Prions of fungi: inherited structures and biological roles

Cited by (231)

Items 101–200 of 231

  1. Fungal biology in the post-genomic era
    Claudio Scazzocchio · 2014 · Fungal Biology and Biotechnology
  2. Regulation of Synaptic Pumilio Function by an Aggregation-Prone Domain
    Anna M. Salazar, Edward J. Silverman, Kaushiki P. Menon, Kai Zinn · 2010 · Journal of Neuroscience
  3. Relationship between Prion Propensity and the Rates of Individual Molecular Steps of Fibril Assembly
    Yiqian Wang, Alexander Kai Buell, Xinyu Wang, Mark Edward Welland, Christopher Martin Dobson, Tuomas P. J. Knowles, Sarah Perrett · 2011 · Journal of Biological Chemistry
  4. Displacement of N/Q-rich Peptides on TiO2Beads Enhances the Depth and Coverage of Yeast Phosphoproteome Analyses
    Evgeny Kanshin, Stephen W. Michnick, Pierre Thibault · 2013 · Journal of Proteome Research
  5. Glycosaminoglycans promote fibril formation by amyloidogenic immunoglobulin light chains through a transient interaction
    Douglas J. Martin, Marina Ramı́rez-Alvarado · 2011 · Biophysical Chemistry
  6. Prions and the proteasome
    Pelagia Deriziotis, Sarah J. Tabrizi · 2008 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  7. Yeast prions form infectious amyloid inclusion bodies in bacteria
    Alba Espargaró, Anna Villar‐Piqué, Raimon Sabaté, Salvador Ventura · 2012 · Microbial Cell Factories
  8. HermesTransposon Mutagenesis Shows [URE3] Prion Pathology Prevented by a Ubiquitin-Targeting Protein: Evidence for Carbon/Nitrogen Assimilation Cross Talk and a Second Function for Ure2p inSaccharomyces cerevisiae
    Herman K. Edskes, Maryam Mukhamedova, Bouke K. Edskes, Reed B. Wickner · 2018 · Genetics
  9. DEF6, a Novel Substrate for the Tec Kinase ITK, Contains a Glutamine-rich Aggregation-prone Region and Forms Cytoplasmic Granules that Co-localize with P-bodies
    Fiona Hey, Nathan Czyzewicz, Peter Jones, Fred Sablitzky · 2012 · Journal of Biological Chemistry
  10. Prion-like properties of disease-relevant proteins in amyotrophic lateral sclerosis
    Stefan Bräuer, Vitaly L. Zimyanin, Andreas Hermann · 2018 · Journal of Neural Transmission
  11. Exploring Protein Misfolding and Aggregate Pathology in Neurodegenerative Diseases: From Molecular Mechanisms to Clinical Interventions
    Joel Theophilus Johnson, Winifred A. Fila, Christian Kosisochukwu Anumudu · 2025 · Applied Sciences
  12. Thermotolerance in S. cerevisiae as a model to study extracellular vesicle biology
    Curtis John Logan, Claire C. Staton, Joshua Oliver, Jeff Bouffard, Thomas David Daniel Kazmirchuk, Melissa Magi, Christopher Leonard Brett · 2024 · Journal of Extracellular Vesicles
  13. A Native‐Like Conformation for the C‐Terminal Domain of the Prion Ure2p within its Fibrillar Form
    Birgit Habenstein, Luc Bousset, Yannick Sourigues, Mehdi Kabani, Antoine Loquet, Beat H. Meier, Ronald Melki, Anja Böckmann · 2012 · Angewandte Chemie International Edition
  14. STITCHER: Dynamic assembly of likely amyloid and prion β‐structures from secondary structure predictions
    Allen W. Bryan, Charles W. O'Donnell, Matthew Ewald Menke, Lenore Cowen, Susan Lee Lindquist, Bonnie Berger · 2011 · Proteins Structure Function and Bioinformatics
  15. Amyloid oligomers: diffuse oligomer‐based transmission of yeast prions
    Hideki Taguchi, Shigeko Kawai‐Noma · 2010 · FEBS Journal
  16. The yeast prion protein Sup35 initiates α-synuclein pathology in mouse models of Parkinson’s disease
    Lanxia Meng, Congcong Liu, Yiming Li, Guiqin Chen, Min Xiong, Ting Yu, Lina Pan, Xingyu Zhang, Lingyan Zhou, Tao Guo et al. · 2023 · Science Advances
  17. Heterologous cross-seeding mimics cross-species prion conversion in a yeast model
    Namitha Vishveshwara, Susan Weiss Liebman · 2009 · BMC Biology
  18. Prion-like proteins and their computational identification in proteomes
    Cristina Batlle, Valentín Iglesias, Susanna Navarro, Salvador Ventura · 2017 · Expert Review of Proteomics
  19. Cost-effectiveness of immunization in The Gambia.
    R L Robertson, S O Foster, Harry F. Hull, P. J. Williams · 1985 · PubMed
  20. Alcohol oxidase (AOX1) from Pichia pastoris is a novel inhibitor of prion propagation and a potential ATPase
    Hong Zhang, Harriët M. Loovers, Li‐Qiong Xu, Mingzhu Wang, Pamela J. E. Rowling, Laura S. Itzhaki, Weimin Gong, Junmei Zhou, Gary W. Jones, Sarah Perrett · 2008 · Molecular Microbiology
  21. Normal levels of ribosome-associated chaperones cure two groups of [PSI+] prion variants
    Moonil Son, Reed B. Wickner · 2020 · Proceedings of the National Academy of Sciences
  22. MED15 prion-like domain forms a coiled-coil responsible for its amyloid conversion and propagation
    Cristina Batlle, Isabel Calvo, Valentín Iglesias, Cian J. Lynch, Marcos Gil-García, Manuel Serrano, Salvador Ventura · 2021 · Communications Biology
  23. [NSI +] determinant has a pleiotropic phenotypic manifestation that is modulated by SUP35, SUP45, and VTS1 genes
    Anton A. Nizhnikov, Zalina M. Magomedova, Aleksandr A. Rubel, Alexandra M. Kondrashkina, Sergey Georgievich Inge-Vechtomov, Alexey P. Galkin · 2012 · Current Genetics
  24. The effects of prion protein proteolysis and disaggregation on the strain properties of hamster scrapie
    Andrea M. Deleault, Nathan R. Deleault, Brent T. Harris, Judy R. Rees, Surachai Supattapone · 2008 · Journal of General Virology
  25. Immunomodulation for prion and prion-related diseases
    Thomas Wısnıewskı, Fernando Goñi · 2010 · Expert Review of Vaccines
  26. Single-particle tracking of quantum dot-conjugated prion proteins inside yeast cells
    Toshikazu Tsuji, Shigeko Kawai‐Noma, Chan‐Gi Pack, Hideki Terajima, Junichiro Yajima, Takayuki Nishizaka, Masataka Kinjo, Hideki Taguchi · 2011 · Biochemical and Biophysical Research Communications
  27. Correction: [SWI+], the Prion Formed by the Chromatin Remodeling Factor Swi1, Is Highly Sensitive to Alterations in Hsp70 Chaperone System Activity
    Justin Keith Hines, Xiaomo Li, Zhiqiang Du, Takashi Higurashi, Liming Li, Elizabeth Anne Craig · 2011 · PLoS Genetics
  28. The sensitive [SWI+] prion
    Justin Keith Hines, Elizabeth Anne Craig · 2011 · Prion
  29. Mass Determination of Entire Amyloid Fibrils by Using Mass Spectrometry
    Tristan Doussineau, Carole Mathevon, Lucie Altamura, Charlotte Vendrely, Philippe Dugourd, Vincent Forge, Rodolphe Antoine · 2015 · Angewandte Chemie
  30. Pernicious Pathogens or Expedient Elements of Inheritance: The Significance of Yeast Prions
    James S. Byers, Daniel F. Jarosz · 2014 · PLoS Pathogens
  31. Sequence specificity and fidelity of prion transmission in yeast
    Kathryn L. Bruce, Yury O. Chernoff · 2011 · Seminars in Cell and Developmental Biology
  32. Insights into the Structure of Amyloid Fibrils
    Karen E. Marshall, Louise C. Serpell · 2009 · The Open Biology Journal
  33. Prions are affected by evolution at two levels
    Reed B. Wickner, Amy Catherine Kelly · 2015 · Cellular and Molecular Life Sciences
  34. Fibres, crystals and polymorphism: the structural promiscuity of amyloidogenic peptides
    Karen E. Marshall, Louise C. Serpell · 2010 · Soft Matter
  35. Amyloids in Site-Specific Autoimmune Reactions and Inflammatory Responses
    Yanmei Huang, Xuezhi Hong, Jian Xing Shen, Li-Jun Geng, Yan-Hong Pan, Wei Ling, Hai‐Lu Zhao · 2020 · Frontiers in Immunology
  36. The Cellular Concentration of the Yeast Ure2p Prion Protein Affects Its Propagation as a Prion
    Myriam Crapeau, Christelle Marchal, Christophe Cullin, Laurent Maillet · 2009 · Molecular Biology of the Cell
  37. Varieties of Living Things: Life at the Intersection of Lineage and Metabolism
    John Dupré, Maureen A. O’Malley · 2013 · History, philosophy and theory of the life sciences
  38. Cellular Prion Protein Role in Cancer Biology: Is It A Potential Therapeutic Target?
    Saba Yousaf, Muhammad Mubeen Ahmad, Siwen Wu, Muhammad Anjum Zia, Ishtiaq Ahmed, Hafiz M.N. Iqbal, Qingyou Liu, Saif ur Rehman · 2022 · Biomedicines
  39. RepA-WH1prionoid
    Rafael Giraldo, Susana Moreno Dı́az de la Espina, M.E. Fernández-Tresguerres, Fátima Gasset-Rosa · 2011 · Prion
  40. C. elegans Models to Study the Propagation of Prions and Prion-Like Proteins
    Carl Alexander Sandhof, Simon Oliver Hoppe, Jessica Tittelmeier, Carmen I. Nussbaum-Krammer · 2020 · Biomolecules
  41. When amyloids become prions
    Raimon Sabaté · 2014 · Prion
  42. Suppression of Polyglutamine Toxicity by the Yeast Sup35 Prion Domain in Drosophila
    Ling-Bo Li, Kexiang Xu, Nancy M. Bonini · 2007 · Journal of Biological Chemistry
  43. Modulation of the Formation of Aβ- and Sup35NM-Based Amyloids by Complex Interplay of Specific and Nonspecific Ion Effects
    Aditi Sharma, Sven Holger Behrens, Yury O. Chernoff, Andreas Sebastian Bommarius · 2018 · The Journal of Physical Chemistry B
  44. Somatic incompatibility and genetic structure of fungal crops in sympatric Atta colombica and Acromyrmex echinatior leaf-cutting ants
    Pepijn W. Kooij, Michael Poulsen, Morten Schiøtt, Jacobus J. Boomsma · 2015 · Fungal ecology
  45. Impact of Amyloid Polymorphism on Prion-Chaperone Interactions in Yeast
    Andrea K. Wegrzynowicz, Sarah C. Miller, Justin Keith Hines · 2019 · Viruses
  46. Innate immunity to prions: anti-prion systems turn a tsunami of prions into a slow drip
    Reed B. Wickner, Herman K. Edskes, Moonil Son, Songsong Wu, Madaleine M Niznikiewicz · 2021 · Current Genetics
  47. A nucleolar protein allows viability in the absence of the essential ER-residing molecular chaperone calnexin
    Pascale B. Beauregard, Renée Guérin, Cynthia L. Turcotte, Susan Lee Lindquist, Luis A. Rokeach · 2009 · Journal of Cell Science
  48. Prions: structure, function, evolution, and disease
    Clara Casey, Roy D. Sleator · 2024 · Archives of Microbiology
  49. Decoding the role of coiled-coil motifs in human prion-like proteins
    Molood Behbahanipour, Javier García‐Pardo, Salvador Ventura · 2021 · Prion
  50. How Do Yeast Cells Contend with Prions?
    Reed B. Wickner, Herman K. Edskes, Moonil Son, Songsong Wu, Madaleine M Niznikiewicz · 2020 · International Journal of Molecular Sciences
  51. Self-propagating amyloid as a critical regulator for diverse cellular functions
    Shinju Sugiyama, Motomasa Tanaka · 2014 · The Journal of Biochemistry
  52. Yeast Prions: Proteins Templating Conformation and an Anti-prion System
    Reed B. Wickner, Herman K. Edskes, David A. Bateman, Anton Gorkovskiy, Yaron Dayani, Evgeny E. Bezsonov, Maryam Mukhamedova · 2015 · PLoS Pathogens
  53. Active conversion to the prion state as a molecular switch for cellular adaptation to environmental stress
    Genjiro Suzuki, Motomasa Tanaka · 2012 · BioEssays
  54. Prion-specific Hsp40 function: The role of the auxilin homolog Swa2
    Emily E. Oliver, Elizabeth M. Troisi, Justin Keith Hines · 2017 · Prion
  55. The yeast protein Ure2p triggers Tau pathology in a mouse model of tauopathy
    Lanxia Meng, Congcong Liu, Miao Liu, Jiehui Chen, Chaoyang Liu, Zhaohui Zhang, Guiqin Chen, Zhentao Zhang · 2023 · Cell Reports
  56. Exposed Hsp70-binding site impacts yeast Sup35 prion disaggregation and propagation
    Howard C.-H. Shen, Yusuke Komi, Yoshiko Nakagawa, Yuji O. Kamatari, Takashi Nomura, Hiromi Kimura, Toshinobu Shida, John Burke, Shingo Tamai, Yasuhiro Ishida et al. · 2024 · Proceedings of the National Academy of Sciences
  57. Septin-Containing Barriers Control the Differential Inheritance of Cytoplasmic Elements
    Alan Michael Tartakoff, Ilya Aylyarov, Purnima Jaiswal · 2012 · Cell Reports
  58. Expanding the yeast prion world
    Genjiro Suzuki, Motomasa Tanaka · 2013 · Prion
  59. Discovering Protein-based Inheritance through Yeast Genetics
    Reed B. Wickner · 2012 · Journal of Biological Chemistry
  60. Bend or break: how biochemically versatile molecules enable metabolic division of labor in clonal microbial communities
    Sriram Varahan, Sunil Laxman · 2021 · Genetics
  61. Patterns of [PSI+] aggregation allow insights into cellular organization of yeast prion aggregates
    Jens Tyedmers · 2012 · Prion
  62. Identity determinants of infectious proteins
    Yury O. Chernoff · 2008 · Proceedings of the National Academy of Sciences
  63. Chaperone functional specificity promotes yeast prion diversity
    Andrea K. Wegrzynowicz, Justin Keith Hines · 2018 · PLoS Pathogens
  64. Biomimetic and bioinspired design of collective systems
    Thomas Schmickl, Karl Crailsheim, Jean‐Louis Deneubourg, José Halloy · 2011 · VU Research Portal
  65. Delayed Encounter of Parental Genomes Can Lead to Aneuploidy in Saccharomyces cerevisiae
    Alan Michael Tartakoff, David Dulce, Elizabeth Landis · 2017 · Genetics
  66. Michler’s hydrol blue elucidates structural differences in prion strains
    Yiling Xiao, Sandra Rocha, Catherine C. Kitts, Anna Reymer, Tamás Beke‐Somfai, Kendra K. Frederick, Bengt Nordén · 2020 · Proceedings of the National Academy of Sciences
  67. The multiple assemblies of VDAC: from conformational heterogeneity to β-aggregation and amyloid formation
    Alexandre Boulbrima, Davina Temple, Georgios Psakis · 2016 · Biochemical Society Transactions
  68. Candida albicans Is Resistant to Polyglutamine Aggregation and Toxicity
    Michelle D. Leach, Taehyung P. Kim, Sonja E. Di Gregorio, Cathy Collins, Zhaolei Zhang, Martin L. Duennwald, Leah E. Cowen · 2017 · G3 Genes Genomes Genetics
  69. Molecular shape as a key source of prebiotic information
    Hugo I. Cruz‐Rosas, Francisco Riquelme, Alejandra Ramírez-Padrón, Thomas Buhse, G. Cocho, Pedro Miramóntes · 2020 · Journal of Theoretical Biology
  70. Amyloids as Sensors and Protectors (ASAP) Hypothesis
    Rachel Petrofes Chapa, Michael A. Emery, Janelle N. Fawver, Ian V.J. Murray · 2012 · Journal of Alzheimer s Disease
  71. The interaction of Hsp104 with yeast prion Sup35 as analyzed by fluorescence cross-correlation spectroscopy
    Shohei Ohta, Shigeko Kawai‐Noma, Akira Kitamura, Chan‐Gi Pack, Masataka Kinjo, Hideki Taguchi · 2013 · Biochemical and Biophysical Research Communications
  72. The fibrils of Ure2p homologs from Saccharomyces cerevisiae and Saccharoymyces paradoxus have similar cross-β structure in both dried and hydrated forms
    Yiqian Wang, Marie N. Bongiovanni, Sally Louise Gras, Sarah Perrett · 2011 · Journal of Structural Biology
  73. Understanding the Small World: The Microbes
    Pompee Chanda, Santa Ram Joshi · 2022 · Springer eBooks
  74. Endogenous Viral Etiology of Prion Diseases
    CLAUDIU I. BANDEA · 2009 · Nature Precedings
  75. A Native‐Like Conformation for the C‐Terminal Domain of the Prion Ure2p within its Fibrillar Form
    Birgit Habenstein, Luc Bousset, Yannick Sourigues, Mehdi Kabani, Antoine Loquet, Beat H. Meier, Ronald Melki, Anja Böckmann · 2012 · Angewandte Chemie
  76. Functional amyloids
    Mansoureh Mirza Agha, Elaheh Tavili, Bahareh Dabirmanesh · 2024 · Progress in molecular biology and translational science
  77. Genome wide association studies and prion disease
    Ana Lukić, Simon Mead · 2011 · Prion
  78. Anti-Prion Systems in Saccharomyces cerevisiae Turn an Avalanche of Prions into a Flurry
    Moonil Son, Reed B. Wickner · 2022 · Viruses
  79. Search for genes influencing the maintenance of the [ISP +] prion-like antisuppressor determinant in yeast with the use of an insertion gene library
    Tatyana M. Rogoza, Olga Viktorovskaya, S. A. Rodionova, M. S. Ivanov, Kirill V. Volkov, Ludmila N Mironova · 2009 · Molecular Biology
  80. Molecular Basis of Prion Diseases
    Jonathan D. F. Wadsworth, John Collinge · 2012 · Elsevier eBooks
  81. Nouvelles formes de maladies à prions chez les ruminants
    Hubert Laude, Vincent Béringue · 2008 · Pathologie Biologie
  82. The SFP1 controls translation termination in Saccharomyces cerevisiae via regulation of Sup35p (eRF3) level
    Polina B. Drozdova, Elina A. Radchenko, Tatyana M. Rogoza, Maria Khokhrina, Ludmila N Mironova · 2013 · Molecular Biology
  83. A New Interpretative Paradigm for Conformational Protein Diseases
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  84. STITCHER: Dynamic assembly of likely amyloid and prion beta-structures from secondary structure predictions
    Allen W. Bryan, Charles William O'Donnell, Matthew Ewald Menke, Lenore Cowen, Susan Lee Lindquist, Bonnie Berger · 2011
  85. New insights into the molecular mechanism of amyloid formation from cysteine scanning
    Li Fei, Sarah Perrett · 2010 · Prion
  86. Amyloid‐Like Fibrils: Origin, Structure, Properties, and Potential Technological Applications
    Pablo Taboada, Sílvia Barbosa, Josué Juárez, Manuel Alatorre‐Meda, Vı́ctor Mosquera · 2013 · Wiley eBooks
  87. Conformational conversion and prion disease
    Liang Shen, Hong‐Fang Ji · 2011 · Nature Reviews Molecular Cell Biology
  88. Anti‐Prion Systems in Saccharomyces cerevisiae
    Reed B. Wickner, Yuho Hayashi, Herman K. Edskes · 2025 · Journal of Neurochemistry
  89. Prion: disease or relief?
    Yury O. Chernoff · 2008 · Nature Cell Biology
  90. Site-specific structural analysis of a yeast prion strain with species-specific seeding activity
    Anna Marie C. Marcelino, Moumita Bhattacharya, Aaron C. Anselmo, Peter M. Tessier · 2011 · Prion
  91. Review: The Prion and its Potentiality
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  92. Amyloids and prions in the light of evolution
    Alexey P. Galkin, Evgeniy I. Sysoev, Anna A. Valina · 2023 · Current Genetics
  93. References
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  94. Determination of growth-phase dependent influences exerted by prions on yeast lipid content using HPTLC—densitometry
    Quang H.D. Bui, J. Sherma, Bernard N. Fried, Justin Keith Hines · 2015 · Acta Chromatographica
  95. When amyloids become prions
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  96. Anti-Prion Systems Block Prion Transmission, Attenuate Prion Generation, Cure Most Prions as They Arise and Limit Prion-Induced Pathology in Saccharomyces cerevisiae
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  97. Hsp40/JDP Requirements for the Propagation of Synthetic Yeast Prions
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  98. Yeast Genetic Structures and Functions
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