All Stories

  1. Author Correction: Emeritus unbound
  2. Emeritus unbound
  3. The chromosomal origin of replication as the basis for the spatio-temporal biology of bacteria
  4. Staphylococcus epidermidis DnaK alters biofilm formation and proteome in Staphylococcus aureus CIP 107093
  5. 60 Years of Studies into the Initiation of Chromosome Replication in Bacteria
  6. Hypothesis: bacteria live on the edge of phase transitions with a cell cycle regulated by a water-clock
  7. Hunting the Cell Cycle Snark
  8. Hunting the Cell Cycle <em>Snark</em>
  9. Perspective Strategies for Interventions in Parkinsonism: Remedying the Neglected Role of TPPP
  10. Hypothesis: bacteria live on the edge of phase transitions with a cell cycle regulated by a water-clock
  11. Science and prizes
  12. Novel Principles and Methods in Bacterial Cell Cycle Physiology: Celebrating the Charles E. Helmstetter Prize in 2022
  13. Open Questions about the Roles of DnaA, Related Proteins, and Hyperstructure Dynamics in the Cell Cycle
  14. Open Questions about the Roles of DnaA, Related Proteins and Hyperstructure Dynamics in the Cell Cycle: a Cobblestone in the Pond?
  15. The Sherpa hypothesis: Phenotype-Preserving Disordered Proteins stabilize the phenotypes of neurons and oligodendrocytes
  16. The Sherpa hypothesis: Phenotype-Protecting Disordered Proteins stabilize the phenotypes of neurons and oligodendrocytes
  17. The roles of nucleoid-associated proteins and topoisomerases in chromosome structure, strand segregation, and the generation of phenotypic heterogeneity in bacteria
  18. 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
  19. Challenges in Discovering Drugs That Target the Protein–Protein Interactions of Disordered Proteins
  20. A Defective Viral Particle Approach to COVID-19
  21. Competitive Coherence Generates Qualia in Bacteria and Other Living Systems
  22. Role of Multifunctional Cytoskeletal Filaments in Coronaviridae Infections: Therapeutic Opportunities for COVID-19 in a Nutshell
  23. Generation of Bacterial Diversity by Segregation of DNA Strands
  24. Hypothesis: nucleoid-associated proteins segregate with a parental DNA strand to generate coherent phenotypic diversity
  25. Emergence of a “Cyclosome” in a Primitive Network Capable of Building “Infinite” Proteins
  26. Does the Semiconservative Nature of DNA Replication Facilitate Coherent Phenotypic Diversity?
  27. Successive Paradigm Shifts in the Bacterial Cell Cycle and Related Subjects
  28. Inter- and intra-cellular diversity of bacterial metabolism
  29. Links between central carbon metabolism and DNA replication
  30. Plant Accommodation to Their Environment: The Role of Specific Forms of Memory
  31. A pension fund for European scientists
  32. Synthetic, Switchable Enzymes
  33. Combining combing and secondary ion mass spectrometry to study DNA on chips using 13C and 15N labeling
  34. Hybolites Revisited
  35. The membrane: transertion as an organizing principle in membrane heterogeneity
  36. Why do bacteria divide?
  37. Modeling of sensing potency of cytoskeletal systems decorated with metabolic enzymes
  38. The Positive Feedback Advantages of Combining Buying and Investing
  39. Extending the Transertion Hypothesis
  40. Molecular complementarity between simple, universal molecules and ions limited phenotype space in the precursors of cells
  41. What Properties of Life Are Universal? Substance-Free, Scale-free Life
  42. The theater management model of plant memory
  43. Scientific Globish: clear enough is good enough
  44. Plasmids as scribbling pads for operon formation and propagation
  45. New approaches to the problem of generating coherent, reproducible phenotypes
  46. Sensor potency of the moonlighting enzyme-decorated cytoskeleton: the cytoskeleton as a metabolic sensor
  47. Membrane heterogeneity created by transertion is a global regulator in bacteria
  48. Hypothesis: Bacteria Control Host Appetites
  49. Chromosome Replication in Escherichia coli: Life on the Scales
  50. How did Metabolism and Genetic Replication Get Married?
  51. Hyperstructure interactions influence the virulence of the type 3 secretion system in yersiniae and other bacteria
  52. The Role of Calcium in the Recall of Stored Morphogenetic Information by Plants
  53. The Mimic Chain Reaction
  54. DNA Movies and Panspermia
  55. Combed Single DNA Molecules Imaged by Secondary Ion Mass Spectrometry
  56. Speculations on the initiation of chromosome replication in Escherichia coli: The dualism hypothesis
  57. Computing with bacterial constituents, cells and populations: from bioputing to bactoputing
  58. Hypothesis: Poly-(R)-3-hydroxybutyrate is a major factor in intraocular pressure
  59. The Eukaryotic Cell Originated in the Integration and Redistribution of Hyperstructures from Communities of Prokaryotic Cells Based on Molecular Complementarity
  60. Hybolites: Novel Therapeutic Tools for Targeting Hyperstructures in Bacteria
  61. Lipoplex nanostructures reveal a general self-organization of nucleic acids
  62. Secretion of MMP-2 and MMP-9 induced by VEGF autocrine loop correlates with clinical features in childhood acute lymphoblastic leukemia
  63. Chemical Microscopy of Biological Samples by Dynamic Mode Secondary Ion Mass Spectrometry (SIMS)
  64. Inner membrane lipids of Escherichia coli form domains
  65. Method for Macromolecular Colocalization Using Atomic Recombination in Dynamic SIMS
  66. A stochastic automaton shows how enzyme assemblies may contribute to metabolic efficiency
  67. Behaviour of bacterial division protein FtsZ under a monolayer with phospholipid domains
  68. Toward a Hyperstructure Taxonomy
  69. Identification and relative quantification of fatty acids in Escherichia coli membranes by gas chromatography/mass spectrometry
  70. The correlation between architecture and mRNA abundance in the genetic regulatory network of Escherichia coli
  71. Question 7: The First Units of Life Were Not Simple Cells
  72. Pharmacological Evidence for Calcium Involvement in the Long-Term Processing of Abiotic Stimuli in Plants
  73. Lipid composition of membranes of Escherichia coli by liquid chromatography/tandem mass spectrometry using negative electrospray ionization
  74. Lipid domain boundaries as prebiotic catalysts of peptide bond formation
  75. Functional Taxonomy of Bacterial Hyperstructures
  76. Steady-state kinetic behaviour of two- or n-enzyme systems made of free sequential enzymes involved in a metabolic pathway
  77. Steady‐state kinetic behaviour of functioning‐dependent structures
  78. On the utility of scale‐free networks
  79. Compositional complementarity and prebiotic ecology in the origin of life
  80. Memory Processes in the Response of Plants to Environmental Signals
  81. Hypercomplexity
  82. Hypothesis: Chemotaxis in <i>Escherichia coli</i> Results from Hyperstructure Dynamics
  83. Introduction to the concept of functioning-dependent structures in living cells
  84. A Logical (Discrete) Formulation for the Storage and Recall of Environmental Signals in Plants
  85. Plant sensitivity to low intensity 105 GHz electromagnetic radiation
  86. Reticulated hyaluronan hydrogels: a model for examining cancer cell invasion in 3D
  87. A hyperstructure approach to mitochondria
  88. Ion condensation and signal transduction
  89. A hypothesis to explain division site selection in Escherichia coli by combining nucleoid occlusion and Min
  90. A strand-specific model for chromosome segregation in bacteria
  91. Modelling autocatalytic networks with artificial microbiology
  92. Biological processes in organised media
  93. Networks as constrained thermodynamic systems
  94. Quasi-periodic behaviour in a model for the lithium-induced, electrical oscillations of frog skin
  95. Hypothesis: A Phospholipid Translocase Couples Lateral and Transverse Bilayer Asymmetries in Dividing Bacteria
  96. Hypothesis: hyperstructures regulate initiation in Escherichia coli and other bacteria
  97. Hyperstructures, genome analysis and I-cells
  98. Chromosome separation and segregation in dinoflagellates andbacteria may depend on liquid crystalline states
  99. Hypothesis: Membrane domains and hyperstructures control bacterial division
  100. A SeqA hyperstructure and its interactions direct the replication and sequestration of DNA
  101. Submolecular Structures in Dipalmytoylphosphatidylethanolamine Langmuir–Blodgett Films Observed by Scanning Force Microscopy
  102. Effects of Calcium and Calcium Chelators on Growth and Morphology of Escherichia coli L-Form NC-7
  103. Long-distance transport, storage and recall of morphogenetic information in plants. The existence of a sort of primitive plant ‘memory’
  104. Effects of glucocorticoids and mineralocorticoids on proliferation and maturation of human peripheral blood stem cells
  105. Hypothesis: Hyperstructures regulate bacterial structure and the cell cycle
  106. Metabolite‐induced metabolons: the activation of transporter–enzyme complexes by substrate binding
  107. The mechanical advantages of DNA
  108. Protein phosphorylation in Escherichia coli L. form NC-7
  109. Modelling Escherichia coli. The concept of competitive coherence
  110. Tyrosine phosphorylation in Escherichia coli
  111. Supracriticality and the prion
  112. A mechanical approach to the distribution and orientation of genes on genetic maps
  113. The universal stress protein, UspA, of Escherichia coli is phosphorylated in response to stasis
  114. Artefactual cleavage of E coli H-NS by omp T
  115. 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
  116. Hypothèse : le modèle du lieu de rencontre pour la maladie des prions
  117. Antiviruses as Therapeutic Agents: A Mathematical Analysis of Their Potential
  118. Elements of a unifying theory of biology
  119. Calcium signalling in bacteria
  120. Electrospray ionization mass spectrometric analysis of phospholipids of Escherichia coli
  121. The Escherichia coli enzoskeleton
  122. Autocatalytic Gene Expression OccursviaTransertion and Membrane Domain Formation and Underlies Differentiation in Bacteria: A Model
  123. Hypothesis: chromosome separation in Escherichia coli involves autocatalytic gene expression, transertion and membrane‐domain formation
  124. Characterization of eukaryotic-like kinase activity inEscherichia coliusing the gene-protein database
  125. Hypothesis: transcriptional sensing and membrane‐domain formation initiate chromosome replication in Escherichia coli
  126. Hypotheses and the regulation of the bacterial cell cycle
  127. Identification of phosphoproteins in Escherichia coli
  128. Relationships between proteasomes and RNA
  129. Immunogold localization of GyrA and GyrB proteins in Escherichia coli
  130. Cloning and Analysis of the Entire Escherichia coli ams Gene
  131. Cell Cycle Control: Prokaryotic Solutions to Eukaryotic Problems?
  132. Designer antiviruses for HIV
  133. Sequestration of Origins of Chromosome Replication in Escherichia coli by Lipid Compartments: The Pocket Hypothesis
  134. Deformations in the cytoplasmic membrane of Escherichia coli direct the synthesis of peptidoglycan. The hernia model
  135. Cloning and analysis of the entire Escherichia coli ams gene
  136. Phospholipid domains determine the spatial organization of the Escherichia coli cell cycle: the membrane tectonics model
  137. A protein kinase C‐like activity in Escherichia coli
  138. A single base change in the acceptor stem of tRNA(3Leu) confers resistance upon Escherichia coli to the calmodulin inhibitor, 48/80.
  139. Calcium in bacteria: a solution to which problem?
  140. Analysis of a myosin-like protein and the role of calcium in the E. coli cell cycle
  141. DNA replication in Escherichia coli is initiated by membrane detachment of oriC
  142. Identification of a 180kD protein in Escherichia coli related to a yeast heavy‐chain myosin
  143. Cytoskeletal elements and calcium: Do they play a role in the Escherichia coli cell cycle?
  144. A calcium flux at the termination of replication triggers cell devision in Escherichia coli
  145. Phospholipid flip-out controls the cell cycle of Escherichia coli
  146. A single calcium flux triggers chromosome replication, segregation and septation in bacteria: a model
  147. DNA replication termination in Escherichia coli parB (a dnaG allele), parA, and gyrB mutants affected in DNA distribution
  148. SOS-independent coupling between DNA replication and cell division in Escherichia coli
  149. Restriction map of Tn7