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The Biochemical Journal
|
August 24, 2006
Multiple forms of copper (II) co-ordination occur throughout the disordered N-terminal region of the prion protein at pH 7.4
Mark A Wells, Clare Jelinska, Laszlo L P Hosszu, et al.
JAMA Neurology
|
November 17, 2015
Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation
Laura Eisenmenger, Marie-Claire Porter, Christopher J Carswell, et al.
Neuron
|
February 3, 2007
Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected mice
Giovanna R Mallucci, Melanie D White, Michael Farmer, et al.
Cells
|
December 24, 2021
NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease Progression
David Mengel, Tze How Mok, Akin Nihat, et al.
The Biochemical Journal
|
July 11, 2006
A reassessment of copper(II) binding in the full-length prion protein
Mark A Wells, Graham S Jackson, Samantha Jones, et al.
Scientific Reports
|
January 25, 2019
Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitro
Cassandra Terry, Robert L Harniman, Jessica Sells, et al.
Prion
|
June 11, 2016
Physical, chemical and kinetic factors affecting prion infectivity
Francesca Properzi, Anjna Badhan, Steffi Klier, et al.
Brain : a Journal of Neurology
|
May 24, 2003
Molecular classification of sporadic Creutzfeldt-Jakob disease
Andrew F Hill, Susan Joiner, Jonathan D F Wadsworth, et al.
The Journal of Biological Chemistry
|
May 15, 2026
Prion propagation is controlled by discrete structural regions of PrP rather than overall stability
Savroop K Bhamra, Parineeta Arora, May Liew, et al.
Brain : a Journal of Neurology
|
February 11, 2020
Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosis
Phillip Smethurst, Emmanuel Risse, Giulia E Tyzack, et al.
Page
of 30
Search research articles
Search
Showing results (141-150 of 295) with videos related to
Sort By:
Page
of 30
The Biochemical Journal
|
August 24, 2006
Multiple forms of copper (II) co-ordination occur throughout the disordered N-terminal region of the prion protein at pH 7.4
Mark A Wells, Clare Jelinska, Laszlo L P Hosszu, et al.
JAMA Neurology
|
November 17, 2015
Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation
Laura Eisenmenger, Marie-Claire Porter, Christopher J Carswell, et al.
Neuron
|
February 3, 2007
Targeting cellular prion protein reverses early cognitive deficits and neurophysiological dysfunction in prion-infected mice
Giovanna R Mallucci, Melanie D White, Michael Farmer, et al.
Cells
|
December 24, 2021
NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease Progression
David Mengel, Tze How Mok, Akin Nihat, et al.
The Biochemical Journal
|
July 11, 2006
A reassessment of copper(II) binding in the full-length prion protein
Mark A Wells, Graham S Jackson, Samantha Jones, et al.
Scientific Reports
|
January 25, 2019
Structural features distinguishing infectious ex vivo mammalian prions from non-infectious fibrillar assemblies generated in vitro
Cassandra Terry, Robert L Harniman, Jessica Sells, et al.
Prion
|
June 11, 2016
Physical, chemical and kinetic factors affecting prion infectivity
Francesca Properzi, Anjna Badhan, Steffi Klier, et al.
Brain : a Journal of Neurology
|
May 24, 2003
Molecular classification of sporadic Creutzfeldt-Jakob disease
Andrew F Hill, Susan Joiner, Jonathan D F Wadsworth, et al.
The Journal of Biological Chemistry
|
May 15, 2026
Prion propagation is controlled by discrete structural regions of PrP rather than overall stability
Savroop K Bhamra, Parineeta Arora, May Liew, et al.
Brain : a Journal of Neurology
|
February 11, 2020
Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosis
Phillip Smethurst, Emmanuel Risse, Giulia E Tyzack, et al.
Page
of 30