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Books on the topic 'Protein misfolding and aggregation'

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Author: Grafiati
Published: 10 December 2022
Last updated: 7 September 2023

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1

Muñoz, Victor, ed. Protein Folding, Misfolding and Aggregation. Cambridge: Royal Society of Chemistry, 2008. http://dx.doi.org/10.1039/9781847558282.

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2

N, Uversky Vladimir, and Fink Anthony L. 1943-, eds. Protein misfolding, aggregation, and conformational diseases. New York, N.Y: Springer Science+Business Media, 2006.

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3

N, Uversky Vladimir, and Fink Anthony L. 1943-, eds. Protein misfolding, aggregation and conformational diseases. New York: Springer, 2006.

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4

N, Uversky Vladimir, and Fink Anthony L. 1943-, eds. Protein misfolding, aggregation and conformational diseases. New York: Springer, 2007.

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5

Uversky, Vladimir N., and Anthony L. Fink, eds. Protein Misfolding, Aggregation, and Conformational Diseases. Boston, MA: Springer US, 2006. http://dx.doi.org/10.1007/b136464.

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6

Uversky, Vladimir N., and Anthony L. Fink, eds. Protein Misfolding, Aggregation, and Conformational Diseases. Boston, MA: Springer US, 2007. http://dx.doi.org/10.1007/978-0-387-36534-3.

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7

Victor, Muñoz, ed. Protein folding, misfolding and aggregation: Classical themes and novel approaches. Cambridge, UK: Royal Society of Chemistry, 2008.

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8

B, O'Doherty Cian, and Byrne Adam C, eds. Protein misfolding. New York: Nova Science Publishers, 2008.

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9

Ramirez-Alvarado, Marina, Jeffery W. Kelly, and Christopher M. Dobson, eds. Protein Misfolding Diseases. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470572702.

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10

Gomes, Cláudio M., ed. Protein Misfolding Diseases. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-8820-4.

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11

Cieplak, Andrzej Stanisław, ed. Protein Aggregation. New York, NY: Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-2597-2.

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12

Protein aggregation. Hauppauge, N.Y: Nova Science Publishers, 2010.

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13

Bross, Peter, and Niels Gregersen. Protein Misfolding and Disease. New Jersey: Humana Press, 2003. http://dx.doi.org/10.1385/1592593941.

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14

Fabian, Heinz, and Dieter Naumann, eds. Protein Folding and Misfolding. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-22230-6.

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15

Gursky, Olga, ed. Lipids in Protein Misfolding. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-17344-3.

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16

Eliezer, David, ed. Protein Amyloid Aggregation. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-2978-8.

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17

Hill, Andrew F., Kevin J. Barnham, Stephen P. Bottomley, and Roberto Cappai, eds. Protein Folding, Misfolding, and Disease. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-60327-223-0.

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18

Ferenc, Orosz, Ovádi Judit 1941-, and SpringerLink (Online service), eds. Protein Folding and Misfolding: Neurodegenerative Diseases. Dordrecht: Springer Netherlands, 2009.

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19

Ovádi, Judit, and Ferenc Orosz, eds. Protein Folding and Misfolding: Neurodegenerative Diseases. Dordrecht: Springer Netherlands, 2009. http://dx.doi.org/10.1007/978-1-4020-9434-7.

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20

Doglia, Silvia Maria, and Marina Lotti, eds. Protein Aggregation in Bacteria. Hoboken, NJ: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118845363.

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21

Peter, Bross, and Gregersen Niels, eds. Protein misfolding and disease: Principles and protocols. Totowa, N.J: Humana Press, 2003.

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22

name, No. Protein misfolding and disease: Principles and protocols. Totowa, NJ: Humana Press, Inc., 2003.

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23

Beckerman, Martin. Fundamentals of Neurodegeneration and Protein Misfolding Disorders. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-22117-5.

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24

Protein folding, misfolding, and disease: Methods and protocols. New York: Humana, 2011.

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25

Schweitzer-Stenner, Reinhard, ed. Protein and Peptide Folding, Misfolding, and Non-Folding. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118183373.

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26

Protein and peptide folding, misfolding, and non-folding. Hoboken, N.J: John Wiley & Sons, 2012.

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27

Bross, Peter, and Niels Gregersen, eds. Protein Misfolding and Cellular Stress in Disease and Aging. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-756-3.

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28

Marina, Ramirez-Alvarado, Kelly Jeffery W, and Dobson C. M, eds. Protein misfolding diseases: Current and emerging principles and therapies. Hoboken, N.J: Wiley, 2010.

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29

1930-, Smith H. J., Simons Claire, and Sewell Robert D. E, eds. Protein misfolding in neurodegenerative diseases: Mechanisms and therapeutic strategies. Boca Raton: Taylor & Francis, 2008.

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30

Protein misfolding and cellular stress in disease and aging: Concepts and protocols. New York: Humana Press, 2010.

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31

Ronald, Wetzel, ed. Amyloid, prions, and other protein aggregates. San Diego, CA: Academic Press, 1999.

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32

Harris, J. Robin, ed. Protein Aggregation and Fibrillogenesis in Cerebral and Systemic Amyloid Disease. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-5416-4.

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33

Uversky, Vladimir, and Yuri Lyubchenko. Bio-Nanoimaging: Protein Misfolding and Aggregation. Elsevier Science & Technology Books, 2013.

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34

Uversky, Vladimir N., and Yuri Lyubchenko. Bio-Nanoimaging: Protein Misfolding and Aggregation. Elsevier Science & Technology Books, 2013.

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35

Sandal, Massimo. Early Stage Protein Misfolding and Amyloid Aggregation. Elsevier Science & Technology, 2017.

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36

Sandal, Massimo. Early Stage Protein Misfolding and Amyloid Aggregation. Elsevier Science & Technology Books, 2017.

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37

Fink, Anthony, and Vladimir N. Uversky. Protein Misfolding, Aggregation and Conformational Diseases : Part A: Protein Aggregation and Conformational Diseases. Springer, 2010.

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38

Protein Misfolding, Aggregation and Conformational Diseases: Part A: Protein Aggregation and Conformational Diseases (Protein Reviews). Springer, 2006.

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39

Williams, Danielle, and Tara L. Pukala. Protein Misfolding, Aggregation and Disease: Insights from Mass Spectrometry. Wiley & Sons, Incorporated, John, 2021.

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40

Williams, Danielle, and Tara L. Pukala. Protein Misfolding, Aggregation and Disease: Insights from Mass Spectrometry. Wiley & Sons, Limited, John, 2021.

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41

Williams, Danielle, and Tara L. Pukala. Protein Misfolding, Aggregation and Disease: Insights from Mass Spectrometry. Wiley & Sons, Incorporated, John, 2021.

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42

Neidle, Stephen, Simon Campbell, David M. J. Lilley, Marius Clore, and Victor Muñoz. Protein Folding, Misfolding and Aggregation: Classical Themes and Novel Approaches. Royal Society of Chemistry, The, 2008.

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43

Fink, Anthony, and Vladimir N. Uversky. Protein Misfolding, Aggregation and Conformational Diseases : Part B: Molecular Mechanisms of Conformational Diseases. Springer, 2010.

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44

Zhou, Huan-Xiang, and Jian-Min Yuan. Biophysics and Biochemistry of Protein Folding and Aggregation: Experimental and Theoretical Studies on Folding, Misfolding, and Self-Assembly of Amyloidogenic Peptides. World Scientific Publishing Co Pte Ltd, 2017.

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45

Protein Misfolding. Elsevier, 2019. http://dx.doi.org/10.1016/s1876-1623(19)x0005-x.

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46

Donev, Rossen. Protein Misfolding. Elsevier Science & Technology, 2020.

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47

Donev, Rossen. Protein Misfolding. Elsevier Science & Technology Books, 2020.

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48

Cummings, Jeffrey L., and Jagan A. Pillai. Neurodegenerative Diseases. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780190233563.003.0001.

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Abstract:
Neurodegenerative diseases (NDDs) are growing in frequency and represent a major threat to public health. Advances in scientific progress have made it clear that NDDs share many underlying processes, including shared intracellular mechanisms such as protein misfolding and aggregation, cell-to-cell prion-like spread, growth factor signaling abnormalities, RNA and DNA disturbances, glial cell changes, and neuronal loss. Transmitter deficits are shared across many types of disorders. Means of studying NDDs with human iPS cells and transgenic models are similar. The progression of NDDs through asymptomatic, prodromal, and manifest stages is shared across disorders. Clinical features of NDDs, including cognitive impairment, disease progression, age-related effects, terminal stages, neuropsychiatric manifestations, and functional disorders and disability, have many common elements. Clinical trials, biomarkers, brain imaging, and regulatory aspects of NDD can share information across NDDs. Disease-modifying and transmitter-based therapeutic interventions, clinical trials, and regulatory approaches to treatments for NDDs are also similar.
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49

Kelly, Jeffery W., Marina Ramirez-Alvarado, and Christopher M. Dobson. Protein Misfolding Diseases. Wiley & Sons, Incorporated, John, 2010.

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50

Gursky, Olga. Lipids in Protein Misfolding. Springer, 2015.

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