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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:

Structural and mechanistic aspects influencing the ADAM10-mediated shedding of the prion protein
Luise Linsenmeier, Behnam Mohammadi, Sebastian Wetzel, et al.
Molecular Neurodegeneration (2018) Vol. 13, Iss. 1
Open Access | Times Cited: 52

Showing 1-25 of 52 citing articles:

Cellular and Molecular Mechanisms of Prion Disease
Christina J. Sigurdson, Jason C. Bartz, Markus Glatzel
Annual Review of Pathology Mechanisms of Disease (2018) Vol. 14, Iss. 1, pp. 497-516
Open Access | Times Cited: 120
Functions of ‘A disintegrin and metalloproteases (ADAMs)’ in the mammalian nervous system
Hung‐En Hsia, Johanna Tüshaus, Tobias Brummer, et al.
Cellular and Molecular Life Sciences (2019) Vol. 76, Iss. 16, pp. 3055-3081
Open Access | Times Cited: 105
Prion Protein: The Molecule of Many Forms and Faces
Valerija Kovač, Vladka Čurin Šerbec
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 3, pp. 1232-1232
Open Access | Times Cited: 33
Prion protein quantification in human cerebrospinal fluid as a tool for prion disease drug development
Sonia M. Vallabh, Chloe K. Nobuhara, Franc Llorens, et al.
Proceedings of the National Academy of Sciences (2019) Vol. 116, Iss. 16, pp. 7793-7798
Open Access | Times Cited: 48
Prion protein glycans reduce intracerebral fibril formation and spongiosis in prion disease
Alejandro M. Sevillano, Patricia Aguilar‐Calvo, Timothy D. Kurt, et al.
Journal of Clinical Investigation (2020) Vol. 130, Iss. 3, pp. 1350-1362
Open Access | Times Cited: 41
Muskelin Coordinates PrPC Lysosome versus Exosome Targeting and Impacts Prion Disease Progression
Frank F. Heisler, Yvonne Pechmann, Ines Wieser, et al.
Neuron (2018) Vol. 99, Iss. 6, pp. 1155-1169.e9
Open Access | Times Cited: 44
GPI-anchor signal sequence influences PrPC sorting, shedding and signalling, and impacts on different pathomechanistic aspects of prion disease in mice
Berta Puig, Hermann C. Altmeppen, Luise Linsenmeier, et al.
PLoS Pathogens (2019) Vol. 15, Iss. 1, pp. e1007520-e1007520
Open Access | Times Cited: 39
Proteolysis of CD44 at the cell surface controls a downstream protease network
Birte Wöhner, Wenjia Li, Sven Hey, et al.
Frontiers in Molecular Biosciences (2023) Vol. 10
Open Access | Times Cited: 12
Human prion diseases and the prion protein – what is the current state of knowledge?
Reinhold Nafe, Christophe Arendt, Elke Hattingen
Translational Neuroscience (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 11
Ligands binding to the prion protein induce its proteolytic release with therapeutic potential in neurodegenerative proteinopathies
Luise Linsenmeier, Behnam Mohammadi, Mohsin Shafiq, et al.
Science Advances (2021) Vol. 7, Iss. 48
Open Access | Times Cited: 24
Prion protein alters viral control and enhances pathology after perinatal cytomegalovirus infection
Dubravka Karner, Daria Kveštak, Paola Kučan Brlić, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 3
Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions
Patricia Aguilar‐Calvo, Alejandro M. Sevillano, Jaidev Bapat, et al.
Acta Neuropathologica (2019) Vol. 139, Iss. 3, pp. 527-546
Open Access | Times Cited: 28
Inhibition of DPAGT1 suppresses HER2 shedding and trastuzumab resistance in human breast cancer
Muwen Yang, Li, Lingzhi Kong, et al.
Journal of Clinical Investigation (2023) Vol. 133, Iss. 14
Open Access | Times Cited: 8
Prion protein modulates endothelial to mesenchyme-like transition in trabecular meshwork cells: Implications for primary open angle glaucoma
Ajay Ashok, Min Hyung Kang, Aaron Wise, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 25
Domain-specific Quantification of Prion Protein in Cerebrospinal Fluid by Targeted Mass Spectrometry
Eric Vallabh Minikel, Eric Kuhn, Alexandra R. Cocco, et al.
Molecular & Cellular Proteomics (2019) Vol. 18, Iss. 12, pp. 2388-2400
Open Access | Times Cited: 25
The prion protein and its ligands: Insights into structure-function relationships
Mohsin Shafiq, Stefano Da Vela, Ladan Amin, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2022) Vol. 1869, Iss. 6, pp. 119240-119240
Open Access | Times Cited: 14
Inducing prion protein shedding as a neuroprotective and regenerative approach in pathological conditions of the brain: from theory to facts.
Andreu Matamoros‐Angles, Behnam Mohammadi, Feizhi Song, et al.
PubMed (2023) Vol. 18, Iss. 9, pp. 1869-1875
Closed Access | Times Cited: 7
N-glycosylation is a potent regulator of prion protein neurotoxicity
Kevin M. Schilling, Pooja Jorwal, Natalia C. Ubilla‐Rodriguez, et al.
Journal of Biological Chemistry (2023) Vol. 299, Iss. 9, pp. 105101-105101
Open Access | Times Cited: 7
TIMP Loss Activates Metalloproteinase-TNFα-DKK1 Axis To Compromise Wnt Signaling and Bone Mass
Yan Chen, Alison Aiken, Sanjay Saw, et al.
Journal of Bone and Mineral Research (2018) Vol. 34, Iss. 1, pp. 182-194
Open Access | Times Cited: 22
Modulation of Immune Responses by Platelet-Derived ADAM10
Stefanie Maurer, Hans‐Georg Kopp, Helmut R. Salih, et al.
Frontiers in Immunology (2020) Vol. 11
Open Access | Times Cited: 19
Cell Surface Processing of CD109 by Meprin β Leads to the Release of Soluble Fragments and Reduced Expression on Extracellular Vesicles
Wiebke Lückstädt, Simon Bub, Tomas Koudelka, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 15
Anchorless risk or released benefit? An updated view on the ADAM10-mediated shedding of the prion protein
Behnam Mohammadi, Feizhi Song, Andreu Matamoros‐Angles, et al.
Cell and Tissue Research (2022) Vol. 392, Iss. 1, pp. 215-234
Open Access | Times Cited: 11
Diminished Neuronal ESCRT-0 Function Exacerbates AMPA Receptor Derangement and Accelerates Prion-Induced Neurodegeneration
Jessica Lawrence, Patricia Aguilar‐Calvo, Daniel Ojeda-Juárez, et al.
Journal of Neuroscience (2023) Vol. 43, Iss. 21, pp. 3970-3984
Open Access | Times Cited: 6
Heparan Sulfated Glypican-4 Is Released from Astrocytes by Proteolytic Shedding and GPI-Anchor Cleavage Mechanisms
Kevin Huang, Sungjin Park
eNeuro (2021) Vol. 8, Iss. 4, pp. ENEURO.0069-21.2021
Open Access | Times Cited: 14
An optimized Western blot assay provides a comprehensive assessment of the physiological endoproteolytic processing of the prion protein
Ilaria Vanni, Floriana Iacobone, Claudia D’Agostino, et al.
Journal of Biological Chemistry (2022) Vol. 299, Iss. 2, pp. 102823-102823
Open Access | Times Cited: 9
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