Cell type-specific transgene expression of the prion protein in Xenopus intermediate pituitary cells (Q46383132)

21 December 2017

title

Cell type-specific transgene expression of the prion protein in Xenopus intermediate pituitary cells (English)

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21 December 2017

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Jos W G van Rosmalen

1

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21 December 2017

Gerard J M Martens

series ordinal

2

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21 December 2017

language of work or name

English

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publication date

1 February 2006

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21 December 2017

published in

FEBS Journal

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21 December 2017

volume

273

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21 December 2017

issue

4

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21 December 2017

page(s)

847-862

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21 December 2017

Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Prion protein is necessary for normal synaptic function

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Cellular phenotyping of secretory and nuclear prion proteins associated with inherited prion diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Mutant prion proteins are partially retained in the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Asparagine-linked glycosylation of the scrapie and cellular prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Scrapie prion protein contains a phosphatidylinositol glycolipid

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Purification and properties of the cellular and scrapie hamster prion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Truncated forms of the human prion protein in normal brain and in prion diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Cholesterol depletion and modification of COOH-terminal targeting sequence of the prion protein inhibit formation of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

A simplified method of generating transgenic Xenopus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Protein tyrosine sulfation, 1993--an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

A cell-specific transgenic approach in Xenopus reveals the importance of a functional p24 system for a secretory cell

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

7B2 is a neuroendocrine chaperone that transiently interacts with prohormone convertase PC2 in the secretory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

High-level expression and characterization of a purified 142-residue polypeptide of the prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

A monomer-dimer equilibrium of a cellular prion protein (PrPC) not observed with recombinant PrP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Semipreparative chromatographic method to purify the normal cellular isoform of the prion protein in nondenatured form.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Mutant PrP is delayed in its exit from the endoplasmic reticulum, but neither wild-type nor mutant PrP undergoes retrotranslocation prior to proteasomal degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Tyrosine sulfation is a trans-Golgi-specific protein modification

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Guanidine hydrochloride extraction and detection of prion proteins in mouse and hamster prion diseases by ELISA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

The secretory granule and pro-opiomelanocortin processing in Xenopus melanotrope cells during background adaptation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Degradation and endoplasmic reticulum retention of unassembled alpha- and beta-subunits of Na,K-ATPase correlate with interaction of BiP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

The appearance of acetylated alpha-tubulin during early development and cellular differentiation in Xenopus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

Biosynthesis of the vacuolar H+-ATPase accessory subunit Ac45 in Xenopus pituitary

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

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/10.1111%2FJ.1742-4658.2006.05118.X

Endocytic Intermediates Involved with the Intracellular Trafficking of a Fluorescent Cellular Prion Protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1742-4658.2006.05118.X

10.1111/J.1742-4658.2006.05118.X

21 January 2018

Identifiers

DOI

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21 December 2017

release_rzf6cxifgff4xexxewpcrobxrq

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/rzf6cxifgff4xexxewpcrobxrq

mapped directly with Wikidata item

24 November 2022

based on heuristic

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21 December 2017