Biology and Genetics of Prions Causing Neurodegeneration

Prusiner, Stanley B.·2013·Annual Review of Genetics

Cited by (455)

Items 101–200 of 455

  1. Transmission Characteristics of Variably Protease-Sensitive Prionopathy
    Silvio Notari, Xiangzhu Xiao, Juan Carlos Espinosa, Yvonne Cohen, Liuting Qing, Patricia Aguilar‐Calvo, Diane Kofskey, Ignazio Calì, Laura Cracco, Qingzhong Kong et al. · 2014 · Emerging infectious diseases
  2. Differential overexpression of SERPINA3 in human prion diseases
    Silvia Vanni, Fabio Moda, Marco Zattoni, Edoardo Bistaffa, Elena De Cecco, Marcello Rossi, Giorgio Giaccone, Fabrizio Tagliavini, Stéphane Haı̈k, J.-P. Deslys et al. · 2017 · Scientific Reports
  3. Motor neuron loss and neuroinflammation in a model of α-synuclein-induced neurodegeneration
    Sorrentino, Zachary A., Xia, Yuxing, Funk, Cory, Riffe, Cara J., Rutherford, Nicola J., Ceballos Diaz, Carolina, Sacino, Amanda N., Price, Nathan D., Golde, Todd E., Giasson, Benoit I. et al. · 2018 · Neurobiology of Disease
  4. Formation and spreading of TDP-43 aggregates in cultured neuronal and glial cells demonstrated by time-lapse imaging
    Tomohiro Ishii, Emiko Kawakami, Kentaro Endo, Hidemi Misawa, Kazuhiko Watabe · 2017 · PLoS ONE
  5. Prion-like Domains in Eukaryotic Viruses
    George V. Tetz, Victor Tetz · 2018 · Scientific Reports
  6. Prion Diseases
    Boon Lead Tee, Erika Mariana Longoria-Ibarrola, Michael D. Geschwind · 2018 · Neurologic Clinics
  7. Prion-Like Characteristics of Polyglutamine-Containing Proteins
    Margaret M.P. Pearce, Ron R. Kopito · 2017 · Cold Spring Harbor Perspectives in Medicine
  8. Recent Advances in Understanding Mammalian Prion Structure: A Mini Review
    Cassandra Terry, Jonathan D. F. Wadsworth · 2019 · Frontiers in Molecular Neuroscience
  9. Dietary Trace Elements and the Pathogenesis of Neurodegenerative Diseases
    Masahiro Kawahara, Midori Kato‐Negishi, Ken‐ichiro Tanaka · 2023 · Nutrients
  10. The Effects of LW-AFC on Intestinal Microbiome in Senescence-Accelerated Mouse Prone 8 Strain, a Mouse Model of Alzheimer’s Disease
    Jianhui Wang, Fuqiang Ye, Xiaorui Cheng, Xiaorui Zhang, Feng Liu, Gang Liu, Ming Ni, Shanyi Qiao, Wenxia Zhou, Yongxiang Zhang · 2016 · Journal of Alzheimer s Disease
  11. Dynamics of oligomer and amyloid fibril formation by yeast prion Sup35 observed by high-speed atomic force microscopy
    Hiroki Konno, Takahiro Watanabe‐Nakayama, Takayuki Uchihashi, Momoko Okuda, Liwen Zhu, Noriyuki Kodera, Yousuke Kikuchi, Toshio Ando, Hideki Taguchi · 2020 · Proceedings of the National Academy of Sciences
  12. TCTP contains a BH3-like domain, which instead of inhibiting, activates Bcl-xL
    Stéphanie Thébault, Morgane Agez, Xiaoke Chi, Johann Stojko, Vincent Cura, Stéphanie B. Telerman, Laurent Maillet, Fabien Gautier, Isabelle M. L. Billas, Catherine Birck et al. · 2016 · Scientific Reports
  13. How an Infection of Sheep Revealed Prion Mechanisms in Alzheimer’s Disease and Other Neurodegenerative Disorders
    Carlson, George A., Prusiner, Stanley B. · 2021 · International Journal of Molecular Sciences
  14. The SH3 domain of Fyn kinase interacts with and induces liquid–liquid phase separation of the low-complexity domain of hnRNPA2
    Joshua Amaya, Veronica H. Ryan, Nicolas Lux Fawzi · 2018 · Journal of Biological Chemistry
  15. Quantitative prediction of electronic absorption spectra of copper(II)–bioligand systems: Validation and applications
    Giuseppe Sciortino, Jean‐Didier Maréchal, István Fábián, Norbert Lihi, Eugenio Garribba · 2019 · Journal of Inorganic Biochemistry
  16. Prion-like Nanofibrils of Small Molecules (PriSM) Selectively Inhibit Cancer Cells by Impeding Cytoskeleton Dynamics
    Yi Kuang, Marcus J. C. Long, Jie Zhou, Junfeng Shi, Yuan Gao, Xu Chen, Lizbeth Hedstrom, Bing Xu · 2014 · Journal of Biological Chemistry
  17. Prions: Beyond a Single Protein
    Alvin S. Das, Wen‐Quan Zou · 2016 · Clinical Microbiology Reviews
  18. Brain aging: A Ianus‐faced player between health and neurodegeneration
    Silvia Vanni, Arianna Colini Baldeschi, Marco Zattoni, Giuseppe Legname · 2019 · Journal of Neuroscience Research
  19. Noncerebral Amyloidoses: Aspects on Seeding, Cross-Seeding, and Transmission.
    G. Westermark, M. Fändrich, K. Lundmark, P. Westermark · 2018 · Cold Spring Harbor Perspectives in Medicine
  20. Endogenous retroviruses and TDP-43 proteinopathy form a sustaining feedback driving intercellular spread of Drosophila neurodegeneration
    Chang, Yung-Heng, Dubnau, Josh · 2023 · Nature Communications
  21. Ligand–Receptor Interaction Catalyzes the Aggregation of Small Molecules To Induce Cell Necroptosis
    Junfeng Shi, Xuewen Du, Huang Yi, Jie Zhou, Dan Yuan, Dongdong Wu, Ye Zhang, Richard Haburcak, Irving R. Epstein, Bing Xu · 2014 · Journal of the American Chemical Society
  22. Long-term memory consolidation: The role of RNA-binding proteins with prion-like domains
    Indulekha P. Sudhakaran, Mani Ramaswami · 2016 · RNA Biology
  23. Pharmacological Agents Targeting the Cellular Prion Protein
    Maria Letizia Barreca, Nunzio Iraci, Silvia Biggi, Violetta Cecchetti, Emiliano Biasini · 2018 · Pathogens
  24. TIA-1 Is a Functional Prion-Like Protein
    Joseph B. Rayman, Eric R. Kandel · 2016 · Cold Spring Harbor Perspectives in Biology
  25. Amyloid-β pathology induced in humans
    Mathias Jucker, Lary C. Walker · 2015 · Nature
  26. Protein Co-Aggregation Related to Amyloids: Methods of Investigation, Diversity, and Classification
    Stanislav A. Bondarev, Kirill S. Antonets, Andrey V. Kajava, Anton A. Nizhnikov, Galina A. Zhouravleva · 2018 · International Journal of Molecular Sciences
  27. Pomegranate as a Possible Treatment in Reducing Risk of Developing Wound Healing, Obesity, Neurodegenerative Disorders, and Diabetes Mellitus
    Manaf AlMatar, Md. Rashedul Islam, Osman Albarri, İşıl Var, Fatih Köksal · 2017 · Mini-Reviews in Medicinal Chemistry
  28. The Iron Metabolism with a Specific Focus on the Functioning of the Nervous System
    Monika Kulaszyńska, Sebastian Kwiatkowski, Karolina Skonieczna‐Żydecka · 2024 · Biomedicines
  29. DFT Protocol for EPR Prediction of Paramagnetic Cu(II) Complexes and Application to Protein Binding Sites
    Giuseppe Sciortino, Giuseppe Lubinu, Jean‐Didier Maréchal, Eugenio Garribba · 2018 · Magnetochemistry
  30. From zinc homeostasis to disease progression: Unveiling the neurodegenerative puzzle
    Yonggang Fan, Ting-Yao Wu, Lingxiao Zhao, Rong‐Jun Jia, Ren Hang, Wen‐Jia Hou, Zhan‐You Wang · 2023 · Pharmacological Research
  31. Functional Prions in the Brain
    Joseph B. Rayman, Eric R. Kandel · 2016 · Cold Spring Harbor Perspectives in Biology
  32. A critical review of the prion hypothesis of human synucleinopathies
    Gültekin Tamgüney, Amos D. Korczyn · 2017 · Cell and Tissue Research
  33. Purkinje Cells Pathology in Alzheimer’s Disease
    Ioannis A. Mavroudis, Foivos E. Petridis, D. Kazis, S. Njau, V. Costa, Stavros J. Baloyannis · 2019 · American Journal of Alzheimers Disease & Other Dementias
  34. Unified theory of Alzheimer’s disease (UTAD): implications for prevention and curative therapy
    Nehls, Michael · 2016 · Journal of Molecular Psychiatry
  35. Feedback control of prion formation and propagation by the ribosome‐associated chaperone complex
    Denis A. Kiktev, Mikhail M. Melomed, Caroline D. Lu, Gary P. Newnam, Yury O. Chernoff · 2015 · Molecular Microbiology
  36. RNA as the stone guest of protein aggregation
    Alexandra Louka, Elsa Zacco, Piero Andrea Temussi, Gian Gaetano Tartaglia, Annalisa Pastore · 2020 · Nucleic Acids Research
  37. Seeding activity of skin misfolded tau as a biomarker for tauopathies
    Zerui Wang, Ling Wu, Maria Gerasimenko, Tricia Gilliland, Zahid Syed Ali Shah, Evalynn Lomax, Yirong Yang, Steven A. Gunzler, Vincenzo Angelo Donadio, Rocco Liguori et al. · 2024 · Molecular Neurodegeneration
  38. CSF biomarkers in neurodegenerative and vascular dementias
    Franc Llorens, Matthias Schmitz, Isidró Ferrer, Inga Zerr · 2016 · Progress in Neurobiology
  39. RNA modulates aggregation of the recombinant mammalian prion protein by direct interaction
    Petar Stefanov Kovachev, Mariana P. B. Gomes, Yraima Cordeiro, Natalia Ferreira, Leticia P. Felix Valadão, Lucas M. Ascari, Luciana Pereira Rangel, Jerson Lima Silva, Suparna Sanyal · 2019 · Scientific Reports
  40. Amyloid Prefibrillar Oligomers: The Surprising Commonalities in Their Structure and Activity
    Marco Diociaiuti, Roberto Bonanni, Ida Cariati, Claudio Frank, Giovanna D’Arcangelo · 2021 · International Journal of Molecular Sciences
  41. Distinct conformers of amyloid beta accumulate in the neocortex of patients with rapidly progressive Alzheimer's disease
    He Liu, Chae Kim, Tracy Haldiman, Christina J. Sigurdson, Sofie Nyström, K. Peter R. Nilsson, Mark L. Cohen, Thomas Wısnıewskı, Per Hammarström, Jiri Safar · 2021 · Journal of Biological Chemistry
  42. Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitro
    Cassandra Terry, Robert L. Harniman, Jessica Sells, Adam Wenborn, Susan Joiner, Helen R. Saibil, Mervyn John Miles, John Collinge, Jonathan D. F. Wadsworth · 2019 · Scientific Reports
  43. Application of yeast to studying amyloid and prion diseases
    Yury O. Chernoff, Anastasia V. Grizel, Aleksandr A. Rubel, Andrew А. Zelinsky, Pavithra Chandramowlishwaran, Tatiana Alexandrovna Chernova · 2020 · Advances in genetics
  44. Clinical update of Jakob–Creutzfeldt disease
    Mee‐Ohk Kim, Michael D. Geschwind · 2015 · Current Opinion in Neurology
  45. Virulent Pseudomonas aeruginosa infection converts antimicrobial amyloids into cytotoxic prions
    Sarah B. Voth, Meredith S. Gwin, C. Michael Francis, Ron Balczon, Dara W. Frank, Jean‐François Pittet, Brant M. Wagener, Stephen A. Moser, Mikhail F. ALEXEYEV, Nicole A. Housley et al. · 2020 · The FASEB Journal
  46. Tau proteinopathies and the prion concept
    2020 · Progress in Molecular Biology and Translational Science
  47. Prion Protein—Antibody Complexes Characterized by Chromatography-Coupled Small-Angle X-Ray Scattering
    Lester G. Carter, Seung Joong Kim, Dina Schneidman‐Duhovny, Jan Stöhr, Guillaume Poncet-Montange, Thomas M Weiss, Hiro Tsuruta, Stanley B. Prusiner, Andrej Šali · 2015 · Biophysical Journal
  48. Untangling a Repetitive Amyloid Sequence: Correlating Biofilm‐Derived and Segmentally Labeled Curli Fimbriae by Solid‐State NMR Spectroscopy
    Tobias Schubeis, Puwei Yuan, Mumdooh A.M. Ahmed, Madhu Nagaraj, Barth‐Jan van Rossum, Christiane Ritter · 2015 · Angewandte Chemie International Edition
  49. The link among microbiota, epigenetics, and disease development
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  50. “Prion-like” seeding and propagation of oligomeric protein assemblies in neurodegenerative disorders
    Silvia Zampar, Sonja E. Di Gregorio, Gustavo Grimmer, Joel C. Watts, Martin Ingelsson · 2024 · Frontiers in Neuroscience
  51. PET imaging of microglia in Alzheimer's disease using copper-64 labeled TREM2 antibodies
    Monireh Shojaei, Rebecca Schaefer, Kai Schlepckow, Lea H. Kunze, Felix L. Struebing, Bettina Brunner, Michael Willem, Laura M. Bartos, Astrid Feiten, Giovanna Palumbo et al. · 2024 · Theranostics
  52. Review: A review on classical and atypical scrapie in caprine: Prion protein gene polymorphisms and their role in the disease
    Ludovica Curcio, Carla Sebastiani, P. Di Lorenzo, Emiliano Lasagna, M. Biagetti · 2016 · animal
  53. Unconventional Secretion and Intercellular Transfer of Mutant Huntingtin
    Bor Luen Tang · 2018 · Cells
  54. Prion-like propagation of α-synuclein in neurodegenerative diseases
    Airi Tarutani, Masato Hasegawa · 2019 · Progress in molecular biology and translational science
  55. Proteins Do Not Replicate, They Precipitate: Phase Transition and Loss of Function Toxicity in Amyloid Pathologies
    Kariem Ezzat, Andrea Sturchio, Alberto Javier Espay · 2022 · Biology
  56. Solid-state NMR: An emerging technique in structural biology of self-assemblies
    Birgit Habenstein, Antoine Loquet · 2015 · Biophysical Chemistry
  57. Prion-like Mechanisms in Alzheimer's Disease
    Ruihua Yin, Lan Tan, Teng Jiang, Jin‐Tai Yu · 2014 · Current Alzheimer Research
  58. Amyloids: Regulators of Metal Homeostasis in the Synapse
    Masahiro Kawahara, Midori Kato‐Negishi, Ken‐ichiro Tanaka · 2020 · Molecules
  59. Prion Protein Biology Through the Lens of Liquid-Liquid Phase Separation
    Aishwarya Agarwal, Samrat Mukhopadhyay · 2021 · Journal of Molecular Biology
  60. Prion disease
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  61. COVID-19 and Neurodegenerative Diseases: Prion-Like Spread and Long-Term Consequences
    Narjes Baazaoui, Khalid Iqbal · 2022 · Journal of Alzheimer s Disease
  62. Aβ seeds and prions: How close the fit?
    Jay Rasmussen, Mathias Jucker, Lary C. Walker · 2017 · Prion
  63. The Role of α-Synuclein in Etiology of Neurodegenerative Diseases
    Daria Krawczuk, Magdalena Groblewska, Jan Mroczko, Izabela Winkel, Barbara Mroczko · 2024 · International Journal of Molecular Sciences
  64. Phosphorylated and aggregated TDP-43 with seeding properties are induced upon mutant Huntingtin (mHtt) polyglutamine expression in human cellular models
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  65. The life of [PSI]
    Brian Cox, Mick F. Tuite · 2017 · Current Genetics
  66. Are fibrinaloid microclots a cause of autoimmunity in Long Covid and other post-infection diseases?
    Douglas Bruce Kell, Etheresia Pretorius · 2023 · Biochemical Journal
  67. The integrated stress response in brain diseases: A double-edged sword for proteostasis and synapses
    Elana R. Lockshin, Nicole Calakos · 2024 · Current Opinion in Neurobiology
  68. Peripheral proteinopathy in neurodegenerative diseases
    Bin Xu, Xia Lei, Ying Yang, Jiayi Yu, Jun Chen, Zhi Xu, Keqiang Ye, Jing Zhang · 2025 · Translational Neurodegeneration
  69. Hsp40 function in yeast prion propagation: Amyloid diversity necessitates chaperone functional complexity
    Zachary A. Sporn, Justin Keith Hines · 2015 · Prion
  70. Glycoform-independent prion conversion by highly efficient, cell-based, protein misfolding cyclic amplification
    Mohammed Moudjou, Jérôme Chapuis, Mériem Mekrouti, Fabienne Reine, Laëtitia Herzog, Pierre Sibille, Hubert Laude, Didier Vilette, Olivier Andréoletti, Human Rézaei et al. · 2016 · Scientific Reports
  71. Glial alterations in human prion diseases
    Marta Monzón, Rodrigo S. Hernández, Moisès Garcés, Rocío Sarasa, Juan José Badiola · 2018 · Medicine
  72. Yeast Models for Amyloids and Prions: Environmental Modulation and Drug Discovery
    Tatiana Alexandrovna Chernova, Yury O. Chernoff, Keith D. Wilkinson · 2019 · Molecules
  73. Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT-P301L mutation
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  74. The amyloid state of proteins: A boon or bane?
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  76. Treatment with a non-toxic, self-replicating anti-prion delays or prevents prion disease in vivo
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  77. Swa2, the yeast homolog of mammalian auxilin, is specifically required for the propagation of the prion variant [ URE 3‐1]
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  78. Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine
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  79. Yeast Models of Prion-Like Proteins That Cause Amyotrophic Lateral Sclerosis Reveal Pathogenic Mechanisms
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  80. On the role of the cellular prion protein in the uptake and signaling of pathological aggregates in neurodegenerative diseases
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  81. Prionoids in amyotrophic lateral sclerosis
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  82. Selective Detection of Misfolded Tau From Postmortem Alzheimer’s Disease Brains
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  83. Prion-based memory of heat stress in yeast
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  84. PIKfyve inhibition blocks endolysosomal escape of α-synuclein fibrils and spread of α-synuclein aggregation
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  85. Autophagy protects against de novo formation of the [PSI+] prion in yeast
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  86. Dual amyloid cross-seeding reveals steric zipper-facilitated fibrillization and pathological links between protein misfolding diseases
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  88. Variant‐specific and reciprocal Hsp40 functions in Hsp104‐mediated prion elimination
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  89. Gene-edited murine cell lines for propagation of chronic wasting disease prions
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  90. Epilepsy and prion diseases: A narrative review
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  94. Vertebrate food products as a potential source of prion-like α-synuclein
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  95. Neurometals in the Pathogenesis of Prion Diseases
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  96. α-Synuclein conformers reveal link to clinical heterogeneity of α-synucleinopathies
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  97. The prion principle and Alzheimer’s disease
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  98. Pathology and function of nuclear amyloid
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  99. So What Have Plant Viruses Ever Done for Virology and Molecular Biology?
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  100. Praja1 RING ‐finger E3 ubiquitin ligase is a common suppressor of neurodegenerative disease‐associated protein aggregation
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