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Additional file 5 of Clinical spectrum of Transthyretin amyloidogenic mutations among diverse population origins

NIAID Data Ecosystem2026-05-01 收录

数据链接：

https://figshare.com/articles/dataset/Additional_file_5_of_Clinical_spectrum_of_Transthyretin_amyloidogenic_mutations_among_diverse_population_origins/26697155 数据链接链接失效反馈

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资源简介：

Supplementary Material 5

应用场景：

创建时间：

2024-03-25

单基因糖尿病

临床遗传学

This dataset contains the supplementary materials for the article titled “ Genetic and Clinical Characteristics of Monogenic Diabetes in Japan: A Nationwide Study by the Japan Diabetes Society,<

Figshare2025-09-06 更新50

Crystal structure of calcium free human gelsolin amyloid mutant D187Y

蛋白质结构解析

淀粉样变性

Crystal structure of calcium free human gelsolin amyloid mutant D187Y Descriptor: Gelsolin Authors: Zorgati, H, Robinson, R.C. Deposit date: 2019-02-05 Release date: 2019-06-12 Last modified: 2023-11-

Protein Data Bank Japan2023-11-22 更新40

Biochemical properties of the two Ig V L domains SMA and LEN.

淀粉样变性

蛋白质序列分析

Amino acid sequence of the VL domains were acquired from the Amyloid Light Chain Database (ALBase Boston university) using the patient ID’s as search. Amino acid differences between LEN and SMA (total

NIAID Data Ecosystem40

Quantitative proteome profiling provides evidence of an activation of the complement cascade in ATTR amyloidosis

蛋白质组学

淀粉样变性

Amyloidosis is a disease group caused by pathological aggregation and deposition of peptides in diverse tissue sites. Apart from the fibril protein, amyloid deposits frequently enclose non-fibrillar c

NIAID Data Ecosystem40

Detection of semenogelin 1 amyloidosis through immunohistochemical staining with novel antiserum developed based on mass spectrometric peptide mapping analysis

生物医学

淀粉样变性

Detection of semenogelin 1 amyloidosis through immunohistochemical staining with novel antiserum developed based on mass spectrometric peptide mapping analysis

DataCite Commons2022-12-29 更新40

Additional file 5 of Clinical spectrum of Transthyretin amyloidogenic mutations among diverse population origins

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