プリオン (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "プリオン" in Japanese language version.

refsWebsite

Global rank Japanese rank

46nih.gov

4^th place

24^th place

34doi.org

2^nd place

6^th place

3pnas.org

1,293^rd place

1,250^th place

1wikimedia.org

low place

1oed.com

360^th place

1,515^th place

1oxforddnb.com

284^th place

1,706^th place

1nobelprize.org

301^st place

644^th place

1sciencemag.org

857^th place

1,005^th place

1cdc.gov

218^th place

712^th place

1sciencedaily.com

993^rd place

2,074^th place

1washingtonpost.com

34^th place

255^th place

1kfu.edu.sa

low place

1bbc.co.uk

8^th place

73^rd place

1hpa.org.uk

low place

1yale.edu

565^th place

1,647^th place

1bseinquiry.gov.uk

low place

1wisc.edu

1,045^th place

2,105^th place

1jbc.org

4,455^th place

3,334^th place

1web.archive.org

1^st place

1livedoor.com

1,049^th place

71^st place

bbc.co.uk

news.bbc.co.uk

(1999-05-28.) "BSE proteins may cause fatal insomnia." (News website.) BBC News. 2007年9月27日閲覧。

bseinquiry.gov.uk

“Normal Function of Prions, Statement to the BSE Inquiry” (PDF). 2009年11月14日閲覧。

cdc.gov

“Prion Diseases”. US Centers for Disease Control. 2007年5月13日閲覧。

doi.org

Prusiner, SB (1982). “Novel proteinaceous infectious particles cause scrapie”. Science 216 (4542): 136–144. doi:10.1126/science.278.5336.245. PMID 6801762.
Aguzzi A (January 2008). “Unraveling prion strains with cell biology and organic chemistry”. Proc. Natl. Acad. Sci., USA 105 (1): 11–2. doi:10.1073/pnas.0710824105. PMC 2224168. PMID 18172195.
Prusiner SB (1998). “Prions”. Proc. Natl. Acad. Sci., USA 95 (23): 13363–83. doi:10.1073/pnas.95.23.13363. PMID 9811807.
Dobson CM (2001). “The structural basis of protein folding and its links with human disease”. Philos. Trans. R. Soc. Lond. B Biol. Sci. 356 (1406): 133–145. doi:10.1098/rstb.2000.0758. PMID 11260793.
Lindquist S, Krobitsch S, Li L and Sondheimer N (2001). “Investigating protein conformation-based inheritance and disease in yeast”. Philos. Trans. R. Soc. Lond. B Biol. Sci. 356 (1406): 169–176. doi:10.1098/rstb.2000.0762. PMID 11260797.
Alper T, Cramp W, Haig D, Clarke M (1967). “Does the agent of scrapie replicate without nucleic acid?”. Nature 214 (5090): 764–6. doi:10.1038/214764a0. PMID 4963878.
Griffith J (1967). “Self-replication and scrapie”. Nature 215 (5105): 1043–4. doi:10.1038/2151043a0. PMID 4964084.
Crick F (1970). “Central dogma of molecular biology”. Nature 227 (5258): 561–3. doi:10.1038/227561a0. PMID 4913914.
Priola, Suzette A.; Chesebro, Bruce; Caughey, Byron (2003). “A View from the Top--Prion Diseases from 10,000 Feet”. Science 300 (5621): 917–919. doi:10.1126/science.1085920. PMID 12738843 2007年1月16日閲覧。.
Hegde RS, Mastrianni JA, Scott MR, Defea KA, Tremblay P, Torchia M, DeArmond SJ, Prusiner SB, Lingappa VR (1998). “A transmembrane form of the prion protein in neurodegenerative disease”. Science 276: 827–834. doi:10.1126/science.279.5352.827. PMID 9452375.
Weissmann, C (2004). “The State of the Prion”. Nature Reviews Microbiology 2: 861–871. doi:10.1038/nrmicro1025. PMID 15494743.
Shorter J, Lindquist S (2005). “Prions as adaptive conduits of memory and inheritance”. Nat Rev Genet 6 (6): 435–50. doi:10.1038/nrg1616. PMID 15931169.
Maglio L, Perez M, Martins V, Brentani R, Ramirez O (2004). “Hippocampal synaptic plasticity in mice devoid of cellular prion protein”. Brain Res Mol Brain Res 131 (1-2): 58–64. doi:10.1016/j.molbrainres.2004.08.004. PMID 15530652.
Zhang CC, Steele AD, Lindquist S, Lodish HF (February 2006). “Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their self-renewal”. Proc. Natl. Acad. Sci. U.S.A. 103 (7): 2184–9. doi:10.1073/pnas.0510577103. PMC 1413720. PMID 16467153.
Belay E. (1999). “Transmissible Spongiform Encephalopathies in Humans”. Annu. Rev. Microbiol. 53: 283–314. doi:10.1146/annurev.micro.53.1.283. PMID 10547693.
Gilch, Sabine, et al. (2001). “Intracellular re-routing of prion protein prevents propagation of PrPSc and delays onset of prion disease”. The EMBO Journal 20 (15): 3957–3966. doi:10.1093/emboj/20.15.3957. PMID 11483499.
Büeler H, Aguzzi A, Sailer A, Greiner R, Autenried P, Aguet M, Weissmann C (1993). “Mice devoid of PrP are resistant to scrapie”. Cell 73 (7): 1339–47. doi:10.1016/0092-8674(93)90360-3. PMID 8100741.
Collinge J (2001). “Prion diseases of humans and animals: their causes and molecular basis”. Annu Rev Neurosci 24: 519–50. doi:10.1146/annurev.neuro.24.1.519. PMID 11283320.
Ironside, JW (2006). “Variant Creutzfeldt-Jakob disease: risk of transmission by blood transfusion and blood therapies”. Haemophilia 12 (s1): 8–15. doi:10.1111/j.1365-2516.2006.01195.x. PMID 16445812.
Telling G, Scott M, Mastrianni J, Gabizon R, Torchia M, Cohen F, DeArmond S, Prusiner S (1995). “Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein”. Cell 83 (1): e93. doi:10.1016/0092-8674(95)90236-8. PMID 7553876.
Johnson C, Pedersen, Chappell R, McKenzie D, Aiken J (2007). “Oral Transmissibility of Prion Disease is Enhanced by Binding to Soil Particles”. PLoS Pathogens 3 (7): e93. doi:10.1371/journal.ppat.0030093. PMID 17616973.
Qin K, O'Donnell M, Zhao R (2006). “Doppel: more rival than double to prion”. Neuroscience 141 (1): 1–8. doi:10.1016/j.neuroscience.2006.04.057. PMID 16781817.
Race RE, Raymond GJ (February 2004). “Inactivation of transmissible spongiform encephalopathy (prion) agents by environ LpH”. J. Virol. 78 (4): 2164–5. doi:10.1128/JVI.78.4.2164-2165.2004. PMC 369477. PMID 14747583.
Collins SJ, Lawson VA, Masters CL (2004). “Transmissible spongiform encephalopathies”. Lancet 363 (9402): 51–61. doi:10.1016/S0140-6736(03)15171-9. PMID 14723996.
Weissmann C, Enari M, Klöhn PC, Rossi D, Flechsig E (2002). “Transmission of prions”. Proc. Natl. Acad. Sci. U.S.A. 99 Suppl 4: 16378–83. doi:10.1073/pnas.172403799. PMID 12181490.
Sutton JM, Dickinson J, Walker JT and Raven NDH (2006). “Methods to Minimize the Risks of Creutzfeldt-Jakob Disease by Surgical Procedures: Where to Set the Standard?”. Clinical Infectious Diseases 43: 757–64. doi:10.1086/507030. PMID 16912952.
Deleault NR, Harris BT, Rees JR, Supattapone S (June 2007). “Formation of native prions from minimal components in vitro”. Proc. Natl. Acad. Sci. U.S.A. 104 (23): 9741–6. doi:10.1073/pnas.0702662104. PMC 1887554. PMID 17535913.
Geoghegan JC, Valdes PA, Orem NR, et al (December 2007). “Selective incorporation of polyanionic molecules into hamster prions”. J. Biol. Chem. 282 (50): 36341–53. doi:10.1074/jbc.M704447200. PMID 17940287.
Manuelidis L (March 2007). “A 25 nm virion is the likely cause of transmissible spongiform encephalopathies”. J. Cell. Biochem. 100 (4): 897–915. doi:10.1002/jcb.21090. PMID 17044041.
Laura Manuelidis, Zhoa-Xue Yu, Nuria Barquero, and Brian Mullins (2007-02-06). “Cells infected with scrapie and Creutzfeldt–Jakob disease agents produce intracellular 25-nm virus-like particles”. Proceedings of the National Academy of Sciences of the United States of America 104 (6): 1965–1970. doi:10.1073/pnas.0610999104. PMID 17267596.
Oesch B, Westaway D, Wälchli M, McKinley M, Kent S, Aebersold R, Barry R, Tempst P, Teplow D, Hood L (1985). “A cellular gene encodes scrapie PrP 27-30 protein”. Cell 40 (4): 735–46. doi:10.1016/0092-8674(85)90333-2. PMID 2859120.
Dong J, Bloom JD, Goncharov V, et al. (November 2007). “Probing the role of PrP repeats in conformational conversion and amyloid assembly of chimeric yeast prions”. The Journal of Biological Chemistry 282 (47): 34204–12. doi:10.1074/jbc.M704952200. PMC 2262835. PMID 17893150 2010年2月28日閲覧。.
Halfmann R, Alberti S, Lindquist S (2010). “Prions, protein homeostasis, and phenotypic diversity”. Trends in Cell Biology. doi:10.1016/j.tcb.2009.12.003. PMID 20071174.
Kuwata K, Nishida N, Matsumoto T, Kamatari YO, Hosokawa-Muto J, Kodama K, Nakamura HK, Kimura K, Kawasaki M, Takakura Y, Shirabe S, Takata J, Kataoka Y, Katamine S. (2007-07-17). “Hot spots in prion protein for pathogenic conversion”. Proc. Natl. Acad. Sci., USA 104 (29): 11921-11926. doi:10.1073/pnas.0702671104.

hpa.org.uk

英国健康保護局 (2005年4月14日). “Agency to test method for the deactivation of prions” (英語). 2005 Press Releases. 2009年11月14日閲覧。

jbc.org

Dong J, Bloom JD, Goncharov V, et al. (November 2007). “Probing the role of PrP repeats in conformational conversion and amyloid assembly of chimeric yeast prions”. The Journal of Biological Chemistry 282 (47): 34204–12. doi:10.1074/jbc.M704952200. PMC 2262835. PMID 17893150 2010年2月28日閲覧。.

kfu.edu.sa

Hussein, Mansour F. and Saud I. Al-Mufarrej. (2004.) "Prion Diseases: A Review; II. Prion Diseases in Man and Animals." Scientific Journal of King Faisal University (Basic and Applied Sciences), vol. 5, no. 2 1425, p. 139. 2007年9月27日閲覧。

livedoor.com

news.livedoor.com

“世界初、プリオンが解剖実習の遺体から発見される感染の危険も”. ライブドアニュース. 2022年6月15日時点のオリジナルよりアーカイブ。2024年9月19日閲覧。

nih.gov

pubmed.ncbi.nlm.nih.gov

Prusiner, SB (1982). “Novel proteinaceous infectious particles cause scrapie”. Science 216 (4542): 136–144. doi:10.1126/science.278.5336.245. PMID 6801762.
Aguzzi A (January 2008). “Unraveling prion strains with cell biology and organic chemistry”. Proc. Natl. Acad. Sci., USA 105 (1): 11–2. doi:10.1073/pnas.0710824105. PMC 2224168. PMID 18172195.
Prusiner SB (1998). “Prions”. Proc. Natl. Acad. Sci., USA 95 (23): 13363–83. doi:10.1073/pnas.95.23.13363. PMID 9811807.
Dobson CM (2001). “The structural basis of protein folding and its links with human disease”. Philos. Trans. R. Soc. Lond. B Biol. Sci. 356 (1406): 133–145. doi:10.1098/rstb.2000.0758. PMID 11260793.
Lindquist S, Krobitsch S, Li L and Sondheimer N (2001). “Investigating protein conformation-based inheritance and disease in yeast”. Philos. Trans. R. Soc. Lond. B Biol. Sci. 356 (1406): 169–176. doi:10.1098/rstb.2000.0762. PMID 11260797.
Alper T, Cramp W, Haig D, Clarke M (1967). “Does the agent of scrapie replicate without nucleic acid?”. Nature 214 (5090): 764–6. doi:10.1038/214764a0. PMID 4963878.
Griffith J (1967). “Self-replication and scrapie”. Nature 215 (5105): 1043–4. doi:10.1038/2151043a0. PMID 4964084.
Crick F (1970). “Central dogma of molecular biology”. Nature 227 (5258): 561–3. doi:10.1038/227561a0. PMID 4913914.
Priola, Suzette A.; Chesebro, Bruce; Caughey, Byron (2003). “A View from the Top--Prion Diseases from 10,000 Feet”. Science 300 (5621): 917–919. doi:10.1126/science.1085920. PMID 12738843 2007年1月16日閲覧。.
Hegde RS, Mastrianni JA, Scott MR, Defea KA, Tremblay P, Torchia M, DeArmond SJ, Prusiner SB, Lingappa VR (1998). “A transmembrane form of the prion protein in neurodegenerative disease”. Science 276: 827–834. doi:10.1126/science.279.5352.827. PMID 9452375.
Brown DR (1997). “The cellular prion protein binds copper in vivo.”. Nature 390: 684–687. PMID 9414160.
Weissmann, C (2004). “The State of the Prion”. Nature Reviews Microbiology 2: 861–871. doi:10.1038/nrmicro1025. PMID 15494743.
Pan KM, Baldwin M, Nguyen J, Gasset M, Serban A, Groth D, Mehlhorn I, Huang Z, Fletterick RJ, Cohen FE, Prusiner, SB (1993-01-01). “Conversion of alpha-helices into beta-sheets features in the formation of scrapie prion protein”. Proc. Natl. Acad. Sci., USA 90 (23): 10962–10966. PMID 7902575.
Brown DR (1999). “Normal prion protein has an activity like that of superoxide dismutase.”. Biochem J 344: 1-15. PMID 10548526.
Shorter J, Lindquist S (2005). “Prions as adaptive conduits of memory and inheritance”. Nat Rev Genet 6 (6): 435–50. doi:10.1038/nrg1616. PMID 15931169.
Maglio L, Perez M, Martins V, Brentani R, Ramirez O (2004). “Hippocampal synaptic plasticity in mice devoid of cellular prion protein”. Brain Res Mol Brain Res 131 (1-2): 58–64. doi:10.1016/j.molbrainres.2004.08.004. PMID 15530652.
Zhang CC, Steele AD, Lindquist S, Lodish HF (February 2006). “Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their self-renewal”. Proc. Natl. Acad. Sci. U.S.A. 103 (7): 2184–9. doi:10.1073/pnas.0510577103. PMC 1413720. PMID 16467153.
Belay E. (1999). “Transmissible Spongiform Encephalopathies in Humans”. Annu. Rev. Microbiol. 53: 283–314. doi:10.1146/annurev.micro.53.1.283. PMID 10547693.
Gilch, Sabine, et al. (2001). “Intracellular re-routing of prion protein prevents propagation of PrPSc and delays onset of prion disease”. The EMBO Journal 20 (15): 3957–3966. doi:10.1093/emboj/20.15.3957. PMID 11483499.
Büeler H, Aguzzi A, Sailer A, Greiner R, Autenried P, Aguet M, Weissmann C (1993). “Mice devoid of PrP are resistant to scrapie”. Cell 73 (7): 1339–47. doi:10.1016/0092-8674(93)90360-3. PMID 8100741.
Collinge J (2001). “Prion diseases of humans and animals: their causes and molecular basis”. Annu Rev Neurosci 24: 519–50. doi:10.1146/annurev.neuro.24.1.519. PMID 11283320.
Ironside, JW (2006). “Variant Creutzfeldt-Jakob disease: risk of transmission by blood transfusion and blood therapies”. Haemophilia 12 (s1): 8–15. doi:10.1111/j.1365-2516.2006.01195.x. PMID 16445812.
Telling G, Scott M, Mastrianni J, Gabizon R, Torchia M, Cohen F, DeArmond S, Prusiner S (1995). “Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein”. Cell 83 (1): e93. doi:10.1016/0092-8674(95)90236-8. PMID 7553876.
Johnson C, Pedersen, Chappell R, McKenzie D, Aiken J (2007). “Oral Transmissibility of Prion Disease is Enhanced by Binding to Soil Particles”. PLoS Pathogens 3 (7): e93. doi:10.1371/journal.ppat.0030093. PMID 17616973.
Qin K, O'Donnell M, Zhao R (2006). “Doppel: more rival than double to prion”. Neuroscience 141 (1): 1–8. doi:10.1016/j.neuroscience.2006.04.057. PMID 16781817.
Race RE, Raymond GJ (February 2004). “Inactivation of transmissible spongiform encephalopathy (prion) agents by environ LpH”. J. Virol. 78 (4): 2164–5. doi:10.1128/JVI.78.4.2164-2165.2004. PMC 369477. PMID 14747583.
Collins SJ, Lawson VA, Masters CL (2004). “Transmissible spongiform encephalopathies”. Lancet 363 (9402): 51–61. doi:10.1016/S0140-6736(03)15171-9. PMID 14723996.
Weissmann C, Enari M, Klöhn PC, Rossi D, Flechsig E (2002). “Transmission of prions”. Proc. Natl. Acad. Sci. U.S.A. 99 Suppl 4: 16378–83. doi:10.1073/pnas.172403799. PMID 12181490.
Sutton JM, Dickinson J, Walker JT and Raven NDH (2006). “Methods to Minimize the Risks of Creutzfeldt-Jakob Disease by Surgical Procedures: Where to Set the Standard?”. Clinical Infectious Diseases 43: 757–64. doi:10.1086/507030. PMID 16912952.
Deleault NR, Harris BT, Rees JR, Supattapone S (June 2007). “Formation of native prions from minimal components in vitro”. Proc. Natl. Acad. Sci. U.S.A. 104 (23): 9741–6. doi:10.1073/pnas.0702662104. PMC 1887554. PMID 17535913.
Geoghegan JC, Valdes PA, Orem NR, et al (December 2007). “Selective incorporation of polyanionic molecules into hamster prions”. J. Biol. Chem. 282 (50): 36341–53. doi:10.1074/jbc.M704447200. PMID 17940287.
Manuelidis L (March 2007). “A 25 nm virion is the likely cause of transmissible spongiform encephalopathies”. J. Cell. Biochem. 100 (4): 897–915. doi:10.1002/jcb.21090. PMID 17044041.
Laura Manuelidis, Zhoa-Xue Yu, Nuria Barquero, and Brian Mullins (2007-02-06). “Cells infected with scrapie and Creutzfeldt–Jakob disease agents produce intracellular 25-nm virus-like particles”. Proceedings of the National Academy of Sciences of the United States of America 104 (6): 1965–1970. doi:10.1073/pnas.0610999104. PMID 17267596.
Oesch B, Westaway D, Wälchli M, McKinley M, Kent S, Aebersold R, Barry R, Tempst P, Teplow D, Hood L (1985). “A cellular gene encodes scrapie PrP 27-30 protein”. Cell 40 (4): 735–46. doi:10.1016/0092-8674(85)90333-2. PMID 2859120.
Dong J, Bloom JD, Goncharov V, et al. (November 2007). “Probing the role of PrP repeats in conformational conversion and amyloid assembly of chimeric yeast prions”. The Journal of Biological Chemistry 282 (47): 34204–12. doi:10.1074/jbc.M704952200. PMC 2262835. PMID 17893150 2010年2月28日閲覧。.
Halfmann R, Alberti S, Lindquist S (2010). “Prions, protein homeostasis, and phenotypic diversity”. Trends in Cell Biology. doi:10.1016/j.tcb.2009.12.003. PMID 20071174.

ncbi.nlm.nih.gov

Aguzzi A (January 2008). “Unraveling prion strains with cell biology and organic chemistry”. Proc. Natl. Acad. Sci., USA 105 (1): 11–2. doi:10.1073/pnas.0710824105. PMC 2224168. PMID 18172195.
Zhang CC, Steele AD, Lindquist S, Lodish HF (February 2006). “Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their self-renewal”. Proc. Natl. Acad. Sci. U.S.A. 103 (7): 2184–9. doi:10.1073/pnas.0510577103. PMC 1413720. PMID 16467153.
"90. Prions - ICTVdB Index of Viruses." (Website.) U.S. National Institutes of Health website.2007年9月27日閲覧。
Race RE, Raymond GJ (February 2004). “Inactivation of transmissible spongiform encephalopathy (prion) agents by environ LpH”. J. Virol. 78 (4): 2164–5. doi:10.1128/JVI.78.4.2164-2165.2004. PMC 369477. PMID 14747583.
Deleault NR, Harris BT, Rees JR, Supattapone S (June 2007). “Formation of native prions from minimal components in vitro”. Proc. Natl. Acad. Sci. U.S.A. 104 (23): 9741–6. doi:10.1073/pnas.0702662104. PMC 1887554. PMID 17535913.

pmc.ncbi.nlm.nih.gov

Aguzzi A (January 2008). “Unraveling prion strains with cell biology and organic chemistry”. Proc. Natl. Acad. Sci., USA 105 (1): 11–2. doi:10.1073/pnas.0710824105. PMC 2224168. PMID 18172195.
Zhang CC, Steele AD, Lindquist S, Lodish HF (February 2006). “Prion protein is expressed on long-term repopulating hematopoietic stem cells and is important for their self-renewal”. Proc. Natl. Acad. Sci. U.S.A. 103 (7): 2184–9. doi:10.1073/pnas.0510577103. PMC 1413720. PMID 16467153.
Race RE, Raymond GJ (February 2004). “Inactivation of transmissible spongiform encephalopathy (prion) agents by environ LpH”. J. Virol. 78 (4): 2164–5. doi:10.1128/JVI.78.4.2164-2165.2004. PMC 369477. PMID 14747583.
Deleault NR, Harris BT, Rees JR, Supattapone S (June 2007). “Formation of native prions from minimal components in vitro”. Proc. Natl. Acad. Sci. U.S.A. 104 (23): 9741–6. doi:10.1073/pnas.0702662104. PMC 1887554. PMID 17535913.
Dong J, Bloom JD, Goncharov V, et al. (November 2007). “Probing the role of PrP repeats in conformational conversion and amyloid assembly of chimeric yeast prions”. The Journal of Biological Chemistry 282 (47): 34204–12. doi:10.1074/jbc.M704952200. PMC 2262835. PMID 17893150 2010年2月28日閲覧。.

nobelprize.org

“The Nobel Prize in Physiology or Medicine 1997”. NobelPrize.org. 2007年5月11日閲覧。

oed.com

IPA: /ˈpriː.ɒn/ 発音^{[ヘルプ/ファイル]}"Prion". Oxford English Dictionary (3rd ed.). Oxford University Press. September 2005. (要購読、またはイギリス公立図書館への会員加入。)。

oxforddnb.com

IPA: /ˈpriː.ɒn/ 発音^{[ヘルプ/ファイル]}"Prion". Oxford English Dictionary (3rd ed.). Oxford University Press. September 2005. (要購読、またはイギリス公立図書館への会員加入。)。

pnas.org

Pan KM, Baldwin M, Nguyen J, Gasset M, Serban A, Groth D, Mehlhorn I, Huang Z, Fletterick RJ, Cohen FE, Prusiner, SB (1993-01-01). “Conversion of alpha-helices into beta-sheets features in the formation of scrapie prion protein”. Proc. Natl. Acad. Sci., USA 90 (23): 10962–10966. PMID 7902575.
Laura Manuelidis, Zhoa-Xue Yu, Nuria Barquero, and Brian Mullins (2007-02-06). “Cells infected with scrapie and Creutzfeldt–Jakob disease agents produce intracellular 25-nm virus-like particles”. Proceedings of the National Academy of Sciences of the United States of America 104 (6): 1965–1970. doi:10.1073/pnas.0610999104. PMID 17267596.
Kuwata K, Nishida N, Matsumoto T, Kamatari YO, Hosokawa-Muto J, Kodama K, Nakamura HK, Kimura K, Kawasaki M, Takakura Y, Shirabe S, Takata J, Kataoka Y, Katamine S. (2007-07-17). “Hot spots in prion protein for pathogenic conversion”. Proc. Natl. Acad. Sci., USA 104 (29): 11921-11926. doi:10.1073/pnas.0702671104.

sciencedaily.com

New York University Medical Center and School of Medicine (2005年5月14日). “Active Vaccine Prevents Mice From Developing Prion Disease”. Science Daily. 2007年5月8日閲覧。

sciencemag.org

Priola, Suzette A.; Chesebro, Bruce; Caughey, Byron (2003). “A View from the Top--Prion Diseases from 10,000 Feet”. Science 300 (5621): 917–919. doi:10.1126/science.1085920. PMID 12738843 2007年1月16日閲覧。.

washingtonpost.com

Weiss, Rick (2007年1月1日). “Scientists Announce Mad Cow Breakthrough.”. The Washington Post 2007年1月1日閲覧. "Scientists said yesterday that they have used genetic engineering techniques to produce the first cattle that may be biologically incapable of getting mad cow disease."

web.archive.org

“世界初、プリオンが解剖実習の遺体から発見される感染の危険も”. ライブドアニュース. 2022年6月15日時点のオリジナルよりアーカイブ。2024年9月19日閲覧。

wikimedia.org

upload.wikimedia.org

IPA: /ˈpriː.ɒn/ 発音^{[ヘルプ/ファイル]}"Prion". Oxford English Dictionary (3rd ed.). Oxford University Press. September 2005. (要購読、またはイギリス公立図書館への会員加入。)。

wisc.edu

ansci.wisc.edu

David L. Thomas. “Genetics of Scrapie resistance in sheep” (word). 2009年11月14日閲覧。

yale.edu

“Pathogenic Virus Found in Mad Cow Cells”. Yale. (2007年2月2日) 2007年2月2日閲覧。