Formation of amyloid fibrils from β-amylase (Q28586287)

31 January 2017

title

Formation of amyloid fibrils from β-amylase (English)

1 reference

31 January 2017

1 reference

GOA release 2020-03-11

author name string

Jian-Chau Luo

1

1 reference

31 January 2017

Shing-Chuen Wang

2

1 reference

31 January 2017

Wei-Bang Jian

3

1 reference

31 January 2017

Chien-Hsing Chen

4

1 reference

31 January 2017

Jaw-Luen Tang

5

1 reference

31 January 2017

Cheng-I. Lee

6

1 reference

31 January 2017

language of work or name

English

0 references

publication date

23 March 2012

1 reference

31 January 2017

1 reference

31 January 2017

volume

586

1 reference

31 January 2017

issue

6

1 reference

31 January 2017

page(s)

680–685

1 reference

The alternative conformations of amyloidogenic proteins and their multi-step assembly pathways

31 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Familial amyloid polyneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Highly promiscuous nature of prion polymerization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Synthetic mammalian prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

NMR structure of the mouse prion protein domain PrP(121-231)

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Amyloid fibril formation by an SH3 domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Designing conditions for in vitro formation of amyloid protofilaments and fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Chemical genetics and cereal starch metabolism: structural basis of the non-covalent and covalent inhibition of barley β-amylase

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

In vitro conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrP(Sc).

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Techniques to study amyloid fibril formation in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Quantifying amyloid by congo red spectral shift assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

The classification and typing of amyloid deposits

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

The peculiar nature of unfolding of the human prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Induction of amyloid fibrils by the C-terminal fragments of TDP-43 in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Real-space refinement of the structure of hen egg-white lysozyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

First experimental transmission of fatal familial insomnia

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Prion protein immunocytochemistry: reliable protocols for the investigation of Creutzfeldt-Jakob disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

The two faces of protein misfolding: gain- and loss-of-function in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

The cellular prion protein mediates neurotoxic signalling of β-sheet-rich conformers independent of prion replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

The most infectious prion protein particles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Naturally secreted oligomers of amyloid beta protein potently inhibit hippocampal long-term potentiation in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

Small non-fibrillar assemblies of amyloid beta-protein bearing the Arctic mutation induce rapid neuritic degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

The structure of amyloid fibrils by electron microscopy and X-ray diffraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2012.01.062

10.1016/J.FEBSLET.2012.01.062

21 January 2018

Identifiers

DOI

1 reference

31 January 2017

1 reference