(Q30797299)

26 June 2017

title

Serum transthyretin monomer in patients with familial amyloid polyneuropathy (English)

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ORCID Public Data File 2021

26 June 2017

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author name string

Sekijima Y

1

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26 June 2017

Tokuda T

2

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26 June 2017

Kametani F

3

1 reference

26 June 2017

Tanaka K

4

1 reference

26 June 2017

Maruyama K

5

1 reference

26 June 2017

Ikeda S

6

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26 June 2017

publication date

1 December 2001

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26 June 2017

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26 June 2017

volume

8

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26 June 2017

issue

4

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26 June 2017

page(s)

257-262

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Structure of prealbumin: secondary, tertiary and quaternary interactions determined by Fourier refinement at 1.8 A

26 June 2017

cites work

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Partial denaturation of transthyretin is sufficient for amyloid fibril formation in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Transthyretin mutation Leu-55-Pro significantly alters tetramer stability and increases amyloidogenicity

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Comparison of Lethal and Nonlethal Transthyretin Variants and Their Relationship to Amyloid Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Usefulness of MALDI/TOF mass spectrometry of immunoprecipitated serum variant transthyretin in the diagnosis of familial amyloid polyneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Characterization of the transthyretin acid denaturation pathways by analytical ultracentrifugation: implications for wild-type, V30M, and L55P amyloid fibril formation

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Comparative stability and clearance of [Met30]transthyretin and [Met119]transthyretin

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

The acid-mediated denaturation pathway of transthyretin yields a conformational intermediate that can self-assemble into amyloid

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

The most pathogenic transthyretin variant, L55P, forms amyloid fibrils under acidic conditions and protofilaments under physiological conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

The amyloidogenic potential of transthyretin variants correlates with their tendency to aggregate in solution

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

The Tetrameric Protein Transthyretin Dissociates to a Non-native Monomer in Solution

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Transthyretin amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Synchrotron X-ray studies suggest that the core of the transthyretin amyloid fibril is a continuous β-sheet helix

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Analysis of x-ray diffraction patterns from amyloid of biopsied vitreous humor and kidney of transthyretin (TTR) Met30 familial amyloidotic polyneuropathy (FAP) patients: axially arrayed TTR monomers constitute the protofilament

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Argentinian patients of European ancestry with familial amyloid polyneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

Transthyretin Met 30 familial amyloid polyneuropathy in China. Usefulness of mass spectrometry for screening a variant TTR in serum

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13506120108993822

10.3109/13506120108993822

21 January 2018

Identifiers

DOI

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26 June 2017

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