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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:

Diverse functions of the prion protein – Does proteolytic processing hold the key?
Luise Linsenmeier, Hermann C. Altmeppen, Sebastian Wetzel, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2017) Vol. 1864, Iss. 11, pp. 2128-2137
Closed Access | Times Cited: 72

Showing 1-25 of 72 citing articles:

Creutzfeldt–Jakob disease and other prion diseases
Inga Zerr, Anna Ladogana, Simon Mead, et al.
Nature Reviews Disease Primers (2024) Vol. 10, Iss. 1
Closed Access | Times Cited: 21
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
Retinal Degeneration and Alzheimer’s Disease: An Evolving Link
Ajay Ashok, Neena Singh, Suman Chaudhary, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 19, pp. 7290-7290
Open Access | Times Cited: 116
Complement 3+-astrocytes are highly abundant in prion diseases, but their abolishment led to an accelerated disease course and early dysregulation of microglia
A. Hartmann, Diego Sepúlveda‐Falla, Indigo V.L. Rose, et al.
Acta Neuropathologica Communications (2019) Vol. 7, Iss. 1
Open Access | Times Cited: 110
Characterization of brain‐derived extracellular vesicles reveals changes in cellular origin after stroke and enrichment of the prion protein with a potential role in cellular uptake
Santra Brenna, Hermann C. Altmeppen, Behnam Mohammadi, et al.
Journal of Extracellular Vesicles (2020) Vol. 9, Iss. 1
Open Access | Times Cited: 71
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
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
Copper drives prion protein phase separation and modulates aggregation
Mariana Juliani do Amaral, Satabdee Mohapatra, Aline Ribeiro Passos, et al.
Science Advances (2023) Vol. 9, Iss. 44
Open Access | Times Cited: 16
Emerging roles of the cellular prion protein (PrPC) and 37/67 kDa laminin receptor (RPSA) interaction in cancer biology
Adriana Limone, Valentina Maggisano, Daniela Sarnataro, et al.
Cellular and Molecular Life Sciences (2023) Vol. 80, Iss. 8
Open Access | Times Cited: 14
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
Albumin Folding Changes Affect the Microfluidic Interfacial Broadening Revealed by Surface Plasmon Resonance
Damiano Calcagno, Maria Luisa Perina, Alessia Distefano, et al.
Chemistry - Methods (2025)
Open Access
Cellular and Molecular Mechanisms Mediated by recPrPC Involved in the Neuronal Differentiation Process of Mesenchymal Stem Cells
Stefano Martellucci, Costantino Santacroce, Francesca Santilli, et al.
International Journal of Molecular Sciences (2019) Vol. 20, Iss. 2, pp. 345-345
Open Access | Times Cited: 33
Melatonin: Regulation of Prion Protein Phase Separation in Cancer Multidrug Resistance
Doris Loh, Russel J. Reıter
Molecules (2022) Vol. 27, Iss. 3, pp. 705-705
Open Access | Times Cited: 17
Prion protein oligomers cause neuronal cytoskeletal damage in rapidly progressive Alzheimer’s disease
Mohsin Shafiq, Saima Zafar, Neelam Younas, et al.
Molecular Neurodegeneration (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 22
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
Transgenic Overexpression of the Disordered Prion Protein N1 Fragment in Mice Does Not Protect Against Neurodegenerative Diseases Due to Impaired ER Translocation
Behnam Mohammadi, Luise Linsenmeier, Mohsin Shafiq, et al.
Molecular Neurobiology (2020) Vol. 57, Iss. 6, pp. 2812-2829
Open Access | Times Cited: 22
On the role of the cellular prion protein in the uptake and signaling of pathological aggregates in neurodegenerative diseases
Giuseppe Legname, Carlo Scialò
Prion (2020) Vol. 14, Iss. 1, pp. 257-270
Open Access | Times Cited: 22
The Cellular Prion Protein and the Hallmarks of Cancer
Sophie Mouillet‐Richard, Alexandre Ghazi, Pierre Laurent‐Puig
Cancers (2021) Vol. 13, Iss. 19, pp. 5032-5032
Open Access | Times Cited: 20
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
Application of the fragment molecular orbital method to discover novel natural products for prion disease
Jiwon Choi, Hyo-Jin Kim, Xuemei Jin, et al.
Scientific Reports (2018) Vol. 8, Iss. 1
Open Access | Times Cited: 21
Programmable DNA Nanodevices for Applications in Neuroscience
Pravin Hivare, Chinmaya Panda, Sharad Gupta, et al.
ACS Chemical Neuroscience (2021) Vol. 12, Iss. 3, pp. 363-377
Closed Access | Times Cited: 16
What Are the Roles of Cellular Prion Protein in Normal and Pathologic Conditions?
Eduardo E. Benarroch
Neurology (2024) Vol. 102, Iss. 7
Closed Access | Times Cited: 2
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
Cell biology of prion strains in vivo and in vitro
Daniel Shoup, Suzette A. Priola
Cell and Tissue Research (2022) Vol. 392, Iss. 1, pp. 269-283
Open Access | Times Cited: 10
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