Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of Bone.

 0 Người đánh giá. Xếp hạng trung bình 0

Tác giả: Dylan Bergen, Eveline Boudin, Paul Coucke, Jan De Beenhouwer, Raphaël De Ridder, Björn De Samber, Antonella Forlino, Chrissy Hammond, Gretl Hendrickx, Yentl Huybrechts, Dries Knapen, Ronald Young Kwon, Geert Mortier, Dorien Schepers, Jan Sijbers, Francesca Tonelli, Qiao Tong, Evelien Van Dijck, Wim Van Hul, Lucia Vergauwen, Anja Verhulst, Andy Willaert, P Eckhard Witten

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: United States : Calcified tissue international , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 707180

The ubiquitin-binding protein p62, encoded by Sequestosome 1 (SQSTM1), is an essential molecular adaptor for selective autophagy. Heterozygous mutations deleting or disrupting the ubiquitin-associated (UBA) domain of p62 have been reported as the major genetic cause for Paget's disease of bone (PDB), the second most common skeletal disease, characterized by hyperactive osteoclasts and focal increases of bone turnover. In this study, we aimed to determine the impact of a similar sqstm1/p62 mutation on the skeleton of zebrafish. We successfully established a sqstm1
Tạo bộ sưu tập với mã QR

THƯ VIỆN - TRƯỜNG ĐẠI HỌC CÔNG NGHỆ TP.HCM

ĐT: (028) 36225755 | Email: tt.thuvien@hutech.edu.vn

Copyright @2024 THƯ VIỆN HUTECH