Imaging of Human Cancer Cells in 3D Collagen Matrices
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
Genetic epidemiology, prevalence, and genotype–phenotype correlations in the Swedish population with osteogenesis imperfecta | European Journal of Human Genetics
Frontiers | New Structural and Single Nucleotide Mutations in Type I and Type II Collagens in Taiwanese Children With Type I and Type II Collagenopathies
Chiral Tartaric Acid Improves Fracture Toughness of Bioactive Brushite– Collagen Bone Cements | ACS Applied Bio Materials
A High-Throughput Assay for Collagen Secretion Suggests an Unanticipated Role for Hsp90 in Collagen Production | Biochemistry
Genotype–phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I | European Journal of Human Genetics
Bone Morphogenetic Protein-1 Processes the NH2-terminal Propeptide, and a Furin-like Proprotein Convertase Processes the COOH-terminal Propeptide of pro-α1(V) Collagen* - Journal of Biological Chemistry
Pseudohypoxic HIF pathway activation dysregulates collagen structure-function in human lung fibrosis | eLife
Interaction of Axonal Chondrolectin with Collagen XIXa1 Is Necessary for Precise Neuromuscular Junction Formation - ScienceDirect
A Genomics-Based Semirational Approach for Expanding the Postbiotic Potential of Collagen Peptides Using Lactobacillaceae | Journal of Agricultural and Food Chemistry
Frontiers | Phenotypic Spectrum and Molecular Basis in a Chinese Cohort of Osteogenesis Imperfecta With Mutations in Type I Collagen
Collagen transport and related pathways in Osteogenesis Imperfecta | SpringerLink
Candidate Cell and Matrix Interaction Domains on the Collagen Fibril, the Predominant Protein of Vertebrates - ScienceDirect
A three-dimensional (3D), serum-free, Collagen Type I system for chondrogenesis of canine bone marrow-derived multipotent stromal cells (cMSCs) | PLOS ONE
Genotype–phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I | European Journal of Human Genetics
Collagen XVII Is Destabilized by a Glycine Substitution Mutation in the Cell Adhesion Domain Col15* - Journal of Biological Chemistry
Polymers | Free Full-Text | A Review of the Effects of Collagen Treatment in Clinical Studies | HTML
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
Four decades in the making: Collagen III and mechanisms of vascular Ehlers Danlos Syndrome - ScienceDirect
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
Clinical Application of NGS Tools in the Diagnosis of Collagenopathies
The triple helix of collagens - an ancient protein structure that enabled animal multicellularity and tissue evolution. - Abstract - Europe PMC
Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin | Scientific Reports
