OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

The myosin interacting-heads motif present in live tarantula muscle explains tetanic and posttetanic phosphorylation mechanisms
Raúl Padrón, Weikang Ma, Sebastian Duno-Miranda, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 117, Iss. 22, pp. 11865-11874
Open Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

The structural OFF and ON states of myosin can be decoupled from the biochemical super- and disordered-relaxed states
Vivek Jani, Taejeong Song, Chengqian Gao, et al.
PNAS Nexus (2024) Vol. 3, Iss. 2
Open Access | Times Cited: 16

Structural basis of the super- and hyper-relaxed states of myosin II
Roger Craig, Raúl Padrón
The Journal of General Physiology (2021) Vol. 154, Iss. 1
Open Access | Times Cited: 66

Cardiac myosin super relaxation (SRX): a perspective on fundamental biology, human disease and therapeutics
Manuel Schmid, Christopher N. Toepfer
Biology Open (2021) Vol. 10, Iss. 2
Open Access | Times Cited: 65

Small Angle X-ray Diffraction as a Tool for Structural Characterization of Muscle Disease
Weikang Ma, Thomas C. Irving
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 6, pp. 3052-3052
Open Access | Times Cited: 50

Exploring the super-relaxed state of myosin in myofibrils from fast-twitch, slow-twitch, and cardiac muscle
Jonathan Walklate, Kerry Y. Kao, Michael Regnier, et al.
Journal of Biological Chemistry (2022) Vol. 298, Iss. 3, pp. 101640-101640
Open Access | Times Cited: 48

Structural OFF/ON transitions of myosin in relaxed porcine myocardium predict calcium-activated force
Weikang Ma, Timothy S. McMillen, Matthew C. Childers, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 5
Open Access | Times Cited: 35

Structure of mavacamten-free human cardiac thick filaments within the sarcomere by cryoelectron tomography
Liang Chen, Jun Liu, Hosna Rastegarpouyani, et al.
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 9
Open Access | Times Cited: 15

Cardiac myosin filaments are directly regulated by calcium
Weikang Ma, Suman Nag, Henry Gong, et al.
The Journal of General Physiology (2022) Vol. 154, Iss. 12
Open Access | Times Cited: 35

Stress-dependent activation of myosin in the heart requires thin filament activation and thick filament mechanosensing
So‐Jin Park‐Holohan, Elisabetta Brunello, Thomas Kampourakis, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 16
Open Access | Times Cited: 40

Two Classes of Myosin Inhibitors, Para-nitroblebbistatin and Mavacamten, Stabilize β-Cardiac Myosin in Different Structural and Functional States
Sampath K. Gollapudi, Weikang Ma, Srinivas Chakravarthy, et al.
Journal of Molecular Biology (2021) Vol. 433, Iss. 23, pp. 167295-167295
Open Access | Times Cited: 34

NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy
Natasha Ranu, Jenni Laitila, Hannah F. Dugdale, et al.
Acta Neuropathologica Communications (2022) Vol. 10, Iss. 1
Open Access | Times Cited: 27

Reduced ATP turnover during hibernation in relaxed skeletal muscle
Cosimo de Napoli, Luisa Schmidt, Mauro Montesel, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access

The myosin II coiled-coil domain atomic structure in its native environment
Hamidreza Rahmani, Wen Ma, Zhongjun Hu, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 14
Open Access | Times Cited: 32

Myosin dynamics during relaxation in mouse soleus muscle and modulation by 2′‐deoxy‐ATP
Weikang Ma, Matthew C. Childers, Jason D. Murray, et al.
The Journal of Physiology (2020) Vol. 598, Iss. 22, pp. 5165-5182
Open Access | Times Cited: 30

Muscle Mechanics and Thick Filament Activation: An Emerging Two-Way Interaction for the Vertebrate Striated Muscle Fine Regulation
Lorenzo Marcucci
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 7, pp. 6265-6265
Open Access | Times Cited: 9

Super-relaxed state of myosin in human skeletal muscle is fiber-type dependent
Lien A. Phung, Aurora D. Foster, Mark S. Miller, et al.
AJP Cell Physiology (2020) Vol. 319, Iss. 6, pp. C1158-C1162
Open Access | Times Cited: 22

Interacting-heads motif explains the X-ray diffraction pattern of relaxed vertebrate skeletal muscle
Natalia A. Koubassova, Andrey K. Tsaturyan, Sergey Y. Bershitsky, et al.
Biophysical Journal (2022) Vol. 121, Iss. 8, pp. 1354-1366
Open Access | Times Cited: 10

Relaxed tarantula skeletal muscle has two ATP energy-saving mechanisms
Weikang Ma, Sebastian Duno-Miranda, Thomas C. Irving, et al.
The Journal of General Physiology (2021) Vol. 153, Iss. 3
Open Access | Times Cited: 13

The regulatory light chain mediates inactivation of myosin motors during active shortening of cardiac muscle
Thomas Kampourakis, Malcolm Irving
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 13

Thick filament activation is different in fast‐ and slow‐twitch skeletal muscle
Henry Gong, Weikang Ma, Michael Regnier, et al.
The Journal of Physiology (2022) Vol. 600, Iss. 24, pp. 5247-5266
Open Access | Times Cited: 9

Structure of the Flight Muscle Thick Filament from the Bumble Bee, Bombus ignitus, at 6 Å Resolution
Jiawei Li, Hamidreza Rahmani, Fatemeh Abbasi Yeganeh, et al.
International Journal of Molecular Sciences (2022) Vol. 24, Iss. 1, pp. 377-377
Open Access | Times Cited: 9

Potentiation of force by extracellular potassium and posttetanic potentiation are additive in mouse fast-twitch muscle in vitro
Kristian Overgaard, William Gittings, Rene Vandenboom
Pflügers Archiv - European Journal of Physiology (2022) Vol. 474, Iss. 6, pp. 637-646
Closed Access | Times Cited: 8

Human skeletal myopathy myosin mutations disrupt myosin head sequestration
Glenn Carrington, Abbi Hau, Sarah Kosta, et al.
JCI Insight (2023) Vol. 8, Iss. 21
Open Access | Times Cited: 4

Mechanisms of a novel regulatory light chain–dependent cardiac myosin inhibitor
Kristina B. Kooiker, Qing-Fen Gan, Ming Yu, et al.
The Journal of General Physiology (2024) Vol. 156, Iss. 10
Closed Access | Times Cited: 1

Frequency-dependent coexistence of muscle fatigue and potentiation assessed by concentric isotonic contractions in human plantar flexors
Alexander M. Zero, Michael T. Paris, Charles L. Rice
Journal of Applied Physiology (2022) Vol. 133, Iss. 2, pp. 490-505
Closed Access | Times Cited: 6

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