Cited by 1,608Cardiomyopathy and Myosin StudiesMuscle Physiology and DisordersCellular Mechanics and Interactions

The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.

Structural Changes in Muscle During Contraction: Interference Microscopy of Living Muscle Fibres

HUXLEY, A. F., NIEDERGERKE, R.·1954·Nature

DOI 10.1038/173971a0

Open this paper in CoChat — free account

Integrity signals

Registry

Crossref · 10.1038/173971a0

Cites

8 of 8 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

The abrupt transition from rest to activity in muscle
Hill, A. V. (1949) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1949.0033 · Cited by 464
The isometric length‐tension diagram of isolated skeletal muscle fibers of the frog
Ramsey, R. W., & Street, S. F. (1940) · Journal of Cellular and Comparative Physiology · doi:10.1002/jcp.1030150103 · Cited by 457
Electron microscope studies of the organisation of the filaments in striated muscle
Huxley, H. E. (1953) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(53)90156-5 · Cited by 304
Elektronenmikroskopische Untersuchungen an Muskelfibrillen bei totaler und partieller Extraktion des L-Myosin
Hasselbach, W. (1953) · Zeitschrift für Naturforschung B · doi:10.1515/znb-1953-0901 · Cited by 61
Die Struktur der quergestreiften, lebenden Muskelfaser des Frosches in Ruhe und während der Kontraktion1
Buchthal, F., Knappeis, G. G., & Lindhard, J. (1936) · Skandinavisches Archiv Für Physiologie · doi:10.1111/j.1748-1716.1936.tb01463.x · Cited by 43
Studies of living muscles. II. Histological changes in single fibers of striated muscle during contraction and clotting
Speidel, C. C. (1939) · American Journal of Anatomy · doi:10.1002/aja.1000650304 · Cited by 42
Diffraction patterns of the frog sartorius and sarcomere behavior under stretch
Sandow, A. (1936) · Journal of Cellular and Comparative Physiology · doi:10.1002/jcp.1030090105 · Cited by 32
Structural changes during contraction in the striped muscle of the frog
Jordan, H. E. (1934) · American Journal of Anatomy · doi:10.1002/aja.1000550106 · Cited by 13

Flagged first, then by citations

Show all 8 references

Research works printed but not linked: 4

Krause, W., “Die motorischen Endplatten der qnergestreiften Muskelfasern” (Hahn, Hannover, 1869). Engelmann, T. W., Pflüg. Arch. ges. Physiol., 23, 571 (1880). Rollett, A., Denkschr. Akad. Wiss. Wien, 58, 41 (1891). Hürthle, K., Pflüg. Arch. ges. Physiol., 126, 1 (1909).
Hill, A. V., Proc. Roy. Soc., B, 136, 399 (1949).
Huxley, A. F., J. Physiol., 117, 52 P (1952).
Jasper, H. H., and Pezard, A., C.R. Acad. Sci., Paris, 198, 499 (1934).

Sorted by citations

Items 901–1,000 of 1,000

Progress in biophysics and molecular biology: A brief history of the journal
Noble, D., Blundell, T. L., & Kohl, P. K. (2018) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2018.11.008 · Cited by 8
Structure of the Thin Filament in Human iPSC-derived Cardiomyocytes and its Response to Heart DiseasePreprint
Woldeyes, R. A., Nishiga, M., Roest, A. S. V., Engel, L., Giri, P., Montenegro, G., Dunn, A. R., Spudich, J. A., Bernstein, D., Schmid, M. F., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.26.564098 · Cited by 8
Program with last minute abstracts of the Padua Days on Muscle and Mobility Medicine, 27 February – 2 March, 2024 (2024Pdm3)
Zampieri, S., Bersch, I., Smeriglio, P., Barbieri, E., Boncompagni, S., Maccarone, M. C., & Carraro, U. (2024) · European Journal of Translational Myology · doi:10.4081/ejtm.2024.12346 · Cited by 8
Beyond calcium: cross-bridge binding regulates titin's contribution to muscle force
Desai, D., Sekhon, A., Tiessen, C., Mebrahtu, A., & Herzog, W. (2025) · Journal of Experimental Biology · doi:10.1242/jeb.250931 · Cited by 7
Levels in Biological Organisms: Hierarchy of Production Mechanisms, Heterarchy of Control Mechanisms
Bechtel, W. (2021) · The Monist · doi:10.1093/monist/onab029 · Cited by 7
Mechanisms and Risk Factors for Premature Ventricular Contraction Induced Cardiomyopathy
Shen, X., Zhu, X., Zuo, L., Liu, X., & Qin, M. (2023) · Reviews in Cardiovascular Medicine · doi:10.31083/j.rcm2412353 · Cited by 7
Glutamate 139 of Tropomyosin is Critical for Cardiac Thin Filament Blocked-State Stabilization
Barry, M. E., Rynkiewicz, M. J., Pavadai, E., Viana, A., Lehman, W., & Moore, J. R. (2023) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2024.01.004 · Cited by 7
Impact of lengthening velocity on the generation of eccentric force by slow-twitch muscle fibers in long stretches
Weidner, S., Tomalka, A., Rode, C., & Siebert, T. (2024) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-024-02991-4 · Cited by 7
Bioelectronic tools for understanding the universal language of electrical signaling across species and kingdoms
Shukla, S., Comerci, C. J., Süel, G. M., & Jahed, Z. (2024) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2024.116843 · Cited by 7
Understanding muscle from its length
Allen, D. G., & Westerblad, H. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.137067 · Cited by 7
Calcium and muscle contraction: the triumph and tragedy of Lewis Victor Heilbrunn
Rall, J. A. (2019) · AJP Advances in Physiology Education · doi:10.1152/advan.00094.2019 · Cited by 7
From “sliding” to “winding” filaments theory: A narrative review of mechanisms behind skeletal muscle contraction
Montesano, P., Palermi, S., Massa, B., & Mazzeo, F. (2020) · Spring Conferences of Sports Science · doi:10.14198/jhse.2020.15.proc3.31 · Cited by 7
A dynamic calcium-force relationship model for sag behavior in fast skeletal muscle
Kim, H., & Heckman, C. J. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011178 · Cited by 7
The Rest-Pause Biceps Curl Exercise Effect on Biceps Brachii Muscle of Women: A Study of Mechanical Responsiveness
Dereshgi, H. A. (2023) · IEEE Access · doi:10.1109/access.2023.3325669 · Cited by 7
Surface-Controlled Properties of Myosin Studied by Electric Field Modulation
van Zalinge, H., Ramsey, L., Aveyard, J., Persson, M., Månsson, A., & Nicolau, D. V. (2015) · Langmuir · doi:10.1021/acs.langmuir.5b01549 · Cited by 7
The unit event of sliding of the chemo-mechanical enzyme composed of myosin and actin with regulatory proteins
Oosawa, F. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.11.186 · Cited by 7
Angle Specific Analysis of Side-to-Side Asymmetry in the Shoulder Rotators
Ruas, C. V., Pinto, R. S., Cadore, E. L., & Brown, L. E. (2015) · Sports · doi:10.3390/sports3030236 · Cited by 7
Skeletal Muscle Excitation–Contraction Coupling
Schneider, M. F., & Hernández‐Ochoa, E. O. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-381510-1.00057-0 · Cited by 7
Muscle sliding filaments
Clarke, M. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2581 · Cited by 7
Physiology of Skeletal Muscle
Windhorst, U., & Mommaerts, W. F. H. M. (1996) · Springer eBooks · doi:10.1007/978-3-642-60946-6_46 · Cited by 7
In Vivo Assessment of Lower Limb Muscle Stress State Based on Shear Wave Elastography
Liu, J., Wang, K., Wu, J., Miao, H., Qian, Z., Ren, L., & Ren, L. (2020) · IEEE Access · doi:10.1109/access.2020.3007145 · Cited by 7
Paraspinal Muscle Contractile Function is Impaired in the ENT1-deficient Mouse Model of Progressive Spine Pathology
Noonan, A. M., Séguin, C. A., & Brown, S. H. M. (2020) · Spine · doi:10.1097/brs.0000000000003882 · Cited by 7
A numerical study of the stiffness of a sarcomere
Forcinito, M. A., Epstein, M., & Herzog, W. (1998) · Journal of Electromyography and Kinesiology · doi:10.1016/s1050-6411(97)00030-8 · Cited by 7
Vitamin D and Skeletal Muscle
Girgis, C. M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809965-0.00035-5 · Cited by 7
An Introduction to Actin and Actin‐Rich Structures
Vogl, A. W., & Guttman, J. A. (2018) · The Anatomical Record · doi:10.1002/ar.23960 · Cited by 7
The Synergic Role of Actomyosin Architecture and Biased Detachment in Muscle Energetics: Insights in Cross Bridge Mechanism beyond the Lever-Arm Swing
Marcucci, L., Fukunaga, H., Yanagida, T., & Iwaki, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22137037 · Cited by 7
Skeletal Muscle
Fung, Y. C. (1993) · Springer eBooks · doi:10.1007/978-1-4757-2257-4_9 · Cited by 7
The time course of early changes in the rate of tension development in electrically‐stimulated frog toe muscle: effects of muscle length, temperature and twitch‐potentiators
Foulks, J. G., & Perry, F. A. (1966) · The Journal of Physiology · doi:10.1113/jphysiol.1966.sp007990 · Cited by 7
Influence of dispersion in myosin filament orientation and anisotropic filament contractions in smooth muscle
Kroon, M. (2010) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2010.11.037 · Cited by 7
Getting to grips with contraction: the interplay of structure and biochemistry
Huxley, H. E. (1998) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(97)01163-8 · Cited by 7
The structure of the vertebrate striated muscle thin filament: a tribute to the contributions of Jean Hanson
Lehman, W., & Craig, R. W. (2004) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-004-3148-z · Cited by 7
A Historical Perspective of Actin Assembly and Its Interactions
Oosawa, F. (2001) · Results and problems in cell differentiation · doi:10.1007/978-3-540-46560-7_2 · Cited by 7
Unfolding transitions in myosin give rise to the double-hyperbolic force velocity relation in muscle
Nielsen, B. (2003) · Journal of Physics Condensed Matter · doi:10.1088/0953-8984/15/18/309 · Cited by 7
Der Stoffwechsel des Herzens
Bing, R. J., & Beuren, A. J. (1959) · Springer eBooks · doi:10.1007/978-3-642-94742-1_2 · Cited by 7
A Periodic Cytoskeletal Lattice in Striated Muscle
Cooke, P. H. (1985) · Springer eBooks · doi:10.1007/978-1-4757-4723-2_9 · Cited by 7
Mechanical Properties and Performance in Skeletal Muscles
Herzog, W. (2000) · Wiley eBooks · doi:10.1002/9780470693797.ch2 · Cited by 7
Mechanical Muscle Models and Their Application to Force and Power Production
Herzog, W., & Ait‐Haddou, R. (2003) · Wiley eBooks · doi:10.1002/9780470757215.ch9 · Cited by 7
Titin Regulation of Active and Passive Force in Skeletal Muscle
DuVall, M. (2015) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/28459 · Cited by 7
Anatomical and physiological considerations in cardiac preservation
Willman, V. L., & Barner, H. B. (1969) · Cryobiology · doi:10.1016/s0011-2240(69)80107-0 · Cited by 7
Conformational relationships between distinct regions in the myosin molecule
SCHAUB, M. C., Watterson, J. G., Loth, K., & Waser, P. G. (1979) · Biochimie · doi:10.1016/s0300-9084(79)80273-4 · Cited by 7
The binding of H-meromyosin on cross-striated myofibrils
Szentkirályi, E. (1961) · Experimental Cell Research · doi:10.1016/0014-4827(61)90082-9 · Cited by 7
ULTRASTRUCTURE OF THAW RIGOR BOVINE MUSCLE
Okubanjo, A. O., Stouffer, J. R., Bensadoun, A., & Sack, W. O. (1975) · Journal of Food Science · doi:10.1111/j.1365-2621.1975.tb12517.x · Cited by 7
Reactivity of myosin to antibodies in cross-striated chick myofibrils II. Contracted muscle
Szent‐Györgyi, A. G., & Holtzer, H. (1963) · Biochimica et Biophysica Acta · doi:10.1016/0006-3002(63)91423-9 · Cited by 7
Variations of reflex parameters and their implications for the control of movements
Capaday, C., & Stein, R. B. (1986) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00051293 · Cited by 7
Contraction Bands: Differences between Physiologically vs. Maximally Activated Single Heart Muscle Cells
Krueger, J. W., & London, B. (1984) · Advances in experimental medicine and biology · doi:10.1007/978-1-4684-4703-3_11 · Cited by 7
The Use of Inotropic Agents in Acute and Chronic Congestive Heart Failure
Sanders, M., Kostis, J. B., & Frishman, W. H. (1989) · Medical Clinics of North America · doi:10.1016/s0025-7125(16)30674-5 · Cited by 7
Towards a model-based estimator of muscle length and force using muscle afferent signals for real time FES control
Coste, C., & Yoshida, K. (2005) · IEEE EUROCON - International Conference on Computer as a Tool (EUROCON) · doi:10.1109/eurcon.2005.1629854 · Cited by 7
A FRET assay to quantitate levels of the human β-cardiac myosin interacting heads motif based on its near-atomic resolution structurePreprint
Goluguri, R. R., Guhathakurta, P., Nandwani, N., Dawood, A., Yakota, S., Roopnarine, O., Thomas, D. D., Spudich, J. A., & Ruppel, K. M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.05.626936 · Cited by 7
Fast myosin binding protein C knockout in skeletal muscle alters length-dependent activation and myofilament structure
Hessel, A. L., Kuehn, M. N., Han, S.-W., Ma, W., Irving, T. C., Momb, B. A., Song, T., Sadayappan, S., Linke, W. A., & Palmer, B. M. (2024) · Communications Biology · doi:10.1038/s42003-024-06265-8 · Cited by 6
Myosin light chain proteins cooperatively promote sarcomere growth in fast-twitch muscle
Adekeye, T. E., Hupper, T., Easterbrooks, T., Teets, E. M., Tomak, E. A., Waterman, S., Sprague, K., White, A., Coffin, M., Tanaka, D. K., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-73861-z · Cited by 7
Structure-Function Relationships in Muscle Fibres: MyoRobot Online Assessment of Muscle Fibre Elasticity and Sarcomere Length Distributions
Haug, M., Ritter, P., Michael, M., Reischl, B., Schürmann, S., Prols, G., & Friedrich, O. (2021) · IEEE Transactions on Biomedical Engineering · doi:10.1109/tbme.2021.3089739 · Cited by 6
Experimental basis of the hypotheses on the mechanism of skeletal muscle contraction.
Grazi, E. (2011) · Europe PMC (PubMed Central) · Cited by 6
Andrew Fielding Huxley (1917–2012)
Huang, C. L.-H. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.238923 · Cited by 6
Thin Filament‐Reconstituted Skinned Muscle Fibers for the Study of Muscle Physiology
Higuchi, S., Tsukasaki, Y., Fukuda, N., Kurihara, S., & Fujita, H. (2011) · BioMed Research International · doi:10.1155/2011/486021 · Cited by 6
Nature’s autonomous oscillators
Mayr, H. G., Yee, J.-H., Mayr, M., & Schnetzler, R. (2012) · Natural Science · doi:10.4236/ns.2012.44034 · Cited by 6
Evidence About the Structural Behaviour of Myosin Crossbridges During Muscle Contraction
Huxley, H. E. (2007) · Springer eBooks · doi:10.1007/978-4-431-38453-3_27 · Cited by 6
Analysis of Differential Proteins in Two Wing-Type Females ofSogatella furcifera(Hemiptera: Delphacidae)
Liang, Z.-Q., Song, S., Liang, S., & Wang, F. (2016) · Journal of Insect Science · doi:10.1093/jisesa/iew024 · Cited by 6
The Contractile Machinery of Skeletal Muscle
Franzini‐Armstrong, C., & Sweeney, H. L. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-381510-1.00058-2 · Cited by 6
Multiscale Modeling and Numerical Simulation of Calcium Cycling in Cardiac Myocytes
Chamakuri, N., Neubert, W., Gilbert, S., Vierheller, J., Warnecke, G., & Falcke, M. (2018) · Multiscale Modeling and Simulation · doi:10.1137/17m1121639 · Cited by 6
Brazilian Jiu-Jitsu fighters present greatest rapid and maximal strength imbalances at extreme elbow angles
Follmer, B., Ruas, C. V., Dellagrana, R. A., de Lima, L. A. P., Pinto, R. S., & Diefenthaeler, F. (2020) · Journal of Bodywork and Movement Therapies · doi:10.1016/j.jbmt.2020.11.013 · Cited by 6
Evaluation of sEMG Signal Features and Segmentation Parameters for Limb Movement Prediction Using a Feedforward Neural Network
Leserri, D., Grimmelsmann, N., Mechtenberg, M., Meyer, H. G., & Schneider, A. (2022) · Mathematics · doi:10.3390/math10060932 · Cited by 6
Introduction
Coluccio, L. M. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-38062-5_1 · Cited by 6
Multiscale Experimental Characterization and Computational Modeling of the Human Aorta
Dalbosco, M., Haspinger, D. C., Li, K., Murtada, S., Pukaluk, A., Rolf‐Pissarczyk, M., Sherifova, S., & Sommer, G. (2022) · Studies in mechanobiology, tissue engineering and biomaterials · doi:10.1007/978-3-030-92339-6_1 · Cited by 6
Extreme-value analysis of intracellular cargo transport by motor proteins
Naoi, T., Kagawa, Y., Nagino, K., Niwa, S., & Hayashi, K. (2024) · Communications Physics · doi:10.1038/s42005-024-01538-4 · Cited by 6
4.29 Bioenergy Conversion
Çatak, J., Semerciöz, A. S., Yalçınkaya, B. H., Yılmaz, B., & Özilgen, M. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809597-3.00447-8 · Cited by 6
Comparative Study of Transcriptome in the Hearts Isolated from Mice, Rats, and Humans
Okada, D., Okamoto, Y., Io, T., Oka, M., Kobayashi, D., Ito, S., Yamada, R., Ishii, K., & Ono, K. (2022) · Biomolecules · doi:10.3390/biom12060859 · Cited by 6
Stretch and Shortening of Skeletal Muscles Activated Along the Ascending Limb of the Force–Length Relation
Rassier, D. E., & Pun, C. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-6366-6_10 · Cited by 6
Motor variability but functional specificity: Demise of the concept of motor commands
Reed, E. S. (1986) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00051517 · Cited by 7
Critérios mecânicos para progressão de exercícios de rotação interna e externa do ombro no plano sagital
Toledo, J., Ribeiro, D. C., & Loss, J. (2007) · Brazilian Journal of Physical Therapy · doi:10.1590/s1413-35552007000100009 · Cited by 6
Entropic Elasticity in the Generation of Muscle Force – A Theoretical Model
Nielsen, B. (2002) · Journal of Theoretical Biology · doi:10.1006/jtbi.2002.3113 · Cited by 6
Ultrastructural and mechanical properties of electrically inexcitable skeletal muscle fibers of the crustacean Atya lanipes
Bonilla, M., García, M. C., Orkand, P. M., & Zuazaga, C. (1992) · Tissue and Cell · doi:10.1016/0040-8166(92)90068-i · Cited by 6
The Effect of Heart Rate, Preload, and Afterload on the Viscoelastic Properties of the Swine Myocardium
Ewert, D. L., Wheeler, B., Doetkott, C. D., Ionan, C. E., Pantalos, G. M., & Koenig, S. C. (2004) · Annals of Biomedical Engineering · doi:10.1114/b:abme.0000039355.53117.6f · Cited by 6
FUNCTIONAL DIFFERENCES OF MYOFIBRILLAR PROTEINS FROM FAST AND SLOW TWITCH MUSCLES1
Foegeding, E. A., & Liu, M. N. (1995) · Journal of Muscle Foods · doi:10.1111/j.1745-4573.1995.tb00561.x · Cited by 6
Chemical Mechanism of Myosin‐Catalyzed ATP Hydrolysis
Webb, M. R., & Trentham, D. R. (1983) · Comprehensive physiology · doi:10.1002/cphy.cp100108 · Cited by 6
Can voluntary movement be understood on the basis of reflex organization?
Ostry, D. J., & Wilkinson, F. E. (1986) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00051499 · Cited by 6
Alterations in the Contracture Band Patterns of Unfrozen and Prerigor Frozen Ovine Muscle Due to Variations in Post‐Mortem Incubation Temperature
Cook, C. F., & Wright, R. G. (1966) · Journal of Food Science · doi:10.1111/j.1365-2621.1966.tb03252.x · Cited by 6
A proposal for the mechanism of muscle contraction at the molecular level
Warner, D. T. (1970) · Journal of Theoretical Biology · doi:10.1016/s0022-5193(70)80019-4 · Cited by 6
Observations on the anisotropic band of cross-striated muscle
de Villafranca, G. W. (1957) · Experimental Cell Research · doi:10.1016/0014-4827(57)90157-x · Cited by 6
Propulsive Torques and Adaptive Reflexes
MacKay, W. A. (1986) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0005144x · Cited by 6
ELECTRONMICROSCOPICAL STUDY OF MUSCLE BIOPSIES FROM HEALTHY YOUNG PEOPLE Methodology and Results
Reske‐Nielsen, E., & Harmsen, A. (1972) · Acta Pathologica Microbiologica Scandinavica Section A Pathology · doi:10.1111/j.1699-0463.1972.tb00304.x · Cited by 6
Muscle Physiology and Contraction Theories
Taggart, J. V., & Podolsky, R. J. (1961) · Circulation · doi:10.1161/01.cir.24.2.399 · Cited by 6
Effect of left atrial filling pressure on the activity of specific myosin isozymes in rat heart.
Kato, N. S., Weisberg, A. S., & Winegrad, S. (1991) · Circulation Research · doi:10.1161/01.res.68.6.1582 · Cited by 6
Controlling the temporal structure of limb movements
Schmidt, R. A. (1986) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00051530 · Cited by 6
Investigating the mechanisms of small extracellular vesicles in cardiovascular disease using the living myocardial slice platform
Koutentaki, F., Nicastro, L., Kelwick, R. J. R., Freemont, P. S., & Terracciano, C. M. (2025) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2025.1697099 · Cited by 5
Engineering anisotropic tissues: from structured scaffolds to magnetic actuation
Demri, N., Descroix, S., & Wilhelm, C. (2026) · Materials Today Bio · doi:10.1016/j.mtbio.2026.103191 · Cited by 5
Mechanisms of Sarcomere Assembly in Muscle Cells Inferred from Sequential Ordering of Myofibril Components
Kolley, F., Sidor, C., Dehapiot, B., Schnorrer, F., & Friedrich, B. M. (2024) · PRX Life · doi:10.1103/prxlife.2.013002 · Cited by 5
An optimized approach to study nanoscale sarcomere structure utilizing super-resolution microscopy with nanobodies
Douglas, C. M., Bird, J. E., Kopinke, D., & Esser, K. A. (2024) · PLoS ONE · doi:10.1371/journal.pone.0300348 · Cited by 5
Mitochondrial Excitation-Energy Coupling in Airway Smooth Muscle
Schaible, N., Delmotte, P. F., & Sieck, G. C. (2014) · Respiratory medicine · doi:10.1007/978-1-4939-0829-5_5 · Cited by 5
Actin turnover protects the cytokinetic contractile ring from structural instability
McDargh, Z. A., Zhu, T., Zhu, H., & O’Shaughnessy, B. (2022) · Journal of Cell Science · doi:10.1242/jcs.259969 · Cited by 5
Predictive Control of Peak Achilles Tendon Force in a Simulated System of the Human Ankle Joint with a Parallel Artificial Actuator During Hopping
Nabipour, M., Sawicki, G. S., & Sartori, M. (2023) · International Conference on Rehabilitation Robotics · doi:10.1109/icorr58425.2023.10304771 · Cited by 5
Invited review: Probing the structures of muscle regulatory proteins using small‐angle solution scattering
Lü, Y., Jeffries, C. M., & Trewhella, J. (2011) · Biopolymers · doi:10.1002/bip.21624 · Cited by 5
Muscle Contraction and Force: the Importance of an Ancillary Network, Nutrient Supply and Waste Removal
Brüggemann, D., Risbo, J., Pierzynowski, S. G., & Harrison, A. P. (2008) · International Journal of Molecular Sciences · doi:10.3390/ijms9081472 · Cited by 5
Skeletal muscle changes due to cerebral palsy
Lieber, R., & Smith, L. (2014) · Elsevier eBooks · doi:10.1016/b978-0-7020-5099-2.00006-6 · Cited by 2
Revisiting a classic: Muscles, Reflexes, and Locomotion by McMahon
Rowen, D. A., Likens, A. D., & Stergiou, N. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-813372-9.00006-3 · Cited by 5
Mathematical and numerical models for the cardiac electromechanical function
Dede’, L., Quarteroni, A. M., & Regazzoni, F. (2021) · Rendiconti Lincei Matematica e Applicazioni · doi:10.4171/rlm/935 · Cited by 5
Effects of shortening velocity on the stiffness to force ratio during isometric force redevelopment suggest mechanisms of residual force depression
Jeong, S., & Nishikawa, K. C. (2023) · Scientific Reports · doi:10.1038/s41598-023-28236-5 · Cited by 5
In vivo imaging of skeletal muscle form and function: 50 years of insight
Blemker, S. S. (2023) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2023.111745 · Cited by 5
Metabolic Myopathies and Related Diseases
Gaspar, B. L., Vasishta, R. K., & Radotra, B. D. (2018) · Springer eBooks · doi:10.1007/978-981-13-1462-9_12 · Cited by 5
Nanomolar ATP binding to single myosin cross-bridges in rigor: a molecular approach to studying myosin ATP kinetics using single human cardiomyocytes
Pandžić, E., Morkel, C. A., Li, A. S., Cooke, R., Whan, R. M., & dos Remedios, C. G. (2020) · Biophysical Reviews · doi:10.1007/s12551-020-00716-2 · Cited by 5
Thermodynamic inconsistency disproves the Suga-Sagawa theory of cardiac energetics
Loiselle, D. S., Taberner, A. J., Tran, K., & Han, J. (2021) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2021.03.002 · Cited by 5

Authors: HUXLEY, A. F., & NIEDERGERKE, R.
Affiliations: University of Cambridge (GB)
Venue: Nature
Publisher: Springer Science and Business Media LLC
Published: 1954-05
Volume: 173
Issue: 4412
Pages: 971-973
ISSN: 0028-0836 (ISSN-L)
1476-4687
DOI: 10.1038/173971a0
OpenAlex: W1975714515
Cited by: 1,608
References: 8
Citations by year: 2026: 29 · 2025: 46 · 2024: 37 · 2023: 50 · 2022: 45 · 2021: 50 · 2020: 49 · 2019: 47 · 2018: 58 · 2017: 54 · 2016: 56 · 2015: 43 · 2014: 42 · 2013: 34 · 2012: 49
FWCI: 18.58
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Nature (publishedVersion)
PubMed (publishedVersion)
Topics: Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiomyopathy and Myosin Studies
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
Keywords: muscle contraction, muscle fiber structure, interference microscopy, sarcomere, sarcomere shortening, sarcomere length
MeSH terms: Humans, Microscopy, Microscopy, Interference, Muscles, Stem Cells, Life

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Structural Changes in Muscle During Contraction: Interference Microscopy of Living Muscle Fibres

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks