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Prion (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Prion" in German language version.

Last modified:

Ref.Un. Ref.Website
Global rank German rank
1917doi.org
2nd place
3rd place
86zdb-katalog.de
107th place
5th place
88nih.gov
5th place
7th place
53nature.com
207th place
227th place
22meduniwien.ac.at
low place
2,800th place
22europa.eu
62nd place
21st place
11leo.org
low place
1,441st place
11oup.com
292nd place
564th place
11annualreviews.org
2,959th place
5,666th place
11pdb.org
low place
low place
11sciencedirect.com
137th place
321st place
11wiley.com
150th place
246th place
11nobelprize.org
265th place
526th place
11mdpi.com
1,887th place
1,072nd place
11frontiersin.org
3,332nd place
1,444th place
11portlandpress.com
low place
low place
11admin.ch
135th place
30th place
11elsevier.com
365th place
435th place
11sciencemag.org
1,019th place
763rd place
11idw-online.de
4,503rd place
303rd place

admin.ch (Global: 135th place; German: 30th place)

bag.admin.ch

annualreviews.org (Global: 2,959th place; German: 5,666th place)

doi.org (Global: 2nd place; German: 3rd place)

  • Adriano Aguzzi, Mathias Heikenwalder: Pathogenesis of prion diseases: current status and future outlook. In: Nature Reviews Microbiology. Band 4, Nr. 10, Oktober 2006, ISSN 1740-1534, S. 765–775, doi:10.1038/nrmicro1492 (nature.com [abgerufen am 9. Dezember 2025]).
  • C. Weissmann, M. Enari, P‐C. Klöhn, D. Rossi, E. Flechsig: Transmission of Prions. In: The Journal of Infectious Diseases. Band 186, s2, Dezember 2002, ISSN 0022-1899, S. S157–S165, doi:10.1086/344575 (oup.com [abgerufen am 9. Dezember 2025]).
  • Matthias Schmitz, Kathrin Dittmar, Franc Llorens, Ellen Gelpi, Isidre Ferrer, Walter J. Schulz-Schaeffer, Inga Zerr: Hereditary Human Prion Diseases: an Update. In: Molecular Neurobiology. Band 54, Nr. 6, 1. August 2017, ISSN 1559-1182, S. 4138–4149, doi:10.1007/s12035-016-9918-y.
  • Adriano Aguzzi, Asvin K. K. Lakkaraju, Karl Frontzek: Toward Therapy of Human Prion Diseases. In: Annual Review of Pharmacology and Toxicology. Band 58, Volume 58, 2018, 6. Januar 2018, ISSN 0362-1642, S. 331–351, doi:10.1146/annurev-pharmtox-010617-052745 (annualreviews.org [abgerufen am 9. Dezember 2025]).
  • K. M. Pan, M Baldwin: Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins. In: Proceedings of the National Academy of Sciences (PNAS). 90. Jahrgang, Nr. 23, 1993, S. 10962–10966, doi:10.1073/pnas.90.23.10962 (englisch, nih.gov [abgerufen am 2. Januar 2026]).
  • Zheng Zhou, Xu Yan: Fibril Formation of the Rabbit/Human/Bovine Prion Proteins. In: Biophysical Journal. 101. Jahrgang, Nr. 6, 2011, S. 1483–1492, doi:10.1016/j.bpj.2011.08.018 (englisch, sciencedirect.com [abgerufen am 2. Januar 2026]).
  • Reed Wickner, Frank Shewmaker: Protein inheritance (prions) based on parallel in-register β-sheet amyloid structures. In: BioEssays. 30. Jahrgang, Nr. 10, 2008, S. 955–964, doi:10.1002/bies.20821 (englisch, wiley.com [abgerufen am 2. Januar 2026]).
  • Claudia Acevedo Morantes, Holger Wille: The Structure of Human Prions: From Biology to Structural Models - Considerations and Pitfalls. In: Viruses. 6. Jahrgang, Nr. 10, 2014, S. 3875–3892, doi:10.3390/v6103875 (englisch, mdpi.com [abgerufen am 2. Januar 2026]).
  • K. A. Schwenke, K. Wagenführ: Kinetics of the reduction of Creutzfeldt-Jakob disease prion seeding activity by steam sterilization support the use of validated 134 °C programmes. In: Journal of Hospital Infection. 132. Jahrgang, Nr. 10, 2023, S. 125–132, doi:10.1016/j.jhin.2022.08.014 (englisch, nih.gov [abgerufen am 2. Januar 2026]).
  • M. J. Jung, D. Pistolesi: Prions, prion diseases and decontamination. In: Igiene e Sanita Pubblica. 59. Jahrgang, Nr. 5, 2003, S. 331–344, doi:10.1016/j.jhin.2022.08.014 (englisch, nih.gov [abgerufen am 2. Januar 2026]).
  • Séverine Martin-Lannerée, Théo Z. Hirsch: PrPC from stem cells to cancer. In: Frontiers in Cell and Developmental Biology. 2. Jahrgang, Nr. 10, 2014, S. 125–132, doi:10.3389/fcell.2014.00055 (englisch, frontiersin.org [abgerufen am 2. Januar 2026]).
  • Giovanna Mde Brito, Fernanda Lupinacci: Loss of prion protein is associated with the development of insulin resistance and obesity. In: Biochemical Journal. 474. Jahrgang, Nr. 17, 2017, S. 2981–2991, doi:10.1042/BCJ20170137 (englisch, portlandpress.com [abgerufen am 2. Januar 2026]).
  • Simone Baiardi, Angela Mammana, Sabina Capellari, Piero Parchi: Human prion disease: molecular pathogenesis, and possible therapeutic targets and strategies. In: Expert Opinion on Therapeutic Targets. Band 27, Nr. 12, 2. Dezember 2023, ISSN 1472-8222, S. 1271–1284, doi:10.1080/14728222.2023.2199923, PMID 37334903.
  • Tikvah Alper, D.A. Haig, M.C. Clarke: The exceptionally small size of the scrapie agent. In: Biochemical and Biophysical Research Communications. Band 22, Nr. 3, S. 278–284, doi:10.1016/0006-291x(66)90478-5 (elsevier.com [abgerufen am 31. Oktober 2017]).
  • Tikvah Alper, W. A. Cramp, D. A. Haig, M. C. Clarke: Does the Agent of Scrapie Replicate without Nucleic Acid ? In: Nature. Band 214, Nr. 5090, 20. Mai 1967, S. 764–766, doi:10.1038/214764a0 (nature.com [abgerufen am 31. Oktober 2017]).
  • R. Latarjet, B. Muel, D. A. Haig, M. C. Clarke, Tikvah Alper: Inactivation of the Scrapie Agent by Near Monochromatic Ultraviolet Light. In: Nature. Band 227, Nr. 5265, 26. September 1970, S. 1341–1343, doi:10.1038/2271341a0 (nature.com [abgerufen am 31. Oktober 2017]).
  • Fei Wang, Xinhe Wang, Chong-Gang Yuan, Jiyan Ma: Generating a Prion with Bacterially Expressed Recombinant Prion Protein. In: Science. Band 327, Nr. 5969, 26. Februar 2010, ISSN 0036-8075, S. 1132–1135, doi:10.1126/science.1183748, PMID 20110469 (sciencemag.org [abgerufen am 31. Oktober 2017]).

elsevier.com (Global: 365th place; German: 435th place)

linkinghub.elsevier.com

  • Tikvah Alper, D.A. Haig, M.C. Clarke: The exceptionally small size of the scrapie agent. In: Biochemical and Biophysical Research Communications. Band 22, Nr. 3, S. 278–284, doi:10.1016/0006-291x(66)90478-5 (elsevier.com [abgerufen am 31. Oktober 2017]).

europa.eu (Global: 62nd place; German: 21st place)

food.ec.europa.eu

frontiersin.org (Global: 3,332nd place; German: 1,444th place)

  • Séverine Martin-Lannerée, Théo Z. Hirsch: PrPC from stem cells to cancer. In: Frontiers in Cell and Developmental Biology. 2. Jahrgang, Nr. 10, 2014, S. 125–132, doi:10.3389/fcell.2014.00055 (englisch, frontiersin.org [abgerufen am 2. Januar 2026]).

idw-online.de (Global: 4,503rd place; German: 303rd place)

leo.org (Global: low place; German: 1,441st place)

dict.leo.org

  • Das Wort prion wird auch als Abkürzung für den von Prusiner verwendeten Begriff proteinaceous infectious particle dargestellt, vgl. proteinaceous im LEO-Wörterbuch

mdpi.com (Global: 1,887th place; German: 1,072nd place)

  • Claudia Acevedo Morantes, Holger Wille: The Structure of Human Prions: From Biology to Structural Models - Considerations and Pitfalls. In: Viruses. 6. Jahrgang, Nr. 10, 2014, S. 3875–3892, doi:10.3390/v6103875 (englisch, mdpi.com [abgerufen am 2. Januar 2026]).

meduniwien.ac.at (Global: low place; German: 2,800th place)

nature.com (Global: 207th place; German: 227th place)

  • Adriano Aguzzi, Mathias Heikenwalder: Pathogenesis of prion diseases: current status and future outlook. In: Nature Reviews Microbiology. Band 4, Nr. 10, Oktober 2006, ISSN 1740-1534, S. 765–775, doi:10.1038/nrmicro1492 (nature.com [abgerufen am 9. Dezember 2025]).
  • Tikvah Alper, W. A. Cramp, D. A. Haig, M. C. Clarke: Does the Agent of Scrapie Replicate without Nucleic Acid ? In: Nature. Band 214, Nr. 5090, 20. Mai 1967, S. 764–766, doi:10.1038/214764a0 (nature.com [abgerufen am 31. Oktober 2017]).
  • R. Latarjet, B. Muel, D. A. Haig, M. C. Clarke, Tikvah Alper: Inactivation of the Scrapie Agent by Near Monochromatic Ultraviolet Light. In: Nature. Band 227, Nr. 5265, 26. September 1970, S. 1341–1343, doi:10.1038/2271341a0 (nature.com [abgerufen am 31. Oktober 2017]).

nih.gov (Global: 5th place; German: 7th place)

ncbi.nlm.nih.gov

  • Stanley B. Prusiner: Novel proteinaceous infectious particles cause scrapie. Science 1982, 216(4542), S. 136–144. PMID 6801762.
  • Simone Baiardi, Angela Mammana, Sabina Capellari, Piero Parchi: Human prion disease: molecular pathogenesis, and possible therapeutic targets and strategies. In: Expert Opinion on Therapeutic Targets. Band 27, Nr. 12, 2. Dezember 2023, ISSN 1472-8222, S. 1271–1284, doi:10.1080/14728222.2023.2199923, PMID 37334903.
  • R. M. Barron u. a.: High titres of TSE infectivity associated with extremely low levels of PrPSc in vivo. In: J Biol Chem. 2007 Oct 8. PMID 17923484
  • P. Piccardo u. a.: Accumulation of prion protein in the brain that is not associated with transmissible disease. In: Proc Natl Acad Sci U S A. 2007 Mar 13;104(11), S. 4712–4717. PMID 17360589.
  • Fei Wang, Xinhe Wang, Chong-Gang Yuan, Jiyan Ma: Generating a Prion with Bacterially Expressed Recombinant Prion Protein. In: Science. Band 327, Nr. 5969, 26. Februar 2010, ISSN 0036-8075, S. 1132–1135, doi:10.1126/science.1183748, PMID 20110469 (sciencemag.org [abgerufen am 31. Oktober 2017]).

pubmed.ncbi.nlm.nih.gov

  • K. A. Schwenke, K. Wagenführ: Kinetics of the reduction of Creutzfeldt-Jakob disease prion seeding activity by steam sterilization support the use of validated 134 °C programmes. In: Journal of Hospital Infection. 132. Jahrgang, Nr. 10, 2023, S. 125–132, doi:10.1016/j.jhin.2022.08.014 (englisch, nih.gov [abgerufen am 2. Januar 2026]).
  • M. J. Jung, D. Pistolesi: Prions, prion diseases and decontamination. In: Igiene e Sanita Pubblica. 59. Jahrgang, Nr. 5, 2003, S. 331–344, doi:10.1016/j.jhin.2022.08.014 (englisch, nih.gov [abgerufen am 2. Januar 2026]).

pmc.ncbi.nlm.nih.gov

  • K. M. Pan, M Baldwin: Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins. In: Proceedings of the National Academy of Sciences (PNAS). 90. Jahrgang, Nr. 23, 1993, S. 10962–10966, doi:10.1073/pnas.90.23.10962 (englisch, nih.gov [abgerufen am 2. Januar 2026]).

nobelprize.org (Global: 265th place; German: 526th place)

oup.com (Global: 292nd place; German: 564th place)

academic.oup.com

  • C. Weissmann, M. Enari, P‐C. Klöhn, D. Rossi, E. Flechsig: Transmission of Prions. In: The Journal of Infectious Diseases. Band 186, s2, Dezember 2002, ISSN 0022-1899, S. S157–S165, doi:10.1086/344575 (oup.com [abgerufen am 9. Dezember 2025]).

pdb.org (Global: low place; German: low place)

portlandpress.com (Global: low place; German: low place)

  • Giovanna Mde Brito, Fernanda Lupinacci: Loss of prion protein is associated with the development of insulin resistance and obesity. In: Biochemical Journal. 474. Jahrgang, Nr. 17, 2017, S. 2981–2991, doi:10.1042/BCJ20170137 (englisch, portlandpress.com [abgerufen am 2. Januar 2026]).

sciencedirect.com (Global: 137th place; German: 321st place)

  • Zheng Zhou, Xu Yan: Fibril Formation of the Rabbit/Human/Bovine Prion Proteins. In: Biophysical Journal. 101. Jahrgang, Nr. 6, 2011, S. 1483–1492, doi:10.1016/j.bpj.2011.08.018 (englisch, sciencedirect.com [abgerufen am 2. Januar 2026]).

sciencemag.org (Global: 1,019th place; German: 763rd place)

science.sciencemag.org

wiley.com (Global: 150th place; German: 246th place)

onlinelibrary.wiley.com

  • Reed Wickner, Frank Shewmaker: Protein inheritance (prions) based on parallel in-register β-sheet amyloid structures. In: BioEssays. 30. Jahrgang, Nr. 10, 2008, S. 955–964, doi:10.1002/bies.20821 (englisch, wiley.com [abgerufen am 2. Januar 2026]).

zdb-katalog.de (Global: 107th place; German: 5th place)

  • Adriano Aguzzi, Mathias Heikenwalder: Pathogenesis of prion diseases: current status and future outlook. In: Nature Reviews Microbiology. Band 4, Nr. 10, Oktober 2006, ISSN 1740-1534, S. 765–775, doi:10.1038/nrmicro1492 (nature.com [abgerufen am 9. Dezember 2025]).
  • C. Weissmann, M. Enari, P‐C. Klöhn, D. Rossi, E. Flechsig: Transmission of Prions. In: The Journal of Infectious Diseases. Band 186, s2, Dezember 2002, ISSN 0022-1899, S. S157–S165, doi:10.1086/344575 (oup.com [abgerufen am 9. Dezember 2025]).
  • Matthias Schmitz, Kathrin Dittmar, Franc Llorens, Ellen Gelpi, Isidre Ferrer, Walter J. Schulz-Schaeffer, Inga Zerr: Hereditary Human Prion Diseases: an Update. In: Molecular Neurobiology. Band 54, Nr. 6, 1. August 2017, ISSN 1559-1182, S. 4138–4149, doi:10.1007/s12035-016-9918-y.
  • Adriano Aguzzi, Asvin K. K. Lakkaraju, Karl Frontzek: Toward Therapy of Human Prion Diseases. In: Annual Review of Pharmacology and Toxicology. Band 58, Volume 58, 2018, 6. Januar 2018, ISSN 0362-1642, S. 331–351, doi:10.1146/annurev-pharmtox-010617-052745 (annualreviews.org [abgerufen am 9. Dezember 2025]).
  • Simone Baiardi, Angela Mammana, Sabina Capellari, Piero Parchi: Human prion disease: molecular pathogenesis, and possible therapeutic targets and strategies. In: Expert Opinion on Therapeutic Targets. Band 27, Nr. 12, 2. Dezember 2023, ISSN 1472-8222, S. 1271–1284, doi:10.1080/14728222.2023.2199923, PMID 37334903.
  • Fei Wang, Xinhe Wang, Chong-Gang Yuan, Jiyan Ma: Generating a Prion with Bacterially Expressed Recombinant Prion Protein. In: Science. Band 327, Nr. 5969, 26. Februar 2010, ISSN 0036-8075, S. 1132–1135, doi:10.1126/science.1183748, PMID 20110469 (sciencemag.org [abgerufen am 31. Oktober 2017]).