(Q33885223)

29 July 2017

title

Transmissible and genetic prion diseases share a common pathway of neurodegeneration (English)

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29 July 2017

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Ramanujan Shankar Hegde

series ordinal

1

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29 July 2017

5

Prusiner SB

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29 July 2017

4

DeArmond SJ

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29 July 2017

Tremblay P

2

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29 July 2017

Groth D

series ordinal

3

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29 July 2017

Lingappa VR

series ordinal

6

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29 July 2017

language of work or name

English

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publication date

1 December 1999

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29 July 2017

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29 July 2017

volume

402

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29 July 2017

issue

6763

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29 July 2017

page(s)

822-826

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https://scigraph.springernature.com/pub.10.1038/45574

29 July 2017

exact match

0 references

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Deadly conformations--protein misfolding in prion disease

21 January 2018

1 reference

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease.

21 January 2018

1 reference

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Straussler-Scheinker syndrome

21 January 2018

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Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents

21 January 2018

1 reference

Inherited prion diseases and transmission to rodents

21 January 2018

1 reference

A transmembrane form of the prion protein in neurodegenerative disease

21 January 2018

1 reference

Separation and properties of cellular and scrapie prion proteins

21 January 2018

1 reference

Pathogenesis of scrapie: study of the temporal development of clinical symptoms, of infectivity titres and scrapie-associated fibrils in brains of hamsters infected intraperitoneally.

21 January 2018

1 reference

Transgenetic studies implicate interactions between homologous PrP isoforms in scrapie prion replication.

21 January 2018

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Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease

21 January 2018

1 reference

Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies

21 January 2018

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The unfolded protein response: an intracellular signalling pathway with many surprising features

21 January 2018

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Quality control in the secretory pathway

21 January 2018

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Regulation of protein topology by trans-acting factors at the endoplasmic reticulum

21 January 2018

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Unusual topogenic sequence directs prion protein biogenesis

21 January 2018

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Scrapie prions selectively modify the stress response in neuroblastoma cells

21 January 2018

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Decreased receptor-mediated calcium response in prion-infected cells correlates with decreased membrane fluidity and IP3 release

21 January 2018

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Synaptic plasticity in the CA1 area of the hippocampus of scrapie-infected mice.

21 January 2018

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Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins

21 January 2018

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Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice.

21 January 2018

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Comparison of scrapie and transmissible mink encephalopathy in hamsters. II. Clinical signs, pathology, and pathogenesis

21 January 2018

1 reference

Encephalopathy in mice produced by inoculation with scrapie brain material.

21 January 2018

1 reference

Molecular genetics of transmissible spongiform encephalopathies

21 January 2018

1 reference

Creutzfeldt-Jakob disease and related transmissible spongiform encephalopathies

21 January 2018

1 reference

Monoclonal antibodies to the cellular and scrapie prion proteins

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1038/45574

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Dimensions Publication ID

29 July 2017

1014361919

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