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Books on the topic 'Priones'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 April 2022

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1

Prion biology: Research and advances. Toronto: Apple Academic Press, 2013.

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2

Prions: Current progress in advanced research. Norfolk, UK: Caister Academic Press, 2013.

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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

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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5

Fatal flaws: How a misfolded protein baffled scientists and changed the way we look at the brain. New Haven: Yale University Press, 2013.

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6

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

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7

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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8

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

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9

Prion diseases of mammals and yeast: Molecular mechanisms and genetic features. New York: Springer, 1997.

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10

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

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11

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

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12

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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13

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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14

Roberts, Lona. Priodas. Caernarfon: Gwasg Pantycelyn, 1998.

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15

Mücke, W. Umwelt und Gesundheit: Aktuelle Themen des umweltbezogenen Gesundheitsschutzes : Persistenz von Prionen in der Umwelt? : Elektronensensibilität diagnostizierbar? : Umweltchemikalien und Hormonsystem. München: Utz Verlag, 2004.

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16

Porson, Richard, and James Scholefield, eds. Euripidis Tragoediae Priores Quatuor. Cambridge: Cambridge University Press, 2009. http://dx.doi.org/10.1017/cbo9780511697449.

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17

Lewis, Elisa. Priodas Branwen. Aberystwyth: Canolfan Astudiaethau Addysg, 2005.

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18

Coppack, Glyn. Abbeys & priories. Stroud, U.K: Tempus, 2006.

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19

Coppack, Glyn. Abbeys & priories. Stroud, Gloucestershire: Amberley, 2009.

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20

Treves, Kathleen. Prior's holt. Bath: Chivers, 1987.

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21

Qu'est-ce qu'un prion? Paris: Le Pommier, 2005.

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22

Max, D. T. The family that couldn't sleep: A medical mystery. New York, NY: Random House, 2007.

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23

Hörnlimann, Beat, Detlev Riesner, and Hans A. Kretzschmar, eds. Prions in Humans and Animals. Berlin, New York: Walter de Gruyter, 2006. http://dx.doi.org/10.1515/9783110200171.

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24

Baker, Harry F. Molecular Pathology of the Prions. New Jersey: Humana Press, 2001. http://dx.doi.org/10.1385/1592591345.

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25

Marc'hadour, Germain, and Jocelyne Malhomme. Prions avec Saint Thomas More. Angers: Editions Moreana, 1997.

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26

Alfred, Gercke. Chrysippea particulam priorem. Lipsiae: Typis B.G. Teubneri, 1991.

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27

Wilde, Oscar. An prionsa sona. [Baile Átha Cliath]: An Gúm, 1986.

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28

Saint-Exupéry, Antoine de. An prionsa beag. Belfast: Lagan Press, 2002.

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29

TROUBLE IN PRIOR'S FORD. [Place of publication not identified]: LITTLE, BROWN, 2015.

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30

Secrets in Prior's Ford. Long Preston: Magna, 2008.

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31

Saiz. Enfermedades Por Priones. Ars Medica, 2006.

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32

Adrogue, Daniel, August Casanovas, and Eduardo E. Smolko. Enfermedades Por Priones. Catalogos, 2004.

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33

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

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34

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

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35

Houston, Eve. Secrets in Prior's Ford (Priors Ford). Little, Brown Book Group, 2008.

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36

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

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37

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

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38

(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). 2nd ed. S. Karger AG (Switzerland), 2004.

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39

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

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40

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

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41

(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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42

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

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43

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

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44

Kitamoto, Tetsuyuki. Prions. Springer, 2008.

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45

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

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46

1963-, Seguin Eve, ed. Infectious processes: Knowledge, discourse, and the politics of prions. Basingstoke, Hampshire: Palgrave Macmillan, 2004.

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47

Seguin, Eve. Infectious Processes: Knowledge, Discourse, and the Politics of Prions (Science, Technology and Medicine in Modern History). Palgrave Macmillan, 2004.

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48

Prions : Molecular and Cellular Biology. Taylor & Francis, 1999.

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49

1955-, Harris David Alan, ed. Prions: Molecular and cellular biology. Wymondham, Norfolk: Horizon Scientific Press, 1999.

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50

Safar, Jiri G. Prion Paradigm of Human Neurodegenerative Diseases Caused by Protein Misfolding. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190233563.003.0005.

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Abstract:

Data accumulated from different laboratories argue that a growing number of proteins causing neurodegeneration share certain characteristics with prions. Prion-like particles were produced from synthetic amyloid beta (Aβ‎) peptides of Alzheimer’s disease (AD), from recombinant α‎-synuclein linked to Parkinson’s disease (PD), and from recombinant tau associated with frontotemporal dementias (FTD). Evidence from human prions reveals that variable disease phenotypes, rates of propagation, and targeting of different brain structures are determined by distinct conformers (strains) of pathogenic prion protein. Recent progress in the development of advanced biophysical tools identified the structural characteristics of Aβ‎ in the brain cortex of phenotypically diverse AD patients and thus allowed an investigation of the prion paradigm of AD. The findings of distinctly structured strains of human brain Aβ‎, forming a unique spectrum of oligomeric particles in the cortex of rapidly progressive cases, implicates these structures in variable rates of propagation in the brain.

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