Candidate Cell and Matrix Interaction Domains on the Collagen Fibril, the Predominant Protein of Vertebrates - ScienceDirect
Marine Drugs | Free Full-Text | Growth Factor-Free Vascularization of Marine-Origin Collagen Sponges Using Cryopreserved Stromal Vascular Fractions from Human Adipose Tissue | HTML
The triple helix of collagens - an ancient protein structure that enabled animal multicellularity and tissue evolution. - Abstract - Europe PMC
Chiral Tartaric Acid Improves Fracture Toughness of Bioactive Brushite– Collagen Bone Cements | ACS Applied Bio Materials
Frontiers | Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen
Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin | Scientific Reports
Frontiers | Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen
A three-dimensional (3D), serum-free, Collagen Type I system for chondrogenesis of canine bone marrow-derived multipotent stromal cells (cMSCs) | PLOS ONE
Pseudohypoxic HIF pathway activation dysregulates collagen structure-function in human lung fibrosis | eLife
Densified Collagen Tubular Grafts for Human Tissue Replacement and Disease Modelling Applications | bioRxiv
Densified Collagen Tubular Grafts for Human Tissue Replacement and Disease Modelling Applications | bioRxiv
Collagen transport and related pathways in Osteogenesis Imperfecta | SpringerLink
Pseudohypoxic HIF pathway activation dysregulates collagen structure-function in human lung fibrosis | eLife
Genotype–phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I | European Journal of Human Genetics
Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers–Danlos syndrome with severe intestinal involvement: a case report | Journal of Medical Case Reports | Full Text
Frontiers | Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen
Collagen XVII Is Destabilized by a Glycine Substitution Mutation in the Cell Adhesion Domain Col15* - Journal of Biological Chemistry
Effect of 3-Hydroxyproline Residues on Collagen Stability | Journal of the American Chemical Society
Collagen Stimulating Effect of Peptide Amphiphile C16–KTTKS on Human Fibroblasts | Molecular Pharmaceutics
Regulation of mineralisation in bone and vascular tissue: a comparative review in: Journal of Endocrinology Volume 248 Issue 2 (2021)
Genetic epidemiology, prevalence, and genotype–phenotype correlations in the Swedish population with osteogenesis imperfecta | European Journal of Human Genetics
Mapping the Ligand-binding Sites and Disease-associated Mutations on the Most Abundant Protein in the Human, Type I Collagen* - Journal of Biological Chemistry
Frontiers | Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen
Polymers | Free Full-Text | A Review of the Effects of Collagen Treatment in Clinical Studies | HTML
Imaging of Human Cancer Cells in 3D Collagen Matrices
Clinical Application of NGS Tools in the Diagnosis of Collagenopathies
