jjray's immune_activation [59 articles] Export

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	Regulation of cytokine signaling and inflammation [My Copy] Cytokine & Growth Factor Reviews, Vol. 13, No. 4-5. ( 2002), pp. 413-421. by Toshitkatsu Hanada, Akihiko Yoshimura posted to cytokine feedback gene_regulation immune_activation inflammation network_motifs nf-kappab review tnf by jjray on 2007-05-14 18:28:18 as along with 1 person LenaBuchner
	Gamma Interferon Responses of CD4 and CD8 T-Cell Subsets Are Quantitatively Different and Independent of Each Other during Pulmonary Mycobacterium bovis BCG Infection [My Copy] Infect. Immun., Vol. 75, No. 5. (1 May 2007), pp. 2244-2252. by Patricia Ngai, Sarah Mccormick, Cherrie Small, et al.Xizhong Zhang, Anna Zganiacz, Naoko Aoki, Zhou Xing posted to cytokine ifn-gamma immune_activation mycobacterium_bovis quantitative_response t_cell by jjray on 2007-04-23 16:47:42 as
	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
	Mycobacterium tuberculosis induces high production of nitric oxide in coordination with production of tumour necrosis factor-alpha in patients with fresh active tuberculosis but not in MDR tuberculosis. [My Copy] Immunol Cell Biol, Vol. 82, No. 4. (August 2004), pp. 377-382. by S. Sharma, M. Sharma, S. Roy, P. Kumar, M. Bose posted to human immune_activation lam nitric_oxide tnf by jjray on 2007-04-16 16:36:27 as
	A brief history of TH17, the first major revision in the TH1/TH2 hypothesis of T cell–mediated tissue damage [My Copy] Nature Medicine, Vol. 13, No. 2. (06 February 2007), pp. 139-145. by Lawrence Steinman posted to immune_activation immune_cell_kinetics inflammation review t_cell theory by jjray on 2007-02-19 22:15:27 as along with 1 person AlfonsoVicenteSuarez
	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
	Dynamic Changes in Pro- and Anti-Inflammatory Cytokine Profiles and Gamma Interferon Receptor Signaling Integrity Correlate with Tuberculosis Disease Activity and Response to Curative Treatment [My Copy] Infect. Immun., Vol. 75, No. 2. (1 February 2007), pp. 820-829. by Edhyana Sahiratmadja, Bachti Alisjahbana, Tjitske de Boer, et al.Iskandar Adnan, Anugrah Maya, Halim Danusantoso, Ronald H. Nelwan, Sangkot Marzuki, Jos W. van der Meer, Reinout van Crevel, Esther van de Vosse, Tom H. Ottenhoff posted to mycobacterium_tuberculosis immune_activation il-10 ifn-gamma human host-pathogen_interaction cytokine by jjray on 2007-01-25 17:48:53 as
	Feedback inhibition of calcineurin and Ras by a dual inhibitory protein Carabin [My Copy] Nature (17 January 2007) by Fan Pan, Luo Sun, David B. Kardian, Katharine A. Whartenby, Drew M. Pardoll, Jun O. Liu posted to quantitative_data network_motifs immune_activation gene_regulation feedback dual_feedback_motif by jjray on 2007-01-25 17:22:02 as along with 1 person and 4 groups jwdietrich MathBio Cybernetics Biomedical_Cybernetics AQUA-FONTIS-Study
	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
	Chemokines and tuberculosis [My Copy] Cytokine & Growth Factor Reviews In Cytokines and Lung Disease, Vol. 14, No. 6. (December 2003), pp. 467-477. by Holly M. Algood, John Chan, Joanne L. Flynn posted to chemokine cytokine gene_regulation granuloma host-pathogen_interaction ifn-gamma immune_activation immune_cell_kinetics lung mycobacterium_tuberculosis pattern_formation review temporal_response by jjray on 2006-10-10 19:38:23 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
	NO suppresses while peroxynitrite sustains NF-kappaB: a paradigm to rationalize cytoprotective and cytotoxic actions attributed to NO. [My Copy] Cardiovascular research, Vol. 63, No. 1. (1 July 2004), pp. 31-40. by Y. Hattori, K. Kasai, S. S. Gross posted to biochemistry feedback immune_activation network_motifs nf-kappab nitric_oxide by jjray on 2006-09-20 20:52:59 as along with 1 person and 1 group HEIRS HEIRS - Environmental Illness Research
	The Ikappa B-NF-kappa B Signaling Module: Temporal Control and Selective Gene Activation [My Copy] Science, Vol. 298, No. 5596. (2002), pp. 1241-1245. by Alexander Hoffmann, Andre Levchenko, Martin L. Scott, David Baltimore posted to immune_activation mathematical_model nf-kappab quantitative_data by jjray on 2006-09-20 20:30:51 as
	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
	A Limited Antigen-Specific Cellular Response Is Sufficient for the Early Control of Mycobacterium tuberculosis in the Lung but Is Insufficient for Long-Term Survival [My Copy] Infect. Immun., Vol. 72, No. 7. (1 July 2004), pp. 3759-3768. by Joanne Turner, Karen M. Dobos, Marc A. Keen, et al.Anthony A. Frank, Stefan Ehlers, Ian M. Orme, John T. Belisle, Andrea M. Cooper posted to cytokine early_immunity ifn-gamma immune_activation inos mycobacterium_tuberculosis by jjray on 2006-09-19 16:16:43 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
	NEGATIVE REGULATION OF TOLL-LIKE RECEPTOR-MEDIATED IMMUNE RESPONSES [My Copy] Nat Rev Immunol, Vol. 5, No. 6. (June 2005), pp. 446-458. by Foo Y. Liew, Damo Xu, Elizabeth K. Brint, Luke A. O'Neill posted to feedback immune_activation lps macrophage_deactivation network_motifs nf-kappab review signaling socs1 toll-like_receptor by jjray on 2006-08-03 16:36:00 as along with 1 person ishakdi
	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
	Role of the NF-kappaB signaling pathway and kappaB cis-regulatory elements on the IRF-1 and iNOS promoter regions in mycobacterial lipoarabinomannan induction of nitric oxide. [My Copy] Infect Immun, Vol. 71, No. 3. (March 2003), pp. 1442-1452. by K. R. Morris, R. D. Lutz, H. S. Choi, T. Kamitani, K. Chmura, E. D. Chan posted to immune_activation inos irf-1 lam mycobacterium_tuberculosis nf-kappab by jjray on 2005-11-08 19:16:56 as
	Mycobacterium tuberculosis heat shock proteins use diverse Toll-like receptor pathways to activate pro-inflammatory signals. [My Copy] J Biol Chem, Vol. 280, No. 22. (3 June 2005), pp. 20961-20967. by Y. Bulut, K. S. Michelsen, L. Hayrapetian, et al.Y. Naiki, R. Spallek, M. Singh, M. Arditi posted to immune_activation mycobacterium_tuberculosis nf-kappab signaling toll-like_receptor by jjray on 2005-11-08 18:59:05 as
	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
	Disseminated tuberculosis in interferon gamma gene-disrupted mice. [My Copy] J Exp Med, Vol. 178, No. 6. (1 December 1993), pp. 2243-2247. by A. M. Cooper, D. K. Dalton, T. A. Stewart, J. P. Griffin, D. G. Russell, I. M. Orme posted to cytokine ifn-gamma immune_activation mycobacterium_tuberculosis by jjray on 2005-11-02 16:21:14 as
	Iron and iron chelating agents modulate Mycobacterium tuberculosis growth and monocyte-macrophage viability and effector functions. [My Copy] FEMS Immunol Med Microbiol, Vol. 45, No. 2. (1 August 2005), pp. 103-112. by L. Cronjé, N. Edmondson, K. D. Eisenach, L. Bornman posted to human_macrophage human_monocyte immune_activation iron metabolism mycobacterium_tuberculosis by jjray on 2005-10-31 21:37:49 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
	Nitric oxide in health and disease of the respiratory system. [My Copy] Physiol Rev, Vol. 84, No. 3. (July 2004), pp. 731-765. by F. L. Ricciardolo, P. J. Sterk, B. Gaston, G. Folkerts posted to human_macrophage human_monocyte immune_activation inos nitric_oxide by jjray on 2005-10-14 20:58:32 as
	Nitric oxide production by human macrophages: there's NO doubt about it. [My Copy] Am J Physiol Lung Cell Mol Physiol, Vol. 282, No. 5. (May 2002) by F. C. Fang, A. Vazquez-Torres posted to human_macrophage human_monocyte immune_activation inos nitric_oxide by jjray on 2005-10-14 20:56:42 as
	Human alveolar macrophages and monocytes as a source and target for nitric oxide. [My Copy] Int Immunopharmacol, Vol. 1, No. 8. (August 2001), pp. 1479-1490. by M. J. Thomassen, M. S. Kavuru posted to human_macrophage human_monocyte immune_activation inos nitric_oxide by jjray on 2005-10-14 20:55:32 as
	The human immune response during cutaneous leishmaniasis: NO problem. [My Copy] Parasitol Today, Vol. 15, No. 8. (August 1999), pp. 342-345. by M. D. Mossalayi, M. Arock, D. Mazier, P. Vincendeau, I. Vouldoukis posted to human_macrophage human_monocyte immune_activation inos leishmania_major nitric_oxide by jjray on 2005-10-14 20:53:48 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
	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
	A model to predict cell-mediated immune regulatory mechanisms during human infection with Mycobacterium tuberculosis. [My Copy] J Immunol, Vol. 166, No. 3. (1 February 2001), pp. 1951-1967. by J. E. Wigginton, D. Kirschner posted to growth_rate ifn-gamma immune_activation immune_cell_kinetics latency lung lymphocyte mathematical_model mycobacterium_tuberculosis quantitative_data by jjray on 2005-08-31 20:47:28 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

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bacteria	291
mathematical_model	257
gene_regulation	255
stochastic	198
signaling	157
evolution	144
mycobacterium_tuberculosis	139
e_coli	134
two-component_system	134
noise	133
network	130
feedback	129
review	103
biophysics	101
gene_expression	85
t_cell	60
immune_activation	59
method	58
biochemistry	56
transcription	56
bacillus_subtilis	54
tnf	53
theory	52
murine_macrophage	51
physics	51
chemokine	50
chemotaxis	48
robustness	44
metabolism	38
network_motifs	38
nitric_oxide	38
quantitative_data	37
sporulation	37
systems_approach	37
thermodynamics	36
bistability	34
simulation	34
dynamical_system	33
phopq	33
spo0	33
phosphorylation	32
ifn-gamma	30
regulatory_t_cell	30
development	29
human_macrophage	29
information	29
kinetics	29
mrna	29
promoter	29
salmonella	29
oscillation	28
granuloma	27
spatial	26
synthetic_biology	26
transcriptional_regulation	26
nf-kappab	25
stability	25
eukaryote	23
macrophage	22
dynamics	21
gillespie_algorithm	21
yeast	21
biochemical_systems_theory	20
complexity	20
growth_rate	20
sigma_factor	20
cytokine	19
iron	19
positive_feedback	19
statistical_mechanics	19
evolutionary_dynamics	18
non-equilibrium	18
apoptosis	17
gene_order	17
opinion	17
sensitivity_analysis	17
toll-like_receptor	17
diffusion	16
history	16
host-pathogen_interaction	16
human_monocyte	16
inos	16
bara	15
chromosome_organization	15
mathematically_controlled_comparison	15
phenotypic_heterogeneity	15
adaptation	14
feedforward	14
game_theory	14
gene_network	14
chemical_reaction	13
computation	13
crosstalk	13
degradation	13
design_principles	13
dna_binding	13
immune_cell_kinetics	13
quantum_mechanics	13
csra	12
response_time	12
sensitivity	12
translation	12
ccl5	11
energy	11
genetics	11
macrophage_activation	11
optimization	11
transcriptional_burst	11
ccl2	10
distribution	10
ecology	10
langevin	10
mathematics	10
mutation	10
neutrophil	10
stress_response	10
textbook	10
3-dimensional_structure	9
atp	9
dna	9
immunology	9
lam	9
lps	9
modularity	9
mouse	9
operon	9
polarity	9
population_genetics	9
recruitment	9
statistical_method	9
statistical_physics	9
brownian_motion	8
cooperativity	8
criticality	8
entropy	8
fokker-planck	8
frequency	8
human	8
hysteresis	8
large_deviations	8
lung	8
mathematical_biology	8
monte_carlo	8
neuroscience	8
parameter	8
phage	8
quorum_sensing	8
recombination	8
statistics	8
temporal_response	8
agent_based	7
chaos	7
delay	7
enzyme	7
intracellular	7
phagocytosis	7
phenotype	7
protein_interactions	7
stem_cell	7
bifurcation	6
canalization	6
conformational_dynamics	6
data_fitting	6
detailed_balance	6
drosophila	6
economics	6
evolvability	6
graph_theory	6
jf	6
macrophage_deactivation	6
multiscale	6
mycobacterium_bovis	6
phagosome	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
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
rare_events	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
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
astrobiology	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
intron	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
phase_transition	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
rnase	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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