127
two-component_system	127
e_coli	114
biophysics	100
review	99
gene_expression	73
t_cell	60
immune_activation	59
biochemistry	55
method	55
transcription	55
bacillus_subtilis	53
tnf	53
murine_macrophage	51
chemokine	50
physics	49
chemotaxis	48
theory	47
robustness	43
network_motifs	38
nitric_oxide	38
metabolism	37
quantitative_data	37
systems_approach	37
sporulation	36
thermodynamics	35
bistability	33
spo0	33
dynamical_system	32
simulation	32
ifn-gamma	30
phopq	30
phosphorylation	30
regulatory_t_cell	30
development	29
human_macrophage	29
information	29
promoter	29
kinetics	28
oscillation	28
granuloma	27
synthetic_biology	26
transcriptional_regulation	26
nf-kappab	25
spatial	25
eukaryote	22
macrophage	22
dynamics	21
gillespie_algorithm	21
salmonella	21
yeast	21
biochemical_systems_theory	20
complexity	20
sigma_factor	20
cytokine	19
growth_rate	19
iron	19
positive_feedback	19
statistical_mechanics	18
apoptosis	17
evolutionary_dynamics	17
gene_order	17
mrna	17
non-equilibrium	17
opinion	17
sensitivity_analysis	17
toll-like_receptor	17
history	16
host-pathogen_interaction	16
human_monocyte	16
inos	16
bara	15
chromosome_organization	15
diffusion	15
mathematically_controlled_comparison	15
phenotypic_heterogeneity	15
adaptation	14
feedforward	14
game_theory	14
chemical_reaction	13
computation	13
crosstalk	13
design_principles	13
dna_binding	13
gene_network	13
immune_cell_kinetics	13
quantum_mechanics	13
csra	12
response_time	12
stability	12
translation	12
ccl5	11
energy	11
genetics	11
macrophage_activation	11
sensitivity	11
transcriptional_burst	11
ccl2	10
distribution	10
ecology	10
langevin	10
mathematics	10
neutrophil	10
optimization	10
stress_response	10
textbook	10
3-dimensional_structure	9
atp	9
dna	9
lam	9
lps	9
modularity	9
mouse	9
mutation	9
population_genetics	9
recruitment	9
statistical_method	9
statistical_physics	9
brownian_motion	8
cooperativity	8
criticality	8
frequency	8
human	8
hysteresis	8
immunology	8
lung	8
mathematical_biology	8
monte_carlo	8
neuroscience	8
operon	8
parameter	8
quorum_sensing	8
recombination	8
statistics	8
temporal_response	8
chaos	7
delay	7
entropy	7
enzyme	7
fokker-planck	7
intracellular	7
phagocytosis	7
protein_interactions	7
stem_cell	7
agent_based	6
bifurcation	6
canalization	6
conformational_dynamics	6
data_fitting	6
detailed_balance	6
drosophila	6
economics	6
evolvability	6
graph_theory	6
jf	6
large_deviations	6
macrophage_deactivation	6
multiscale	6
mycobacterium_bovis	6
phagosome	6
phenotype	6
philosophy_of_science	6
population	6
power_law	6
protein_folding	6
socs1	6
synergistic_signals	6
timescale	6
transcriptional_reprogramming	6
algorithm	5
biology_as_engineering	5
ergodic	5
fluid_flow	5
geometric	5
inflammation	5
mechanism	5
necrosis	5
pattern_formation	5
prokaryote	5
ratchet	5
receptor	5
rni	5
signaling_cascade	5
sos	5
stat1	5
tor	5
antagonist	4
bursting	4
cell_polarization	4
chemical_physics	4
commentary	4
cxcl9	4
cxcr3	4
degradation	4
dose_response	4
dynamic_range	4
editorial	4
epistasis	4
fitness_landscape	4
fluctuation-dissipation	4
genome	4
irf-1	4
kinetic_proofreading	4
latency	4
markov_chain	4
mutual_information	4
network_inference	4
pathogen_killing	4
persister	4
phylogeny	4
protein_binding	4
rate	4
repressilator	4
shea-ackers	4
steady_state	4
synergistic	4
tau_leap	4
zero-order_ultrasensitivity	4
analysis	3
antibiotics	3
bayesian_inference	3
b_cell	3
book	3
ccr5	3
cell_cycle	3
cell_division	3
co-culture	3
competence	3
correlation	3
ctl	3
data	3
demand_theory	3
differential_equations	3
early_immunity	3
endothelium	3
extrinsic_noise	3
ferritin	3
flow_cytometry	3
foxp3	3
fractal	3
gibbs	3
hamiltonian	3
heat_shock	3
historical_contingency	3
lymphocyte	3
mode-of-control	3
mutational_entropy	3
neural_network	3
nucleus	3
phobr	3
physical_limit	3
potential	3
probability	3
random_walk	3
reaction-diffusion	3
receptor_binding	3
replicator_equation	3
roi	3
scale-free	3
shannon_entropy	3
siderophore	3
signal_specificity	3
single_cell	3
spin_glass	3
threshold_signal	3
timing	3
trade-off	3
tsc	3
adhesion_molecules	2
adiabatic_elimination	2
artificial_evolution	2
autocrine_paracrine	2
binding_constant	2
biological_uncertainty_principle	2
bliss_independence	2
boolean_network	2
bottleneck	2
brownian_dynamics	2
ccr2	2
cell_size	2
chemistry	2
chemokine_paradox	2
chromatin	2
convergent_evolution	2
cooperation	2
copy_number	2
cost-benefit	2
cytoplasm	2
database	2
deconvolution	2
dense_overlapping_regulon	2
dimerization	2
dual_feedback_motif	2
endothelial_cell	2
es_cell	2
flexibility	2
fluorescence	2
fragility	2
genetic_linkage	2
global_regulator	2
goldbeter-koshland	2
hierarchy	2
horizontal_gene_transfer	2
ider	2
intrinsic_protein_disorder	2
in_vitro	2
labile_iron_pool	2
macrodomain	2
macrophage_mtb_moi_upper_limit	2
mammalian	2
microarray	2
microenvironment	2
molecular_crowding	2
motif_compositions	2
mutational_robustness	2
nadph_phagocyte_oxidase	2
nonlinear	2
notes	2
nucleosome	2
numerical_methods	2
ornsteinuhlenbeck	2
overexpression	2
pde	2
periodic	2
photosynthesis	2
physical_chemistry	2
piecewise_power-law	2
poisson_process	2
polymer	2
proportion	2
rare_events	2
rat	2
rate_saturation	2
rat_macrophage	2
regulon	2
rrna	2
secretion	2
spectral	2
statistical_model	2
statistical_sensitivity	2
strong_inference	2
survival_strategy	2
systems_biology	2
time_series	2
tumor	2
turbulence	2
type-1_ifn	2
ultrasensitivity	2
uncertainty_principle	2
writing	2
antibody	1
approximation	1
behavior	1
branching_process	1
causality	1
c_elegans	1
cell_turn_angle	1
cellular_automaton	1
clinical	1
codon_bias	1
coherent_coupling	1
component_relevance_ranking	1
convolution	1
cxcl11	1
cytochrome_oxidase	1
cytotoxic	1
dendritic_cell	1
deterministic	1
dna_replication	1
drift	1
eigenworm	1
elongation	1
endoplasmic_reticulum	1
equilibrium	1
ess	1
estimation	1
falsification	1
fasl	1
fdr	1
filter	1
focal_secretion	1
formyl_peptides	1
free_energy	1
genetic_variation	1
gfp	1
gradient	1
granular_dynamics	1
group_selection	1
half-life	1
hilbert_space	1
hiv	1
homeostatic_circuit	1
hormesis	1
il-10	1
il-12	1
il-2	1
induction	1
infliximab	1
inhertiance	1
iron_percent_acquisition	1
islets_of_langerhans	1
just-in-time	1
kinetic_insulation	1
kolmogorov_complexity	1
kolmogorov-smirnov	1
laplace_transform	1
lattice	1
leishmania_major	1
lhs	1
limit_cycle	1
lip	1
lipid_domain	1
localization	1
lymph_node	1
manhattan_project	1
mass-action	1
maximum_likelihood	1
memristor	1
met-leu-phe	1
metropolis-hastings	1
metropolis_rule	1
michaelis-menten	1
microfluidics	1
migration	1
mitochondria	1
mixed_feedback	1
molecular_dynamics	1
motility	1
mtsa-10	1
multimerization	1
mycobacteria	1
mycobacterium_marinum	1
mycobacterium_smegmatis	1
myd88	1
myosin	1
myxobacteria	1
neutral_evolution	1
nkt	1
non-human_primate	1
organization	1
overshoot	1
oxidative_stress	1
percolation	1
phase_coherence	1
phenotypic_mutation	1
philosophy	1
pleiotropy	1
potts_model	1
ppar-gamma	1
propensity	1
proteasome	1
protein_export	1
protein_function	1
proteome	1
quantitative_response	1
quantum_field_theory	1
rapamycin	1
reciprocal_adaptation	1
refseq	1
relativity	1
ribosome	1
rna	1
sampling	1
sde	1
series	1
siphon	1
sirna	1
smoluchowski_diffusion	1
speculation	1
stochastic_resonance	1
stoichiometry	1
substrate_competition	1
supercoiling	1
superoxide	1
superstatistics	1
symbolic_dynamics	1
szilard	1
tgfbeta	1
th1	1
time	1
transcriptional_attentuation	1
transendothelial_migration	1
triad	1
volume	1

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