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Books on the topic 'Prione'

Author: Grafiati

Published: 9 March 2023

Last updated: 11 March 2023

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1

C, Telling Glenn, ed. Prions and prion diseases: Current perspectives. Norfolk, Eng: Horizon Bioscience, 2004.

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2

Zhang, Jiapu. Molecular Structures and Structural Dynamics of Prion Proteins and Prions. Dordrecht: Springer Netherlands, 2015. http://dx.doi.org/10.1007/978-94-017-7318-8.

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3

Prusiner, Stanley B., ed. Prions Prions Prions. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-60983-1.

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4

Lewis, Patrick A. Prions. Washington, DC, USA: American Chemical Society, 2022. http://dx.doi.org/10.1021/acsinfocus.7e5002.

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5

Kitamoto, Tetsuyuki, ed. Prions. Tokyo: Springer-Verlag, 2005. http://dx.doi.org/10.1007/4-431-29402-3.

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6

Lawson, Victoria A., ed. Prions. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7244-9.

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7

Kleopatra, Ferla, ed. Priene. Cambridge, Mass: Harvard University Press, 2004.

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8

Kleopatra, Ferla, ed. Priene. 2nd ed. Athens, Greece: Foundation of the Hellenic World, 2005.

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9

Schweizer, Laurent. Prions: Roman. Paris: Seuil, 2004.

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10

Baker, Harry F., and Rosalind M. Ridley. Prion Diseases. New Jersey: Humana Press, 1996. http://dx.doi.org/10.1385/0896033422.

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11

Tatzelt, Jörg, ed. Prion Proteins. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-24067-6.

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12

Groschup, Martin H., and Hans A. Kretzschmar, eds. Prion Diseases. Vienna: Springer Vienna, 2000. http://dx.doi.org/10.1007/978-3-7091-6308-5.

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13

Liberski, Pawel P., ed. Prion Diseases. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7211-1.

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14

F, Baker Harry, and Ridley Rosalind M, eds. Prion diseases. Totowa, N.J: Humana Press, 1996.

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15

Winslow, Caughey Byron, ed. Prion proteins. San Diego: Academic Press, 2001.

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16

MD, Collinge John, and Palmer Mark S, eds. Prion diseases. Oxford: Oxford University Press, 1997.

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17

service), SpringerLink (Online, ed. Prion Proteins. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2011.

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18

Priene, Miletos, Didyma. Ankara: Keskin Color Kartpostalcilik, 1993.

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19

Zou, Wen-Quan, and Pierluigi Gambetti, eds. Prions and Diseases. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-5305-5.

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20

Zou, Wen-Quan, and Pierluigi Gambetti, eds. Prions and Diseases. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-5338-3.

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21

Zou, Wen-Quan, and Pierluigi Gambetti, eds. Prions and Diseases. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-20565-1.

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22

Zou, Wen-Quan, and Pierluigi Gambetti. Prions and diseases. New York: Springer, 2013.

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23

Hill, Andrew F., ed. Prion Protein Protocols. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-234-2.

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24

Blümel, Wolfgang. Die Inschriften von Priene. Bonn: Habelt, 2014.

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25

I racconti del Prione: Antologia del 2o premio nazionale di narrativa "Il Prione," 1994. La Spezia: Giacché, 1994.

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26

I racconti del Prione: Antologia del 3. premio nazionale di narrativa "Il Prione," 1995 : Premio speciale teatro. La Spezia: Giacché, 1995.

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27

Verdier, Jean-Michel. Prions and Prion Diseases: New Developments. Nova Science Publishers, Incorporated, 2012.

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28

Telling, Glenn. Prions and Prion Diseases: Current Perspectives (Horizonbioscience). Taylor & Francis, 2004.

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29

Cashman, Neil. Prions and Prion Diseases (Neurological Disease and Therapy). Informa Healthcare, 2009.

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30

Prusiner, Stanley B. Prions Prions Prions. Springer London, Limited, 2012.

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31

Prusiner, Stanley B. Prions Prions Prions. Springer Berlin / Heidelberg, 2011.

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32

Zhang, Jiapu. Molecular Structures and Structural Dynamics of Prion Proteins and Prions: Mechanism Underlying the Resistance to Prion Diseases. Springer, 2015.

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33

Zhang, Jiapu. Molecular Structures and Structural Dynamics of Prion Proteins and Prions: Mechanism Underlying the Resistance to Prion Diseases. Springer, 2016.

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34

Prions, Prions, Prions (Current Topics in Microbiology and Immunology). Springer, 1996.

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35

Soto, Claudio. Prions. Taylor & Francis Group, 2019.

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36

Rabenau, H. F., J. Cinatl, and H. W. Doerr, eds. Prions. S. Karger AG, 2000. http://dx.doi.org/10.1159/isbn.978-3-318-00622-3.

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37

Rabenau, H. F., J. Cinatl, and H. W. Doerr, eds. Prions. S. Karger AG, 2004. http://dx.doi.org/10.1159/isbn.978-3-318-01032-9.

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38

Meyer, Harriet S. Prions. Oxford University Press, 2009. http://dx.doi.org/10.1093/jama/9780195176339.022.528.

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39

Kitamoto, Tetsuyuki. Prions. Springer, 2008.

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40

Gleason, Holly. Prine on Prine: Interviews and Encounters with John Prine. Chicago Review Press, Incorporated, 2022.

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41

Gleason, Holly. Prine on Prine: Interviews and Encounters with John Prine. Chicago Review Press, Incorporated, 2022.

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42

Gleason, Holly. Prine on Prine: Interviews and Encounters with John Prine. Chicago Review Press, Incorporated, 2022.

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43

Gleason, Holly. Prine on Prine: Interviews and Encounters with John Prine. Chicago Review Press, Incorporated, 2022.

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44

Peaseland, John. Prion. Independently Published, 2017.

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45

Peaseland, John. Prion. Lulu Press, Inc., 2014.

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46

Subbarao, Italo, and Ed Hsu. Prion. 2012.

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47

Legname, Giuseppe, and Silvia Vanni. Prion Protein. Elsevier Science & Technology Books, 2017.

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48

Prion Proteins. Springer Berlin / Heidelberg, 2013.

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49

Mastrianni, James A., and Joshuae G. Gallardo. Prion Diseases. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0166.

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Abstract:

Prion diseases are transmissible fatal neurodegenerative disorders resulting from the accumulation of misfolded prion protein. Although primarily sporadic diseases, 5% to 10% result from a mutation of the prion protein gene (PRNP), and less than 1% occur from exposure to prions. The current family of prion diseases includes Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker disease (GSS), fatal insomnia (FI), variant CJD (vCJD), and variably protease-sensitive prionopathy (VPSPr). Kuru is a disease of historical interest that was transmitted through cannibalistic rituals. Iatrogenic CJD (iCJD) is the result of secondary transmission of prion disease from contaminated biologicals.

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50

Knight, Richard. Prion disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0319.

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Abstract:

Prion diseases (also known as transmissible spongiform encephalopathies (TSEs)) affect animals and humans, although only the human diseases will be discussed in this chapter. Despite TSEs having somewhat disparate causes and effects, there are unifying features: TSEs are brain diseases with neurodegenerative pathology, which is typically associated with spongiform change, and, most characteristically, there is tissue deposition of an abnormal structural form of the prion protein. Some of the TSEs are naturally acquired infections and, while others are not, they are potentially transmissible in certain circumstances.

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