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The molecular basis of corneal transparency

https://doi.org/10.1016/j.exer.2010.06.021
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archopht.123.6.741openalex-snapshot
Histologic, Ultrastructural, and Immunofluorescent Evaluation of Human Laser-Assisted In Situ Keratomileusis Corneal Wounds
inferredcites →https://doi.org/10.1001/archopht.1958.00940080130016openalex-snapshot
Incorporation of S35 in Healing Wounds in Normal and Devitalized Corneas
inferredcites →https://doi.org/10.1001/archopht.1988.01060130900049openalex-snapshot
Diamond Burring and Surgical Keratectomy
inferredcites →https://doi.org/10.1001/archopht.1989.01070010917041openalex-snapshot
Corneal Stromal Wound Healing in Rabbits After 193-nm Excimer Laser Surface Ablation
inferredcites →https://doi.org/10.1002/dvdy.21579openalex-snapshot
Development of the corneal stroma, and the collagen–proteoglycan associations that help define its structure and function
inferredcites →https://doi.org/10.1002/jcp.1030510102openalex-snapshot
Corneal development. I. Corneal transparency
inferredcites →https://doi.org/10.1002/jcp.1041380103openalex-snapshot
L‐ascorbic acid 2‐phosphate stimulates collagen accumulation, cell proliferation, and formation of a three‐dimensional tissuelike substance by skin fibroblasts
inferredcites →https://doi.org/10.1002/jcp.1041630108openalex-snapshot
Three patterns of cytokine expression potentially involved in epithelial‐fibroblast interactions of human ocular surface
inferredcites →https://doi.org/10.1002/pmic.200700137openalex-snapshot
Proteomic analysis of rabbit tear fluid: Defensin levels after an experimental corneal wound are correlated to wound closure
inferredcites →https://doi.org/10.1006/exer.1993.1081openalex-snapshot
Regulation of Corneal Collagen Fibrillogenesis In Vitro by Corneal Proteoglycan (Lumican and Decorin) Core Proteins
inferredcites →https://doi.org/10.1006/exer.1998.0511openalex-snapshot
Extracellular Matrix Changes in Human Corneas After Radial Keratotomy
inferredcites →https://doi.org/10.1006/exer.1998.0540openalex-snapshot
Proteoglycan Distribution During Healing of Corneal Stromal Wounds in Chick
inferredcites →https://doi.org/10.1006/exer.1999.0789openalex-snapshot
Expression of the Keratan Sulfate Proteoglycans Lumican, Keratocan and Osteoglycin/Mimecan During Chick Corneal Development
inferredcites →https://doi.org/10.1006/exer.2000.0926openalex-snapshot
Kinetics of Keratocyte Proliferation in Response to Epithelial Debridement
inferredcites →https://doi.org/10.1006/exer.2001.0999openalex-snapshot
Human Tear Fluid PDGF-BB, TNF-α and TGF-β1 vs Corneal Haze and Regeneration of Corneal Epithelium and Subbasal Nerve Plexus after PRK
inferredcites →https://doi.org/10.1007/s000180050048openalex-snapshot
Independent modulation of collagen fibrillogenesis by decorin and lumican
inferredcites →https://doi.org/10.1007/s00441-009-0844-4openalex-snapshot
Collagens
inferredcites →https://doi.org/10.1016/0003-9861(83)90532-5openalex-snapshot
Proteoglycan changes during restoration of transparency in corneal scars
inferredcites →https://doi.org/10.1016/0003-9861(92)90562-bopenalex-snapshot
cDNA clone to chick corneal chondroitin/dermatan sulfate proteoglycan reveals identity to decorin
inferredcites →https://doi.org/10.1016/0012-1606(71)90104-7openalex-snapshot
Hyaluronate production and removal during corneal development in the chick
inferredcites →https://doi.org/10.1016/0012-1606(77)90304-9openalex-snapshot
Regeneration of corneal tissue
inferredcites →https://doi.org/10.1016/0012-1606(86)90130-2openalex-snapshot
Keratan sulfate proteoglycan during embryonic development of the chicken cornea
inferredcites →https://doi.org/10.1016/0304-4165(75)90202-0openalex-snapshot
The hydration of proteoglycans of bovine cornea
inferredcites →https://doi.org/10.1016/j.ajo.2006.03.064openalex-snapshot
A Second Decorin Frame Shift Mutation in a Family With Congenital Stromal Corneal Dystrophy
inferredcites →https://doi.org/10.1016/j.exer.2005.08.012openalex-snapshot
Focus on Molecules: Lumican
inferredcites →https://doi.org/10.1016/j.exer.2005.09.009openalex-snapshot
Focus on Molecules: Keratocan (KERA)
inferredcites →https://doi.org/10.1016/j.exer.2005.11.020openalex-snapshot
Focus on Molecules: CHST6 (carbohydrate sulfotransferase 6; corneal N-acetylglucosamine-6-sulfotransferase)
inferredcites →https://doi.org/10.1016/j.exer.2007.12.004openalex-snapshot
IGF-II is present in bovine corneal stroma and activates keratocytes to proliferate in vitro
inferredcites →https://doi.org/10.1016/j.exer.2008.02.001openalex-snapshot
Topical interleukin-1 receptor antagonist inhibits inflammatory cell infiltration into the cornea
inferredcites →https://doi.org/10.1016/j.exer.2008.09.010openalex-snapshot
Increased stromal extracellular matrix synthesis and assembly by insulin activated bovine keratocytes cultured under agarose
inferredcites →https://doi.org/10.1016/j.exer.2009.03.010openalex-snapshot
IGF-II and collagen expression by keratocytes during postnatal development
inferredcites →https://doi.org/10.1016/j.semcdb.2007.09.015openalex-snapshot
Corneal crystallins and the development of cellular transparency
inferredcites →https://doi.org/10.1016/s0002-9394(14)74608-2openalex-snapshot
A Refractive and Histopathologic Study of Excimer Laser Keratectomy in Primates
inferredcites →https://doi.org/10.1016/s0014-4835(03)00160-xopenalex-snapshot
Isolation of a putative keratocyte activating factor from the corneal stroma
inferredcites →https://doi.org/10.1016/s0014-4835(61)80017-1openalex-snapshot
Glycosaminoglycans in corneal regeneration
inferredcites →https://doi.org/10.1016/s0021-9258(18)48424-4openalex-snapshot
Proteoglycan-Lb, a small dermatan sulfate proteoglycan expressed in embryonic chick epiphyseal cartilage, is structurally related to osteoinductive factor.
inferredcites →https://doi.org/10.1016/s0021-9258(18)48500-6openalex-snapshot
cDNA to chick lumican (corneal keratan sulfate proteoglycan) reveals homology to the small interstitial proteoglycan gene family and expression in muscle and intestine.
inferredcites →https://doi.org/10.1016/s0021-9258(18)55489-2openalex-snapshot
Proteoglycan biosynthesis by human corneas from patients with types 1 and 2 macular corneal dystrophy.
inferredcites →https://doi.org/10.1016/s0021-9258(18)94204-3openalex-snapshot
Analysis of the Proteoglycans Synthesized by Corneal Explants from Embryonic Chicken
inferredcites →https://doi.org/10.1016/s0021-9258(19)46970-6openalex-snapshot
Collagen fibril formation. Optimal in vitro conditions and preliminary kinetic results.
inferredcites →https://doi.org/10.1016/s0021-9258(19)86322-6openalex-snapshot
Characterization and biosynthesis of proteoglycans of corneal stroma from rhesus monkey.
inferredcites →https://doi.org/10.1016/s0022-5320(78)90017-5openalex-snapshot
Biochemical and ultrastructural changes in collagen during corneal wound healing
inferredcites →https://doi.org/10.1016/s1542-0124(12)70128-3openalex-snapshot
Growth Factor, Cytokine and Protease Interactions During Corneal Wound Healing
inferredcites →https://doi.org/10.1038/75664openalex-snapshot
Mutations in KERA, encoding keratocan, cause cornea plana
inferredcites →https://doi.org/10.1073/pnas.0605441103openalex-snapshot
Matrix morphogenesis in cornea is mediated by the modification of keratan sulfate by GlcNAc 6- O -sulfotransferase
inferredcites →https://doi.org/10.1073/pnas.77.6.3705openalex-snapshot
Macular corneal dystrophy: failure to synthesize a mature keratan sulfate proteoglycan.
inferredcites →https://doi.org/10.1073/pnas.93.9.4219openalex-snapshot
Myofibroblasts differentiate from fibroblasts when plated at low density.
inferredcites →https://doi.org/10.1074/jbc.271.16.9759openalex-snapshot
Molecular Cloning and Tissue Distribution of Keratocan
inferredcites →https://doi.org/10.1074/jbc.272.44.28089openalex-snapshot
Mimecan, the 25-kDa Corneal Keratan Sulfate Proteoglycan, Is a Product of the Gene Producing Osteoglycin
inferredcites →https://doi.org/10.1074/jbc.273.16.9615openalex-snapshot
Identification of the N-Linked Oligosaccharide Sites in Chick Corneal Lumican and Keratocan That Receive Keratan Sulfate
inferredcites →https://doi.org/10.1074/jbc.m107596200openalex-snapshot
Proteoglycan Expression during Transforming Growth Factor β-induced Keratocyte-Myofibroblast Transdifferentiation
inferredcites →https://doi.org/10.1074/jbc.m301169200openalex-snapshot
Keratocan-deficient Mice Display Alterations in Corneal Structure
inferredcites →https://doi.org/10.1074/jbc.m303292200openalex-snapshot
Keratocyte Phenotype Mediates Proteoglycan Structure
inferredcites →https://doi.org/10.1074/jbc.m409622200openalex-snapshot
Type V Collagen Controls the Initiation of Collagen Fibril Assembly
inferredcites →https://doi.org/10.1074/jbc.m504724200openalex-snapshot
Maintenance of the Keratocyte Phenotype during Cell Proliferation Stimulated by Insulin
inferredcites →https://doi.org/10.1074/jbc.m511528200openalex-snapshot
Murine Model of the Ehlers-Danlos Syndrome
inferredcites →https://doi.org/10.1074/jbc.m609280200openalex-snapshot
A Rapid Transient Increase in Hyaluronan Synthase-2 mRNA Initiates Secretion of Hyaluronan by Corneal Keratocytes in Response to Transforming Growth Factor β
inferredcites →https://doi.org/10.1074/jbc.m806590200openalex-snapshot
Genetic Evidence for the Coordinated Regulation of Collagen Fibrillogenesis in the Cornea by Decorin and Biglycan
inferredcites →https://doi.org/10.1076/ceyr.17.3.286.5212openalex-snapshot
TGF-ßs stimulate cell proliferation via an autocrine production of FGF-2 in corneal stromal fibroblasts
inferredcites →https://doi.org/10.1083/jcb.141.5.1277openalex-snapshot
Lumican Regulates Collagen Fibril Assembly: Skin Fragility and Corneal Opacity in the Absence of Lumican
inferredcites →https://doi.org/10.1089/dna.1990.9.303openalex-snapshot
Molecular Cloning of a Novel Bone-Forming Compound: Osteoinductive Factor
inferredcites →https://doi.org/10.1093/glycob/10.10.951openalex-snapshot
MINI REVIEW Keratan sulfate: structure, biosynthesis, and function
inferredcites →https://doi.org/10.1097/00003226-199209000-00014openalex-snapshot
Ultrastructural Effect of L-Ascorbic Acid 2-Phosphate on Cultured Keratocytes
inferredcites →https://doi.org/10.1097/00003226-199609000-00011openalex-snapshot
Induction of ??-Smooth Muscle Actin Expression and Myofibroblast Transformation in Cultured Corneal Keratocytes
inferredcites →https://doi.org/10.1097/00003226-199711000-00012openalex-snapshot
Alterations of Corneal Extracellular Matrix After Multiple Refractive Procedures
inferredcites →https://doi.org/10.1097/00003226-200003000-00012openalex-snapshot
The Keratocyte Network of Human Cornea: A Three-Dimensional Study Using Confocal Laser Scanning Fluorescence Microscopy
inferredcites →https://doi.org/10.1111/j.1365-2567.2008.02868.xopenalex-snapshot
Turnover of bone marrow‐derived cells in the irradiated mouse cornea
inferredcites →https://doi.org/10.1111/j.1600-0420.2005.00439.xopenalex-snapshot
Expression of basic fibroblast growth factor in rabbit corneal alkali wounds in the presence and absence of granulocytes
inferredcites →https://doi.org/10.1113/jphysiol.1957.sp005758openalex-snapshot
The structure and transparency of the cornea
inferredcites →https://doi.org/10.1113/jphysiol.1973.sp010325openalex-snapshot
Wave‐length dependencies of light scattering in normal and cold swollen rabbit corneas and their structural implications*
inferredcites →https://doi.org/10.1146/annurev.biochem.67.1.609openalex-snapshot
MATRIX PROTEOGLYCANS: From Molecular Design to Cellular Function
inferredcites →https://doi.org/10.1167/iovs.02-1188openalex-snapshot
Molecular Mechanisms Controlling the Fibrotic Repair Phenotype in Cornea: Implications for Surgical Outcomes
inferredcites →https://doi.org/10.1167/iovs.04-0804openalex-snapshot
Congenital Stromal Dystrophy of the Cornea Caused by a Mutation in the Decorin Gene
inferredcites →https://doi.org/10.1167/iovs.04-1405openalex-snapshot
Serum-Free Spheroid Culture of Mouse Corneal Keratocytes
inferredcites →https://doi.org/10.1167/iovs.05-0325openalex-snapshot
An X-Ray Diffraction Study of Corneal Structure in Mimecan-Deficient Mice
inferredcites →https://doi.org/10.1167/iovs.06-0612openalex-snapshot
Stimulation of Collagen Synthesis by Insulin and Proteoglycan Accumulation by Ascorbate in Bovine Keratocytes In Vitro
inferredcites →https://doi.org/10.1167/iovs.06-1216openalex-snapshot
Morphologic Characterization of Organized Extracellular Matrix Deposition by Ascorbic Acid–Stimulated Human Corneal Fibroblasts
inferredcites →https://doi.org/10.1167/iovs.06-1323openalex-snapshot
Keratan Sulfate Glycosaminoglycan and the Association with Collagen Fibrils in Rudimentary Lamellae in the Developing Avian Cornea
inferredcites →https://doi.org/10.1167/iovs.08-3077openalex-snapshot
The Effect of Growth Factor Signaling on Keratocytes In Vitro and Its Relationship to the Phases of Stromal Wound Repair
inferredcites →https://doi.org/10.1242/jcs.01731openalex-snapshot
Procollagen trafficking, processing and fibrillogenesis
inferredcites →https://doi.org/10.1242/jcs.106.2.685openalex-snapshot
Keratocyte networks visualised in the living cornea using vital dyes
inferredcites →https://doi.org/10.1242/jcs.95.4.649openalex-snapshot
Collagen fibrillogenesis in vitro: interaction of types I and V collagen regulates fibril diameter
inferredcites →https://doi.org/10.1364/ao.10.000459openalex-snapshot
Theory of Transparency of the Eye

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Special senses
inferred← citeshttps://doi.org/10.1002/9781119047919.ch7openalex-snapshot
Diseases of the cornea
inferred← citeshttps://doi.org/10.1002/9781119617228.ch52openalex-snapshot
Ocular Physiology and Vision in the Equine Neonate
inferred← citeshttps://doi.org/10.1002/9781119782285.ch5openalex-snapshot
Diseases of the Equine Cornea
inferred← citeshttps://doi.org/10.1002/9783527652273.ch20openalex-snapshot
Tissue Analogs by the Assembly of Engineered Hydrogel Blocks
inferred← citeshttps://doi.org/10.1002/9783527825820.ch5openalex-snapshot
Hierarchical Peptide‐ and Protein‐Based Biomaterials: From Molecular Structure to Directed Self‐assembly and Applications
inferred← citeshttps://doi.org/10.1002/adbi.202400571openalex-snapshot
Current and Future Cornea Chip Models for Advancing Ophthalmic Research and Therapeutics
inferred← citeshttps://doi.org/10.1002/adhm.201701434openalex-snapshot
Natural Biomaterials for Corneal Tissue Engineering, Repair, and Regeneration
inferred← citeshttps://doi.org/10.1002/adhm.202100972openalex-snapshot
Mechanical Properties of Bioengineered Corneal Stroma
inferred← citeshttps://doi.org/10.1002/adma.201503986openalex-snapshot
Progress in Corneal Stromal Repair: From Tissue Grafts and Biomaterials to Modular Supramolecular Tissue‐Like Assemblies
inferred← citeshttps://doi.org/10.1002/dvdy.43openalex-snapshot
Transcriptomic analysis of differential gene expression during chick periocular neural crest differentiation into corneal cells
inferred← citeshttps://doi.org/10.1002/glia.23102openalex-snapshot
Corneal epithelial cells function as surrogate Schwann cells for their sensory nerves
inferred← citeshttps://doi.org/10.1002/jbio.202200022openalex-snapshot
Longitudinal assessment of the effect of alkali burns on corneal biomechanical properties using optical coherence elastography
inferred← citeshttps://doi.org/10.1002/jbm.b.34808openalex-snapshot
Cell sheet technology: Influence of culture conditions on in vitro‐cultivated corneal stromal tissue for regenerative therapies of the ocular surface
inferred← citeshttps://doi.org/10.1002/jemt.22180openalex-snapshot
Ultrastructural features of corneas with pellucid marginal degeneration
inferred← citeshttps://doi.org/10.1002/jemt.24293openalex-snapshot
Morphogenetic events influencing corneal maturation, development, and transparency: Light and electron microscopic study
inferred← citeshttps://doi.org/10.1002/mabi.201100341openalex-snapshot
Controlled Cell Proliferation on an Electrochemically Engineered Collagen Scaffold
inferred← citeshttps://doi.org/10.1002/sctm.19-0173openalex-snapshot
Adult tissue–derived neural crest-like stem cells: Sources, regulatory networks, and translational potential
inferred← citeshttps://doi.org/10.1002/sctm.19-0306openalex-snapshot
Corneal stromal stem cells restore transparency after N2 injury in mice
inferred← citeshttps://doi.org/10.1002/stem.1100openalex-snapshot
Concise Review: Stem Cells in the Corneal Stroma
inferred← citeshttps://doi.org/10.1002/stem.1541openalex-snapshot
Differentiation Potential of Limbal Fibroblasts and Bone Marrow Mesenchymal Stem Cells to Corneal Epithelial Cells
inferred← citeshttps://doi.org/10.1002/tcr.201200012openalex-snapshot
Assembly of Bacteriophage into Functional Materials
inferred← citeshttps://doi.org/10.1002/term.1859openalex-snapshot
In-body tissue-engineered collagenous connective tissue membranes (BIOSHEETs) for potential corneal stromal substitution
inferred← citeshttps://doi.org/10.1002/term.2283openalex-snapshot
Low oxygen tension and macromolecular crowding accelerate extracellular matrix deposition in human corneal fibroblast culture
inferred← citeshttps://doi.org/10.1002/term.2316openalex-snapshot
Corneal keratocyte transition to mesenchymal stem cell phenotype and reversal using serum-free medium supplemented with fibroblast growth factor-2, transforming growth factor-β3 and retinoic acid
inferred← citeshttps://doi.org/10.1002/term.2363openalex-snapshot
Scaffold-free tissue engineering of functional corneal stromal tissue
inferred← citeshttps://doi.org/10.1002/term.2621openalex-snapshot
Mimicking corneal stroma using keratocyte‐loaded photopolymerizable methacrylated gelatin hydrogels
inferred← citeshttps://doi.org/10.1007/978-1-0716-0599-8_11openalex-snapshot
Fabrication of Corneal Extracellular Matrix-Derived Hydrogels
inferred← citeshttps://doi.org/10.1007/978-1-0716-0599-8_5openalex-snapshot
A Guide to the Development of Human CorneaOrganoids from Induced Pluripotent Stem Cells in Culture
inferred← citeshttps://doi.org/10.1007/978-1-0716-0845-6_15openalex-snapshot
Corneal Repair Models in Mice: Epithelial/Mechanical Versus Stromal/Chemical Injuries
inferred← citeshttps://doi.org/10.1007/978-1-4471-2476-4_13openalex-snapshot
The Corneal Disc
inferred← citeshttps://doi.org/10.1007/978-3-030-01304-2_23openalex-snapshot
Applied Anatomy of the Corneal Stroma
inferred← citeshttps://doi.org/10.1007/978-3-030-01304-2_7openalex-snapshot
Corneal Stromal Stem Cell: Methods for Ex Vivo Expansion
inferred← citeshttps://doi.org/10.1007/978-3-030-11425-1_30openalex-snapshot
Eye
inferred← citeshttps://doi.org/10.1007/978-3-030-40146-7_2openalex-snapshot
Keratan Sulphate in the Tumour Environment
inferred← citeshttps://doi.org/10.1007/978-3-030-76525-5_13openalex-snapshot
The Corneal Disc
inferred← citeshttps://doi.org/10.1007/978-3-031-65422-0_1openalex-snapshot
Morphology of the Human Cornea as Displayed by in Vivo and Ex Vivo Imaging Techniques
inferred← citeshttps://doi.org/10.1007/978-3-031-70835-0_2openalex-snapshot
Osteogenesis Imperfecta and Related Diseases: Collagen I Alterations in Skeletal and Extraskeletal Tissues
inferred← citeshttps://doi.org/10.1007/978-3-031-93677-7_8openalex-snapshot
Mechanisms of Corneal Epithelial Homeostasis, Repair, and Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-18530-9_20openalex-snapshot
Concept of Reversible Corneal Refractive Surgery (Lenticule Reimplantation)
inferred← citeshttps://doi.org/10.1007/978-3-319-24052-7_2openalex-snapshot
Anatomy and Physiology: Considerations in Relation to Transplantation
inferred← citeshttps://doi.org/10.1007/978-3-319-25498-2_5openalex-snapshot
The Biochemistry of the Eye
inferred← citeshttps://doi.org/10.1007/978-3-319-33299-4_14openalex-snapshot
DSC for Ocular Regeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-33720-3_13openalex-snapshot
Stem Cell Applications in Corneal Regeneration and Wound Repair
inferred← citeshttps://doi.org/10.1007/978-3-642-16712-6_84openalex-snapshot
Proteoglycans
inferred← citeshttps://doi.org/10.1007/978-3-642-35943-9_84-1openalex-snapshot
Proteoglycans
inferred← citeshttps://doi.org/10.1007/978-3-642-38419-6_1openalex-snapshot
Einführung
inferred← citeshttps://doi.org/10.1007/978-981-10-3554-8_8openalex-snapshot
Scaffolds Reinforced by Fibers or Tubes for Soft Tissue Repair
inferred← citeshttps://doi.org/10.1007/978-981-16-4667-6_5openalex-snapshot
Gel-Inks for 3D Printing in Corneal Tissue Engineering
inferred← citeshttps://doi.org/10.1007/978-981-287-846-5_3openalex-snapshot
The Cornea and Sclera
inferred← citeshttps://doi.org/10.1007/s00109-019-01827-4openalex-snapshot
Substance P induces fibrotic changes through activation of the RhoA/ROCK pathway in an in vitro human corneal fibrosis model
inferred← citeshttps://doi.org/10.1007/s00210-019-01711-5openalex-snapshot
Apoptotic effects of norfloxacin on corneal endothelial cells
inferred← citeshttps://doi.org/10.1007/s00347-018-0667-3openalex-snapshot
Korneale Densitometrie
inferred← citeshttps://doi.org/10.1007/s00414-025-03692-yopenalex-snapshot
Study of microstructural changes in cornea under different stresses using a custom-made 100 kHz swept-source optical coherence tomography imaging system
inferred← citeshttps://doi.org/10.1007/s00417-014-2783-3openalex-snapshot
Cytotoxic activity and degradation patterns of structural proteins by corneal isolates of Acanthamoeba spp
inferred← citeshttps://doi.org/10.1007/s00417-020-05058-zopenalex-snapshot
NF-κB, iNOS, IL-6, and collagen 1 and 5 expression in healthy and keratoconus corneal fibroblasts after 0.1% riboflavin UV-A illumination
inferred← citeshttps://doi.org/10.1007/s00417-024-06601-yopenalex-snapshot
Expression of matrix metalloproteinases and their inhibitors in corneal stromal fibroblasts and keratocytes from healthy and keratoconus corneas
inferred← citeshttps://doi.org/10.1007/s00441-015-2233-5openalex-snapshot
Collagens and proteoglycans of the cornea: importance in transparency and visual disorders
inferred← citeshttps://doi.org/10.1007/s00441-016-2372-3openalex-snapshot
Proteins of the corneal stroma: importance in visual function
inferred← citeshttps://doi.org/10.1007/s00441-018-2934-7openalex-snapshot
Basement membranes in the cornea and other organs that commonly develop fibrosis
inferred← citeshttps://doi.org/10.1007/s10096-020-03980-yopenalex-snapshot
First report of a new corneal pathogen: Phaeoacremonium parasiticum
inferred← citeshttps://doi.org/10.1007/s10517-023-05976-yopenalex-snapshot
Studying the Proliferative Activity of Human Corneal Stromal Cell Populations
inferred← citeshttps://doi.org/10.1007/s10561-013-9372-2openalex-snapshot
A portable device for measuring donor corneal transparency in eye banks
inferred← citeshttps://doi.org/10.1007/s10616-019-00349-8openalex-snapshot
Gelam honey promotes ex vivo corneal fibroblasts wound healing
inferred← citeshttps://doi.org/10.1007/s10633-013-9396-8openalex-snapshot
Next-generation sequencing analysis of gene regulation in the rat model of retinopathy of prematurity
inferred← citeshttps://doi.org/10.1007/s10719-011-9358-xopenalex-snapshot
Lumican is a major small leucine-rich proteoglycan (SLRP) in Atlantic cod (Gadus morhua L.) skeletal muscle
inferred← citeshttps://doi.org/10.1007/s10792-022-02226-4openalex-snapshot
Investigation of the effect of solution pH value on rabbit corneal stroma biomechanics
inferred← citeshttps://doi.org/10.1007/s10792-024-03034-8openalex-snapshot
Biochemical component analysis of human myopic corneal stroma using the Raman spectrum
inferred← citeshttps://doi.org/10.1007/s11033-026-12342-4openalex-snapshot
Comparative phenotypic and molecular characterization of primary, sv40-immortalized, and commercial human corneal keratocytes reveals a passage-dependent optimal window for in vitro applications
inferred← citeshttps://doi.org/10.1007/s11426-014-5083-1openalex-snapshot
Biomaterials for refractive correction: corneal onlays and inlays
inferred← citeshttps://doi.org/10.1007/s12079-014-0230-1openalex-snapshot
The integrin needle in the stromal haystack: emerging role in corneal physiology and pathology
inferred← citeshttps://doi.org/10.1007/s12195-011-0186-7openalex-snapshot
Human Corneal Keratocyte Response to Micro- and Nano-Gratings on Chitosan and PDMS
inferred← citeshttps://doi.org/10.1007/s12541-021-00615-wopenalex-snapshot
Multi-scale Fabrication Techniques of Collagen Hydrogel for Developing Physiological 3D In vitro Barrier Model
inferred← citeshttps://doi.org/10.1007/s13346-018-0541-5openalex-snapshot
Controlled delivery of pirfenidone through vitamin E-loaded contact lens ameliorates corneal inflammation
inferred← citeshttps://doi.org/10.1007/s40123-026-01381-6openalex-snapshot
Scheimpflug Photography-Based Evaluation of Structural Iris Changes Across Keratoconus Stages in Comparison with Healthy Eyes
inferred← citeshttps://doi.org/10.1007/s40135-026-00353-0openalex-snapshot
Corneal Regeneration Using Induced Pluripotent Stem Cells: Stem Cell-based Corneal Cell Therapy
inferred← citeshttps://doi.org/10.1007/s40674-021-00187-wopenalex-snapshot
Insights Into the Preclinical Models of SSc
inferred← citeshttps://doi.org/10.1007/s40883-020-00159-xopenalex-snapshot
Antheraea mylitta Silk Films Support Corneal Re-epithelialisation as Inlay Grafts in Large-Sized Corneal Defect
inferred← citeshttps://doi.org/10.1016/b978-0-08-100147-9.00007-9openalex-snapshot
Collagen scaffolds for corneal regeneration
inferred← citeshttps://doi.org/10.1016/b978-0-12-391448-4.00016-2openalex-snapshot
Eye and Associated Glands
inferred← citeshttps://doi.org/10.1016/b978-0-12-401717-7.00031-9openalex-snapshot
Vitamin C Functions in the Cornea
inferred← citeshttps://doi.org/10.1016/b978-0-12-401730-6.00011-9openalex-snapshot
Neural Crest Cells in Ocular Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-800159-2.00038-5openalex-snapshot
Ocular Toxicity of Chemical Warfare Agents
inferred← citeshttps://doi.org/10.1016/b978-0-12-815245-4.00036-3openalex-snapshot
New Ultra-Structural Aspects of Cornea: Significance of Ascorbate Micronutrient Deficiency
inferred← citeshttps://doi.org/10.1016/b978-0-12-817876-8.00006-1openalex-snapshot
Gene editing for the cornea
inferred← citeshttps://doi.org/10.1016/b978-0-12-819090-6.00036-2openalex-snapshot
Ocular toxicity of chemical warfare agents
inferred← citeshttps://doi.org/10.1016/b978-0-12-819713-4.00004-9openalex-snapshot
Stem cell therapies in ocular repair, regeneration, and diseases
inferred← citeshttps://doi.org/10.1016/b978-0-443-13820-1.00115-8openalex-snapshot
Cornea Overview
inferred← citeshttps://doi.org/10.1016/b978-0-443-13820-1.00137-7openalex-snapshot
Corneal Wound Healing: Optical Clarity, Cytokines and Growth Factors, Matrix Metalloproteinases
inferred← citeshttps://doi.org/10.1016/b978-0-443-13820-1.00205-xopenalex-snapshot
The Corneal Stroma
inferred← citeshttps://doi.org/10.1016/b978-0-443-13820-1.00206-1openalex-snapshot
Corneal Epithelium: Cell Biology and Basic Science
inferred← citeshttps://doi.org/10.1016/b978-0-443-36643-7.00020-2openalex-snapshot
Biomaterials for corneal endothelial cell transplantation
inferred← citeshttps://doi.org/10.1016/b978-0-7020-4691-9.00002-9openalex-snapshot
Clinical embryology and development of the eye
inferred← citeshttps://doi.org/10.1016/b978-0-7020-6616-0.00003-7openalex-snapshot
Clinical embryology and development of the eye
inferred← citeshttps://doi.org/10.1016/b978-0-7020-6660-3.00002-2openalex-snapshot
Anterior Eye
inferred← citeshttps://doi.org/10.1016/b978-0-7020-8427-0.00002-7openalex-snapshot
Anterior Eye
inferred← citeshttps://doi.org/10.1016/b978-1-4557-0737-9.00020-5openalex-snapshot
Structure, Function, and Pathology of Bruch's Membrane
inferred← citeshttps://doi.org/10.1016/b978-84-9022-649-0.50009-0openalex-snapshot
Factores que influyen sobre la biomecánica corneal
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2015.04.002openalex-snapshot
Stem Cells in the Cornea
inferred← citeshttps://doi.org/10.1016/j.actbio.2012.05.004openalex-snapshot
Corneal reinforcement using an acellular dermal matrix for an analysis of biocompatibility, mechanical properties, and transparency
inferred← citeshttps://doi.org/10.1016/j.actbio.2015.04.018openalex-snapshot
Development of human corneal epithelium on organized fibrillated transparent collagen matrices synthesized at high concentration
inferred← citeshttps://doi.org/10.1016/j.actbio.2015.06.007openalex-snapshot
Optimization of optical and mechanical properties of real architecture for 3-dimensional tissue equivalents: Towards treatment of limbal epithelial stem cell deficiency
inferred← citeshttps://doi.org/10.1016/j.actbio.2018.06.005openalex-snapshot
Cell-laden and orthogonal-multilayer tissue-engineered corneal stroma induced by a mechanical collagen microenvironment and transplantation in a rabbit model
inferred← citeshttps://doi.org/10.1016/j.actbio.2023.09.002openalex-snapshot
Human cornea-derived extracellular matrix hydrogel for prevention of post-traumatic corneal scarring: A translational approach
inferred← citeshttps://doi.org/10.1016/j.addr.2026.115905openalex-snapshot
Spatial patterning of biomimetic signals in corneal regeneration
inferred← citeshttps://doi.org/10.1016/j.ajo.2013.06.025openalex-snapshot
Transepithelial Riboflavin/Ultraviolet. A Corneal Cross-linking in Keratoconus: Morphologic Studies on Human Corneas
inferred← citeshttps://doi.org/10.1016/j.ajo.2020.02.002openalex-snapshot
In Vivo Corneal Confocal Microscopy and Histopathology of Keratitis Fugax Hereditaria From a Pathogenic Variant in NLRP3
inferred← citeshttps://doi.org/10.1016/j.ajoc.2018.02.010openalex-snapshot
Improvement of chronic corneal opacity in ocular surface disease with prosthetic replacement of the ocular surface ecosystem (PROSE) treatment
inferred← citeshttps://doi.org/10.1016/j.ajpath.2013.04.001openalex-snapshot
Intracellularly-Retained Decorin Lacking the C-Terminal Ear Repeat Causes ER Stress
inferred← citeshttps://doi.org/10.1016/j.ajpath.2013.05.025openalex-snapshot
Notch Signal Regulates Corneal Endothelial-to-Mesenchymal Transition
inferred← citeshttps://doi.org/10.1016/j.ajpath.2017.04.002openalex-snapshot
Antifibrotic Actions of Peroxisome Proliferator-Activated Receptor γ Ligands in Corneal Fibroblasts Are Mediated by β-Catenin–Regulated Pathways
inferred← citeshttps://doi.org/10.1016/j.ajpath.2021.08.016openalex-snapshot
Collagen XIV Is an Intrinsic Regulator of Corneal Stromal Structure and Function
inferred← citeshttps://doi.org/10.1016/j.ajpath.2021.10.016openalex-snapshot
The Neuropeptide Alpha-Melanocyte–Stimulating Hormone Is Critical for Corneal Endothelial Cell Protection and Graft Survival after Transplantation
inferred← citeshttps://doi.org/10.1016/j.ajpath.2023.09.007openalex-snapshot
The Neuropeptide α-Melanocyte–Stimulating Hormone Prevents Persistent Corneal Edema following Injury
inferred← citeshttps://doi.org/10.1016/j.ajpath.2025.12.005openalex-snapshot
Keratocyte Depletion by Genetic Manipulation Re-creates Corneal Ectasia in a Mouse Model
inferred← citeshttps://doi.org/10.1016/j.asej.2023.102292openalex-snapshot
Corneal elevation topographic maps assessing different diseases detection: A review
inferred← citeshttps://doi.org/10.1016/j.autrev.2015.12.001openalex-snapshot
The autoimmune diseases of the eyes
inferred← citeshttps://doi.org/10.1016/j.bbiosy.2023.100083openalex-snapshot
Optimization and evaluation of oxygen-plasma-modified, aligned, poly (Є-caprolactone) and silk fibroin nanofibrous scaffold for corneal stromal regeneration
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.10.107openalex-snapshot
Semaphorin 3A potentiates the profibrotic effects of transforming growth factor-β1 in the cornea
inferred← citeshttps://doi.org/10.1016/j.bioactmat.2024.07.008openalex-snapshot
Oriented cellulose hydrogel: Directed tissue regeneration for reducing corneal leukoplakia and managing fungal corneal ulcers
inferred← citeshttps://doi.org/10.1016/j.bioelechem.2014.08.023openalex-snapshot
Dielectric relaxation of normothermic and hypothermic rat corneas
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2013.08.061openalex-snapshot
Modulation of keratocyte phenotype by collagen fibril nanoarchitecture in membranes for corneal repair
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2013.12.078openalex-snapshot
Corneal stromal bioequivalents secreted on patterned silk substrates
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2021.121320openalex-snapshot
Exosomes-loaded thermosensitive hydrogels for corneal epithelium and stroma regeneration
inferred← citeshttps://doi.org/10.1016/j.bpj.2020.08.040openalex-snapshot
ECM Stiffness Controls the Activation and Contractility of Corneal Keratocytes in Response to TGF-β1
inferred← citeshttps://doi.org/10.1016/j.carbpol.2026.125469openalex-snapshot
Characterizing structure-function relationships for a homogeneous, highly 6-O-sulfated keratan sulfate from bovine cornea: collagen binding and anti-inflammatory potential
inferred← citeshttps://doi.org/10.1016/j.clae.2022.101795openalex-snapshot
The research progress on the molecular mechanism of corneal cross-linking in keratoconus treatment
inferred← citeshttps://doi.org/10.1016/j.clae.2025.102425openalex-snapshot
The impact of soft contact lenses on the corneal neuromediators and optical quality in high myopia
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2011.10.007openalex-snapshot
Implications of the alpha dispersion for studies on interaction of tobacco smoke – Corneal tissue
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2016.08.011openalex-snapshot
Analysis of cornea curvature using radial basis functions – Part I: Methodology
inferred← citeshttps://doi.org/10.1016/j.cyto.2011.12.022openalex-snapshot
The role of cytokines and pathogen recognition molecules in fungal keratitis – Insights from human disease and animal models
inferred← citeshttps://doi.org/10.1016/j.drudis.2018.10.017openalex-snapshot
Interplay between hereditary and environmental factors to establish an in vitro disease model of keratoconus
inferred← citeshttps://doi.org/10.1016/j.exer.2011.10.004openalex-snapshot
Sphere formation from corneal keratocytes and phenotype specific markers
inferred← citeshttps://doi.org/10.1016/j.exer.2011.12.022openalex-snapshot
Interleukin-1 receptor role in the viability of corneal myofibroblasts
inferred← citeshttps://doi.org/10.1016/j.exer.2012.03.015openalex-snapshot
Individual versus collective fibroblast spreading and migration: Regulation by matrix composition in 3D culture
inferred← citeshttps://doi.org/10.1016/j.exer.2013.07.016openalex-snapshot
Hydration dependent biomechanical properties of the corneal stroma
inferred← citeshttps://doi.org/10.1016/j.exer.2014.08.001openalex-snapshot
Regulation of corneal stroma extracellular matrix assembly
inferred← citeshttps://doi.org/10.1016/j.exer.2014.09.003openalex-snapshot
Mechanical interactions and crosstalk between corneal keratocytes and the extracellular matrix
inferred← citeshttps://doi.org/10.1016/j.exer.2014.09.013openalex-snapshot
Cellular and extracellular matrix modulation of corneal stromal opacity
inferred← citeshttps://doi.org/10.1016/j.exer.2015.01.014openalex-snapshot
Corneal stroma microfibrils
inferred← citeshttps://doi.org/10.1016/j.exer.2015.07.009openalex-snapshot
Myofibroblasts
inferred← citeshttps://doi.org/10.1016/j.exer.2015.09.010openalex-snapshot
Development of a novel in vivo corneal fibrosis model in the dog
inferred← citeshttps://doi.org/10.1016/j.exer.2016.08.015openalex-snapshot
Small leucine-rich repeat proteoglycans in corneal inflammation and wound healing
inferred← citeshttps://doi.org/10.1016/j.exer.2017.04.007openalex-snapshot
Effects of MMP12 on cell motility and inflammation during corneal epithelial repair
inferred← citeshttps://doi.org/10.1016/j.exer.2017.05.003openalex-snapshot
Epithelial basement membrane injury and regeneration modulates corneal fibrosis after pseudomonas corneal ulcers in rabbits
inferred← citeshttps://doi.org/10.1016/j.exer.2018.09.004openalex-snapshot
Nidogen-2: Location and expression during corneal wound healing
inferred← citeshttps://doi.org/10.1016/j.exer.2019.01.001openalex-snapshot
Decorin antagonizes corneal fibroblast migration via caveolae-mediated endocytosis of epidermal growth factor receptor
inferred← citeshttps://doi.org/10.1016/j.exer.2019.03.012openalex-snapshot
APP processing and metabolism in corneal fibroblasts and epithelium as a potential biomarker for Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.exer.2019.107704openalex-snapshot
Dynamic changes of the extracellular matrix during corneal wound healing
inferred← citeshttps://doi.org/10.1016/j.exer.2019.107705openalex-snapshot
Is sex a biological variable in corneal wound healing?
inferred← citeshttps://doi.org/10.1016/j.exer.2019.107709openalex-snapshot
Corneal injury: Clinical and molecular aspects
inferred← citeshttps://doi.org/10.1016/j.exer.2019.107772openalex-snapshot
Cell-independent matrix configuration in early corneal development
inferred← citeshttps://doi.org/10.1016/j.exer.2020.107933openalex-snapshot
Requirement for the collagen receptor Endo180 in collagen gel contraction mediated by corneal fibroblasts
inferred← citeshttps://doi.org/10.1016/j.exer.2020.107935openalex-snapshot
Two-year observation of morphologic and histopathologic changes in the monkey cornea following small incision allogenic lenticule implantation
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108062openalex-snapshot
Keratocyte biology
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108089openalex-snapshot
Corneal wound healing
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108127openalex-snapshot
Modeling the cornea in 3-dimensions: Current and future perspectives
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108137openalex-snapshot
Composition, structure and function of the corneal stroma
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108192openalex-snapshot
Tissue engineered ultra-thin descemet stripping corneal endothelial layers using porcine cornea and stem cells
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108218openalex-snapshot
Biological effects of mitomycin C on late corneal haze stromal fibrosis following PRK
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108228openalex-snapshot
Keratocyte mechanobiology
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108229openalex-snapshot
Corneal fibroblasts: Function and markers
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108303openalex-snapshot
Fibroblastic and bone marrow-derived cellularity in the corneal stroma
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108325openalex-snapshot
TGFβ1 and TGFβ2 proteins in corneas with and without stromal fibrosis: Delayed regeneration of apical epithelial growth factor barrier and the epithelial basement membrane in corneas with stromal fibrosis
inferred← citeshttps://doi.org/10.1016/j.exer.2020.108357openalex-snapshot
Optical transmittance and ultrastructure of SMILE-derived lenticules subjected to three different preservative methods
inferred← citeshttps://doi.org/10.1016/j.exer.2021.108611openalex-snapshot
Inhibition of enhancer of zeste homolog 2 prevents corneal myofibroblast transformation in vitro
inferred← citeshttps://doi.org/10.1016/j.exer.2021.108617openalex-snapshot
The role of peroxisome proliferator-activated receptors in healthy and diseased eyes
inferred← citeshttps://doi.org/10.1016/j.exer.2022.108933openalex-snapshot
Decorin regulates collagen fibrillogenesis during corneal wound healing in mouse in vivo
inferred← citeshttps://doi.org/10.1016/j.exer.2022.109062openalex-snapshot
Pathogenesis of keratoconus: NRF2-antioxidant, extracellular matrix and cellular dysfunctions
inferred← citeshttps://doi.org/10.1016/j.exer.2022.109112openalex-snapshot
ECM stiffness modulates the proliferation but not the motility of primary corneal keratocytes in response to PDGF-BB
inferred← citeshttps://doi.org/10.1016/j.exer.2022.109205openalex-snapshot
Localization of phosphatidylinositol phosphate 5 kinase γ, phospholipase β3 and diacylglycerol kinase ζ in corneal epithelium in comparison with conjunctival epithelium of mice
inferred← citeshttps://doi.org/10.1016/j.exer.2023.109395openalex-snapshot
Progress towards a standardized model of ocular sulfur mustard injury for therapeutic testing
inferred← citeshttps://doi.org/10.1016/j.exer.2023.109641openalex-snapshot
Effect of adlay seed extract on inflammation and fibrogenesis in human corneal activated keratocytes at transcriptional level
inferred← citeshttps://doi.org/10.1016/j.exer.2024.110162openalex-snapshot
Macromolecular crowding agent dependent extracellular matrix deposition and growth factor retention in human corneal fibroblast cultures
inferred← citeshttps://doi.org/10.1016/j.exer.2024.110181openalex-snapshot
Role of sulfated GAGs in shear mechanical properties of human and porcine cornea
inferred← citeshttps://doi.org/10.1016/j.exer.2025.110321openalex-snapshot
Riboflavin-UV crosslinking of the cornea: Wound healing and biomechanics
inferred← citeshttps://doi.org/10.1016/j.exer.2025.110529openalex-snapshot
Matrix molecules associated with both regulation of inflammation and pathogenic outcomes associated with the surface of the lens in the eyes of EAU mice
inferred← citeshttps://doi.org/10.1016/j.exer.2025.110816openalex-snapshot
Single cell RNA-seq characterization of non-fibrotic stromal wound repopulation in the rabbit
inferred← citeshttps://doi.org/10.1016/j.gca.2011.11.041openalex-snapshot
Calculation of the standard molal thermodynamic properties of crystalline peptides
inferred← citeshttps://doi.org/10.1016/j.heliyon.2026.e45295openalex-snapshot
Characterization of transparent self-healing gelatin-adipic acid dihydrazide-alginate dialdehyde hydrogel for application in corneal stroma regeneration
inferred← citeshttps://doi.org/10.1016/j.ijleo.2018.06.132openalex-snapshot
Optical transmittance of cornea during the embryonic development of chick
inferred← citeshttps://doi.org/10.1016/j.intimp.2015.05.039openalex-snapshot
Acetylcholine enhances keratocyte proliferation through muscarinic receptor activation
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104038openalex-snapshot
Zeb1 regulation of wound-healing-induced inflammation in alkali-damaged corneas
inferred← citeshttps://doi.org/10.1016/j.isci.2026.116130openalex-snapshot
Topical rewetting restores the autoimmune-damaged corneal stroma
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.102537openalex-snapshot
Insights into the biochemical and biophysical mechanisms mediating the longevity of the transparent optics of the eye lens
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2013.03.013openalex-snapshot
An experimental and theoretical analysis of unconfined compression of corneal stroma
inferred← citeshttps://doi.org/10.1016/j.jbiomech.2024.112360openalex-snapshot
The effect of enzymatic GAG degradation on transverse shear properties of porcine cornea
inferred← citeshttps://doi.org/10.1016/j.jcrs.2014.07.029openalex-snapshot
Evaluation of hydration effects on tensile properties of bovine corneas
inferred← citeshttps://doi.org/10.1016/j.jcrs.2016.08.031openalex-snapshot
Immunohistochemical study of corneal inflammation after femtosecond laser clear corneal incisions or manual surgery
inferred← citeshttps://doi.org/10.1016/j.jcrs.2016.10.025openalex-snapshot
Comparison of the performance and safety of 2 ophthalmic viscosurgical devices in cataract surgery
inferred← citeshttps://doi.org/10.1016/j.jcyt.2015.08.003openalex-snapshot
Effect of culture medium on propagation and phenotype of corneal stroma–derived stem cells
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2014.03.011openalex-snapshot
The relation between hydration and mechanical behavior of bovine cornea in tension
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2022.105300openalex-snapshot
Effect of corneal collagen crosslinking on viscoelastic shear properties of the cornea
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2024.106437openalex-snapshot
Multiscale characterization of electrospun non-wovens for corneal regeneration: Impact of microstructure on mechanical, optical and biological properties
inferred← citeshttps://doi.org/10.1016/j.jmbbm.2025.107303openalex-snapshot
Collagen fibril organization and its association with glycosaminoglycans in human, pig, and mouse cornea
inferred← citeshttps://doi.org/10.1016/j.jprot.2011.04.032openalex-snapshot
Proteome profiling of wild type and lumican-deficient mouse corneas
inferred← citeshttps://doi.org/10.1016/j.jsb.2011.03.015openalex-snapshot
Electron tomography reveals multiple self-association of chondroitin sulphate/dermatan sulphate proteoglycans in Chst5-null mouse corneas
inferred← citeshttps://doi.org/10.1016/j.jtos.2015.12.006openalex-snapshot
Stem Cells in the Limbal Stroma
inferred← citeshttps://doi.org/10.1016/j.jtos.2020.07.020openalex-snapshot
Decellularized porcine cornea-derived hydrogels for the regeneration of epithelium and stroma in focal corneal defects
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