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:

Myomaker and Myomerger Work Independently to Control Distinct Steps of Membrane Remodeling during Myoblast Fusion
Evgenia Leikina, Dilani G. Gamage, Vikram Prasad, et al.
Developmental Cell (2018) Vol. 46, Iss. 6, pp. 767-780.e7
Open Access | Times Cited: 143

Showing 1-25 of 143 citing articles:

How cells fuse
Nicolás G. Brukman, Berna Uygur, Benjamin Podbilewicz, et al.
The Journal of Cell Biology (2019) Vol. 218, Iss. 5, pp. 1436-1451
Open Access | Times Cited: 162

TGFβ signaling curbs cell fusion and muscle regeneration
Francesco Girardi, Anissa Taleb, Majid Ebrahimi, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 110

Cell Fusion: Merging Membranes and Making Muscle
Michael J. Petrany, Douglas P. Millay
Trends in Cell Biology (2019) Vol. 29, Iss. 12, pp. 964-973
Open Access | Times Cited: 114

Mechanisms regulating myoblast fusion: A multilevel interplay
Lilya Lehka, Maria Jolanta Rędowicz
Seminars in Cell and Developmental Biology (2020) Vol. 104, pp. 81-92
Closed Access | Times Cited: 109

ERK1/2 inhibition promotes robust myotube growth via CaMKII activation resulting in myoblast-to-myotube fusion
Tamar Eigler, Giulia Zarfati, Emmanuel Amzallag, et al.
Developmental Cell (2021) Vol. 56, Iss. 24, pp. 3349-3363.e6
Open Access | Times Cited: 75

Extracellular vesicle fusion visualized by cryo-electron microscopy
Mattia I. Morandi, Petro Busko, Efrat Ozer-Partuk, et al.
PNAS Nexus (2022) Vol. 1, Iss. 4
Open Access | Times Cited: 50

Classification of domains in predicted structures of the human proteome
R. Dustin Schaeffer, Jing Zhang, Lisa N. Kinch, et al.
Proceedings of the National Academy of Sciences (2023) Vol. 120, Iss. 12
Open Access | Times Cited: 29

Microproteins: Overlooked regulators of physiology and disease
Keira R. Hassel, Omar Brito‐Estrada, Catherine A. Makarewich
iScience (2023) Vol. 26, Iss. 6, pp. 106781-106781
Open Access | Times Cited: 28

Skeletal muscle: molecular structure, myogenesis, biological functions, and diseases
Lan‐Ting Feng, Zhi‐Nan Chen, Huijie Bian
MedComm (2024) Vol. 5, Iss. 7
Open Access | Times Cited: 13

Hallmarks of regeneration
Kenneth D. Poss, Elly M. Tanaka
Cell stem cell (2024) Vol. 31, Iss. 9, pp. 1244-1261
Closed Access | Times Cited: 10

The regulatory role of Myomaker and Myomixer–Myomerger–Minion in muscle development and regeneration
Bide Chen, Wenjing You, Yizhen Wang, et al.
Cellular and Molecular Life Sciences (2019) Vol. 77, Iss. 8, pp. 1551-1569
Open Access | Times Cited: 65

Role of damage and management in muscle hypertrophy: Different behaviors of muscle stem cells in regeneration and hypertrophy
So‐ichiro Fukada, Takayuki Akimoto, Athanassia Sotiropoulos
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2020) Vol. 1867, Iss. 9, pp. 118742-118742
Open Access | Times Cited: 57

The Fertilization Enigma: How Sperm and Egg Fuse
Victoria E. Deneke, Andrea Pauli
Annual Review of Cell and Developmental Biology (2021) Vol. 37, Iss. 1, pp. 391-414
Closed Access | Times Cited: 48

Myomerger promotes fusion pore by elastic coupling between proximal membrane leaflets and hemifusion diaphragm
Gonen Golani, Evgenia Leikina, Kamran Melikov, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 45

Regulation of the myoblast fusion reaction for muscle development, regeneration, and adaptations
Douglas P. Millay
Experimental Cell Research (2022) Vol. 415, Iss. 2, pp. 113134-113134
Open Access | Times Cited: 37

Cell Fusion-Related Proteins and Signaling Pathways, and Their Roles in the Development and Progression of Cancer
Hao Zhang, Hong Ma, Xiaohui Yang, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 9
Open Access | Times Cited: 33

Discovery of archaeal fusexins homologous to eukaryotic HAP2/GCS1 gamete fusion proteins
David Moi, Shunsuke Nishio, Xiaohui Li, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 33

Cell surface-bound La protein regulates the cell fusion stage of osteoclastogenesis
Jarred M. Whitlock, Evgenia Leikina, Kamran Melikov, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 22

Intrinsic signalling factors associated with cancer cell-cell fusion
Thomas Dittmar, Ralf Hass
Cell Communication and Signaling (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 17

Enveloped viruses pseudotyped with mammalian myogenic cell fusogens target skeletal muscle for gene delivery
Sajedah M. Hindi, Michael J. Petrany, Elena Greenfeld, et al.
Cell (2023) Vol. 186, Iss. 10, pp. 2062-2077.e17
Open Access | Times Cited: 17

The fusogenic synapse at a glance
Ji Hoon Kim, Elizabeth H. Chen
Journal of Cell Science (2019) Vol. 132, Iss. 18
Open Access | Times Cited: 49

Fusogenic Reoviruses and Their Fusion-Associated Small Transmembrane (FAST) Proteins
Roy Duncan
Annual Review of Virology (2019) Vol. 6, Iss. 1, pp. 341-363
Open Access | Times Cited: 48

Cell–Cell Fusion and the Roads to Novel Properties of Tumor Hybrid Cells
Mareike Sieler, Julian Weiler, Thomas Dittmar
Cells (2021) Vol. 10, Iss. 6, pp. 1465-1465
Open Access | Times Cited: 34

SIX1 reprograms myogenic transcription factors to maintain the rhabdomyosarcoma undifferentiated state
Jessica Y. Hsu, Etienne Danis, Stephanie Nance, et al.
Cell Reports (2022) Vol. 38, Iss. 5, pp. 110323-110323
Open Access | Times Cited: 28

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