(Q24294784)

Amyloid beta precursor protein

GOA release 2020-03-11

1 reference

identical protein binding

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Marco Gobbi

1

Marco

Gobbi

1 reference

1 May 2024

Laura Colombo

2

Laura

Colombo

1 reference

1 May 2024

Michela Morbin

3

Michela

Morbin

1 reference

1 May 2024

Giulia Mazzoleni

4

Giulia

Mazzoleni

1 reference

1 May 2024

Elena Accardo

5

Elena

Accardo

1 reference

1 May 2024

Marco Vanoni

6

Marco

Vanoni

1 reference

1 May 2024

Elena Del Favero

7

Elena

Del Favero

1 reference

1 May 2024

Laura Cantù

8

Laura

Cantù

1 reference

1 May 2024

Daniel A Kirschner

9

Daniel A

Kirschner

1 reference

1 May 2024

Claudia Manzoni

10

Claudia

Manzoni

1 reference

1 May 2024

Marten Beeg

11

Marten

Beeg

1 reference

1 May 2024

Paolo Ceci

12

Paolo

Ceci

1 reference

1 May 2024

Paolo Ubezio

13

Paolo

Ubezio

1 reference

1 May 2024

Gianluigi Forloni

14

Gianluigi

Forloni

1 reference

1 May 2024

Fabrizio Tagliavini

15

Fabrizio

Tagliavini

1 reference

1 May 2024

Mario Salmona

16

Mario

Salmona

1 reference

Journal of Biological Chemistry

1 May 2024

language of work or name

English

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publication date

13 January 2006

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published in

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volume

281

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issue

2

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page(s)

843-9

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cites work

Molecular biology of prion diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Shattuck lecture--neurodegenerative diseases and prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Recombinant scrapie-like prion protein of 106 amino acids is soluble

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Structural properties of Gerstmann-Straussler-Scheinker disease amyloid protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Protein folding and misfolding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Alzheimer's disease amyloid propagation by a template-dependent dock-lock mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Reversible in vitro growth of Alzheimer disease beta-amyloid plaques by deposition of labeled amyloid peptide

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Using inducible vectors to study intracellular trafficking of GFP-tagged steroid/nuclear receptors in living cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Kinetic modeling and determination of reaction constants of Alzheimer's beta-amyloid fibril extension and dissociation using surface plasmon resonance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Kinetic analysis of beta-amyloid fibril elongation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Pathway complexity of prion protein assembly into amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

An unusual soluble beta-turn-rich conformation of prion is involved in fibril formation and toxic to neuronal cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Tetracycline affects abnormal properties of synthetic PrP peptides and PrP(Sc) in vitro.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Chemistry for the analysis of protein-protein interactions: rapid and efficient cross-linking triggered by long wavelength light

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Amyloid beta-protein oligomerization: prenucleation interactions revealed by photo-induced cross-linking of unmodified proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Amyloid beta -protein (Abeta) assembly: Abeta 40 and Abeta 42 oligomerize through distinct pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Binding of prion proteins to lipid membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Bovine prion protein as a modulator of protein kinase CK2

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Oligomeric Aip2p/Dld2p modifies the protein conformation of both properly folded and misfolded substrates in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Characterization and polyanion-binding properties of purified recombinant prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Quinoline derivatives are therapeutic candidates for transmissible spongiform encephalopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Prion protein stimulates tissue-type plasminogen activator-mediated plasmin generation via a lysine-binding site on kringle 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Is the prion domain of soluble Ure2p unstructured?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Autocatalytic conversion of recombinant prion proteins displays a species barrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

Immobilization of proteins to a carboxymethyldextran-modified gold surface for biospecific interaction analysis in surface plasmon resonance sensors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

7 January 2021

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

7 January 2021

Kinetic intermediate in the folding of human prion protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

7 January 2021

Both lysine-clusters of the NH2-terminal prion-protein fragment PrP23-110 are essential for t-PA mediated plasminogen activation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M506164200

7 January 2021

release_sbxq5i42nvgkrb4gzdqdpkjwpq

Identifiers

DOI

10.1074/JBC.M506164200

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Fatcat ID

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