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Regulation of Contraction by the Thick Filaments in Skeletal Muscle

https://doi.org/10.1016/j.bpj.2017.09.037

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Towards a molecular understanding of titin.

inferredcites →https://doi.org/10.1006/jmbi.1996.0800openalex-snapshot

Steric-model for activation of muscle thin filaments

inferredcites →https://doi.org/10.1007/bf00713257openalex-snapshot

The maximum velocity of shortening during the early phases of the contraction in frog single muscle fibres

inferredcites →https://doi.org/10.1007/bf01753571openalex-snapshot

The ultrastructural location of C-protein, X-protein and H-protein in rabbit muscle

inferredcites →https://doi.org/10.1007/s00424-004-1363-5openalex-snapshot

Sarcomeric determinants of striated muscle relaxation kinetics

inferredcites →https://doi.org/10.1007/s10974-012-9291-zopenalex-snapshot

Structure, interactions and function of the N-terminus of cardiac myosin binding protein C (MyBP-C): who does what, with what, and to whom?

inferredcites →https://doi.org/10.1007/s12551-011-0044-9openalex-snapshot

The role of the myosin ATPase activity in adaptive thermogenesis by skeletal muscle

inferredcites →https://doi.org/10.1007/s12551-012-0067-xopenalex-snapshot

Cardiac myosin binding protein-C: redefining its structure and function

inferredcites →https://doi.org/10.1016/0014-5793(77)80560-7openalex-snapshot

The significance of the slow dissociation of divalent metal ions from myosin ‘regulatory’ light chains

inferredcites →https://doi.org/10.1016/0022-2836(73)90222-2openalex-snapshot

X-ray evidence for radial cross-bridge movement and for the sliding filament model in actively contracting skeletal muscle

inferredcites →https://doi.org/10.1016/0022-2836(73)90527-5openalex-snapshot

Structural role of tropomyosin in muscle regulation: Analysis of the X-ray diffraction patterns from relaxed and contracting muscles

inferredcites →https://doi.org/10.1016/0022-2836(75)90094-7openalex-snapshot

X-ray evidence for conformational changes in the myosin filaments of vertebrate striated muscle

inferredcites →https://doi.org/10.1016/0022-2836(82)90253-4openalex-snapshot

Time-resolved X-ray diffraction studies of the myosin layer-line reflections during muscle contraction

inferredcites →https://doi.org/10.1016/0022-2836(86)90158-0openalex-snapshot

Structural changes during activation of frog muscle studied by time-resolved X-ray diffraction

inferredcites →https://doi.org/10.1016/0306-3623(86)90238-7openalex-snapshot

Energetic aspects of muscle contraction

inferredcites →https://doi.org/10.1016/0955-0674(91)90171-topenalex-snapshot

Regulation of cytoplasmic and smooth muscle myosin

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Clusters of bound Ca2+ initiate contraction in fast skeletal muscle

inferredcites →https://doi.org/10.1016/j.bpj.2008.09.022openalex-snapshot

Dynamics of Thin-Filament Activation in Rabbit Skeletal Muscle Fibers Examined by Time-Resolved X-Ray Diffraction

inferredcites →https://doi.org/10.1016/j.bpj.2009.01.049openalex-snapshot

Stabilization of Helical Order in the Thick Filaments by Blebbistatin: Further Evidence of Coexisting Multiple Conformations of Myosin

inferredcites →https://doi.org/10.1016/j.bpj.2010.04.021openalex-snapshot

Monitoring the Structural Behavior of Troponin and Myoplasmic Free Ca2+ Concentration during Twitch of Frog Skeletal Muscle

inferredcites →https://doi.org/10.1016/j.bpj.2014.07.075openalex-snapshot

The Myosin Inhibitor Blebbistatin Stabilizes the Super-Relaxed State in Skeletal Muscle

inferredcites →https://doi.org/10.1016/j.bpj.2015.06.038openalex-snapshot

The Conformation of Myosin Heads in Relaxed Skeletal Muscle: Implications for Myosin-Based Regulation

inferredcites →https://doi.org/10.1016/j.bpj.2015.12.024openalex-snapshot

Compliance Accelerates Relaxation in Muscle by Allowing Myosin Heads to Move Relative to Actin

inferredcites →https://doi.org/10.1016/j.bpj.2016.05.021openalex-snapshot

A Perspective on the Role of Myosins as Mechanosensors

inferredcites →https://doi.org/10.1016/j.bpj.2016.11.005openalex-snapshot

Force Responses and Sarcomere Dynamics of Cardiac Myofibrils Induced by Rapid Changes in [Pi]

inferredcites →https://doi.org/10.1016/j.cell.2007.09.045openalex-snapshot

Skeletal Muscle Performance Determined by Modulation of Number of Myosin Motors Rather Than Motor Force or Stroke Size

inferredcites →https://doi.org/10.1016/j.jmb.2008.09.007openalex-snapshot

Structural Changes in the Muscle Thin Filament during Contractions Caused by Single and Double Electrical Pulses

inferredcites →https://doi.org/10.1016/j.jmb.2008.10.013openalex-snapshot

Three-Dimensional Reconstruction of Tarantula Myosin Filaments Suggests How Phosphorylation May Regulate Myosin Activity

inferredcites →https://doi.org/10.1016/j.jmb.2011.06.051openalex-snapshot

Slow Myosin ATP Turnover in the Super-Relaxed State in Tarantula Muscle

inferredcites →https://doi.org/10.1016/s0006-3495(02)73974-xopenalex-snapshot

Relaxation Kinetics Following Sudden Ca2+ Reduction in Single Myofibrils from Skeletal Muscle

inferredcites →https://doi.org/10.1016/s0006-3495(93)81110-xopenalex-snapshot

Regulation of the interaction between actin and myosin subfragment 1: evidence for three states of the thin filament

inferredcites →https://doi.org/10.1016/s0006-3495(94)80728-3openalex-snapshot

X-ray diffraction measurements of the extensibility of actin and myosin filaments in contracting muscle

inferredcites →https://doi.org/10.1016/s0006-3495(94)80729-5openalex-snapshot

X-ray diffraction evidence for the extensibility of actin and myosin filaments during muscle contraction

inferredcites →https://doi.org/10.1016/s0006-3495(95)80278-xopenalex-snapshot

Passive tension in cardiac muscle: contribution of collagen, titin, microtubules, and intermediate filaments

inferredcites →https://doi.org/10.1016/s0006-3495(96)79293-7openalex-snapshot

Myosin light chain phosphorylation affects the structure of rabbit skeletal muscle thick filaments

inferredcites →https://doi.org/10.1016/s0006-3495(97)78262-6openalex-snapshot

Temperature-induced structural changes in the myosin thick filament of skinned rabbit psoas muscle

inferredcites →https://doi.org/10.1016/s0006-3495(99)77308-xopenalex-snapshot

Ca2+ and Cross-Bridge-Induced Changes in Troponin C in Skinned Skeletal Muscle Fibers: Effects of Force Inhibition

inferredcites →https://doi.org/10.1016/s0021-9258(17)39206-2openalex-snapshot

Phosphorylation of smooth muscle myosin at two distinct sites by myosin light chain kinase.

inferredcites →https://doi.org/10.1016/s0021-9258(18)50392-6openalex-snapshot

The calcium binding properties of phosphorylated and unphosphorylated cardiac and skeletal myosins.

inferredcites →https://doi.org/10.1016/s0021-9258(18)62075-7openalex-snapshot

Reconstitution of Troponin Activity from Three Protein Components

inferredcites →https://doi.org/10.1016/s0021-9258(18)89724-1openalex-snapshot

Kinetic studies of calcium binding to regulatory complexes from skeletal muscle.

inferredcites →https://doi.org/10.1016/s0022-2836(67)80046-9openalex-snapshot

The low-angle X-ray diagram of vertebrate striated muscle and its behaviour during contraction and rigor

inferredcites →https://doi.org/10.1016/s0065-3233(04)71005-0openalex-snapshot

The Molecular Mechanism of Muscle Contraction

inferredcites →https://doi.org/10.1016/s0096-4174(18)30128-8openalex-snapshot

Muscle Structure and Theories of Contraction

inferredcites →https://doi.org/10.1016/s1097-2765(03)00096-0openalex-snapshot

In Situ Orientations of Protein Domains

inferredcites →https://doi.org/10.1017/s0033583500001190openalex-snapshot

Control of muscle contraction

inferredcites →https://doi.org/10.1038/75890openalex-snapshot

Conformation of the myosin motor during force generation in skeletal muscle

inferredcites →https://doi.org/10.1038/nature02380openalex-snapshot

The myosin motor in muscle generates a smaller and slower working stroke at higher load

inferredcites →https://doi.org/10.1038/nature03920openalex-snapshot

Atomic model of a myosin filament in the relaxed state

inferredcites →https://doi.org/10.1038/nature15727openalex-snapshot

Force generation by skeletal muscle is controlled by mechanosensing in myosin filaments

inferredcites →https://doi.org/10.1038/nature18295openalex-snapshot

Cryo-EM structure of a human cytoplasmic actomyosin complex at near-atomic resolution

inferredcites →https://doi.org/10.1038/ncomms13281openalex-snapshot

Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle

inferredcites →https://doi.org/10.1038/newbio238097a0openalex-snapshot

Cooperation within Actin Filament in Vertebrate Skeletal Muscle

inferredcites →https://doi.org/10.1038/newbio244152a0openalex-snapshot

X-ray Diffraction of Muscle labelled with Antibody to C-Protein

inferredcites →https://doi.org/10.1042/bj1710165openalex-snapshot

Reaction mechanism of the magnesium ion-dependent adenosine triphosphatase of frog muscle myosin and subfragment 1

inferredcites →https://doi.org/10.1073/pnas.0605430103openalex-snapshot

Structural changes in troponin in response to Ca 2+ and myosin binding to thin filaments during activation of skeletal muscle

inferredcites →https://doi.org/10.1073/pnas.0707846105openalex-snapshot

Conservation of the regulated structure of folded myosin 2 in species separated by at least 600 million years of independent evolution

inferredcites →https://doi.org/10.1073/pnas.0708912105openalex-snapshot

Three-dimensional structure of vertebrate cardiac muscle myosin filaments

inferredcites →https://doi.org/10.1073/pnas.071051098openalex-snapshot

Three-dimensional image reconstruction of dephosphorylated smooth muscle heavy meromyosin reveals asymmetry in the interaction between myosin heads and placement of subfragment 2

inferredcites →https://doi.org/10.1073/pnas.0909468107openalex-snapshot

Myosin ATP turnover rate is a mechanism involved in thermogenesis in resting skeletal muscle fibers

inferredcites →https://doi.org/10.1073/pnas.1018330108openalex-snapshot

Motion of myosin head domains during activation and force development in skeletal muscle

inferredcites →https://doi.org/10.1073/pnas.1103216108openalex-snapshot

Direct visualization of myosin-binding protein C bridging myosin and actin filaments in intact muscle

inferredcites →https://doi.org/10.1073/pnas.1212708110openalex-snapshot

Atomic model of the human cardiac muscle myosin filament

inferredcites →https://doi.org/10.1073/pnas.1218462110openalex-snapshot

Structural basis of the relaxed state of a Ca 2+ -regulated myosin filament and its evolutionary implications

inferredcites →https://doi.org/10.1073/pnas.1316001111openalex-snapshot

Myosin-binding protein C displaces tropomyosin to activate cardiac thin filaments and governs their speed by an independent mechanism

inferredcites →https://doi.org/10.1073/pnas.1321868111openalex-snapshot

Structural dynamics of troponin during activation of skeletal muscle

inferredcites →https://doi.org/10.1073/pnas.1413922112openalex-snapshot

Myosin binding protein-C activates thin filaments and inhibits thick filaments in heart muscle cells

inferredcites →https://doi.org/10.1073/pnas.1522236113openalex-snapshot

Phosphorylation and calcium antagonistically tune myosin-binding protein C’s structure and function

inferredcites →https://doi.org/10.1073/pnas.1602776113openalex-snapshot

Myosin light chain phosphorylation enhances contraction of heart muscle via structural changes in both thick and thin filaments

inferredcites →https://doi.org/10.1073/pnas.2235652100openalex-snapshot

Calcium-dependent molecular spring elements in the giant protein titin

inferredcites →https://doi.org/10.1073/pnas.95.9.5383openalex-snapshot

Phosphorylation of a twitchin-related protein controls catch and calcium sensitivity of force production in invertebrate smooth muscle

inferredcites →https://doi.org/10.1074/jbc.m808850200openalex-snapshot

The Myosin-binding Protein C Motif Binds to F-actin in a Phosphorylation-sensitive Manner

inferredcites →https://doi.org/10.1074/jbc.r110.198697openalex-snapshot

Signaling to Myosin Regulatory Light Chain in Sarcomeres

inferredcites →https://doi.org/10.1085/jgp.106.5.957openalex-snapshot

Nucleotide turnover rate measured in fully relaxed rabbit skeletal muscle myofibrils.

inferredcites →https://doi.org/10.1085/jgp.66.1.1openalex-snapshot

Regulation of muscular contraction. Distribution of actin control and myosin control in the animal kingdom.

inferredcites →https://doi.org/10.1091/mbc.e08-02-0206openalex-snapshot

Head–Head and Head–Tail Interaction: A General Mechanism for Switching Off Myosin II Activity in Cells

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The structural basis of muscle contraction

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Adenosine diphosphate and strain sensitivity in myosin motors

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Smooth muscle myosin: regulation and properties

inferredcites →https://doi.org/10.1101/sqb.1973.037.01.046openalex-snapshot

Structural Changes in the Actin- and Myosin-eontaining Filaments during Contraction

inferredcites →https://doi.org/10.1113/expphysiol.1996.sp003971openalex-snapshot

The relationship between the intracellular Ca2+ transient and the isometric twitch force in frog muscle fibres

inferredcites →https://doi.org/10.1113/jp273299openalex-snapshot

Minimum number of myosin motors accounting for shortening velocity under zero load in skeletal muscle

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On the increase in rate of heat production caused by stretch in frog's skeletal muscle

inferredcites →https://doi.org/10.1113/jphysiol.1968.sp008672openalex-snapshot

Tension due to interaction between the sliding filaments in resting striated muscle. the effect of stimulation

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Muscular contraction.

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Aerobic recovery metabolism following a single isometric tetanus in frog sartorius muscle at 0 degrees C.

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Tension responses to sudden length change in stimulated frog muscle fibres near slack length

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Force‐velocity relation in normal and nitrate‐treated frog single muscle fibres during rise of tension in an isometric tetanus.

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High‐energy phosphate metabolism and energy liberation associated with rapid shortening in frog skeletal muscle

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Laser diffraction studies of sarcomere dynamics during ‘isometric’ relaxation in isolated muscle fibres of the frog

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Transient tension changes initiated by laser temperature jumps in rabbit psoas muscle fibres.

inferredcites →https://doi.org/10.1113/jphysiol.1991.sp018689openalex-snapshot

C‐protein limits shortening velocity of rabbit skeletal muscle fibres at low levels of Ca2+ activation.

inferredcites →https://doi.org/10.1113/jphysiol.1992.sp019163openalex-snapshot

Reversal of the cross‐bridge force‐generating transition by photogeneration of phosphate in rabbit psoas muscle fibres.

inferredcites →https://doi.org/10.1113/jphysiol.1994.sp020237openalex-snapshot

Variation in myoplasmic Ca2+ concentration during contraction and relaxation studied by the indicator fluo‐3 in frog muscle fibres.

inferredcites →https://doi.org/10.1113/jphysiol.2002.032185openalex-snapshot

Energy storage during stretch of active single fibres from frog skeletal muscle

inferredcites →https://doi.org/10.1113/jphysiol.2006.115394openalex-snapshot

Structural changes in the myosin filament and cross‐bridges during active force development in single intact frog muscle fibres: stiffness and X‐ray diffraction measurements

inferredcites →https://doi.org/10.1113/jphysiol.2007.138693openalex-snapshot

Impact of temperature on cross‐bridge cycling kinetics in rat myocardium

inferredcites →https://doi.org/10.1113/jphysiol.2008.164707openalex-snapshot

Calcium‐ and myosin‐dependent changes in troponin structure during activation of heart muscle

inferredcites →https://doi.org/10.1113/jphysiol.2009.176222openalex-snapshot

Structural changes in myosin motors and filaments during relaxation of skeletal muscle

inferredcites →https://doi.org/10.1113/jphysiol.2013.257410openalex-snapshot

The working stroke of the myosin II motor in muscle is not tightly coupled to release of orthophosphate from its active site

inferredcites →https://doi.org/10.1113/jphysiol.2013.267849openalex-snapshot

Sarcomere‐length dependence of myosin filament structure in skeletal muscle fibres of the frog

inferredcites →https://doi.org/10.1126/sciadv.1600058openalex-snapshot

Structure of myosin filaments from relaxed Lethocerus flight muscle by cryo-EM at 6 Å resolution

inferredcites →https://doi.org/10.1126/science.164.3886.1356openalex-snapshot

The Mechanism of Muscular Contraction

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The latch-bridge hypothesis of smooth muscle contraction

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Myosin light chain phosphorylation in vertebrate striated muscle: regulation and function

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Energetic Aspects of Muscle Contraction

inferredcites →https://doi.org/10.1152/physrev.2000.80.2.853openalex-snapshot

Regulation of Contraction in Striated Muscle

inferredcites →https://doi.org/10.1155/2010/612482openalex-snapshot

Roles of Titin in the Structure and Elasticity of the Sarcomere

inferredcites →https://doi.org/10.1161/01.res.0000012222.70819.64openalex-snapshot

Hypertrophic Cardiomyopathy in Cardiac Myosin Binding Protein-C Knockout Mice

inferredcites →https://doi.org/10.1161/01.res.0000096363.85588.9aopenalex-snapshot

Loaded Shortening, Power Output, and Rate of Force Redevelopment Are Increased With Knockout of Cardiac Myosin Binding Protein-C

inferredcites →https://doi.org/10.1161/01.res.0000127175.21818.c2openalex-snapshot

Cardiac Myosin Binding Protein C

inferredcites →https://doi.org/10.1161/01.res.0000222059.54917.efopenalex-snapshot

Activation of Myocardial Contraction by the N-Terminal Domains of Myosin Binding Protein-C

inferredcites →https://doi.org/10.1161/01.res.86.1.51openalex-snapshot

Myosin Binding Protein C, a Phosphorylation-Dependent Force Regulator in Muscle That Controls the Attachment of Myosin Heads by Its Interaction With Myosin S2

inferredcites →https://doi.org/10.1529/biophysj.108.137067openalex-snapshot

Blebbistatin Stabilizes the Helical Order of Myosin Filaments by Promoting the Switch 2 Closed State

inferredcites →https://doi.org/10.2170/jjphysiol.48.421openalex-snapshot

Cytoplasmic Free Concentrations of Ca2+ and Mg2+ in Skeletal Muscle Fibers at Rest and during Contraction.

inferredcites →https://doi.org/10.2170/physiolsci.rv005408openalex-snapshot

Physiological Functions of the Giant Elastic Protein Titin in Mammalian Striated Muscle

inferredcites →https://doi.org/10.3389/fcvm.2016.00021openalex-snapshot

A Review of the Giant Protein Titin in Clinical Molecular Diagnostics of Cardiomyopathies

inferredcites →https://doi.org/10.3389/fphys.2016.00410openalex-snapshot

MYBPC1, an Emerging Myopathic Gene: What We Know and What We Need to Learn

inferredcites →https://doi.org/10.3389/fphys.2016.00427openalex-snapshot

Mechanosensing in Myosin Filament Solves a 60 Years Old Conflict in Skeletal Muscle Modeling between High Power Output and Slow Rise in Tension

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Mechanisms of Frank-Starling law of the heart and stretch activation in striated muscles may have a common molecular origin

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The effect of muscle length on post-tetanic potentiation of C57BL/6 and skMLCK−/− mouse EDL muscles

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Cryo-electron tomography of intact cardiac muscle reveals myosin binding protein-C linking myosin and actin filaments

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Temperature dependence of activation of thick and thin filaments in skeletal and cardiac muscles

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Disease mutations in striated muscle myosins

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Structural changes in troponin during activation of skeletal and heart muscle determined in situ by polarised fluorescence

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The role of the myosin dimer in the contractility of the heart

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Closing the therapeutic loop

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Cooperative & competitive binding of anti-myosin tail antibodies revealed by super-resolution microscopy

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The effects of inorganic phosphate on contractile function of slow skeletal muscle fibres are length-dependent

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Thick Filament Length Changes in Muscle Have Both Elastic and Structural Components

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Omecamtiv Mecarbil Slows Myosin Kinetics in Skinned Rat Myocardium at Physiological Temperature

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A Parallel Ratchet-Stroke Mechanism Leads to an Optimum Force for Molecular Motor Function

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Interacting-heads motif explains the X-ray diffraction pattern of relaxed vertebrate skeletal muscle

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Myosins may know when to hold and when to fold

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inferred← citeshttps://doi.org/10.1016/j.bpr.2026.100268openalex-snapshot

Drosophila jump muscle myofibrils: A new tool for investigating activation and relaxation

inferred← citeshttps://doi.org/10.1016/j.clinbiomech.2025.106544openalex-snapshot

Performance across the isokinetic velocity spectrum: Interpretation for individuals after anterior cruciate ligament reconstruction

inferred← citeshttps://doi.org/10.1016/j.cplett.2026.142652openalex-snapshot

EMD simulations for visualization of torsional strain dynamics in the γ subunit of ATP synthase

inferred← citeshttps://doi.org/10.1016/j.eml.2026.102532openalex-snapshot

Antagonistic coupling of Z-disc perforation and thick-filament mechano-sensing shapes supercontracting muscle mechanics

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.01.048openalex-snapshot

Dose-response relationship between dietary nitrate intake and nitric oxide congeners in various blood compartments and skeletal muscle: Differential effects on skeletal muscle torque and velocity

inferred← citeshttps://doi.org/10.1016/j.jbc.2023.105565openalex-snapshot

The biochemically defined super relaxed state of myosin—A paradox

inferred← citeshttps://doi.org/10.1016/j.jbiomech.2025.112744openalex-snapshot

Effect of pre-activation force on active force generation in skeletal muscle

inferred← citeshttps://doi.org/10.1016/j.mehy.2023.111023openalex-snapshot

The potential role of the myosin head for strength gain in hypertrophied muscle

inferred← citeshttps://doi.org/10.1016/j.niox.2022.04.001openalex-snapshot

Nitric oxide and skeletal muscle contractile function

inferred← citeshttps://doi.org/10.1016/j.sbi.2022.102391openalex-snapshot

Cryo-electron microscopy analysis of myosin at work and at rest

inferred← citeshttps://doi.org/10.1016/j.tox.2026.154452openalex-snapshot

Polystyrene microplastics induce skeletal muscle atrophy through disruption of anabolic signaling and mitochondrial function

inferred← citeshttps://doi.org/10.1016/j.ydbio.2023.04.002openalex-snapshot

Slow myosin heavy chain 1 is required for slow myofibril and muscle fibre growth but not for myofibril initiation

inferred← citeshttps://doi.org/10.1016/j.yjmcc.2021.02.009openalex-snapshot

The effect of variable troponin C mutation thin filament incorporation on cardiac muscle twitch contractions

inferred← citeshttps://doi.org/10.1017/s1431927620015871openalex-snapshot

CryoEM Structure of Drosophila Flight Muscle Thick Filaments at 7Å Resolution

inferred← citeshttps://doi.org/10.1021/acs.nanolett.8b02989openalex-snapshot

Nanothermometry Reveals Calcium-Induced Remodeling of Myosin

inferred← citeshttps://doi.org/10.1038/s41467-018-06191-4openalex-snapshot

Hypertrophic cardiomyopathy disease results from disparate impairments of cardiac myosin function and auto-inhibition

inferred← citeshttps://doi.org/10.1038/s41467-021-25601-8openalex-snapshot

The regulatory light chain mediates inactivation of myosin motors during active shortening of cardiac muscle

inferred← citeshttps://doi.org/10.1038/s41467-023-43538-yopenalex-snapshot

Discovery of a novel cardiac-specific myosin modulator using artificial intelligence-based virtual screening

inferred← citeshttps://doi.org/10.1038/s41467-024-46957-7openalex-snapshot

Myosin-binding protein C regulates the sarcomere lattice and stabilizes the OFF states of myosin heads

inferred← citeshttps://doi.org/10.1038/s41467-026-75106-5openalex-snapshot

Bioinspired electrochemical artificial muscles with low voltage redox triggering and spontaneous contraction

inferred← citeshttps://doi.org/10.1038/s41569-024-01063-5openalex-snapshot

Functional control of myosin motors in the cardiac cycle

inferred← citeshttps://doi.org/10.1038/s41586-023-06690-5openalex-snapshot

Structure of the native myosin filament in the relaxed cardiac sarcomere

inferred← citeshttps://doi.org/10.1038/s41586-023-06691-4openalex-snapshot

Cryo-EM structure of the human cardiac myosin filament

inferred← citeshttps://doi.org/10.1038/s41598-022-21425-8openalex-snapshot

Sarcomere dynamics revealed by a myofilament integrated FRET-based biosensor in live skeletal muscle fibers

inferred← citeshttps://doi.org/10.1038/s42003-022-04184-0openalex-snapshot

The force of the myosin motor sets cooperativity in thin filament activation of skeletal muscles

inferred← citeshttps://doi.org/10.1038/s42003-024-06265-8openalex-snapshot

Fast myosin binding protein C knockout in skeletal muscle alters length-dependent activation and myofilament structure

inferred← citeshttps://doi.org/10.1073/pnas.1809540115openalex-snapshot

Deciphering the super relaxed state of human β-cardiac myosin and the mode of action of mavacamten from myosin molecules to muscle fibers

inferred← citeshttps://doi.org/10.1073/pnas.1920632117openalex-snapshot

Myosin filament-based regulation of the dynamics of contraction in heart muscle

inferred← citeshttps://doi.org/10.1073/pnas.2023706118openalex-snapshot

Stress-dependent activation of myosin in the heart requires thin filament activation and thick filament mechanosensing

inferred← citeshttps://doi.org/10.1073/pnas.2024151118openalex-snapshot

The myosin II coiled-coil domain atomic structure in its native environment

inferred← citeshttps://doi.org/10.1073/pnas.2207615120openalex-snapshot

Structural OFF/ON transitions of myosin in relaxed porcine myocardium predict calcium-activated force

inferred← citeshttps://doi.org/10.1073/pnas.2209441119openalex-snapshot

Titin force in muscle cells alters lattice order, thick and thin filament protein formation

inferred← citeshttps://doi.org/10.1073/pnas.2302837120openalex-snapshot

Activation of skeletal muscle is controlled by a dual-filament mechano-sensing mechanism

inferred← citeshttps://doi.org/10.1073/pnas.2311883121openalex-snapshot

Structure of mavacamten-free human cardiac thick filaments within the sarcomere by cryoelectron tomography

inferred← citeshttps://doi.org/10.1073/pnas.2416324122openalex-snapshot

Dual-filament regulation of relaxation in mammalian fast skeletal muscle

inferred← citeshttps://doi.org/10.1073/pnas.2504562122openalex-snapshot

A FRET assay to monitor different structural states of human β-cardiac myosin including the interacting-heads motif

inferred← citeshttps://doi.org/10.1073/pnas.2535527123openalex-snapshot

Subsarcomeric regulation of thin and thick filaments in skeletal muscle myofibrils

inferred← citeshttps://doi.org/10.1074/jbc.ra118.001938openalex-snapshot

Dilated cardiomyopathy myosin mutants have reduced force-generating capacity

inferred← citeshttps://doi.org/10.1080/02640414.2026.2705723openalex-snapshot

Intermuscular coordination adaptations to strength training: Insights from muscle synergy analysis during squats with different loads

inferred← citeshttps://doi.org/10.1085/jgp.201812165openalex-snapshot

Nebulin and titin modulate cross-bridge cycling and length-dependent calcium sensitivity

inferred← citeshttps://doi.org/10.1085/jgp.201812210openalex-snapshot

Myosin lever arm orientation in muscle determined with high angular resolution using bifunctional spin labels

inferred← citeshttps://doi.org/10.1085/jgp.201812288openalex-snapshot

Toward an understanding of the regulation of myofibrillar function

inferred← citeshttps://doi.org/10.1085/jgp.201912323openalex-snapshot

The enduring relationship between myosin enzymatic activity and the speed of muscle contraction

inferred← citeshttps://doi.org/10.1085/jgp.201912424openalex-snapshot

Low temperature traps myosin motors of mammalian muscle in a refractory state that prevents activation

inferred← citeshttps://doi.org/10.1085/jgp.201912444openalex-snapshot

A case for reduced energy utilization associated with spatial disorder of myosin in skeletal muscle

inferred← citeshttps://doi.org/10.1085/jgp.201912446openalex-snapshot

The mechanism of thin filament regulation: Models in conflict?

inferred← citeshttps://doi.org/10.1085/jgp.202012604openalex-snapshot

Multiscale modeling of twitch contractions in cardiac trabeculae

inferred← citeshttps://doi.org/10.1085/jgp.202012713openalex-snapshot

Dependence of thick filament structure in relaxed mammalian skeletal muscle on temperature and interfilament spacing

inferred← citeshttps://doi.org/10.1085/jgp.202012729openalex-snapshot

Making waves: A proposed new role for myosin-binding protein C in regulating oscillatory contractions in vertebrate striated muscle

inferred← citeshttps://doi.org/10.1085/jgp.202112896openalex-snapshot

Myosin motors that cannot bind actin leave their folded OFF state on activation of skeletal muscle

inferred← citeshttps://doi.org/10.1085/jgp.202113012openalex-snapshot

Structural basis of the super- and hyper-relaxed states of myosin II

inferred← citeshttps://doi.org/10.1085/jgp.202113029openalex-snapshot

Cooling intact and demembranated trabeculae from rat heart releases myosin motors from their inhibited conformation

inferred← citeshttps://doi.org/10.1085/jgp.202213087openalex-snapshot

Single-molecule imaging reveals how mavacamten and PKA modulate ATP turnover in skeletal muscle myofibrils

inferred← citeshttps://doi.org/10.1085/jgp.202213265openalex-snapshot

Calcium activation through thick and thin?

inferred← citeshttps://doi.org/10.1085/jgp.202213276openalex-snapshot

Myosin-binding protein C stabilizes, but is not the sole determinant of SRX myosin in cardiac muscle

inferred← citeshttps://doi.org/10.1085/jgp.202313393openalex-snapshot

Dependence of myosin filament structure on intracellular calcium concentration in skeletal muscle

inferred← citeshttps://doi.org/10.1085/jgp.202313414openalex-snapshot

Myosin and tropomyosin–troponin complementarily regulate thermal activation of muscles

inferred← citeshttps://doi.org/10.1085/jgp.202313494openalex-snapshot

Changing face of contractile activation in striated muscle at physiological temperature

inferred← citeshttps://doi.org/10.1085/jgp.202413545openalex-snapshot

Calcium has a direct effect on thick filament activation in porcine myocardium

inferred← citeshttps://doi.org/10.1085/jgp.202413678openalex-snapshot

Myosin binding protein-C modulates loaded sarcomere shortening in rodent permeabilized cardiac myocytes

inferred← citeshttps://doi.org/10.1085/jgp.202413722openalex-snapshot

Modeling cardiac contractile cooperativity across species

inferred← citeshttps://doi.org/10.1088/1361-6528/abe6c7openalex-snapshot

Nanomaterials and their applications on bio-inspired wearable electronics

inferred← citeshttps://doi.org/10.1093/pnasnexus/pgae039openalex-snapshot

The structural OFF and ON states of myosin can be decoupled from the biochemical super- and disordered-relaxed states

inferred← citeshttps://doi.org/10.1098/rsif.2021.0585openalex-snapshot

Geometric frustration in the myosin superlattice of vertebrate muscle

inferred← citeshttps://doi.org/10.1101/2020.08.20.259283openalex-snapshot

Phosphate binding induced force-reversal occurs via slow backward cycling of cross-bridges

inferred← citeshttps://doi.org/10.1101/2022.09.16.22279894openalex-snapshot

Intraoperative phrenic stimulation offsets diaphragm fiber weakness during cardiothoracic surgery

inferred← citeshttps://doi.org/10.1101/2023.04.11.536274openalex-snapshot

Cryo-EM structure of the human cardiac myosin filament

inferred← citeshttps://doi.org/10.1101/2023.04.11.536387openalex-snapshot

In situ structures from relaxed cardiac myofibrils reveal the organization of the muscle thick filament

inferred← citeshttps://doi.org/10.1101/2023.05.15.540775openalex-snapshot

Human light meromyosin mutations linked to skeletal myopathies disrupt the coiled coil structure and myosin head sequestration

inferred← citeshttps://doi.org/10.1101/2023.09.10.556972openalex-snapshot

Myosin-binding protein C forms C-links and stabilizes OFF states of myosin

inferred← citeshttps://doi.org/10.1101/2023.10.18.562891openalex-snapshot

The structural OFF and ON states of myosin can be decoupled from the biochemical super-relaxed and disordered-relaxed states

inferred← citeshttps://doi.org/10.1101/2024.06.06.597809openalex-snapshot

An atomistic model of myosin interacting heads motif dynamics and their modification by 2’-deoxy-ADP

inferred← citeshttps://doi.org/10.1101/2024.12.05.626936openalex-snapshot

A FRET assay to quantitate levels of the human β-cardiac myosin interacting heads motif based on its near-atomic resolution structure

inferred← citeshttps://doi.org/10.1101/2025.10.31.685881openalex-snapshot

Biophysical model for predicting muscle short-range stiffness during movement

inferred← citeshttps://doi.org/10.1101/2025.11.21.689690openalex-snapshot

Sub-sarcomeric regulation of thin and thick filaments in skeletal muscle myofibrils

inferred← citeshttps://doi.org/10.1101/2025.11.24.689918openalex-snapshot

Piperine activates the thick filament of resting rat skeletal muscle, enhancing dynamic contractility in a fibre-type-dependent manner

inferred← citeshttps://doi.org/10.1101/cshperspect.a041477openalex-snapshot

The Diversity of Skeletal Muscle Fiber Types

inferred← citeshttps://doi.org/10.1103/physreve.105.034405openalex-snapshot

Parallel path mechanisms lead to nonmonotonic force-velocity curves and an optimum load for molecular motor function

inferred← citeshttps://doi.org/10.1107/s205327332209934xopenalex-snapshot

Cardiac myosin filaments are directly regulated by calcium

inferred← citeshttps://doi.org/10.1111/apha.13425openalex-snapshot

Chaperone co‐inducer BGP‐15 mitigates early contractile dysfunction of the soleus muscle in a rat ICU model

inferred← citeshttps://doi.org/10.1111/asj.13226openalex-snapshot

Myosin: Formation and maintenance of thick filaments

inferred← citeshttps://doi.org/10.1111/bph.70247openalex-snapshot

Transcriptional and functional effects of mavacamten in multiple porcine and human models with hypertrophic cardiomyopathy

inferred← citeshttps://doi.org/10.1113/jp280402openalex-snapshot

Myosin dynamics during relaxation in mouse soleus muscle and modulation by 2′‐deoxy‐ATP

inferred← citeshttps://doi.org/10.1113/jp280664openalex-snapshot

A bright light on myosin to study skeletal muscle relaxation

inferred← citeshttps://doi.org/10.1113/jp283048openalex-snapshot

Activation of the myosin motors in fast‐twitch muscle of the mouse is controlled by mechano‐sensing in the myosin filaments

inferred← citeshttps://doi.org/10.1113/jp283574openalex-snapshot

Thick filament activation is different in fast‐ and slow‐twitch skeletal muscle

inferred← citeshttps://doi.org/10.1113/jp286072openalex-snapshot

Differences in thick filament activation in fast rodent skeletal muscle and slow porcine cardiac muscle

inferred← citeshttps://doi.org/10.1113/jp287434openalex-snapshot

Load‐dependence of the activation of myosin filaments in heart muscle

inferred← citeshttps://doi.org/10.1113/jp289201openalex-snapshot

Myosin‐binding protein C slows cardiac myofibril relaxation kinetics

inferred← citeshttps://doi.org/10.1113/jp290232openalex-snapshot

Distinct distributions of myosin motor conformations during contraction of slow and fast skeletal muscle

inferred← citeshttps://doi.org/10.1113/jp290962openalex-snapshot

Piperine disrupts the OFF state of the resting thick filament of rat skeletal muscle, enhancing dynamic contractility in a fibre‐type‐dependent manner

inferred← citeshttps://doi.org/10.1126/sciadv.abo7622openalex-snapshot

Mavacamten, a precision medicine for hypertrophic cardiomyopathy: From a motor protein to patients

inferred← citeshttps://doi.org/10.1146/annurev-physiol-042222-022728openalex-snapshot

Regulating Striated Muscle Contraction: Through Thick and Thin

inferred← citeshttps://doi.org/10.1152/japplphysiol.00788.2018openalex-snapshot

Muscle thixotropy—where are we now?

inferred← citeshttps://doi.org/10.1152/physrev.00014.2023openalex-snapshot

Mechanisms of myosin II force generation: insights from novel experimental techniques and approaches

inferred← citeshttps://doi.org/10.1172/jci.insight.172322openalex-snapshot

Human skeletal myopathy myosin mutations disrupt myosin head sequestration

inferred← citeshttps://doi.org/10.1172/jci.insight.178131openalex-snapshot

Myosin folding boosts solubility in cardiac muscle sarcomeres

inferred← citeshttps://doi.org/10.1172/jci172599openalex-snapshot

A Laing distal myopathy–associated proline substitution in the β-myosin rod perturbs myosin cross-bridging activity

inferred← citeshttps://doi.org/10.1242/jeb.247436openalex-snapshot

On the rate-limiting dynamics of force development in muscle

inferred← citeshttps://doi.org/10.1242/jeb.252866openalex-snapshot

Repeated stretch–shortening cycles enhance force and work despite brief deactivation between cycles

inferred← citeshttps://doi.org/10.12794/metadc2179318openalex-snapshot

Anti-S2 Peptides and Antibodies Binding Effect on Myosin S2 and Anti-S2 Peptide's Ability to Reach the Cardiomyocytes in vivo and Interfere in Muscle Contraction

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1014748openalex-snapshot

Cross-bridge model for predicting muscle short-range stiffness during movement

inferred← citeshttps://doi.org/10.1371/journal.pone.0320936openalex-snapshot

Intraoperative phrenic nerve stimulation to prevent diaphragm fiber weakness during thoracic surgery

inferred← citeshttps://doi.org/10.18203/2320-6012.ijrms20240691openalex-snapshot

Significance of calcium: its correlation with red and white muscle contraction, fatigue and potential

inferred← citeshttps://doi.org/10.20517/rdodj.2024.34openalex-snapshot

The necessity for skeletal muscle contractile assays to assess treatment efficacy in DMD

inferred← citeshttps://doi.org/10.20944/preprints202507.2317.v1openalex-snapshot

Myosin Heads and Thick Filaments: Recent and Older Experiments and Hypotheses

inferred← citeshttps://doi.org/10.2139/ssrn.5051285openalex-snapshot

Dose-Response Relationship between Dietary Nitrate Intake and Nitric Oxide Congeners in Various Blood Compartments and Skeletal Muscle: Differential Effects on Skeletal Muscle Torque and Velocity

inferred← citeshttps://doi.org/10.25026/jsk.v5i6.2216openalex-snapshot

Studi Komparatif Efektivitas Mckenzie Exercises dan William Flexion Exercises pada Myogenic Low Back Pain

inferred← citeshttps://doi.org/10.26508/lsa.202000823openalex-snapshot

CryoEM structure ofDrosophilaflight muscle thick filaments at 7 Å resolution

inferred← citeshttps://doi.org/10.32469/10355/85774openalex-snapshot

Skeletal muscle weakness and mitochondrial dysfunction in the osteogenesis imperfecta murine (oim) model

inferred← citeshttps://doi.org/10.32469/10355/91015openalex-snapshot

Molecular regulation of sarcomere function

inferred← citeshttps://doi.org/10.3389/fphys.2018.00736openalex-snapshot

Thick Filament Mechano-Sensing in Skeletal and Cardiac Muscles: A Common Mechanism Able to Adapt the Energetic Cost of the Contraction to the Task

inferred← citeshttps://doi.org/10.3389/fphys.2019.00316openalex-snapshot

The Effect of the Stretch-Shortening Cycle in the Force–Velocity Relationship and Its Association With Physical Function in Older Adults With COPD

inferred← citeshttps://doi.org/10.3389/fphys.2019.00769openalex-snapshot

On the Shape of the Force-Velocity Relationship in Skeletal Muscles: The Linear, the Hyperbolic, and the Double-Hyperbolic

inferred← citeshttps://doi.org/10.3389/fphys.2020.00144openalex-snapshot

Cycling Cross-Bridges Contribute to Thin Filament Activation in Human Slow-Twitch Fibers

inferred← citeshttps://doi.org/10.3389/fphys.2020.01043openalex-snapshot

Multiscale Modeling of Cardiovascular Function Predicts That the End-Systolic Pressure Volume Relationship Can Be Targeted via Multiple Therapeutic Strategies

inferred← citeshttps://doi.org/10.3389/fphys.2022.947206openalex-snapshot

Effects of omecamtiv mecarbil on the contractile properties of skinned porcine left atrial and ventricular muscles

inferred← citeshttps://doi.org/10.3389/fphys.2023.1170396openalex-snapshot

Editorial: Recent Advances on Myocardium Physiology, Volume II

inferred← citeshttps://doi.org/10.3389/fphys.2024.1476876openalex-snapshot

Phosphate rebinding induces force reversal via slow backward cycling of cross-bridges

inferred← citeshttps://doi.org/10.3390/biom14010069openalex-snapshot

Leveraging Biomaterial Platforms to Study Aging-Related Neural and Muscular Degeneration

inferred← citeshttps://doi.org/10.3390/biomedicines13030703openalex-snapshot

Thick-Filament-Based Regulation and the Determinants of Force Generation

inferred← citeshttps://doi.org/10.3390/ijms19092643openalex-snapshot

Myosin Head Configurations in Resting and Contracting Murine Skeletal Muscle

inferred← citeshttps://doi.org/10.3390/ijms22137037openalex-snapshot

The Synergic Role of Actomyosin Architecture and Biased Detachment in Muscle Energetics: Insights in Cross Bridge Mechanism beyond the Lever-Arm Swing

inferred← citeshttps://doi.org/10.3390/ijms23063052openalex-snapshot

Small Angle X-ray Diffraction as a Tool for Structural Characterization of Muscle Disease

inferred← citeshttps://doi.org/10.3390/ijms232314517openalex-snapshot

EMD-57033 Augments the Contractility in Porcine Myocardium by Promoting the Activation of Myosin in Thick Filaments

inferred← citeshttps://doi.org/10.3390/ijms232416223openalex-snapshot

Cardiac Sarcomere Signaling in Health and Disease

inferred← citeshttps://doi.org/10.3390/ijms24076265openalex-snapshot

Muscle Mechanics and Thick Filament Activation: An Emerging Two-Way Interaction for the Vertebrate Striated Muscle Fine Regulation

inferred← citeshttps://doi.org/10.3390/ijms24108474openalex-snapshot

Using Multiscale Simulations as a Tool to Interpret Equatorial X-ray Fiber Diffraction Patterns from Skeletal Muscle

inferred← citeshttps://doi.org/10.3390/ijms25084546openalex-snapshot

Developmental, Physiological and Phylogenetic Perspectives on the Expression and Regulation of Myosin Heavy Chains in Craniofacial Muscles

inferred← citeshttps://doi.org/10.3390/proteomes7020025openalex-snapshot

Characterization of Contractile Proteins from Skeletal Muscle Using Gel-Based Top-Down Proteomics

inferred← citeshttps://doi.org/10.3410/f.733814468.793563791openalex-snapshot

Faculty Opinions recommendation of Deciphering the super relaxed state of human β-cardiac myosin and the mode of action of mavacamten from myosin molecules to muscle fibers.

inferred← citeshttps://doi.org/10.3969/j.issn.1673-4254.2018.06.16openalex-snapshot

[AMPK regulates mitochondrial oxidative stress in C2C12 myotubes induced by electrical stimulations of different intensities].

inferred← citeshttps://doi.org/10.4081/ejtm.2020.9311openalex-snapshot

Muscle hypertrophy and muscle strength: dependent or independent variables? A provocative review

inferred← citeshttps://doi.org/10.4162/nrp.2025.19.4.511openalex-snapshot

Yuja peel hot water extract protects against dexamethasone-induced skeletal muscle atrophy through the PI3K-Akt-mTOR/FoxO3α signaling pathway

inferred← citeshttps://doi.org/10.4172/2167-7956.1000162openalex-snapshot

Effect of Electrical Stimulation at Different Time on Mitochondrial Function of C2C12 Myotubes

inferred← citeshttps://doi.org/10.64898/2026.02.16.706210openalex-snapshot

Myosin Filaments of Vertebrate Skeletal and Cardiac Muscle are Highly Similar, but not Identical

inferred← citeshttps://doi.org/10.64898/2026.05.18.726029openalex-snapshot

Porcine Left Atrial and Ventricular Thick Filaments Exhibit Distinct Resting Structures and Calcium-dependent Responses

inferred← citeshttps://doi.org/10.70675/97b47775z4ab8z4850z8140z5b58f48edb7copenalex-snapshot

Effect of velocity on force production capabilities during single and repeated high-intensity exercises

inferred← citeshttps://doi.org/10.7554/elife.107730openalex-snapshot

Probing relaxed myosin states in hypertrophic cardiomyopathy by second harmonic-generation microscopy

inferred← citeshttps://doi.org/10.7554/elife.107730.1openalex-snapshot

Probing relaxed myosin states in hypertrophic cardiomyopathy by second harmonic-generation microscopy

inferred← citeshttps://doi.org/10.7554/elife.107730.3openalex-snapshot

Probing relaxed myosin states in hypertrophic cardiomyopathy by second harmonic-generation microscopy

inferred← citeshttps://doi.org/10.7554/elife.63703openalex-snapshot

To lie or not to lie: Super-relaxing with myosins

inferred← citeshttps://doi.org/10.7554/elife.64107openalex-snapshot

Graded titin cleavage progressively reduces tension and uncovers the source of A-band stability in contracting muscle

inferred← citeshttps://doi.org/10.7554/elife.68211openalex-snapshot

Myosin-based regulation of twitch and tetanic contractions in mammalian skeletal muscle

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.