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SEARCH FOR QUANTUM AND CLASSICAL MODES OF INFORMATION PROCESSING IN MICROTUBULES: IMPLICATIONS FOR “THE LIVING STATE”
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0169(1998)40:2<183::aid-cm7>3.0.co;2-gopenalex-snapshot
Altered drug resistance of microtubules in cells exposed to infrared light pulses: Are microtubules the “nerves” of cells?
inferredcites →https://doi.org/10.1002/(sici)1097-4644(199704)65:1<114::aid-jcb12>3.0.co;2-kopenalex-snapshot
Mechanical continuity and reversible chromosome disassembly within intact genomes removed from living cells
inferredcites →https://doi.org/10.1002/(sici)1522-2594(200005)43:5<627::aid-mrm2>3.0.co;2-jopenalex-snapshot
Intermolecular zero-quantum coherence imaging of the human brain
inferredcites →https://doi.org/10.1002/bip.360340114openalex-snapshot
Solitary wave dynamics as a mechanism for explaining the internal motion during microtubule growth
inferredcites →https://doi.org/10.1002/qua.560020505openalex-snapshot
Long‐range coherence and energy storage in biological systems
inferredcites →https://doi.org/10.1002/qua.560370206openalex-snapshot
Coherence in disordered condensed matter. III: H+ and OH− ionic conductance and proton transfer reactions in aqueous solutions
inferredcites →https://doi.org/10.1006/jmbi.1996.0757openalex-snapshot
Motor domains of kinesin and ncd interact with microtubule protofilaments with the same binding geometry
inferredcites →https://doi.org/10.1006/jtbi.1995.0105openalex-snapshot
Ferroelectric behavior in microtubule dipole lattices: Implications for information processing, signaling and assembly/disassembly
inferredcites →https://doi.org/10.1007/978-1-4899-1727-0_9openalex-snapshot
Structure and Function in the Tubulin Dimer and the Role of the Acidic Carboxyl Terminus
inferredcites →https://doi.org/10.1007/bf01342185openalex-snapshot
Quantum mechanical hamiltonian models of turing machines
inferredcites →https://doi.org/10.1016/0006-291x(85)90642-4openalex-snapshot
Intermembrane linkage mediated by tubulin
inferredcites →https://doi.org/10.1016/0022-5193(73)90233-6openalex-snapshot
Microtubule theory of sensory transduction
inferredcites →https://doi.org/10.1016/0022-5193(82)90137-0openalex-snapshot
Information processing in microtubules
inferredcites →https://doi.org/10.1016/0167-2789(84)90259-8openalex-snapshot
Cellular automata in cytoskeletal lattices
inferredcites →https://doi.org/10.1016/0167-2789(90)90093-5openalex-snapshot
Computational connectionism within neurons: A model of cytoskeletal automata subserving neural networks
inferredcites →https://doi.org/10.1016/0263-7855(96)00009-4openalex-snapshot
MOLMOL: A program for display and analysis of macromolecular structures
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Quantum optical coherence in cytoskeletal microtubules: implications for brain function
inferredcites →https://doi.org/10.1016/0309-1651(82)90001-7openalex-snapshot
A model for the microtubule organizing activity of the centrosomes and kinetochores in mammalian cells
inferredcites →https://doi.org/10.1016/0960-0779(94)90056-6openalex-snapshot
Amplification of superpositional effects through electronic-conformational interactions
inferredcites →https://doi.org/10.1016/0968-0004(83)90039-7openalex-snapshot
Biochemistry, 2nd edition
inferredcites →https://doi.org/10.1016/1011-1344(93)80042-8openalex-snapshot
Light-induced photon emission by mammalian cells
inferredcites →https://doi.org/10.1016/s0006-3495(94)81014-8openalex-snapshot
Control of cytoskeletal mechanics by extracellular matrix, cell shape, and mechanical tension
inferredcites →https://doi.org/10.1016/s0022-5320(70)90062-6openalex-snapshot
Microtubules in the heliozoan axopodium
inferredcites →https://doi.org/10.1016/s0074-7696(08)62454-7openalex-snapshot
Role of the Cytoskeleton in Genome Regulation and Cancer
inferredcites →https://doi.org/10.1016/s0167-2789(01)00332-3openalex-snapshot
Electron self-trapping in a discrete two-dimensional lattice
inferredcites →https://doi.org/10.1016/s0303-2647(01)00183-6openalex-snapshot
Conduction pathways in microtubules, biological quantum computation, and consciousness
inferredcites →https://doi.org/10.1016/s0378-4274(98)00162-3openalex-snapshot
Anesthesia, consciousness and hydrophobic pockets—a unitary quantum hypothesis of anesthetic action
inferredcites →https://doi.org/10.1016/s0730-725x(00)00133-8openalex-snapshot
Functional magnetic resonance imaging with intermolecular multiple-quantum coherences
inferredcites →https://doi.org/10.1016/s1011-1344(00)00078-6openalex-snapshot
Analogous features of delayed luminescence from Acetabularia acetabulum and some solid state systems
inferredcites →https://doi.org/10.1016/s1011-1344(99)00048-2openalex-snapshot
‘Simultaneous’ measurements of delayed luminescence and chloroplast organization in Acetabularia acetabulum
inferredcites →https://doi.org/10.1016/s1364-6613(00)01774-5openalex-snapshot
A quantum approach to visual consciousness
inferredcites →https://doi.org/10.1021/bi00449a028openalex-snapshot
Cold depolymerization of microtubules to double rings: geometric stabilization of assemblies
inferredcites →https://doi.org/10.1021/ja991855iopenalex-snapshot
Evidence of Electron Transfer from Peptides to DNA: Oxidation of DNA-Bound Tryptophan Using the Flash-Quench Technique
inferredcites →https://doi.org/10.1038/2281093a0openalex-snapshot
Long Range Coherence and the Action of Enzymes
inferredcites →https://doi.org/10.1038/300487a0openalex-snapshot
Molecular mechanisms of general anaesthesia
inferredcites →https://doi.org/10.1038/34465openalex-snapshot
Structure of the αβ tubulin dimer by electron crystallography
inferredcites →https://doi.org/10.1063/1.882757openalex-snapshot
The Feynman Processor: Quantum Entanglement and the Computing Revolution
inferredcites →https://doi.org/10.1073/pnas.72.11.4211openalex-snapshot
The extraordinary dielectric properties of biological materials and the action of enzymes.
inferredcites →https://doi.org/10.1073/pnas.89.17.8288openalex-snapshot
Rudimentary form of cellular "vision".
inferredcites →https://doi.org/10.1073/pnas.94.3.849openalex-snapshot
Demonstration of mechanical connections between integrins, cytoskeletal filaments, and nucleoplasm that stabilize nuclear structure
inferredcites →https://doi.org/10.1093/nar/20.suppl.2019openalex-snapshot
The SWISS-PROT protein sequence data bank
inferredcites →https://doi.org/10.1093/nar/25.1.31openalex-snapshot
The SWISS-PROT protein sequence data bank and its supplement TrEMBL
inferredcites →https://doi.org/10.1093/oso/9780198519737.001.0001openalex-snapshot
The Emperor's New Mind
inferredcites →https://doi.org/10.1098/rsta.1998.0254openalex-snapshot
Quantum computation in brain microtubules? The Penrose–Hameroff ‘Orch OR‘ model of consciousness
inferredcites →https://doi.org/10.1098/rsta.1998.0255openalex-snapshot
Dielectric polarization, electrical conduction, information processing and quantum computation in microtubules. Are they plausible?
inferredcites →https://doi.org/10.1098/rsta.1998.0256openalex-snapshot
Quantum computation, entanglement and state reduction
inferredcites →https://doi.org/10.1103/physreva.57.3229openalex-snapshot
Experimental demonstration of quantum correlations over more than 10 km
inferredcites →https://doi.org/10.1103/physreve.58.6333openalex-snapshot
Mössbauer effect as a possible tool in detecting nonlinear excitations in microtubules
inferredcites →https://doi.org/10.1103/physreve.61.4194openalex-snapshot
Importance of quantum decoherence in brain processes
inferredcites →https://doi.org/10.1103/physreve.64.031902openalex-snapshot
Delayed luminescence of biological systems arising from correlated many-soliton states
inferredcites →https://doi.org/10.1103/physreve.65.051912openalex-snapshot
Molecular gyroscopes and biological effects of weak extremely low-frequency magnetic fields
inferredcites →https://doi.org/10.1103/physreve.65.061901openalex-snapshot
Quantum computation in brain microtubules: Decoherence and biological feasibility
inferredcites →https://doi.org/10.1103/physrevlett.49.91openalex-snapshot
Experimental Realization of Einstein-Podolsky-Rosen-Bohm Gedankenexperiment : A New Violation of Bell's Inequalities
inferredcites →https://doi.org/10.1111/j.1550-7408.1977.tb05273.xopenalex-snapshot
Gradionation: Hypothesis for Positioning and Patterning*
inferredcites →https://doi.org/10.1111/j.1749-6632.1974.tb26778.xopenalex-snapshot
THE ELECTRET EFFECT IN BONE AND BIOPOLYMERS AND THE BOUND‐WATER PROBLEM*
inferredcites →https://doi.org/10.1111/j.1749-6632.1974.tb26780.xopenalex-snapshot
PYROELECTRIC AND PIEZOELECTRIC PROPERTIES OF VERTEBRATES
inferredcites →https://doi.org/10.1111/j.1749-6632.1986.tb38445.xopenalex-snapshot
ATP‐Dependent Gelation Contraction of Microtubules in Vitro
inferredcites →https://doi.org/10.1111/j.1749-6632.2001.tb05709.xopenalex-snapshot
Consciousness, the Brain, and Spacetime Geometry
inferredcites →https://doi.org/10.1126/science.1067680openalex-snapshot
Long-Range Interactions Within a Nonnative Protein
inferredcites →https://doi.org/10.1126/science.272.5260.425openalex-snapshot
Response : Does Macroscopic Quantum Coherence Occur in Ferritin?
inferredcites →https://doi.org/10.1126/science.7539156openalex-snapshot
Anharmonic Wave Functions of Proteins: Quantum Self-Consistent Field Calculations of BPTI
inferredcites →https://doi.org/10.1142/s0192415x74000213openalex-snapshot
Ch'i: A Neural Hologram? Microtubules, Bioholography, and Acupuncture
inferredcites →https://doi.org/10.1523/jneurosci.14-05-02818.1994openalex-snapshot
Changes in microtubule number and length during axon differentiation
inferredcites →https://doi.org/10.4324/9780429494116-14openalex-snapshot
Bose-Einstein Condensation and Liquid Helium
inferredcites →https://doi.org/10.7939/r3nc5sj5jopenalex-snapshot
A study of the interactions between electromagnetic fields and microtubules: ferroelectric effects, signal transduction and electronic conduction
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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