Position of single amino acid substitutions in the collagen triple helix determines their effect on structure of collagen fibrils-Reference-Cited by-同舟云学术

Position of single amino acid substitutions in the collagen triple helix determines their effect on structure of collagen fibrils

Published:2004-12 Issue:3 Volume:148 Page:326-337
ISSN:1047-8477
Container-title:Journal of Structural Biology
language:en
Short-container-title:Journal of Structural Biology

Author:

Steplewski Andrzej,Ito Hidetoshi,Rucker Eileen,Brittingham Raymond J.,Alabyeva Tatiana,Gandhi Milind,Ko Frank K.,Birk David E.,Jimenez Sergio A.,Fertala Andrzej

Publisher

Elsevier BV

Subject

Structural Biology

Reference48 articles.

1. Collagen II containing a Cys substitution for Arg-alpha1-519. Analysis by atomic force microscopy demonstrates that mutated monomers alter the topography of the surface of collagen II fibrils;Adachi;Matrix Biol.,1999

2. Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia;Ala-Kokko;Proc. Natl. Acad. Sci. USA,1990

3. Skeletal abnormalities and ultrastructural changes of cartilage in transgenic mice expressing a collagen II gene (COL2A1) with a Cys for Arg-alpha1-519 substitution;Arita;Osteoarthritis Cartilage,2002

4. Collagen fibrillogenesis in vitro: interaction of types I and V collagen regulates fibril diameter;Birk;J Cell Sci.,1990

5. Collagen type I and type V are present in the same fibril in the avian corneal stroma;Birk;J Cell Biol.,1988

Cited by 41 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. The application of human medical image-based finite element analysis in the construction of mouse osteoarthritis models;Heliyon;2024-02

2. The Application of Finite Element Analysis in the Construction of Mouse Osteoarthritis Models;2023

3. De novo mutation in COL2A1 leads to lethal foetal skeletal dysplasia;Bone;2021-12

4. Novel variants in COL2A1 causing rare spondyloepiphyseal dysplasia congenita;Molecular Genetics & Genomic Medicine;2020-01-23

5. Clinical and Molecular Characterization and Discovery of Novel Genetic Mutations of Chinese Patients with COL2A1-related Dysplasia;International Journal of Biological Sciences;2020