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Books on the topic 'Prion'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

1942-, Prusiner Stanley B., and Ridley Rosalind M, eds. Prion biology and diseases. Cold Spring Harbor Laboratory Press, 1999.

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1942-, Prusiner Stanley B., ed. Prion biology and diseases. 2nd ed. Cold Spring Harbor Laboratory Press, 2004.

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3

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

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4

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

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5

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

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6

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

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7

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

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8

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

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9

Winslow, Caughey Byron, ed. Prion proteins. Academic Press, 2001.

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10

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

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11

F, Baker Harry, and Ridley Rosalind M, eds. Prion diseases. Humana Press, 1996.

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12

F, Hill A., ed. Prion protein protocols. Humana, 2008.

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13

F, Baker Harry, ed. Molecular and cellular pathology in prion disease. Humana Press, 2001.

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14

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

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15

O, Morrison Douglas R., North Atlantic Treaty Organization. Scientific Affairs Division., and NATO Advanced Research Workshop on Prions and Brain Diseases in Animals and Humans (1996 : Erice, Italy), eds. Prions and brain diseases in animals and humans. Plenum Press, in cooperation with NATO Scientific Affairs Division, 1998.

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16

Science, Institute of Medicine (U S. ). Committee on Transmissible Spongiform Encephalopathies: Assessment of Relevant. Advancing prion science: Guidance for the national prion research program. National Academies Press, 2004.

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17

Dr, Soto Claudio, ed. Prions: The new biology of proteins. CRC/Taylor & Francis, 2006.

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18

Lehmann, Sylvain, and Jacques Grassi, eds. Techniques in Prion Research. Birkhäuser Basel, 2004. http://dx.doi.org/10.1007/978-3-0348-7949-1.

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19

Brown, David R., ed. Neurodegeneration and Prion Disease. Springer-Verlag, 2005. http://dx.doi.org/10.1007/b103635.

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20

PhD, Brown David R., ed. Neurodegeneration and prion disease. Springer Science+Business Media, 2005.

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21

1965-, Lehmann Sylvain, and Grassi Jacques 1951-, eds. Techniques in prion research. Birkhäuser, 2004.

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22

Béringue, Vincent. Prion Biology. Taylor & Francis Group, 2021.

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23

Prusiner, Stanley B. Prion Biology and Diseases. Cold Spring Harbor Laboratory Press, 1999.

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24

Peaseland, John. Prion. Independently Published, 2017.

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25

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

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26

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

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27

(Editor), Holger F. Rabenau, Jindrich Cinatl (Editor), and Hans Wilhelm Doerr (Editor), eds. Prions: A Challenge for Science, Medicine and Public Health System (Contributions to Microbiology, Vol. 7). S. Karger Publishers (USA), 2001.

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28

(Collaborator), Detlev Riesner, Hans Kretzschmar (Collaborator), and Beat Hornlimann (Editor), eds. Prions in Humans and Animals. Walter de Gruyter, 2006.

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29

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

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30

Kitamoto, Tetsuyuki. Prions: Food and Drug Safety. Springer, 2005.

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31

Kitamoto, Tetsuyuki. Prions. Springer, 2008.

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32

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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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. Iatrogen

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33

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

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34

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

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35

Prusiner, Stanley B. Prion Biology. Cold Spring Harbor Laboratory Press, 2017.

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36

Prion Protein. Elsevier, 2017. http://dx.doi.org/10.1016/s1877-1173(17)x0007-0.

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37

Bain, Darrell. Prion Promises. Double Dragon Publishing, 2005.

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38

Prusiner, Stanley B. Prion Diseases. Oxford University Press, 2017.

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39

Ridley, Rosalind M., and Harry F. Baker. Prion Diseases. Humana Press, 2013.

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40

Berg, Diane, and David Rough. Prion-4. Independently Published, 2018.

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41

Prion Catalogue. Prion Books Ltd (formerly Multimedia Books Ltd), 1999.

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42

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

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43

Liberski, Pawel. Prion Diseases. Humana Press, 2017.

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44

Davis, Garrett. Prion Paradigm. Davis, Garrett, 2022.

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45

Miller, Robert A. Prion Madness. Publishers Circulation Corp., 1998.

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46

Caughey, Byron. Prion Proteins. Elsevier Science & Technology Books, 2001.

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47

Tatzelt, Jörg. Prion Proteins. Springer, 2011.

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48

Liberski, Pawel P. Prion Diseases. Springer New York, 2018.

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49

Prion Proteins. Springer Berlin / Heidelberg, 2013.

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50

Prion Biology. Cold Spring Harbor Laboratory Press, 2017.

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