All Stories

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