Metabolomics analysis for diagnosis and biomarker discovery of transthyretin amyloidosis
Author:
Affiliation:
1. Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden
2. Wallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden
Funder
Region of Västerbotten
Swedish Heart-Lung Foundation
Swedish Research Council
Knut and Alice Wallenberg Foundation
Patients’ Organisations FAMY, FAMY Norrbotten and AMYL
Publisher
Informa UK Limited
Subject
Internal Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/13506129.2021.1958775
Reference46 articles.
1. Loss of gastric interstitial cells of Cajal in patients with hereditary transthyretin amyloidosis
2. Amyloid Cardiomyopathy in Hereditary Transthyretin V30M Amyloidosis - Impact of Sex and Amyloid Fibril Composition
3. Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient
4. The Acid-Mediated Denaturation Pathway of Transthyretin Yields a Conformational Intermediate That Can Self-Assemble into Amyloid
5. Tetramer Dissociation and Monomer Partial Unfolding Precedes Protofibril Formation in Amyloidogenic Transthyretin Variants
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