BiP binds type I procollagen pro alpha chains with mutations in the carboxyl-terminal propeptide synthesized by cells from patients with osteogenesis imperfecta.-Reference-Cited by-同舟云学术

BiP binds type I procollagen pro alpha chains with mutations in the carboxyl-terminal propeptide synthesized by cells from patients with osteogenesis imperfecta.

Published:1993-08 Issue:24 Volume:268 Page:18226-18233
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Chessler S.D.,Byers P.H.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference45 articles.

1. Osteogenesis imperfecta: translation of mutation to phenotype.

2. Mutations in collagen genes: causes of rare and some common diseases in humans

3. Protein Folding: Deciphering the Second Half of the Genetic Code.;Byers,1990

4. Regulation of Protein Export From the Endoplasmic Reticulum

5. Protein Disulphide Isomerase, A Multifunctional Endoplasmic Reticulum Protein

Cited by 95 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. ER procollagen storage defect without coupled unfolded protein response drives precocious arthritis;Life Science Alliance;2024-07-09

2. Profibrotic COVID-19 subphenotype exhibits enhanced localized ER-dependent HSP47+ expression in cardiac myofibroblasts in situ;Journal of Molecular and Cellular Cardiology;2023-12

3. Chondrodysplasia-inducingCOL2A1p.Gly1170Ser causes an ER storage defect without associated unfolded protein response in a human cartilage model;2023-10-20

4. Collagen (I) homotrimer potentiates the osteogenesis imperfecta (oim) mutant allele and reduces survival in male mice;Disease Models & Mechanisms;2022-09-01

5. ER, Mitochondria, and ISR Regulation by mt‐HSP70 and ATF5 upon Procollagen Misfolding in Osteoblasts;Advanced Science;2022-08-21