All Stories

  1. Hypothesis: bacteria live on the edge of phase transitions with a cell cycle regulated by a water-clock
  2. Hunting the Cell Cycle Snark
  3. Perspective Strategies for Interventions in Parkinsonism: Remedying the Neglected Role of TPPP
  4. Hypothesis: bacteria live on the edge of phase transitions with a cell cycle regulated by a water-clock
  5. Science and prizes
  6. Novel Principles and Methods in Bacterial Cell Cycle Physiology: Celebrating the Charles E. Helmstetter Prize in 2022
  7. Open Questions about the Roles of DnaA, Related Proteins, and Hyperstructure Dynamics in the Cell Cycle
  8. Open Questions about the Roles of DnaA, Related Proteins and Hyperstructure Dynamics in the Cell Cycle: a Cobblestone in the Pond?
  9. The Sherpa hypothesis: Phenotype-Preserving Disordered Proteins stabilize the phenotypes of neurons and oligodendrocytes
  10. The Sherpa hypothesis: Phenotype-Protecting Disordered Proteins stabilize the phenotypes of neurons and oligodendrocytes
  11. The roles of nucleoid-associated proteins and topoisomerases in chromosome structure, strand segregation, and the generation of phenotypic heterogeneity in bacteria
  12. The Ring World: Eversion of Small Double-Stranded Polynucleotide Circlets at the Origin of DNA Double Helix, RNA Polymerization, Triplet Code, Twenty Amino Acids, and Strand Asymmetry
  13. Challenges in Discovering Drugs That Target the Protein–Protein Interactions of Disordered Proteins
  14. A Defective Viral Particle Approach to COVID-19
  15. Competitive Coherence Generates Qualia in Bacteria and Other Living Systems
  16. Role of Multifunctional Cytoskeletal Filaments in Coronaviridae Infections: Therapeutic Opportunities for COVID-19 in a Nutshell
  17. Generation of Bacterial Diversity by Segregation of DNA Strands
  18. Hypothesis: nucleoid-associated proteins segregate with a parental DNA strand to generate coherent phenotypic diversity
  19. Emergence of a “Cyclosome” in a Primitive Network Capable of Building “Infinite” Proteins
  20. Does the Semiconservative Nature of DNA Replication Facilitate Coherent Phenotypic Diversity?
  21. Successive Paradigm Shifts in the Bacterial Cell Cycle and Related Subjects
  22. Inter- and intra-cellular diversity of bacterial metabolism
  23. Links between central carbon metabolism and DNA replication
  24. A pension fund for European scientists
  25. Synthetic, Switchable Enzymes
  26. Combining combing and secondary ion mass spectrometry to study DNA on chips using 13C and 15N labeling
  27. Hybolites Revisited
  28. The membrane: transertion as an organizing principle in membrane heterogeneity
  29. Why do bacteria divide?
  30. Modeling of sensing potency of cytoskeletal systems decorated with metabolic enzymes
  31. Molecular complementarity between simple, universal molecules and ions limited phenotype space in the precursors of cells
  32. What Properties of Life Are Universal? Substance-Free, Scale-free Life
  33. The theater management model of plant memory
  34. Scientific Globish: clear enough is good enough
  35. Plasmids as scribbling pads for operon formation and propagation
  36. New approaches to the problem of generating coherent, reproducible phenotypes
  37. Sensor potency of the moonlighting enzyme-decorated cytoskeleton: the cytoskeleton as a metabolic sensor
  38. Membrane heterogeneity created by transertion is a global regulator in bacteria
  39. Hypothesis: Bacteria Control Host Appetites
  40. Chromosome Replication in Escherichia coli: Life on the Scales
  41. How did Metabolism and Genetic Replication Get Married?
  42. Hyperstructure interactions influence the virulence of the type 3 secretion system in yersiniae and other bacteria
  43. The Role of Calcium in the Recall of Stored Morphogenetic Information by Plants
  44. The Mimic Chain Reaction
  45. DNA Movies and Panspermia
  46. Combed Single DNA Molecules Imaged by Secondary Ion Mass Spectrometry
  47. Speculations on the initiation of chromosome replication in Escherichia coli: The dualism hypothesis
  48. Computing with bacterial constituents, cells and populations: from bioputing to bactoputing
  49. Hypothesis: Poly-(R)-3-hydroxybutyrate is a major factor in intraocular pressure
  50. The Eukaryotic Cell Originated in the Integration and Redistribution of Hyperstructures from Communities of Prokaryotic Cells Based on Molecular Complementarity
  51. Hybolites: Novel Therapeutic Tools for Targeting Hyperstructures in Bacteria
  52. Lipoplex nanostructures reveal a general self-organization of nucleic acids
  53. Secretion of MMP-2 and MMP-9 induced by VEGF autocrine loop correlates with clinical features in childhood acute lymphoblastic leukemia
  54. Chemical Microscopy of Biological Samples by Dynamic Mode Secondary Ion Mass Spectrometry (SIMS)
  55. Inner membrane lipids of Escherichia coli form domains
  56. Method for Macromolecular Colocalization Using Atomic Recombination in Dynamic SIMS
  57. A stochastic automaton shows how enzyme assemblies may contribute to metabolic efficiency
  58. Behaviour of bacterial division protein FtsZ under a monolayer with phospholipid domains
  59. Toward a Hyperstructure Taxonomy
  60. Identification and relative quantification of fatty acids in Escherichia coli membranes by gas chromatography/mass spectrometry
  61. The correlation between architecture and mRNA abundance in the genetic regulatory network of Escherichia coli
  62. Question 7: The First Units of Life Were Not Simple Cells
  63. Pharmacological Evidence for Calcium Involvement in the Long-Term Processing of Abiotic Stimuli in Plants
  64. Lipid composition of membranes of Escherichia coli by liquid chromatography/tandem mass spectrometry using negative electrospray ionization
  65. Lipid domain boundaries as prebiotic catalysts of peptide bond formation
  66. Functional Taxonomy of Bacterial Hyperstructures
  67. Steady-state kinetic behaviour of two- or n-enzyme systems made of free sequential enzymes involved in a metabolic pathway
  68. Steady‐state kinetic behaviour of functioning‐dependent structures
  69. On the utility of scale‐free networks
  70. Compositional complementarity and prebiotic ecology in the origin of life
  71. Memory Processes in the Response of Plants to Environmental Signals
  72. Hypercomplexity
  73. Hypothesis: Chemotaxis in <i>Escherichia coli</i> Results from Hyperstructure Dynamics
  74. Introduction to the concept of functioning-dependent structures in living cells
  75. A Logical (Discrete) Formulation for the Storage and Recall of Environmental Signals in Plants
  76. Plant sensitivity to low intensity 105 GHz electromagnetic radiation
  77. Reticulated hyaluronan hydrogels: a model for examining cancer cell invasion in 3D
  78. A hyperstructure approach to mitochondria
  79. Ion condensation and signal transduction
  80. A hypothesis to explain division site selection in Escherichia coli by combining nucleoid occlusion and Min
  81. A strand-specific model for chromosome segregation in bacteria
  82. Modelling autocatalytic networks with artificial microbiology
  83. Biological processes in organised media
  84. Networks as constrained thermodynamic systems
  85. Quasi-periodic behaviour in a model for the lithium-induced, electrical oscillations of frog skin
  86. Hypothesis: A Phospholipid Translocase Couples Lateral and Transverse Bilayer Asymmetries in Dividing Bacteria
  87. Hypothesis: hyperstructures regulate initiation in Escherichia coli and other bacteria
  88. Hyperstructures, genome analysis and I-cells
  89. Chromosome separation and segregation in dinoflagellates andbacteria may depend on liquid crystalline states
  90. Hypothesis: Membrane domains and hyperstructures control bacterial division
  91. A SeqA hyperstructure and its interactions direct the replication and sequestration of DNA
  92. Submolecular Structures in Dipalmytoylphosphatidylethanolamine Langmuir–Blodgett Films Observed by Scanning Force Microscopy
  93. Effects of Calcium and Calcium Chelators on Growth and Morphology of Escherichia coli L-Form NC-7
  94. Long-distance transport, storage and recall of morphogenetic information in plants. The existence of a sort of primitive plant ‘memory’
  95. Effects of glucocorticoids and mineralocorticoids on proliferation and maturation of human peripheral blood stem cells
  96. Hypothesis: Hyperstructures regulate bacterial structure and the cell cycle
  97. Metabolite‐induced metabolons: the activation of transporter–enzyme complexes by substrate binding
  98. The mechanical advantages of DNA
  99. Protein phosphorylation in Escherichia coli L. form NC-7
  100. Modelling Escherichia coli. The concept of competitive coherence
  101. Tyrosine phosphorylation in Escherichia coli
  102. Supracriticality and the prion
  103. A mechanical approach to the distribution and orientation of genes on genetic maps
  104. The universal stress protein, UspA, of Escherichia coli is phosphorylated in response to stasis
  105. Artefactual cleavage of E coli H-NS by omp T
  106. Do bacteria sing? Sonic intercellular communication between bacteria may reflect electromagnetic intracellular communication involving coherent collective vibrational modes that could integrate enzyme activities and gene expression
  107. Hypothèse : le modèle du lieu de rencontre pour la maladie des prions
  108. Antiviruses as Therapeutic Agents: A Mathematical Analysis of Their Potential
  109. Elements of a unifying theory of biology
  110. Calcium signalling in bacteria
  111. Electrospray ionization mass spectrometric analysis of phospholipids of Escherichia coli
  112. The Escherichia coli enzoskeleton
  113. Autocatalytic Gene Expression OccursviaTransertion and Membrane Domain Formation and Underlies Differentiation in Bacteria: A Model
  114. Hypothesis: chromosome separation in Escherichia coli involves autocatalytic gene expression, transertion and membrane‐domain formation
  115. Characterization of eukaryotic-like kinase activity inEscherichia coliusing the gene-protein database
  116. Hypothesis: transcriptional sensing and membrane‐domain formation initiate chromosome replication in Escherichia coli
  117. Hypotheses and the regulation of the bacterial cell cycle
  118. Identification of phosphoproteins in Escherichia coli
  119. Relationships between proteasomes and RNA
  120. Immunogold localization of GyrA and GyrB proteins in Escherichia coli
  121. Cloning and Analysis of the Entire Escherichia coli ams Gene
  122. Cell Cycle Control: Prokaryotic Solutions to Eukaryotic Problems?
  123. Designer antiviruses for HIV
  124. Sequestration of Origins of Chromosome Replication in Escherichia coli by Lipid Compartments: The Pocket Hypothesis
  125. Deformations in the cytoplasmic membrane of Escherichia coli direct the synthesis of peptidoglycan. The hernia model
  126. Cloning and analysis of the entire Escherichia coli ams gene
  127. Phospholipid domains determine the spatial organization of the Escherichia coli cell cycle: the membrane tectonics model
  128. A protein kinase C‐like activity in Escherichia coli
  129. A single base change in the acceptor stem of tRNA(3Leu) confers resistance upon Escherichia coli to the calmodulin inhibitor, 48/80.
  130. Calcium in bacteria: a solution to which problem?
  131. Analysis of a myosin-like protein and the role of calcium in the E. coli cell cycle
  132. DNA replication in Escherichia coli is initiated by membrane detachment of oriC
  133. Identification of a 180kD protein in Escherichia coli related to a yeast heavy‐chain myosin
  134. Cytoskeletal elements and calcium: Do they play a role in the Escherichia coli cell cycle?
  135. A calcium flux at the termination of replication triggers cell devision in Escherichia coli
  136. Phospholipid flip-out controls the cell cycle of Escherichia coli
  137. A single calcium flux triggers chromosome replication, segregation and septation in bacteria: a model
  138. DNA replication termination in Escherichia coli parB (a dnaG allele), parA, and gyrB mutants affected in DNA distribution
  139. SOS-independent coupling between DNA replication and cell division in Escherichia coli
  140. Restriction map of Tn7