Published in J Biol Chem on November 09, 2001
Collagen structure and stability. Annu Rev Biochem (2009) 4.62
New perspectives on osteogenesis imperfecta. Nat Rev Endocrinol (2011) 3.97
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans. Hum Mutat (2007) 3.93
Collagen fibrillogenesis: fibronectin, integrins, and minor collagens as organizers and nucleators. Curr Opin Cell Biol (2008) 2.50
Collagen fibril architecture, domain organization, and triple-helical conformation govern its proteolysis. Proc Natl Acad Sci U S A (2008) 2.13
Influence of type I collagen surface density on fibroblast spreading, motility, and contractility. Biophys J (2003) 1.97
Candidate cell and matrix interaction domains on the collagen fibril, the predominant protein of vertebrates. J Biol Chem (2008) 1.92
A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders. J Clin Invest (2005) 1.68
Functional impact of missense variants in BRCA1 predicted by supervised learning. PLoS Comput Biol (2006) 1.49
Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships. Hum Mol Genet (2008) 1.42
Rapid Quantification of 3D Collagen Fiber Alignment and Fiber Intersection Correlations with High Sensitivity. PLoS One (2015) 1.41
ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta. PLoS Genet (2008) 1.37
Nonlinear optical imaging to evaluate the impact of obesity on mammary gland and tumor stroma. Mol Imaging (2007) 1.36
Inhibition of cancer cell invasion and metastasis by genistein. Cancer Metastasis Rev (2010) 1.29
The metabolism of proline as microenvironmental stress substrate. J Nutr (2008) 1.28
Mapping of SPARC/BM-40/osteonectin-binding sites on fibrillar collagens. J Biol Chem (2008) 1.21
Biominerals--hierarchical nanocomposites: the example of bone. Wiley Interdiscip Rev Nanomed Nanobiotechnol (2010) 1.20
Identification and structural analysis of type I collagen sites in complex with fibronectin fragments. Proc Natl Acad Sci U S A (2009) 1.17
Biomaterials that regulate growth factor activity via bioinspired interactions. Adv Funct Mater (2011) 1.16
The powerful functions of peptide-based bioactive matrices for regenerative medicine. Ann Biomed Eng (2014) 1.15
Amelogenin-collagen interactions regulate calcium phosphate mineralization in vitro. J Biol Chem (2010) 1.14
Collagen fibril surface displays a constellation of sites capable of promoting fibril assembly, stability, and hemostasis. Connect Tissue Res (2010) 1.14
Spatio-temporal modification of collagen scaffolds mediated by triple helical propensity. Biomacromolecules (2008) 1.13
Phosphoproteomics of collagen receptor networks reveals SHP-2 phosphorylation downstream of wild-type DDR2 and its lung cancer mutants. Biochem J (2013) 1.08
Synthesis and biological applications of collagen-model triple-helical peptides. Org Biomol Chem (2010) 1.05
Collagens as biomaterials. J Mater Sci Mater Med (2008) 1.04
Natural variation in four human collagen genes across an ethnically diverse population. Genomics (2008) 1.03
Effects of fibronectin and laminin on structural, mechanical and transport properties of 3D collageneous network. J Mater Sci Mater Med (2007) 1.02
Caffey disease: new perspectives on old questions. Bone (2013) 1.02
Structural and mechanical differences between collagen homo- and heterotrimers: relevance for the molecular origin of brittle bone disease. Biophys J (2012) 1.02
The influence of specific binding of collagen-silk chimeras to silk biomaterials on hMSC behavior. Biomaterials (2012) 1.01
Effects of genotype and dietary fish oil replacement with vegetable oil on the intestinal transcriptome and proteome of Atlantic salmon (Salmo salar). BMC Genomics (2012) 0.98
Recombinant collagen studies link the severe conformational changes induced by osteogenesis imperfecta mutations to the disruption of a set of interchain salt bridges. J Biol Chem (2008) 0.96
Collagen concentration and biomechanical properties of samples from the lower uterine cervix in relation to age and parity in non-pregnant women. Reprod Biol Endocrinol (2010) 0.94
Inhibition of collagen fibrillogenesis by cells expressing soluble extracellular domains of DDR1 and DDR2. J Mol Biol (2009) 0.94
NMR conformational and dynamic consequences of a gly to ser substitution in an osteogenesis imperfecta collagen model peptide. J Biol Chem (2009) 0.94
Role of the netrin-like domain of procollagen C-proteinase enhancer-1 in the control of metalloproteinase activity. J Biol Chem (2010) 0.93
Self-Assembly for the Synthesis of Functional Biomaterials. Acta Mater (2013) 0.93
Computational analysis of bovine alpha-1 collagen sequences. Bioinformation (2013) 0.90
Preserved Proteins from Extinct Bison latifrons Identified by Tandem Mass Spectrometry; Hydroxylysine Glycosides are a Common Feature of Ancient Collagen. Mol Cell Proteomics (2015) 0.89
Implications for collagen binding from the crystallographic structure of fibronectin 6FnI1-2FnII7FnI. J Biol Chem (2010) 0.89
Non-enzymatic glycation of type I collagen diminishes collagen-proteoglycan binding and weakens cell adhesion. J Cell Biochem (2008) 0.88
Control of crosslinking for tailoring collagen-based scaffolds stability and mechanics. Acta Biomater (2015) 0.87
Collagen-binding peptidoglycans: a biomimetic approach to modulate collagen fibrillogenesis for tissue engineering applications. Tissue Eng Part A (2009) 0.86
Definition of the native and denatured type II collagen binding site for fibronectin using a recombinant collagen system. J Biol Chem (2013) 0.86
Regulation of collagen fibrillogenesis by cell-surface expression of kinase dead DDR2. J Mol Biol (2008) 0.86
Probing the 3-D structure, dynamics, and stability of bacterial collagenase collagen binding domain (apo- versus holo-) by limited proteolysis MALDI-TOF MS. J Am Soc Mass Spectrom (2011) 0.85
PPARgamma and Proline Oxidase in Cancer. PPAR Res (2008) 0.85
Conformational dynamics accompanying the proteolytic degradation of trimeric collagen I by collagenases. J Am Chem Soc (2012) 0.85
Variation in the helical structure of native collagen. PLoS One (2014) 0.84
Osteogenesis imperfecta model peptides: incorporation of residues replacing Gly within a triple helix achieved by renucleation and local flexibility. Biophys J (2011) 0.84
Bone tissue engineering with a collagen-hydroxyapatite scaffold and culture expanded bone marrow stromal cells. J Biomed Mater Res B Appl Biomater (2014) 0.84
Mimicking the nanostructure of bone matrix to regenerate bone. Mater Today (Kidlington) (2013) 0.82
Bone matrix osteonectin limits prostate cancer cell growth and survival. Matrix Biol (2012) 0.82
A novel role of the Sp/KLF transcription factor KLF11 in arresting progression of endometriosis. PLoS One (2013) 0.82
Topographical guidance of 3D tumor cell migration at an interface of collagen densities. Phys Biol (2013) 0.82
Collagen's triglycine repeat number and phylogeny suggest an interdomain transfer event from a Devonian or Silurian organism into Trichodesmium erythraeum. J Mol Evol (2008) 0.82
The role of collagen crosslinks in ageing and diabetes - the good, the bad, and the ugly. Muscles Ligaments Tendons J (2014) 0.82
Structural insights from (15)N relaxation data for an anisotropic collagen peptide. J Am Chem Soc (2009) 0.82
Prospects and limitations of the rational engineering of fibrillar collagens. Protein Sci (2003) 0.82
Osteogenesis imperfecta missense mutations in collagen: structural consequences of a glycine to alanine replacement at a highly charged site. Biochemistry (2011) 0.81
Synthesis of Cell-Adhesive Anisotropic Multifunctional Particles by Stop Flow Lithography and Streptavidin-Biotin Interactions. Langmuir (2015) 0.81
Designed triple-helical peptides as tools for collagen biochemistry and matrix engineering. Philos Trans R Soc Lond B Biol Sci (2007) 0.81
Collagen scaffolds in bone sialoprotein-mediated bone regeneration. ScientificWorldJournal (2013) 0.80
Lysyl Hydroxylase 2 Is Secreted by Tumor Cells and Can Modify Collagen in the Extracellular Space. J Biol Chem (2016) 0.79
Fibrillar collagen assembled in the presence of glycosaminoglycans to constitute bioartificial stem cell niches in vitro. J Mater Sci Mater Med (2005) 0.79
Preferential sites for intramolecular glucosepane cross-link formation in type I collagen: A thermodynamic study. Matrix Biol (2015) 0.79
Development of hydrogels and biomimetic regulators as tissue engineering scaffolds. Membranes (Basel) (2012) 0.79
Should we use cells, biomaterials, or tissue engineering for cartilage regeneration? Stem Cell Res Ther (2016) 0.79
Analysis of cell migration within a three-dimensional collagen matrix. J Vis Exp (2014) 0.78
Chick tendon fibroblast transcriptome and shape depend on whether the cell has made its own collagen matrix. Sci Rep (2015) 0.78
Influence of the microenvironment on cell fate determination and migration. Physiol Genomics (2014) 0.78
Strategies for regeneration of components of nervous system: scaffolds, cells and biomolecules. Regen Biomater (2015) 0.78
Molecular dynamics simulations of the full triple helical region of collagen type I provide an atomic scale view of the protein's regional heterogeneity. Pac Symp Biocomput (2011) 0.78
Rapid three-dimensional quantification of voxel-wise collagen fiber orientation. Biomed Opt Express (2015) 0.78
Plant-derived human collagen scaffolds for skin tissue engineering. Tissue Eng Part A (2013) 0.78
Micro/Nano Multilayered Scaffolds of PLGA and Collagen by Alternately Electrospinning for Bone Tissue Engineering. Nanoscale Res Lett (2016) 0.78
Precise Tuning of Facile One-Pot Gelatin Methacryloyl (GelMA) Synthesis. Sci Rep (2016) 0.77
Anti-Photoaging Effects of Angelica acutiloba Root Ethanol Extract in Human Dermal Fibroblasts. Toxicol Res (2017) 0.77
Local amino acid sequence patterns dominate the heterogeneous phenotype for the collagen connective tissue disease Osteogenesis Imperfecta resulting from Gly mutations. J Struct Biol (2015) 0.77
Antioxidant Activity and Anti-wrinkle Effects of Aceriphyllum rossii Leaf Ethanol Extract. Toxicol Res (2015) 0.77
Biopolymers and supramolecular polymers as biomaterials for biomedical applications. MRS Bull (2015) 0.77
Candidate prognostic markers in breast cancer: focus on extracellular proteases and their inhibitors. Breast Cancer (Dove Med Press) (2014) 0.77
New tricks for "old" domains: how novel architectures and promiscuous hubs contributed to the organization and evolution of the ECM. Genome Biol Evol (2014) 0.77
Advances in progenitor cell therapy using scaffolding constructs for central nervous system injury. Stem Cell Rev (2009) 0.77
Anti-aging effects of Piper cambodianum P. Fourn. extract on normal human dermal fibroblast cells and a wound-healing model in mice. Clin Interv Aging (2016) 0.76
pH-responsive collagen fibrillogenesis in confined droplets induced by vapour diffusion. J Mater Sci Mater Med (2014) 0.76
Intrinsically disordered proteins and biomineralization. Matrix Biol (2016) 0.76
Control of Collagen Stability and Heterotrimer Specificity through Repulsive Electrostatic Interactions. Biomolecules (2013) 0.76
Self-assembled peptide-based nanostructures: Smart nanomaterials toward targeted drug delivery. Nano Today (2016) 0.76
The genome-wide role of HSF-1 in the regulation of gene expression in Caenorhabditis elegans. BMC Genomics (2016) 0.76
Actinidain-hydrolyzed type I collagen reveals a crucial amino acid sequence in fibril formation. J Biol Chem (2010) 0.76
Valorisation of Biowastes for the Production of Green Materials Using Chemical Methods. Top Curr Chem (J) (2017) 0.75
Bone marker gene expression in calvarial bones: different bone microenvironments. J Biol Res (Thessalon) (2017) 0.75
Utilization of Molecular Dynamics Simulation Coupled with Experimental Assays to Optimize Biocompatibility of an Electrospun PCL/PVA Scaffold. PLoS One (2017) 0.75
Effects of hydrotalcite combined with esomeprazole on gastric ulcer healing quality: A clinical observation study. World J Gastroenterol (2017) 0.75
Demethyleneberberine Protects against Hepatic Fibrosis in Mice by Modulating NF-κB Signaling. Int J Mol Sci (2016) 0.75
Distribution bias analysis of germline and somatic single-nucleotide variations that impact protein functional site and neighboring amino acids. Sci Rep (2017) 0.75
Characterization of a liver organoid tissue composed of hepatocytes and fibroblasts in dense collagen fibrils. Tissue Eng Part A (2013) 0.75
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans. Hum Mutat (2007) 3.93
Regulation of cardiovascular development and integrity by the heart of glass-cerebral cavernous malformation protein pathway. Nat Med (2009) 2.12
Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database. Hum Mutat (2003) 2.10
Candidate cell and matrix interaction domains on the collagen fibril, the predominant protein of vertebrates. J Biol Chem (2008) 1.92
Occupational and genetic risk factors associated with intervertebral disc disease. Spine (Phila Pa 1976) (2007) 1.74
Endorepellin, a novel inhibitor of angiogenesis derived from the C terminus of perlecan. J Biol Chem (2002) 1.67
Association between interleukin 1 gene cluster polymorphisms and bilateral distal interphalangeal osteoarthritis. J Rheumatol (2009) 1.52
Serum antibodies against intact human collagen IX are elevated at onset of rheumatoid arthritis but are not related to development of erosions. J Rheumatol (2008) 1.45
Angiogenesis in collagen I requires alpha2beta1 ligation of a GFP*GER sequence and possibly p38 MAPK activation and focal adhesion disassembly. J Biol Chem (2003) 1.36
Radial perivascular retinal degeneration: a key to the clinical diagnosis of an ocular variant of Stickler syndrome with minimal or no systemic manifestations. Am J Ophthalmol (2002) 1.28
Heterozygous mutations in the LDL receptor-related protein 5 (LRP5) gene are associated with primary osteoporosis in children. J Bone Miner Res (2005) 1.27
Interleukin 1 polymorphisms and intervertebral disc degeneration. Epidemiology (2004) 1.24
The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degeneration. Spine (Phila Pa 1976) (2005) 1.24
Sp1 and Sp3 transcription factors mediate interleukin-1 beta down-regulation of human type II collagen gene expression in articular chondrocytes. J Biol Chem (2003) 1.21
COL9A3 gene polymorphism and obesity in intervertebral disc degeneration of the lumbar spine: evidence of gene-environment interaction. Spine (Phila Pa 1976) (2002) 1.19
Altered integration of matrilin-3 into cartilage extracellular matrix in the absence of collagen IX. Mol Cell Biol (2005) 1.19
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1. Eur J Hum Genet (2003) 1.10
Heparan sulfate proteoglycans: a GAGgle of skeletal-hematopoietic regulators. Dev Dyn (2008) 1.10
Genetic variations in IL6 associate with intervertebral disc disease characterized by sciatica. Pain (2005) 1.08
Intervertebral disc degeneration in relation to the COL9A3 and the IL-1ss gene polymorphisms. Eur Spine J (2005) 1.07
Genetic susceptibility of intervertebral disc degeneration among young Finnish adults. BMC Med Genet (2011) 1.05
Characterization of recombinant amino-terminal NC4 domain of human collagen IX: interaction with glycosaminoglycans and cartilage oligomeric matrix protein. J Biol Chem (2004) 1.05
Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients. Hum Mutat (2004) 1.05
Missense and nonsense mutations in the alternatively-spliced exon 2 of COL2A1 cause the ocular variant of Stickler syndrome. Hum Mutat (2008) 1.04
Oto-spondylo-megaepiphyseal dysplasia (OSMED): clinical and radiological findings in sibs homozygous for premature stop codon mutation in the COL11A2 gene. Am J Med Genet A (2006) 1.03
Genetic factors are associated with modic changes in endplates of lumbar vertebral bodies. Spine (Phila Pa 1976) (2008) 1.03
Novel mutations in the small leucine-rich repeat protein/proteoglycan (SLRP) genes in high myopia. Hum Mutat (2007) 1.03
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity. BMC Med Genet (2012) 1.00
Down-regulation of human type II collagen gene expression by transforming growth factor-beta 1 (TGF-beta 1) in articular chondrocytes involves SP3/SP1 ratio. J Biol Chem (2002) 0.99
Genetic risk factors of disc degeneration among 12-14-year-old Danish children: a population study. Int J Mol Epidemiol Genet (2010) 0.99
Clinical and radiographic findings in multiple epiphyseal dysplasia caused by MATN3 mutations: description of 12 patients. Am J Med Genet A (2004) 0.98
A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathies. Am J Med Genet A (2007) 0.96
Mutations in the known genes are not the major cause of MED; distinctive phenotypic entities among patients with no identified mutations. Eur J Hum Genet (2005) 0.96
Structural and functional characterization of recombinant matrilin-3 A-domain and implications for human genetic bone diseases. J Biol Chem (2007) 0.96
Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia. Eur J Hum Genet (2003) 0.95
Genetic predisposition for femoral neck stress fractures in military conscripts. BMC Genet (2010) 0.93
A stop codon mutation in COL11A2 induces exon skipping and leads to non-ocular Stickler syndrome. Am J Med Genet A (2004) 0.93
Finer linkage mapping of a primary hip osteoarthritis susceptibility locus on chromosome 6. Eur J Hum Genet (2002) 0.93
Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene. Am J Hum Genet (2010) 0.93
A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome. Am J Med Genet A (2011) 0.93
Is the interleukin-6 haplotype a prognostic factor for sciatica? Eur J Pain (2008) 0.92
Common interleukin-6 promoter variants associate with the more severe forms of distal interphalangeal osteoarthritis. Arthritis Res Ther (2008) 0.91
The fibril-associated collagen IX provides a novel mechanism for cell adhesion to cartilaginous matrix. J Biol Chem (2004) 0.91
Radiologic phenotypes in lumbar MR imaging for a gene defect in the COL9A3 gene of type IX collagen. Radiology (2003) 0.91
Univariate and bivariate variance component linkage analysis of a whole-genome scan for loci contributing to bone mineral density. Eur J Hum Genet (2005) 0.91
Association between the aggrecan gene variable number of tandem repeats polymorphism and intervertebral disc degeneration. Spine (Phila Pa 1976) (2007) 0.88
Non-enzymatic glycation of type I collagen diminishes collagen-proteoglycan binding and weakens cell adhesion. J Cell Biochem (2008) 0.88
Magnetic resonance imaging findings in relation to the COL9A2 tryptophan allele among patients with sciatica. Spine (Phila Pa 1976) (2002) 0.87
A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family. Hum Hered (2005) 0.86
Procollagen with skipping of alpha 1(I) exon 41 has lower binding affinity for alpha 1(I) C-telopeptide, impaired in vitro fibrillogenesis, and altered fibril morphology. J Biol Chem (2001) 0.85
Rare variations in WNT3A and DKK1 may predispose carriers to primary osteoporosis. Eur J Med Genet (2012) 0.84
Analysis of an ascidian integrin provides new insight into early evolution of collagen recognition. FEBS Lett (2007) 0.81
Trimerization of collagen IX alpha-chains does not require the presence of the COL1 and NC1 domains. Biochem J (2008) 0.81
Analysis of the COL3A1 gene in patients with spontaneous cervical artery dissections. J Neurol (2002) 0.80
Gender difference in genetic association between IL1A variant and early lumbar disc degeneration: a three-year follow-up. Int J Mol Epidemiol Genet (2012) 0.78
Putative susceptibility locus on chromosome 21q for lumbar disc disease (LDD) in the Finnish population. J Bone Miner Res (2007) 0.78
Germline mosacism in Shprintzen-Goldberg syndrome. Am J Med Genet A (2012) 0.78
Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2. Am J Med Genet A (2012) 0.77
The collagen V homotrimer [alpha1(V)](3) production is unexpectedly favored over the heterotrimer [alpha1(V)](2)alpha2(V) in recombinant expression systems. J Biomed Biotechnol (2010) 0.76
Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy? Genet Med (2012) 0.76
Absence of TGFBR2 mutations in patients with spontaneous spinal CSF leaks and intracranial hypotension. J Headache Pain (2008) 0.75
Wolf-Hirschhorn syndrome and ectrodactyly: New findings and a review of the literature. Am J Med Genet A (2010) 0.75
A new syndromic craniosynostosis with involvement of the spine, long bones, pelvis, and digits: molecular genetic and array analysis. Clin Dysmorphol (2012) 0.75