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1 | (12) |
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1 | (3) |
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Isoform Machinery for Speeding Up Information Transfer |
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4 | (1) |
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Troponin C Isoforms in Speeding Up Contractile Function |
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5 | (1) |
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Coadaptation of Energy Demand and Energy Supply Pathways |
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6 | (4) |
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Coadaptation and Metabolic Isozymes: the LDH Archetype |
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10 | (1) |
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Coadaptation and Emergent Properties |
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11 | (2) |
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Chapter 2 Nerve-to-Muscle Signals |
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13 | (18) |
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How the Signals Get There |
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13 | (1) |
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14 | (1) |
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Acetylcholine: the Signal to Go |
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15 | (1) |
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ACh Release Depends Upon Ca++ Channels |
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15 | (1) |
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ACh-Induced Depolarization Depends on End-Plate Channels |
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16 | (1) |
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Structure of End-Plate Channels |
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17 | (2) |
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End-Plate Channel Isoforms |
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19 | (1) |
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Localization of End-Plate Channels |
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19 | (1) |
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Synaptic Transmission Time |
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20 | (1) |
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Muscle (and Nerve) Action Potentials Depend on Na+ and K+ Channels |
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21 | (1) |
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Structure of Na+ Channels |
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21 | (1) |
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22 | (2) |
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Localization of Na+ Channels |
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24 | (1) |
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Isoforms of Delayed Rectifier K+ Channels |
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24 | (1) |
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Excitation-Contraction Coupling |
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25 | (3) |
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28 | (1) |
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E-C Coupling in Fast- and Slow-Twitch Muscles |
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29 | (1) |
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Facilitating Role of Calsequestrin |
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30 | (1) |
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Chapter 3 Design of Nerve-to-Muscle Information Systems |
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31 | (10) |
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31 | (1) |
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Channels Are Extremely Efficient Catalysts |
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31 | (2) |
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Channel Densities Are Usually Rather Low |
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33 | (1) |
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Channel Densities May Be Adjusted Upward |
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34 | (1) |
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Design Criteria for Presynaptic Signaling Processes |
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35 | (1) |
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Design Criteria for Postsynaptic Signal Transduction |
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36 | (1) |
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Design Criteria for Na+ Channel Functions |
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37 | (1) |
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Design Criteria for TT and SR Ca++ Channels |
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38 | (1) |
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Overall Design Principles for Nerve-to-Muscle Information Flow Systems |
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39 | (2) |
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Chapter 4 Energy Demand of Muscle Machines |
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41 | (18) |
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41 | (1) |
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The Sarcomere: the Basic Contractile Unit |
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42 | (1) |
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Sliding Filament Model of Contraction |
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43 | (1) |
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Taking Myosin Apart to Identify Functional Domains |
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44 | (1) |
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Globular and Filamentous Forms of Actin |
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45 | (1) |
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ATPase Coupling with Filament Movement |
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45 | (2) |
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Troponin and Tropomyosin Mediate Ca++ Regulation of Muscle Contraction |
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47 | (2) |
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Adaptable vs. Conservative Aspects of Contractile Components |
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49 | (3) |
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Myosin Isoforms: Patterns and Distribution |
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49 | (1) |
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50 | (1) |
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51 | (1) |
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51 | (1) |
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Co-occurrence of Specific Contractile Isoforms |
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51 | (1) |
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Excitation-Contraction (EC) Coupling: Decoupling of Ca+4 Channel and Ca+ 4 Pump Functions of the SR |
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52 | (1) |
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52 | (1) |
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Co-occurrence of Contractile and Regulatory Protein Isoforms |
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52 | (1) |
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Role of Actomyosin ATPase in Adaptation of Muscle Function |
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53 | (1) |
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In Solution, Actomyosin ATPases Are Highly Adapted Catalysts |
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53 | (1) |
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Diffusion Limitation of Enzyme Function Can Be Circumvented |
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54 | (1) |
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The Contractile Cycle as a Channeled Reaction Sequence |
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55 | (2) |
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Evidence For Preferential Access To and From Actomyosin ATPase |
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57 | (1) |
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Minimizing Ca++ Diffusion-Based Limits |
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57 | (2) |
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Chapter 5 Return to the Precontraction State |
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59 | (10) |
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59 | (1) |
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Ca++ ATPase and Sarcoplasmic Reticulum (SR) Structure |
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59 | (1) |
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Ca++ ATPase Catalytic Cycle |
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60 | (1) |
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Model of Ca+t ATPase Structure |
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61 | (1) |
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Two Ca++ ATPase Genes: Two (or More) Ca++ ATPase Isoforms |
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62 | (1) |
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Two Ca++ ATPases: Differences and Homologies |
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62 | (1) |
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Coadaptation and Design Properties of SR Ca++ ATPases |
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62 | (1) |
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Na+K+ ATPase and the Na+ Pump |
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63 | (1) |
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Na+K+ ATPase Catalytic Cycle |
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64 | (1) |
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64 | (1) |
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Minimal Design Criteria for Na+K4 ATPase as an Ion Pump |
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65 | (1) |
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Na+ Pump Isoforms Based on a and B Subunit Polymorphism |
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65 | (1) |
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Functional Significance of Na+ Pump Isoforms |
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66 | (1) |
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Magnitude of the Postexercise Na+K+ Imbalance |
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66 | (1) |
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Short-Term Na+K+ ATPase Regulatory Mechanisms |
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66 | (1) |
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Long-Term Na+K+ ATPase Regulatory Mechanisms |
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67 | (1) |
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Muscle Na+K+ ATPase Functional Design Considerations |
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67 | (2) |
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Chapter 6 Supplying Muscle Machines with Energy |
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69 | (26) |
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69 | (1) |
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Three Basic ATP-Synthesizing Pathways in Muscle |
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69 | (5) |
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74 | (1) |
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The Nature of Effective Phosphagens |
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74 | (3) |
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74 | (1) |
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74 | (1) |
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Phosphagens "Buffer" ATP Content |
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75 | (1) |
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76 | (1) |
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Osmotic or Ionic Effects of Phosphagen Mobilization |
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76 | (1) |
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Ancillary Roles of Phosphagens |
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76 | (1) |
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Phosphagens: Their Pros and Cons |
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77 | (1) |
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77 | (9) |
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Glycogen---An Ideal Fermentable Fuel |
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78 | (1) |
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ATP Yields of Anaerobic Pathways |
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78 | (1) |
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Turning on Anaerobic Glycolysis: Hormones and Neurotransmitters |
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78 | (2) |
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Turning on Anaerobic Glycolysis: Enzyme and Isozyme Function |
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80 | (2) |
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The Problem of Anaerobic End Products |
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82 | (1) |
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Upper Glycolytic Limits in Muscle: A Coadaptation Problem |
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83 | (3) |
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86 | (9) |
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Nature of Endogenous Aerobic Fuels |
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87 | (1) |
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ATP Yields of Aerobic Pathways |
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87 | (1) |
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End Products of Aerobic Metabolism |
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87 | (2) |
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Nature of Exogenous Fuels of Aerobic Muscle Metabolism |
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89 | (1) |
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Storage Sites of Exogenous Fuels |
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89 | (1) |
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Flux Rates Sustainable by Exogenous Fuels |
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90 | (1) |
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Regulating Fluxes of Exogenous Fuels |
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91 | (2) |
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Coordinating Aerobic and Glycolytic Pathways |
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93 | (2) |
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Chapter 7 Integrating Atp Supply and Demand |
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95 | (24) |
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Quantifying Energy Coupling |
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95 | (1) |
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Energy Coupling in Anaerobically-Driven Muscles |
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96 | (1) |
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Human Muscle at Maximum Aerobic Work Rates |
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97 | (1) |
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Setting the ATP Demand: V vs S or S vs V |
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97 | (2) |
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Gastrocnemius of the Laboratory Rat |
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99 | (1) |
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Biceps and Soleus of the Laboratory Cat |
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99 | (2) |
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Gracilis and Gastrocnemius of the Laboratory Dog |
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101 | (1) |
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Gastrocnemius of the Laboratory Rabbit |
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101 | (1) |
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Biceps Femoris of the Greyhound---Canine Super-Athlete |
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102 | (1) |
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Leg Muscle of the Thoroughbred---Equine Super-Athlete |
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102 | (1) |
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Calf Muscle of Variably Adapted Humans |
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103 | (1) |
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Serving a Small Muscle Mass with a Large Cardiac Output |
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103 | (1) |
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Flight Muscle of Insects---Champion Animal Athletes |
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104 | (1) |
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Thermally Driven Change in ATP Turnover Rates |
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105 | (1) |
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Pathway Intermediates and the Latent Enzyme Concept |
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105 | (3) |
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Exogenous Control of Energy Coupling |
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108 | (1) |
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Oxygen Sensing in Regulation of ATP Turnover |
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109 | (6) |
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O2 Sensing---Possible Pathways and Mechanisms |
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115 | (1) |
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Controlling the Physical State of ICF |
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116 | (3) |
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Chapter 8 Isoform Definition of Muscle Machines |
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119 | (18) |
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119 | (1) |
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Denning Muscle Fiber Types |
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119 | (2) |
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Nature's Fastest Oxidative Muscles: One Isoform Combination to the Exclusion of All Others? |
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121 | (3) |
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Fish White Muscle: An Anaerobic Type of Muscle Displaying Exceptional Compositional Homogeneity |
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124 | (1) |
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Sound-Producing Muscles: Structurally Homogeneous Muscles Designed for High Frequency, Not Power Output |
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125 | (2) |
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Rattler Muscle of the Rattlesnake |
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127 | (1) |
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Brain Heater Organ: A Structurally Homogeneous Muscle Designed for Thermogenesis, Not Power Output |
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127 | (3) |
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Electroplax: A Structurally Homogeneous Kind of Muscle Designed for Electrical Discharge, Not Power Output |
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130 | (1) |
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Why Muscles Specialize into So Few Different Fiber Types |
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130 | (2) |
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Glycolytic Function in Chronic Hypobaric Hypoxia |
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132 | (1) |
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Role of MDH and LDH in Chronic Hypobaric Hypoxia |
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132 | (1) |
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Role of LDH Isozymes in Chronic Hypobaric Hypoxia |
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133 | (1) |
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The Fixed Nature of the Lactate Paradox in Andean Natives |
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134 | (1) |
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Isoform Basis for Plasticity of Muscle Function |
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134 | (1) |
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The Issue of Emergent Properties |
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135 | (2) |
References |
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137 | |