Transthyretin mutations in health and disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference55 articles.
1. Transthyretin Leu 68 in a form of cardiac amyloidosis
2. Characterization of a basic transthyretin variant - TTR Arg 102 - in the German population
3. Two transthyretin variants (TTR Ala-49 and TTR Gln-89) in two sicilian kindreds with hereditary amyloidosis
4. Transthyretin ALA 71: A new transthyretin variant in a Spanish family with familial amyloidotic polyneuropathy
5. Paraffin oil protected high resolution hybrid isoelectric focusing for the demonstration of substitutions of neutral amino acids in denatured proteins: The case of four human transthyretin (prealbumin) variants associated with familial amyloidotic polyneuropathy
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1. Identification of the interfacial regions in misfolded transthyretin oligomers;Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics;2024-09
2. Transthyretin mutagenesis: impact on amyloidogenesis and disease;Critical Reviews in Clinical Laboratory Sciences;2024-06-07
3. Defensin-based therapeutic peptide design in attenuating V30M TTR-induced Familial Amyloid Polyneuropathy;3 Biotech;2023-06-08
4. Theoretical investigations of TTR derived aggregation-prone peptides’ potential to biochemically attenuate the amyloidogenic propensities of V30 M TTR amyloid fibrils;Journal of the Indian Chemical Society;2023-02
5. Molecular Tweezers: Supramolecular Hosts with Broad-Spectrum Biological Applications;Pharmacological Reviews;2022-12-22
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