(Q46025414)

18 December 2017

title

Structural studies of the scrapie prion protein using mass spectrometry and amino acid sequencing. (English)

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18 December 2017

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7

Prusiner SB

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18 December 2017

Stahl N

1

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18 December 2017

Baldwin MA

2

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18 December 2017

Teplow DB

3

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18 December 2017

Hood L

4

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18 December 2017

Gibson BW

5

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18 December 2017

Burlingame AL

6

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18 December 2017

language of work or name

English

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publication date

1 March 1993

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18 December 2017

published in

Biochemistry

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18 December 2017

volume

32

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18 December 2017

issue

8

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18 December 2017

page(s)

1991-2002

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18 December 2017

describes a project that uses

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Assignment of the human and mouse prion protein genes to homologous chromosomes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

daughterless, a Drosophila gene essential for both neurogenesis and sex determination, has sequence similarities to myc and the achaete-scute complex

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Temporary and permanent modifications to a single strain of mouse scrapie on transmission to rats and hamsters

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

In vivo chemical modification of proteins (post-translational modification).

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Scrapie: A Prototype Slow Infection

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Subcellular distribution and physicochemical properties of scrapie-associated precursor protein and relationship with scrapie agent

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Separation and properties of cellular and scrapie prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Techniques in the detection and characterization of phosphoramidate-containing proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Creutzfeldt-Jakob disease prion proteins in human brains

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Identification of a gene which controls the incubation period of some strains of scrapie agent in mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Molecular pathology of scrapie-associated fibril protein (PrP) in mouse brain affected by the ME7 strain of scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Purification and properties of the cellular and scrapie hamster prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Further purification and characterization of scrapie prions

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

The Scrapie Agent: Evidence Against its Dependence for Replication on Intrinsic Nucleic Acid

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Fibrils from brains of cows with new cattle disease contain scrapie-associated protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

A 'unified theory' of prion propagation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Turn prediction in proteins using a pattern-matching approach

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Differential release of cellular and scrapie prion proteins from cellular membranes by phosphatidylinositol-specific phospholipase C.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Purification and properties of the cellular prion protein from Syrian hamster brain

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

William Hunting and The Veterinary Record.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Isolation and structural studies of the intact scrapie agent protein.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

A prion protein missense variant is integrated in kuru plaque cores in patients with Gerstmann‐Sträussler syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Scrapie prions aggregate to form amyloid-like birefringent rods

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Experimental transmission of a Kuru-like syndrome to chimpanzees

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Purification and structural studies of a major scrapie prion protein.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Conservation of infectivity in purified fibrillary extracts of scrapie-infected hamster brain after sequential enzymatic digestion or polyacrylamide gel electrophoresis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Scrapie prion protein contains a phosphatidylinositol glycolipid

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Molecular mass, biochemical composition, and physicochemical behavior of the infectious form of the scrapie precursor protein monomer

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Scrapie and cellular prion proteins differ in their kinetics of synthesis and topology in cultured cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

A dementing illness associated with a novel insertion in the prion protein gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Scrapie PrP 27-30 is a sialoglycoprotein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Asparagine-linked glycosylation of the scrapie and cellular prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

A model for RNA editing in kinetoplastid mitochondria: "guide" RNA molecules transcribed from maxicircle DNA provide the edited information

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

RNA editing in brain controls a determinant of ion flow in glutamate-gated channels

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

A cellular gene encodes scrapie PrP 27-30 protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Insertion in prion protein gene in familial Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Scrapie prion rod formation in vitro requires both detergent extraction and limited proteolysis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Unconventional Viruses and the Origin and Disappearance of Kuru

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Biological evidence that scrapie agent has an independent genome.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Identification of a protein that purifies with the scrapie prion.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Three hamster species with different scrapie incubation times and neuropathological features encode distinct prion proteins

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Does the agent of scrapie replicate without nucleic acid?

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Acquisition of protease resistance by prion proteins in scrapie-infected cells does not require asparagine-linked glycosylation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

The exceptionally small size of the scrapie agent

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

A micromethod for complete removal of dodecyl sulfate from proteins by ion-pair extraction

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Estimation of scrapie nucleic acid MW from standard curves for virus sensitivity to ionizing radiation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Synthesis and trafficking of prion proteins in cultured cells

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Protein splicing converts the yeast TFP1 gene product to the 69-kD subunit of the vacuolar H(+)-adenosine triphosphatase

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Diagnosis of Creutzfeldt-Jakob disease by Western blot identification of marker protein in human brain tissue.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Diversity of oligosaccharide structures linked to asparagines of the scrapie prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

A prion protein variant in a family with the telencephalic form of Gerstmann-Straussler-Scheinker syndrome

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Electrophoretic properties of the scrapie agent in agarose gels

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

PrP and the scrapie agent

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Glycosylinositol phospholipid anchors of the scrapie and cellular prion proteins contain sialic acid

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Thiocyanate and hydroxyl ions inactivate the scrapie agent

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Perturbation of the secondary structure of the scrapie prion protein under conditions that alter infectivity

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Scrapie prion liposomes and rods exhibit target sizes of 55,000 Da.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Molecular biology of prion diseases

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Distinct prion proteins in short and long scrapie incubation period mice

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Permethylation and tandem mass spectrometry of oligosaccharides having free hexosamine: analysis of the glycoinositol phospholipid anchor glycan from the scrapie prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Identification of glycoinositol phospholipid linked and truncated forms of the scrapie prion protein

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Further analysis of nucleic acids in purified scrapie prion preparations by improved return refocusing gel electrophoresis

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Novel proteinaceous infectious particles cause scrapie

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Transmissible mink encephalopathy (TME) in Chinese hamsters: identification of two strains of TME and comparisons with scrapie.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/BI00059A016

Identifiers

DOI

10.1021/BI00059A016

1 reference

18 December 2017

1 reference

18 December 2017