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	Isolation ofrpoBMutations Causing Rifampicin Resistance inBacillus subtilisSpores Exposed to Simulated Martian Surface Conditions [My Copy] Astrobiology, Vol. 8, No. 6. (December 2008), pp. 1159-1167. by Amy E. Perkins, Andrew C. Schuerger, Wayne L. Nicholson posted to sporulation mutation bacteria bacillus_subtilis astrobiology by jjray on 2009-11-13 20:58:11 as
	Bacillus subtilis spreads by surfing on waves of surfactant [My Copy] Proceedings of the National Academy of Sciences, Vol. 106, No. 43. (27 October 2009), pp. 18109-18113. by Thomas E. Angelini, Marcus Roper, Roberto Kolter, David A. Weitz, Michael P. Brenner posted to spatial motility mathematical_model bacteria bacillus_subtilis by jjray on 2009-10-14 15:37:22 as
	Partial penetrance facilitates developmental evolution in bacteria [My Copy] Nature, Vol. 460, No. 7254. (05 July 2009), pp. 510-514. by Avigdor Eldar, Vasant K. Chary, Panagiotis Xenopoulos, et al.Michelle E. Fontes, Oliver C. Loson, Jonathan Dworkin, Patrick J. Piggot, Michael B. Elowitz posted to bacillus_subtilis bacteria development evolution sporulation by jjray on 2009-07-22 19:35:25 as along with 8 people and 1 group ellarond bpcusack psique absterga biomcgary maren phoenixzxl jbhiatt Journal picks
	Single cell analysis of gene expression patterns of competence development and initiation of sporulation in Bacillus subtilis grown on chemically defined media [My Copy] Journal of Applied Microbiology, Vol. 101, No. 3. (September 2006), pp. 531-541. by J. W. Veening, W. K. Smits, L. W. Hamoen, O. P. Kuipers posted to bacillus_subtilis bacteria bistability flow_cytometry spo0 sporulation by jjray on 2009-05-13 16:00:37 as
	Timing and genetic regulation of commitment to sporulation in Bacillus subtilis [My Copy] Microbiology, Vol. 142, No. 12. (1 December 1996), pp. 3445-3452. by George F. Parker, Richard A. Daniel, Jeffery Errington posted to bacillus_subtilis bacteria bistability hysteresis spo0 sporulation by jjray on 2009-05-11 20:46:24 as
	Bet-hedging and epigenetic inheritance in bacterial cell development [My Copy] Proceedings of the National Academy of Sciences (6 March 2008), 0700463105. by Jan-Willem Veening, Eric J. Stewart, Thomas W. Berngruber, Francois Taddei, Oscar P. Kuipers, Leendert W. Hamoen posted to bacillus_subtilis bacteria bistability spo0 sporulation by jjray on 2009-05-08 23:17:49 as along with 2 people Retchless madhadron
	Phosphatases modulate the bistable sporulation gene expression pattern in Bacillus subtilis [My Copy] Molecular Microbiology, Vol. 56, No. 6. (June 2005), pp. 1481-1494. by Jan-Willem Veening, Leendert W. Hamoen, Oscar P. Kuipers posted to bacillus_subtilis bacteria bistability signaling spo0 sporulation by jjray on 2009-05-08 23:17:27 as along with 2 people Winzer margaritis
	Negative regulation of Bacillus subtilis sporulation by the spo0E gene product. [My Copy] Journal of bacteriology, Vol. 173, No. 8. (April 1991), pp. 2514-2520. by M. Perego, J. A. Hoch posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:08:28 as
	Mutational dissociation of the positive and negative regulatory properties of the Spo0A sporulation transcription factor of Bacillus subtilis. [My Copy] Gene, Vol. 100 (April 1991), pp. 207-212. by M. Perego, J. J. Wu, G. B. Spiegelman, J. A. Hoch posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:08:21 as
	Spo0A activates and represses its own synthesis by binding at its dual promoters. [My Copy] Biochimie, Vol. 74, No. 7-8. (g 1992), pp. 619-626. by M. A. Strauch, K. A. Trach, J. Day, J. A. Hoch posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:08:15 as
	Subunit composition and domain structure of the Spo0A sporulation transcription factor of Bacillus subtilis. [My Copy] The Journal of biological chemistry, Vol. 269, No. 24. (17 June 1994), pp. 16977-16982. by J. K. Grimsley, R. B. Tjalkens, M. A. Strauch, et al.T. H. Bird, G. B. Spiegelman, Z. Hostomsky, J. M. Whiteley, J. A. Hoch posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:07:57 as
	The major role of Spo0A in genetic competence is to downregulate abrB, an essential competence gene. [My Copy] Journal of bacteriology, Vol. 177, No. 12. (June 1995), pp. 3601-3605. by J. Hahn, M. Roggiani, D. Dubnau posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:07:37 as
	The Spo0A protein of Bacillus subtilis inhibits transcription of the abrB gene without preventing binding of the polymerase to the promoter. [My Copy] The Journal of biological chemistry, Vol. 271, No. 19. (10 May 1996), pp. 11455-11461. by E. A. Greene, G. B. Spiegelman posted to bacillus_subtilis bacteria gene_regulation promoter spo0 sporulation by jjray on 2009-04-28 20:07:26 as
	Feedback loops involving Spo0A and AbrB in in vitro transcription of the genes involved in the initiation of sporulation in Bacillus subtilis. [My Copy] Journal of biochemistry, Vol. 124, No. 1. (July 1998), pp. 98-104. by M. Fujita, Y. Sadaie posted to bacillus_subtilis bacteria feedback gene_regulation spo0 sporulation by jjray on 2009-04-28 20:07:11 as
	Identification of a second region of the Spo0A response regulator of Bacillus subtilis required for transcription activation. [My Copy] Journal of bacteriology, Vol. 182, No. 15. (August 2000), pp. 4352-4355. by D. A. Rowe-Magnus, M. J. Richer, G. B. Spiegelman posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:06:59 as
	Multiple histidine kinases regulate entry into stationary phase and sporulation in Bacillus subtilis. [My Copy] Molecular microbiology, Vol. 38, No. 3. (November 2000), pp. 535-542. by M. Jiang, W. Shao, M. Perego, J. A. Hoch posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:06:51 as
	AbrB and Spo0E control the proper timing of sporulation in Bacillus subtilis. [My Copy] Curr Microbiol, Vol. 48, No. 4. (April 2004), pp. 262-269. by S. H. Shafikhani, T. Leighton posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:06:43 as along with 1 person mhucka
	Bacillus subtilis transcriptional regulators interaction. [My Copy] Biotechnology letters, Vol. 26, No. 5. (March 2004), pp. 403-407. by A. Sánchez, J. Olmos posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:06:37 as
	The DNA-binding specificity of the Bacillus anthracis AbrB protein. [My Copy] Microbiology (Reading, England), Vol. 151, No. Pt 6. (June 2005), pp. 1751-1759. by M. A. Strauch, P. Ballar, A. J. Rowshan, K. L. Zoller posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:06:30 as
	Spo0A-dependent activation of an extended -10 region promoter in Bacillus subtilis. [My Copy] Journal of bacteriology, Vol. 188, No. 4. (February 2006), pp. 1411-1418. by G. Chen, A. Kumar, T. H. Wyman, C. P. Moran posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:06:06 as
	A derepression system based on the Bacillus subtilis sporulation pathway offers dynamic control of heterologous gene expression. [My Copy] Applied and environmental microbiology, Vol. 73, No. 7. (April 2007), pp. 2390-2393. by R. Nijland, J. W. Veening, O. P. Kuipers posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:05:58 as
	Parallel pathways of repression and antirepression governing the transition to stationary phase in Bacillus subtilis. [My Copy] Proceedings of the National Academy of Sciences of the United States of America, Vol. 105, No. 40. (7 October 2008), pp. 15547-15552. by A. V. Banse, A. Chastanet, L. Rahn-Lee, E. C. Hobbs, R. Losick posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:05:43 as
	Insights into the nature of DNA binding of AbrB-like transcription factors. [My Copy] Structure (London, England : 1993), Vol. 16, No. 11. (12 November 2008), pp. 1702-1713. by D. M. Sullivan, B. G. Bobay, D. J. Kojetin, et al.R. J. Thompson, M. Rance, M. A. Strauch, J. Cavanagh posted to 3-dimensional_structure bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:05:29 as
	The Spo0A regulon of Bacillus subtilis. [My Copy] Mol Microbiol, Vol. 50, No. 5. (December 2003), pp. 1683-1701. by V. Molle, M. Fujita, S. T. Jensen, et al.P. Eichenberger, J. E. González-Pastor, J. S. Liu, R. Losick posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:04:40 as along with 2 people Winzer mhucka
	Structure of the gene for the transition state regulator, abrB: regulator synthesis is controlled by the spo0A sporulation gene in Bacillus subtilis. [My Copy] Molecular microbiology, Vol. 2, No. 6. (November 1988), pp. 689-699. by M. Perego, G. B. Spiegelman, J. A. Hoch posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:04:30 as
	The transition state transcription regulator abrB of Bacillus subtilis is a DNA binding protein. [My Copy] The EMBO journal, Vol. 8, No. 5. (May 1989), pp. 1615-1621. by M. A. Strauch, G. B. Spiegelman, M. Perego, W. C. Johnson, D. Burbulys, J. A. Hoch posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-28 20:04:04 as
	A positive feedback loop controls transcription of the spoOF gene, a component of the sporulation phosphorelay in Bacillus subtilis. [My Copy] Molecular microbiology, Vol. 7, No. 6. (March 1993), pp. 967-974. by M. A. Strauch, J. J. Wu, R. H. Jonas, J. A. Hoch posted to bacillus_subtilis bacteria gene_regulation promoter sigma_factor spo0 sporulation by jjray on 2009-04-28 17:45:59 as
	Bacillus subtilis early sporulation genes kinA, spo0F, and spo0A are transcribed by the RNA polymerase containing sigma H. [My Copy] J Bacteriol, Vol. 174, No. 9. (May 1992), pp. 2771-2778. by M. Predich, G. Nair, I. Smith posted to bacillus_subtilis bacteria gene_regulation promoter sigma_factor spo0 sporulation by jjray on 2009-04-28 17:45:53 as along with 1 person mhucka
	Transcriptional regulation of the spo0F gene of Bacillus subtilis. [My Copy] Journal of bacteriology, Vol. 168, No. 2. (November 1986), pp. 870-877. by M. Lewandoski, E. Dubnau, I. Smith posted to bacillus_subtilis bacteria gene_regulation promoter sigma_factor spo0 sporulation by jjray on 2009-04-28 17:45:47 as
	Complete sequence and transcriptional analysis of the spo0F region of the Bacillus subtilis chromosome. [My Copy] Journal of bacteriology, Vol. 170, No. 9. (September 1988), pp. 4194-4208. by K. Trach, J. W. Chapman, P. Piggot, D. LeCoq, J. A. Hoch posted to bacillus_subtilis bacteria gene_regulation promoter sigma_factor spo0 sporulation by jjray on 2009-04-28 17:45:40 as
	Temporal and selective association of multiple sigma factors with RNA polymerase during sporulation in Bacillus subtilis. [My Copy] Genes to cells : devoted to molecular & cellular mechanisms, Vol. 5, No. 2. (February 2000), pp. 79-88. by M. Fujita posted to bacillus_subtilis bacteria gene_regulation sigma_factor spo0 sporulation by jjray on 2009-04-27 20:47:04 as
	Translational attenuation of the Bacillus subtilis spo0B cistron by an RNA structure encompassing the initiation region. [My Copy] Nucleic acids research, Vol. 26, No. 3. (1 February 1998), pp. 824-830. by M. Asayama, K. Saito, Y. Kobayashi posted to bacillus_subtilis bacteria spo0 sporulation translation by jjray on 2009-04-27 20:05:49 as
	Differential regulation of spo0A transcription in Bacillus subtilis: glucose represses promoter switching at the initiation of sporulation. [My Copy] J. Bacteriol., Vol. 173, No. 8. (1 April 1991), pp. 2625-2632. by T. Chibazakura, F. Kawamura, H. Takahashi posted to bacillus_subtilis bacteria gene_regulation promoter spo0 sporulation by jjray on 2009-04-27 20:04:26 as
	Complexity in bacterial cell–cell communication: Quorum signal integration and subpopulation signaling in the Bacillus subtilis phosphorelay [My Copy] Proceedings of the National Academy of Sciences (20 April 2009) by Ilka B. Bischofs, Joshua A. Hug, Aiwen W. Liu, Denise M. Wolf, Adam P. Arkin posted to bacillus_subtilis bacteria complexity quorum_sensing signaling sporulation by jjray on 2009-04-21 17:07:04 as along with 4 people trfield coela kalvala Winzer
	Synergistic Kinetic Interactions between Components of the Phosphorelay Controlling Sporulation in Bacillus subtilis† [My Copy] Biochemistry, Vol. 37, No. 5. (1 February 1998), pp. 1365-1375. by Charles E. Grimshaw, Shaoming Huang, Conrad G. Hanstein, et al.Mark A. Strauch, David Burbulys, Ling Wang, James A. Hoch, John M. Whiteley posted to bacillus_subtilis bacteria quantitative_data signaling spo0 sporulation by jjray on 2009-04-20 23:02:20 as
	High- and Low-Threshold Genes in the Spo0A Regulon of Bacillus subtilis [My Copy] J. Bacteriol., Vol. 187, No. 4. (15 February 2005), pp. 1357-1368. by Masaya Fujita, Jose E. Gonzalez-Pastor, Richard Losick posted to bacillus_subtilis bacteria gene_regulation spo0 sporulation by jjray on 2009-04-20 21:04:00 as
	Transient heterogeneity in extracellular protease production by Bacillus subtilis [My Copy] Mol Syst Biol, Vol. 4 (15 April 2008) by Jan-Willem Veening, Oleg A. Igoshin, Robyn T. Eijlander, Reindert Nijland, Leendert W. Hamoen, Oscar P. Kuipers posted to bacillus_subtilis bistability feedback stochastic by jjray on 2009-04-07 17:19:22 as along with 4 people Winzer balabu margaritis brianb
	The Bacillus subtilis SIN Operon: An Evolvable Network Motif. [My Copy] Genetics, Vol. 169, No. 3. (30 March 2005), pp. 1187-1202. by Christopher A. Voigt, Denise Wolf, Adam P. Arkin posted to bacillus_subtilis bacteria chromosome_organization evolvability gene_expression network_motifs operon by jjray on 2009-03-23 22:52:19 as along with 5 people and 1 group camster rklancer lingchong dbikard heliopais dbk-lab
	RNA-based regulation of genes of tryptophan synthesis and degradation, in bacteria. [My Copy] RNA (New York, N.Y.), Vol. 13, No. 8. (August 2007), pp. 1141-1154. by C. Yanofsky posted to bacillus_subtilis bacteria e_coli metabolism review by jjray on 2009-01-07 20:59:35 as along with 1 person stk
	The sigma factors of Bacillus subtilis. [My Copy] Microbiol Rev, Vol. 59, No. 1. (March 1995), pp. 1-30. by W. G. Haldenwang posted to bacillus_subtilis gene_regulation review sigma_factor by jjray on 2008-12-29 19:53:39 as along with 1 person mhucka
	Cys303 in the Histidine Kinase PhoR Is Crucial for the Phosphotransfer Reaction in the PhoPR Two-Component System in Bacillus subtilis [My Copy] J. Bacteriol., Vol. 189, No. 2. (15 January 2007), pp. 410-421. by Amr Eldakak, Marion F. Hulett posted to bacillus_subtilis bacteria biochemistry phosphorylation two-component_system by jjray on 2008-12-11 20:16:19 as
	Spatial organization of a replicating bacterial chromosome [My Copy] Proceedings of the National Academy of Sciences (2008) by Idit A. Berlatzky, Alex Rouvinski, Sigal Ben-Yehuda posted to bacillus_subtilis bacteria chromosome_organization dna spatial by jjray on 2008-09-09 16:09:05 as
	Bacillus subtilis PhoP binds to the phoB tandem promoter exclusively within the phosphate starvation-inducible promoter [My Copy] J. Bacteriol., Vol. 179, No. 20. (1 October 1997), pp. 6302-6310. by W. Liu, F. M. Hulett posted to atp bacillus_subtilis gene_regulation phosphorylation two-component_system by jjray on 2008-08-22 19:34:32 as
	Decay of Activated Bacillus subtilis Pho Response Regulator, PhoP~P, Involves the PhoR~P Intermediate [My Copy] Biochemistry, Vol. 38, No. 31. (3 August 1999), pp. 10119-10125. by L. Shi, W. Liu, F. M. Hulett posted to atp bacillus_subtilis bacteria phosphorylation two-component_system by jjray on 2008-08-20 19:03:33 as
	Lipid Localization in Bacterial Cells through Curvature-Mediated Microphase Separation [My Copy] Biophys. J., Vol. 95, No. 3. (1 August 2008), pp. 1034-1049. by Ranjan Mukhopadhyay, Kerwyn C. Huang, Ned S. Wingreen posted to bacillus_subtilis bacteria biophysics e_coli lipid_domain sporulation by jjray on 2008-07-21 22:58:35 as
	Genome-wide survey of mRNA half-lives in Bacillus subtilis identifies extremely stable mRNAs. [My Copy] Molecular genetics and genomics : MGG, Vol. 269, No. 5. (August 2003), pp. 706-714. by G. Hambraeus, C. von Wachenfeldt, L. Hederstedt posted to bacillus_subtilis half-life mrna parameter by jjray on 2008-01-15 20:26:09 as along with 1 person madhadron
	A metabolic sensor governing cell size in bacteria. [My Copy] Cell, Vol. 130, No. 2. (27 July 2007), pp. 335-347. by R. B. Weart, A. H. Lee, A. C. Chien, D. P. Haeusser, N. S. Hill, P. A. Levin posted to bacillus_subtilis cell_size growth_rate by jjray on 2008-01-15 20:20:50 as along with 2 people aswin margaritis
	An excitable gene regulatory circuit induces transient cellular differentiation. [My Copy] Nature, Vol. 440, No. 7083. (23 March 2006), pp. 545-550. by Gürol M. Süel, Jordi Garcia-Ojalvo, Louisa M. Liberman, Michael B. Elowitz posted to bacillus_subtilis competence gene_regulation noise stochastic by jjray on 2008-01-15 20:14:01 as along with 14 people and 1 group yyfwuhan ashishanand megraw dswan rklancer alexg madhadron balabu nickluscombe comb dbikard mhucka margaritis paurue EBI-regulation
	Tunability and noise dependence in differentiation dynamics. [My Copy] Science (New York, N.Y.), Vol. 315, No. 5819. (23 March 2007), pp. 1716-1719. by Gurol M. Suel, Rajan P. Kulkarni, Jonathan Dworkin, Jordi Garcia-Ojalvo, Michael B. Elowitz posted to bacillus_subtilis competence noise stochastic by jjray on 2008-01-15 20:10:13 as along with 5 people and 2 groups samubernard lauresultan dbikard margaritis zwang Centre de Recherches Interdisciplinaires SynBioSys
	Molecular level stochastic model for competence cycles in Bacillus subtilis [My Copy] Proceedings of the National Academy of Sciences, Vol. 104, No. 45. (6 November 2007), pp. 17582-17587. by Daniel Schultz, Ben, Jose N. Onuchic, Peter G. Wolynes posted to bacillus_subtilis competence mathematical_model stochastic by jjray on 2008-01-15 20:00:36 as along with 3 people balabu lshaw margaritis

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bacteria	292
mathematical_model	257
gene_regulation	256
stochastic	198
signaling	157
evolution	145
mycobacterium_tuberculosis	139
e_coli	134
two-component_system	134
noise	133
network	131
feedback	129
review	103
biophysics	101
gene_expression	85
t_cell	60
immune_activation	59
method	58
biochemistry	57
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
phopq	34
simulation	34
dynamical_system	33
spo0	33
phosphorylation	32
ifn-gamma	30
regulatory_t_cell	30
salmonella	30
development	29
human_macrophage	29
information	29
kinetics	29
mrna	29
promoter	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
modularity	10
mutation	10
neutrophil	10
stress_response	10
textbook	10
3-dimensional_structure	9
atp	9
dna	9
immunology	9
lam	9
lps	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
graph_theory	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
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
neutral_evolution	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
amino_acid	1
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
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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