Targeted Disruption of Decorin Leads to Abnormal Collagen Fibril Morphology and Skin Fragility

Collagen fibrillogenesis in vitro: interaction of types I and V collagen regulates fibril diameter

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Myofibroblasts and mechano-regulation of connective tissue remodelling

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Microfibrillar structure of type I collagen in situ

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Lumican regulates collagen fibril assembly: skin fragility and corneal opacity in the absence of lumican

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Glycosaminoglycans and their proteoglycans: host‐associated molecular patterns for initiation and modulation of inflammation

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Molecular aspects of skin ageing

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Type V collagen controls the initiation of collagen fibril assembly

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The regulatory roles of small leucine‐rich proteoglycans in extracellular matrix assembly

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Molecular and cellular biology of alveolar bone

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Topically Applied Vitamin C Enhances the mRNA Level of Collagens I and III, Their Processing Enzymes and Tissue Inhibitor of Matrix Metalloproteinase 1 in the Human Dermis11Part of this work was presented in poster form at the American Academy of Dermatology, San Francisco, CA, March 10–15, 2000.

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Ehlers-Danlos syndromes and Marfan syndrome

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Mechanoregulation of the Myofibroblast in Wound Contraction, Scarring, and Fibrosis: Opportunities for New Therapeutic Intervention

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Dermal extracellular matrix molecules in skin development, homeostasis, wound regeneration and diseases

Huang, J., Heng, S., Zhang, W., Liu, Y., Xia, T., Ji, C., & Zhang, L.-J. (2022) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2022.02.027 · Cited by 238

The Ehlers-Danlos syndrome: on beyond collagens

Mao, J.-R., & Bristow, J. (2001) · Journal of Clinical Investigation · doi:10.1172/jci12881 · Cited by 233

Transparency, swelling and scarring in the corneal stroma

Meek, K. M., Leonard, D. W., Connon, C. J., Dennis, S., & Khan, S. (2003) · Eye · doi:10.1038/sj.eye.6700574 · Cited by 230

Tobacco smoke causes premature skin aging

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Genetic evidence for the coordinated regulation of collagen fibrillogenesis in the cornea by decorin and biglycan

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Decorin Binds Near the C Terminus of Type I Collagen

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Circadian control of the secretory pathway maintains collagen homeostasis

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Extracellular matrix signaling through growth factor receptors during wound healing

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Classical Ehlers-Danlos Syndrome Caused by a Mutation in Type I Collagen

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Tendon properties in relation to muscular activity and physical training

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Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome

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Stromal and hematopoietic cells in secondary lymphoid organs: partners in immunity

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Matrix molecules and skin biology

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Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder

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The use of X-ray scattering techniques to determine corneal ultrastructure

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The Extracellular Matrix in Wound Healing: A Closer Look at Therapeutics for Chronic Wounds

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Musculocontractural Ehlers-Danlos Syndrome (former EDS type VIB) and adducted thumb clubfoot syndrome (ATCS) represent a single clinical entity caused by mutations in the dermatan-4-sulfotransferase 1 encoding CHST14 gene

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Expression of Glycosaminoglycans and Small Proteoglycans in Wounds: Modulation by the Tripeptide–Copper Complex Glycyl-L-Histidyl-L-Lysine-Cu2+

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Defective glycosylation of decorin and biglycan, altered collagen structure, and abnormal phenotype of the skin fibroblasts of an Ehlers–Danlos syndrome patient carrying the novel Arg270Cys substitution in galactosyltransferase I (β4GalT-7)

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Vitamin C–squalene bioconjugate promotes epidermal thickening and collagen production in human skin

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Mammalian Skeletogenesis and Extracellular Matrix. What can We Learn from Knockout Mice?

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Collagen fibril assembly during postnatal development and dysfunctional regulation in the lumican-deficient murine cornea

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The matricellular protein periostin contributes to proper collagen function and is downregulated during skin aging

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Prdm5 Regulates Collagen Gene Transcription by Association with RNA Polymerase II in Developing Bone

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Fibromodulin regulates collagen fibrillogenesis during peripheral corneal development

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Serpina3n attenuates granzyme B-mediated decorin cleavage and rupture in a murine model of aortic aneurysm

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Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel B3GALT6 mutations

Ritelli, M., Chiarelli, N., Zoppi, N., Dordoni, C., Quinzani, S., Traversa, M., Venturini, M., Calzavara-Pinton, P., & Colombi, M. (2015) · Molecular Genetics and Metabolism Reports · doi:10.1016/j.ymgmr.2014.11.005 · Cited by 37

A personal voyage through the proteoglycan field

Lindahl, U. (2014) · Matrix Biology · doi:10.1016/j.matbio.2014.01.001 · Cited by 28

Elongated dermatan sulphate in post-inflammatory healing skin distributes among collagen fibrils separated by enlarged interfibrillar gaps

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Galactosaminoglycan Function and Oligosaccharide Structure Determination

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Organotypic cultures as aging associated disease models

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Different architectures of collagen fibrils enforce different fibrillogenesis mechanisms

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Genetics of the Ehlers–Danlos syndrome: More than collagen disorders

Van Damme, T., Syx, D., Coucke, P., Symoens, S., De Paepe, A., & Malfait, F. (2015) · Expert Opinion on Orphan Drugs · doi:10.1517/21678707.2015.1022528 · Cited by 4

Three-Dimensional Modeling of CpG DNA Binding with Matrix Lumican Shows Leucine-Rich Repeat Motif Involvement as in TLR9-CpG DNA Interactions

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