Published in Connect Tissue Res on August 18, 2011
Proteomic analysis reveals age-related changes in tendon matrix composition, with age- and injury-specific matrix fragmentation. J Biol Chem (2014) 1.13
Targeted deletion of collagen V in tendons and ligaments results in a classic Ehlers-Danlos syndrome joint phenotype. Am J Pathol (2015) 0.87
Collagen V localizes to pericellular sites during tendon collagen fibrillogenesis. Matrix Biol (2013) 0.80
Dissection of the human multipotent adult progenitor cell secretome by proteomic analysis. Stem Cells Transl Med (2013) 0.77
Genome-wide analysis identifies differential promoter methylation of Leprel2, Foxf1, Mmp25, Igfbp6, and Peg12 in murine tendinopathy. J Orthop Res (2016) 0.75
Empirical statistical model to estimate the accuracy of peptide identifications made by MS/MS and database search. Anal Chem (2002) 35.30
A statistical model for identifying proteins by tandem mass spectrometry. Anal Chem (2003) 29.58
Resistance of cell membranes to different detergents. Proc Natl Acad Sci U S A (2003) 3.57
Procollagen trafficking, processing and fibrillogenesis. J Cell Sci (2005) 3.54
Decorin regulates assembly of collagen fibrils and acquisition of biomechanical properties during tendon development. J Cell Biochem (2006) 2.71
Collagen fibrillogenesis: fibronectin, integrins, and minor collagens as organizers and nucleators. Curr Opin Cell Biol (2008) 2.50
Type V collagen controls the initiation of collagen fibril assembly. J Biol Chem (2004) 2.34
Polymerization of type I and III collagens is dependent on fibronectin and enhanced by integrins alpha 11beta 1 and alpha 2beta 1. J Biol Chem (2002) 2.26
Extracellular compartments in matrix morphogenesis: collagen fibril, bundle, and lamellar formation by corneal fibroblasts. J Cell Biol (1984) 2.19
Differential expression of lumican and fibromodulin regulate collagen fibrillogenesis in developing mouse tendons. J Cell Biol (2000) 2.19
Coalignment of plasma membrane channels and protrusions (fibripositors) specifies the parallelism of tendon. J Cell Biol (2004) 2.19
Collagen fibrillogenesis in situ: fibril segments undergo post-depositional modifications resulting in linear and lateral growth during matrix development. Dev Dyn (1995) 2.17
Development of tendon structure and function: regulation of collagen fibrillogenesis. J Musculoskelet Neuronal Interact (2005) 1.93
Surfaceome of Leptospira spp. Infect Immun (2005) 1.90
Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition. Nat Genet (2002) 1.60
Collagen XI nucleates self-assembly and limits lateral growth of cartilage fibrils. J Biol Chem (2000) 1.58
Vascular smooth muscle cells orchestrate the assembly of type I collagen via alpha2beta1 integrin, RhoA, and fibronectin polymerization. Am J Pathol (2003) 1.37
Control of extracellular matrix assembly by syndecan-2 proteoglycan. J Cell Sci (2000) 1.37
Murine model of the Ehlers-Danlos syndrome. col5a1 haploinsufficiency disrupts collagen fibril assembly at multiple stages. J Biol Chem (2006) 1.35
Toward the complete membrane proteome: high coverage of integral membrane proteins through transmembrane peptide detection. Mol Cell Proteomics (2005) 1.26
Tenascin-X, collagen, elastin, and the Ehlers-Danlos syndrome. Am J Med Genet C Semin Med Genet (2005) 1.16
Regulation of collagen fibril nucleation and initial fibril assembly involves coordinate interactions with collagens V and XI in developing tendon. J Biol Chem (2011) 1.14
Structural requirements for fibromodulin binding to collagen and the control of type I collagen fibrillogenesis--critical roles for disulphide bonding and the C-terminal region. Eur J Biochem (1998) 1.05
Collagen fibrillogenesis in tendon development: current models and regulation of fibril assembly. Birth Defects Res C Embryo Today (2008) 1.03
Localizing matrix metalloproteinase activities in the pericellular environment. FEBS J (2010) 1.03
Multiple signaling pathways mediate compaction of collagen matrices by EGF-stimulated fibroblasts. Exp Cell Res (2006) 1.00
Hyaluronan and CD44: strategic players for cell-matrix interactions during chondrogenesis and matrix assembly. Birth Defects Res C Embryo Today (2003) 0.99
Reduced type I collagen utilization: a pathogenic mechanism in COL5A1 haplo-insufficient Ehlers-Danlos syndrome. J Cell Biochem (2004) 0.96
Interactions of syndecan-1 and heparin with human collagens. Glycobiology (1994) 0.95
Collagen receptor integrins: rising to the challenge. Curr Drug Targets (2008) 0.90
How many potentially secreted proteins are contained in a bacterial genome? Gene (1999) 0.89
Focus on molecules: collagens V and XI. Exp Eye Res (2010) 0.87
Collagen fibrils forming in developing tendon show an early and abrupt limitation in diameter at the growing tips. J Mol Biol (1998) 0.83
Decorin regulates assembly of collagen fibrils and acquisition of biomechanical properties during tendon development. J Cell Biochem (2006) 2.71
Targeted ablation of the abcc6 gene results in ectopic mineralization of connective tissues. Mol Cell Biol (2005) 2.64
Type V collagen controls the initiation of collagen fibril assembly. J Biol Chem (2004) 2.34
The molecular basis of corneal transparency. Exp Eye Res (2010) 2.08
Keratocan, a cornea-specific keratan sulfate proteoglycan, is regulated by lumican. J Biol Chem (2005) 1.83
Genetic evidence for the coordinated regulation of collagen fibrillogenesis in the cornea by decorin and biglycan. J Biol Chem (2009) 1.79
Keratocan-deficient mice display alterations in corneal structure. J Biol Chem (2003) 1.74
A role for MEK kinase 1 in TGF-beta/activin-induced epithelium movement and embryonic eyelid closure. EMBO J (2003) 1.72
Influence of decorin and biglycan on mechanical properties of multiple tendons in knockout mice. J Biomech Eng (2005) 1.71
A syndrome of joint laxity and impaired tendon integrity in lumican- and fibromodulin-deficient mice. J Biol Chem (2002) 1.64
Structural abnormalities of the cornea and lid resulting from collagen V mutations. Invest Ophthalmol Vis Sci (2006) 1.53
Biologically active decorin is a monomer in solution. J Biol Chem (2003) 1.40
Mechanical, compositional, and structural properties of the post-natal mouse Achilles tendon. Ann Biomed Eng (2011) 1.40
Decorin expression is important for age-related changes in tendon structure and mechanical properties. Matrix Biol (2012) 1.39
Murine model of the Ehlers-Danlos syndrome. col5a1 haploinsufficiency disrupts collagen fibril assembly at multiple stages. J Biol Chem (2006) 1.35
Secretion and organization of a cornea-like tissue in vitro by stem cells from human corneal stroma. Invest Ophthalmol Vis Sci (2007) 1.35
The regulatory roles of small leucine-rich proteoglycans in extracellular matrix assembly. FEBS J (2013) 1.33
Stem cell therapy restores transparency to defective murine corneas. Stem Cells (2009) 1.32
Type XIV Collagen Regulates Fibrillogenesis: PREMATURE COLLAGEN FIBRIL GROWTH AND TISSUE DYSFUNCTION IN NULL MICE. J Biol Chem (2009) 1.32
Partial restoration of the keratocyte phenotype to bovine keratocytes made fibroblastic by serum. Invest Ophthalmol Vis Sci (2002) 1.32
Collagen fibril assembly during postnatal development and dysfunctional regulation in the lumican-deficient murine cornea. Dev Dyn (2006) 1.29
Fhit interaction with ferredoxin reductase triggers generation of reactive oxygen species and apoptosis of cancer cells. J Biol Chem (2008) 1.22
Ocular and scleral alterations in gene-targeted lumican-fibromodulin double-null mice. Invest Ophthalmol Vis Sci (2003) 1.21
Influence of decorin on the mechanical, compositional, and structural properties of the mouse patellar tendon. J Biomech Eng (2012) 1.20
Fibulin-2 is dispensable for mouse development and elastic fiber formation. Mol Cell Biol (2007) 1.16
Regulation of procollagen amino-propeptide processing during mouse embryogenesis by specialization of homologous ADAMTS proteases: insights on collagen biosynthesis and dermatosparaxis. Development (2006) 1.16
Regulation of collagen fibril nucleation and initial fibril assembly involves coordinate interactions with collagens V and XI in developing tendon. J Biol Chem (2011) 1.14
Effect of age and proteoglycan deficiency on collagen fiber re-alignment and mechanical properties in mouse supraspinatus tendon. J Biomech Eng (2013) 1.13
Effect of latanoprost on the expression of matrix metalloproteinases and their tissue inhibitors in human trabecular meshwork cells. Invest Ophthalmol Vis Sci (2006) 1.12
Functional knockout of the matrilin-3 gene causes premature chondrocyte maturation to hypertrophy and increases bone mineral density and osteoarthritis. Am J Pathol (2006) 1.11
Type XII collagen regulates osteoblast polarity and communication during bone formation. J Cell Biol (2011) 1.06
Dysfunctional tendon collagen fibrillogenesis in collagen VI null mice. Matrix Biol (2010) 1.06
Targeted inactivation of murine laminin gamma2-chain gene recapitulates human junctional epidermolysis bullosa. J Invest Dermatol (2003) 1.06
Regional differences in stem cell/progenitor cell populations from the mouse achilles tendon. Tissue Eng Part A (2012) 1.03
The roles of types XII and XIV collagen in fibrillogenesis and matrix assembly in the developing cornea. J Cell Biochem (2002) 1.03
Procollagen C proteinase enhancer 1 genes are important determinants of the mechanical properties and geometry of bone and the ultrastructure of connective tissues. Mol Cell Biol (2006) 1.01
Collagen V is a dominant regulator of collagen fibrillogenesis: dysfunctional regulation of structure and function in a corneal-stroma-specific Col5a1-null mouse model. J Cell Sci (2011) 1.00
Fibromodulin regulates collagen fibrillogenesis during peripheral corneal development. Dev Dyn (2010) 0.98
Reduced type I collagen utilization: a pathogenic mechanism in COL5A1 haplo-insufficient Ehlers-Danlos syndrome. J Cell Biochem (2004) 0.96
Position of single amino acid substitutions in the collagen triple helix determines their effect on structure of collagen fibrils. J Struct Biol (2004) 0.96
Collagen fibril growth during chicken tendon development: matrix metalloproteinase-2 and its activation. Cell Tissue Res (2009) 0.94
Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice. Hum Mol Genet (2013) 0.93
Procollagen VII self-assembly depends on site-specific interactions and is promoted by cleavage of the NC2 domain with procollagen C-proteinase. Biochemistry (2003) 0.91
Increased stromal extracellular matrix synthesis and assembly by insulin activated bovine keratocytes cultured under agarose. Exp Eye Res (2008) 0.91
COL6A3 protein deficiency in mice leads to muscle and tendon defects similar to human collagen VI congenital muscular dystrophy. J Biol Chem (2013) 0.91
The fibril-associated collagen IX provides a novel mechanism for cell adhesion to cartilaginous matrix. J Biol Chem (2004) 0.91
Mechanical, compositional, and structural properties of the mouse patellar tendon with changes in biglycan gene expression. J Orthop Res (2013) 0.90
Recapitulation of the Achilles tendon mechanical properties during neonatal development: a study of differential healing during two stages of development in a mouse model. J Orthop Res (2011) 0.90
Mechanical property changes during neonatal development and healing using a multiple regression model. J Biomech (2012) 0.90
Single amino acid substitutions in procollagen VII affect early stages of assembly of anchoring fibrils. J Biol Chem (2004) 0.89
Analysis of expression of matrix metalloproteinases and tissue inhibitors of metalloproteinases in human ciliary body after latanoprost. Invest Ophthalmol Vis Sci (2006) 0.89
Collagen fibril formation in a wound healing model. J Struct Biol (2002) 0.88
The tendon injury response is influenced by decorin and biglycan. Ann Biomed Eng (2013) 0.88
Validation of an empirical damage model for aging and in vivo injury of the murine patellar tendon. J Biomech Eng (2013) 0.88
Non-enzymatic glycation of type I collagen diminishes collagen-proteoglycan binding and weakens cell adhesion. J Cell Biochem (2008) 0.88
Structure, physiology, and biochemistry of collagens. Adv Exp Med Biol (2014) 0.88
Pathophysiological mechanisms of autosomal dominant congenital stromal corneal dystrophy: C-terminal-truncated decorin results in abnormal matrix assembly and altered expression of small leucine-rich proteoglycans. Am J Pathol (2011) 0.87
Targeted expression of a lumican transgene rescues corneal deficiencies in lumican-null mice. Mol Vis (2007) 0.87
Role of Cys41 in the N-terminal domain of lumican in ex vivo collagen fibrillogenesis by cultured corneal stromal cells. Biochem J (2003) 0.87
Focus on molecules: collagens V and XI. Exp Eye Res (2010) 0.87
Differential expression of type XII collagen in developing chicken metatarsal tendons. J Anat (2003) 0.86
Collagen dysregulation in the dermis of the Sagg/+ mouse: a loose skin model. J Invest Dermatol (2006) 0.85
Proteome profiling of wild type and lumican-deficient mouse corneas. J Proteomics (2011) 0.85
A mouse model for dominant collagen VI disorders: heterozygous deletion of Col6a3 Exon 16. J Biol Chem (2014) 0.83
Regulatory role of collagen V in establishing mechanical properties of tendons and ligaments is tissue dependent. J Orthop Res (2015) 0.82
Association of type XII collagen with regions of increased stability and keratocyte density in the cornea. Exp Eye Res (2002) 0.82
Collagen XIV is important for growth and structural integrity of the myocardium. J Mol Cell Cardiol (2012) 0.82
Complete primary structure and genomic organization of the mouse Col14a1 gene. Matrix Biol (2004) 0.82
Enhanced cell accumulation and collagen processing by keratocytes cultured under agarose and in media containing IGF-I, TGF-β or PDGF. Matrix Biol (2010) 0.81
Intracellularly-retained decorin lacking the C-terminal ear repeat causes ER stress: a cell-based etiological mechanism for congenital stromal corneal dystrophy. Am J Pathol (2013) 0.81
Abnormal corneal endothelial maturation in collagen XII and XIV null mice. Invest Ophthalmol Vis Sci (2013) 0.80
Tendon proper- and peritenon-derived progenitor cells have unique tenogenic properties. Stem Cell Res Ther (2014) 0.80
The location-specific role of proteoglycans in the flexor carpi ulnaris tendon. Connect Tissue Res (2013) 0.79
Mouse models in tendon and ligament research. Adv Exp Med Biol (2014) 0.79
Focus on molecules: decorin. Exp Eye Res (2010) 0.79
Intolerance of short arm cast wear by patients with claustrophobia: case report. J Hand Surg Am (2010) 0.79
Complete primary structure and genomic organization of the mouse Col14a1 gene. Matrix Biol (2003) 0.76
Two-stage hierarchical modeling for analysis of subpopulations in conditional distributions. J Appl Stat (2011) 0.75
Is it time to reexamine KDOQI aluminum guidelines? Am J Kidney Dis (2006) 0.75
Fhit interaction with ferredoxin reductase triggers generation of reactive oxygen species and apoptosis of cancer cells. J Biol Chem (2017) 0.75