(Q40783039)

23 September 2017

title

Mutant prion proteins are partially retained in the endoplasmic reticulum (English)

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23 September 2017

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endoplasmic reticulum

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author name string

Ivanova L

1

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23 September 2017

Barmada S

2

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23 September 2017

Kummer T

3

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23 September 2017

Harris DA

4

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23 September 2017

language of work or name

English

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publication date

29 August 2001

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Journal of Biological Chemistry

23 September 2017

number of pages

13

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based on heuristic

inferred from page(s)

published in

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23 September 2017

volume

276

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23 September 2017

issue

45

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23 September 2017

page(s)

42409-42421

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https://api.crossref.org/works/10.1074%2FJBC.M106928200

23 September 2017

1 reference

Influence of amino acid substitutions related to inherited human prion diseases on the thermodynamic stability of the cellular prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Familial mutations and the thermodynamic stability of the recombinant human prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Prion protein NMR structure and familial human spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Solution structure of the E200K variant of human prion protein. Implications for the mechanism of pathogenesis in familial prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

A Mutant Prion Protein Displays an Aberrant Membrane Association When Expressed in Cultured Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Mutant and infectious prion proteins display common biochemical properties in cultured cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Prion proteins carrying pathogenic mutations are resistant to phospholipase cleavage of their glycolipid anchors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Abnormal properties of prion protein with insertional mutations in different cell types

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Noncytopathic Sindbis virus RNA vectors for heterologous gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Insulin-sensitive targeting of the GLUT4 glucose transporter in L6 myoblasts is conferred by its COOH-terminal cytoplasmic tail

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Measurement of cytosolic, mitochondrial, and Golgi pH in single living cells with green fluorescent proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Lectin-binding sites as markers of Golgi subcompartments: proximal-to-distal maturation of oligosaccharides

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Rab7: a key to lysosome biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

FACS-optimized mutants of the green fluorescent protein (GFP)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Giantin, a novel conserved Golgi membrane protein containing a cytoplasmic domain of at least 350 kDa

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Sequestration of GPI-anchored proteins in caveolae triggered by cross-linking

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

GPI-anchored proteins are organized in submicron domains at the cell surface.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

A glycolipid-anchored prion protein is endocytosed via clathrin-coated pits.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Secretory protein trafficking and organelle dynamics in living cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Setting the standards: quality control in the secretory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Cellular defenses against unfolded proteins: a cell biologist thinks about neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Stress signaling from the lumen of the endoplasmic reticulum: coordination of gene transcriptional and translational controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

A transmembrane form of the prion protein contains an uncleaved signal peptide and is retained in the endoplasmic Reticulum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

The Metabolism and Imaging in Live Cells of the Bovine Prion Protein in Its Native Form or Carrying Single Amino Acid Substitutions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Prions of yeast and fungi. Proteins as genetic material

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Identification of intermediate steps in the conversion of a mutant prion protein to a scrapie-like form in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Nerve growth factor-induced differentiation does not alter the biochemical properties of a mutant prion protein expressed in PC12 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Prion Protein Aggregation Reverted by Low Temperature in Transfected Cells Carrying a Prion Protein Gene Mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Proteasomal Degradation and N-terminal Protease Resistance of the Codon 145 Mutant Prion Protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

The Chaperone Protein BiP Binds to a Mutant Prion Protein and Mediates Its Degradation by the Proteasome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Effect of the D178N Mutation and the Codon 129 Polymorphism on the Metabolism of the Prion Protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

Ubiquitin and the control of protein fate in the secretory and endocytic pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M106928200

21 January 2018

Identifiers

DOI

10.1074/JBC.M106928200

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23 September 2017

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