The toxicity of antiprion antibodies is mediated by the flexible tail of the prion protein (Q27685314)

18

0 references

Simone Hornemann

6

object named as

Simone Hornemann

0 references

Paweł P. Liberski

16

object named as

Pawel P Liberski

0 references

author name string

Tiziana Sonati

1

0 references

Jeppe Falsig

3

0 references

Pravas Kumar Baral

4

0 references

Tracy O'Connor

5

0 references

Sine Yaganoglu

7

0 references

Bei Li

8

0 references

Uli S Herrmann

9

0 references

Barbara Wieland

10

0 references

Mridula Swayampakula

11

0 references

Muhammad Hafizur Rahman

12

0 references

Dipankar Das

13

0 references

Nat Kav

14

0 references

Roland Riek

15

0 references

Michael N G James

Normal host prion protein necessary for scrapie-induced neurotoxicity.

17

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language of work or name

English

0 references

publication date

5 September 2013

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published in

Nature

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volume

501

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issue

7465

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page(s)

102-6

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cites work

1 reference

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Prion pathogenesis is faithfully reproduced in cerebellar organotypic slice cultures.

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Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis.

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Lethal recessive myelin toxicity of prion protein lacking its central domain

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Prions: protein aggregation and infectious diseases

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NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231).

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Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

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NMR solution structure of the human prion protein

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Three-dimensional structures of prion proteins

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Prion protein devoid of the octapeptide repeat region restores susceptibility to scrapie in PrP knockout mice.

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Axonal prion protein is required for peripheral myelin maintenance

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Calpain and caspase: can you tell the difference?

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Oxidative stress in neurodegeneration and available means of protection.

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NOX enzymes in the central nervous system: from signaling to disease

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Manganese-enhanced magnetic resonance imaging (MEMRI): methodological and practical considerations

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Hydroxytyrosol: from laboratory investigations to future clinical trials.

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Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production

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Biological and biochemical characterization of mice expressing prion protein devoid of the octapeptide repeat region after infection with prions

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Neurological illness in transgenic mice expressing a prion protein with an insertional mutation.

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Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene.

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Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

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Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease

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Prion protein interaction with the C-terminal SH3 domain of Grb2 studied using NMR and optical spectroscopy

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Cerebellar granule cell Cre recombinase expression

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Post-natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration

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Truncated Prion Protein and Doppel Are Myelinotoxic in the Absence of Oligodendrocytic PrPC

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Intrinsic resistance of oligodendrocytes to prion infection.

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Experimental autoimmune encephalomyelitis repressed by microglial paralysis.

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Intracranial adeno-associated virus-mediated delivery of anti-pan amyloid beta, amyloid beta40, and amyloid beta42 single-chain variable fragments attenuates plaque pathology in amyloid precursor protein mice.

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Fractionated manganese injections: effects on MRI contrast enhancement and physiological measures in C57BL/6 mice

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Comparative evaluation of two purification methods of anti-CD19-c-myc-His6-Cys scFv

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IgM and IgA anti-erythrocyte autoantibodies induce anemia in a mouse model through multivalency-dependent hemagglutination but not through complement activation.

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Prion protein library of recombinant constructs for structural biology

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Attenuated T2 relaxation by mutual cancellation of dipole-dipole coupling and chemical shift anisotropy indicates an avenue to NMR structures of very large biological macromolecules in solution

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Crystallization and preliminary X-ray diffraction analysis of prion protein bound to the Fab fragment of the POM1 antibody

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An automated system to mount cryo-cooled protein crystals on a synchrotron beam line, using compact sample cassettes and a small-scale robot

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Web-Ice: integrated data collection and analysis for macromolecular crystallography

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Blu-Ice and the Distributed Control System: software for data acquisition and instrument control at macromolecular crystallography beamlines

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Processing of X-ray diffraction data collected in oscillation mode

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MOLREP: an Automated Program for Molecular Replacement

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Identifiers

DOI

10.1038/NATURE12402

1 reference

Consolidated OpenCitations Corpus – April 2017

journals/nature/SonatiRFBOHYLHW13

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

1022995825

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

23903654

1 reference

Consolidated OpenCitations Corpus – April 2017