Identification of a novel transthyretin Thr59Lys/Arg104His. A case of compound heterozygosity in a Chinese patient diagnosed with familial transthyretin amyloidosis-Reference-Cited by-同舟云学术

Identification of a novel transthyretin Thr59Lys/Arg104His. A case of compound heterozygosity in a Chinese patient diagnosed with familial transthyretin amyloidosis

Published:2002-01 Issue:2 Volume:9 Page:134-140
ISSN:1350-6129
Container-title:Amyloid
language:en
Short-container-title:Amyloid

Author:

Lim Amareth¹,Prokaeva Tatiana¹,Connors Lawreen H.²,Falk Rodney H.³,Skinner Martha³,Costello Catherine E.⁴

Affiliation:

1. Mass Spectrometry Resource, Boston University School of Medicine, Boston, MA, 02118, USA

2. Department of Biochemistry, Boston University School of Medicine, Boston, MA, 02118, USA

3. Department of Medicine, Boston University School of Medicine, Boston, MA, 02118, USA

4. Amyloid Treatment and Research Program, Boston University School of Medicine, Boston, MA, 02118, USA

Publisher

Informa UK Limited

Subject

Internal Medicine

Link

https://www.tandfonline.com/doi/pdf/10.3109/13506120208995246

Reference33 articles.

1. Dissection of multi-protein complexes using mass spectrometry: Subunit interactions in transthyretin and retinol-binding protein complexes

2. The Acid-Mediated Denaturation Pathway of Transthyretin Yields a Conformational Intermediate That Can Self-Assemble into Amyloid

3. Tertiary structures of amyloidogenic and non-amyloidogenic transthyretin variants: new model for amyloid fibril formation

4. Capture of a Dimeric Intermediate during Transthyretin Amyloid Formation

5. Tetramer Dissociation and Monomer Partial Unfolding Precedes Protofibril Formation in Amyloidogenic Transthyretin Variants

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