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Mutations in KERA, encoding keratocan, cause cornea plana

https://doi.org/10.1038/75664
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What this work says

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

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The Human Decorin Gene: Intron-Exon Organization, Discovery of Two Alternatively Spliced Exons in the 5′ Untranslated Region, and Mapping of the Gene to Chromosome 12q23
inferredcites →https://doi.org/10.1006/geno.1993.1023openalex-snapshot
Human Decorin Gene: Intron-Exon Junctions and Chromosomal Localization
inferredcites →https://doi.org/10.1006/geno.1995.1258openalex-snapshot
Linkage Disequilibrium Mapping of the Cornea Plana Congenita Gene CNA2
inferredcites →https://doi.org/10.1006/geno.1996.0643openalex-snapshot
Characterization of Human DSPG3, a Small Dermatan Sulfate Proteoglycan
inferredcites →https://doi.org/10.1006/jmbi.1997.0951openalex-snapshot
Prediction of complete gene structures in human genomic DNA
inferredcites →https://doi.org/10.1016/0888-7543(95)80213-6openalex-snapshot
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis
inferredcites →https://doi.org/10.1016/s0945-053x(98)90070-1openalex-snapshot
Leucine-rich repeat glycoproteins of the extracellular matrix
inferredcites →https://doi.org/10.1034/j.1600-0420.1998.760215.xopenalex-snapshot
Autosomal recessive cornea plana. A clinical and genetic study of 78 cases in Finland
inferredcites →https://doi.org/10.1038/sj.ejhg.5200338openalex-snapshot
Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease
inferredcites →https://doi.org/10.1073/pnas.88.24.11261openalex-snapshot
Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach.
inferredcites →https://doi.org/10.1074/jbc.270.37.21942openalex-snapshot
The Human Lumican Gene
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.273.35.22584openalex-snapshot
The Cloning of Mouse Keratocan cDNA and Genomic DNA and the Characterization of Its Expression during Eye Development
inferredcites →https://doi.org/10.1083/jcb.62.3.815openalex-snapshot
EPITHELIAL COLLAGENS AND GLYCOSAMINOGLYCANS IN THE EMBRYONIC CORNEA
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1101/gr.6.4.249openalex-snapshot
Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12.
inferredcites →https://doi.org/10.1101/gr.9.5.449openalex-snapshot
Genomic Characterization of Human DSPG3
inferredcites →https://doi.org/10.1111/j.1399-0004.1973.tb01924.xopenalex-snapshot
Congenital cornea plana in Finland
inferredcites →https://doi.org/10.1126/science.286.5447.2169openalex-snapshot
Functional Human Corneal Equivalents Constructed from Cell Lines
inferredcites →https://doi.org/10.1136/jmg.33.2.116openalex-snapshot
The genetics of cornea plana congenita.
inferredcites →https://doi.org/10.1385/1-59259-247-3:25openalex-snapshot
Radiation Hybrid (RH) Mapping of Human Smooth Muscle-Restricted Genes
inferredcites →https://doi.org/10.3109/10425179909033939openalex-snapshot
Structure and Sequence of the Gene Encoding Human Keratocan
inferredcites →https://doi.org/10.3109/13816819709057116openalex-snapshot
Autosomal dominant cornea plana: Clinical findings in a Cuban family and a review of the literature

What points at this work

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

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Identification of Sexually Dimorphic Genes in Pectoral Fin as Molecular Markers for Assessing the Sex of Japanese Silver Eels (Anguilla japonica).
inferred← citeshttps://doi.org/10.1001/archopht.123.9.1248openalex-snapshot
Clinical and Molecular Characterization of a Family With Autosomal Recessive Cornea Plana
inferred← citeshttps://doi.org/10.1001/archopht.124.9.1371openalex-snapshot
Further Information Regarding KERA and Recessive Cornea Plana
inferred← citeshttps://doi.org/10.1001/archopht.124.9.1372openalex-snapshot
Further Information Regarding KERA and Recessive Cornea Plana—Reply
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Complex Trait Genetics of Refractive Error
inferred← citeshttps://doi.org/10.1002/0471203076.emm1133openalex-snapshot
Osteoglycin
inferred← citeshttps://doi.org/10.1002/9780470015902.a0005821.pub2openalex-snapshot
Chromosome 12
inferred← citeshttps://doi.org/10.1002/9783527624522.ch7openalex-snapshot
Modelle zur Entwicklungsgenetik des Auges: Mausmutanten mit angeborenen Augenerkrankungen
inferred← citeshttps://doi.org/10.1002/adbi.201800327openalex-snapshot
Functional Consequences of Keratan Sulfate Sulfation in Electrosensory Tissues and in Neuronal Regulation
inferred← citeshttps://doi.org/10.1002/dvdy.22216openalex-snapshot
Fibromodulin regulates collagen fibrillogenesis during peripheral corneal development
inferred← citeshttps://doi.org/10.1002/dvdy.24435openalex-snapshot
Development of myotendinous‐like junctions that anchor cardiac valves requires fibromodulin and lumican
inferred← citeshttps://doi.org/10.1002/humu.10019openalex-snapshot
Database for the mutations of the Finnish disease heritage
inferred← citeshttps://doi.org/10.1002/ijc.22701openalex-snapshot
Identification of a novel noncoding RNA gene, NAMA, that is downregulated in papillary thyroid carcinoma with BRAF mutation and associated with growth arrest
inferred← citeshttps://doi.org/10.1002/stem.91openalex-snapshot
Stem Cell Therapy Restores Transparency to Defective Murine Corneas
inferred← citeshttps://doi.org/10.1006/dbio.2002.0732openalex-snapshot
The Homeobox Gene Six3 Is a Potential Regulator of Anterior Segment Formation in the Chick Eye
inferred← citeshttps://doi.org/10.1007/978-3-030-42634-7_326openalex-snapshot
Corneal Dysgeneses, Dystrophies, and Degenerations
inferred← citeshttps://doi.org/10.1007/978-3-031-81743-4_2openalex-snapshot
Contribution of Proteoglycans to the Multiscale Structure and Function of Soft Tissues
inferred← citeshttps://doi.org/10.1007/978-3-319-55298-9_6openalex-snapshot
Corneal Diseases in Children: Congenital Anomalies
inferred← citeshttps://doi.org/10.1007/978-3-319-90495-5_326-1openalex-snapshot
Corneal Dysgeneses, Dystrophies, and Degenerations
inferred← citeshttps://doi.org/10.1007/978-3-540-68632-3_21openalex-snapshot
Congenital Ocular Malformations
inferred← citeshttps://doi.org/10.1007/978-3-642-16555-9_6openalex-snapshot
Small Leucine-Rich Proteoglycans
inferred← citeshttps://doi.org/10.1007/978-3-642-55694-4_5openalex-snapshot
Lexikalischer Teil
inferred← citeshttps://doi.org/10.1007/978-3-662-43382-9_3openalex-snapshot
Cornea
inferred← citeshttps://doi.org/10.1007/978-981-16-5217-2_13openalex-snapshot
Zebrafish: A Metamorphosis in Ophthalmological Research—A Literature Review
inferred← citeshttps://doi.org/10.1007/978-981-96-7890-7_4openalex-snapshot
Regulatory Role and Significance of Class II SLRPs: Fibromodulin, Lumican, Osteoadherin, PRELP, and Keratocan
inferred← citeshttps://doi.org/10.1007/978-981-96-7890-7_8openalex-snapshot
Biological Basis Behind Molecular Fragmentation of SLRPs as DAMPs
inferred← citeshttps://doi.org/10.1007/bf03401852openalex-snapshot
Keratocan Expression Is Increased in the Stroma of Keratoconus Corneas
inferred← citeshttps://doi.org/10.1007/s00018-004-4353-zopenalex-snapshot
A genetic perspective on myopia
inferred← citeshttps://doi.org/10.1007/s00018-005-5187-zopenalex-snapshot
Structural analysis of leucine-rich-repeat variants in proteins associated with human diseases
inferred← citeshttps://doi.org/10.1007/s00018-009-0228-7openalex-snapshot
Structural and biochemical aspects of keratan sulphate in the cornea
inferred← citeshttps://doi.org/10.1007/s00347-003-0808-0openalex-snapshot
Genexpression bei Keratokonus
inferred← citeshttps://doi.org/10.1007/s00417-002-0562-zopenalex-snapshot
Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene
inferred← citeshttps://doi.org/10.1007/s00418-007-0332-4openalex-snapshot
Differential expression of the keratan sulphate proteoglycan, keratocan, during chick corneal embryogenesis
inferred← citeshttps://doi.org/10.1007/s00439-002-0877-1openalex-snapshot
The Finnish disease heritage III: the individual diseases
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/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/s10792-011-9490-4openalex-snapshot
Cornea plana associated with open-angle glaucoma: a case report
inferred← citeshttps://doi.org/10.1007/s11914-021-00708-5openalex-snapshot
The Osteocyte Transcriptome: Discovering Messages Buried Within Bone
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/s12079-021-00616-4openalex-snapshot
Sequence features, structure, ligand interaction, and diseases in small leucine rich repeat proteoglycans
inferred← citeshttps://doi.org/10.1016/b978-0-12-374169-1.00011-4openalex-snapshot
Mouse Models of the Cornea and Lens
inferred← citeshttps://doi.org/10.1016/b978-0-12-384878-9.00007-8openalex-snapshot
Toward a Better Understanding of Human Eye Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-816222-4.00013-7openalex-snapshot
Genetics of keratoconus
inferred← citeshttps://doi.org/10.1016/b978-0-323-04835-4.50011-2openalex-snapshot
Shape, structure, and biomechanical properties
inferred← citeshttps://doi.org/10.1016/b978-0-323-06387-6.00008-8openalex-snapshot
Cornea and Sclera
inferred← citeshttps://doi.org/10.1016/b978-0-323-06387-6.00019-2openalex-snapshot
Molecular Genetics of Corneal Disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-65414-2.00005-2openalex-snapshot
Genetic Abnormalities of the Cornea
inferred← citeshttps://doi.org/10.1016/b978-012436636-7/50198-1openalex-snapshot
Cornea
inferred← citeshttps://doi.org/10.1016/j.ajo.2005.09.024openalex-snapshot
Clinical and Molecular Characterization of a Patient With an Interstitial Deletion of Chromosome 12q15-q23 and Peripheral Corneal Abnormalities
inferred← citeshttps://doi.org/10.1016/j.ajoc.2026.102514openalex-snapshot
Cataract surgery with autosomal recessive cornea plana caused by a novel KERA mutation
inferred← citeshttps://doi.org/10.1016/j.ajpath.2011.07.026openalex-snapshot
Pathophysiological Mechanisms of Autosomal Dominant Congenital Stromal Corneal Dystrophy
inferred← citeshttps://doi.org/10.1016/j.ajpath.2024.10.017openalex-snapshot
A Core of Keratocan-Negative Cells Survives in Old Corneal Scars
inferred← citeshttps://doi.org/10.1016/j.bbcan.2023.189029openalex-snapshot
ASPORIN: A root of the matter in tumors and their host environment
inferred← citeshttps://doi.org/10.1016/j.exer.2005.09.009openalex-snapshot
Focus on Molecules: Keratocan (KERA)
inferred← citeshttps://doi.org/10.1016/j.exer.2010.06.021openalex-snapshot
The molecular basis of corneal transparency
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.2016.08.015openalex-snapshot
Small leucine-rich repeat proteoglycans in corneal inflammation and wound healing
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.jfo.2015.10.015openalex-snapshot
Cornea plana : à propos d’un cas et revue de la littérature
inferred← citeshttps://doi.org/10.1016/j.jfo.2025.104587openalex-snapshot
Severe corneal flattening in bilateral cornea plana
inferred← citeshttps://doi.org/10.1016/j.jsb.2009.01.009openalex-snapshot
Ultrastructural changes in the retinopathy, globe enlarged (rge) chick cornea
inferred← citeshttps://doi.org/10.1016/j.jtos.2023.06.013openalex-snapshot
Small leucine rich proteoglycans: Biology, function and their therapeutic potential in the ocular surface
inferred← citeshttps://doi.org/10.1016/j.jtos.2023.08.008openalex-snapshot
Glycosaminoglycans: Roles in wound healing, formation of corneal constructs and synthetic corneas
inferred← citeshttps://doi.org/10.1016/j.jtos.2024.11.007openalex-snapshot
Matrix glycosaminoglycans and proteoglycans in human cornea organoids and similarities with fetal corneal stages
inferred← citeshttps://doi.org/10.1016/j.jtos.2026.06.013openalex-snapshot
Impact of the loss of tenascin X on tissue architecture and wound healing of the murine corneal stroma
inferred← citeshttps://doi.org/10.1016/j.mad.2005.05.005openalex-snapshot
Protection against hydrogen peroxide-induced cell death in cultured human retinal pigment epithelial cells by 17β-estradiol: A differential gene expression profile
inferred← citeshttps://doi.org/10.1016/j.matbio.2014.01.004openalex-snapshot
Interclass small leucine-rich repeat proteoglycan interactions regulate collagen fibrillogenesis and corneal stromal assembly
inferred← citeshttps://doi.org/10.1016/j.matbio.2015.02.003openalex-snapshot
Proteoglycan form and function: A comprehensive nomenclature of proteoglycans
inferred← citeshttps://doi.org/10.1016/j.matbio.2017.12.006openalex-snapshot
Small leucine-rich proteoglycans and matrix metalloproteinase-14: Key partners?
inferred← citeshttps://doi.org/10.1016/j.matbio.2023.10.001openalex-snapshot
Molecular cues for immune cells from small leucine-rich repeat proteoglycans in their extracellular matrix-associated and free forms
inferred← citeshttps://doi.org/10.1016/j.ophtha.2006.04.026openalex-snapshot
Recessive Cornea Plana in the Kingdom of Saudi Arabia
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2023.101192openalex-snapshot
Posterior corneoscleral limbus: Architecture, stem cells, and clinical implications
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2024.101288openalex-snapshot
Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms
inferred← citeshttps://doi.org/10.1016/j.sjbs.2021.08.019openalex-snapshot
Ultrastructural study of collagen fibrils, proteoglycans and lamellae of the cornea treated with iontophoresis – UVA cross-linking and hypotonic riboflavin solution
inferred← citeshttps://doi.org/10.1016/j.survophthal.2007.02.001openalex-snapshot
Sclerocornea and Cornea Plana Are Distinct Entities
inferred← citeshttps://doi.org/10.1016/s0021-5155(03)00072-8openalex-snapshot
Cornea with Peters' anomaly: perturbed differentiation of corneal cells and abnormal extracellular matrix in the corneal stroma
inferred← citeshttps://doi.org/10.1016/s0246-0343(07)44094-1openalex-snapshot
Génétique et œil
inferred← citeshttps://doi.org/10.1016/s1542-0124(12)70003-4openalex-snapshot
The Use of Transgenic and Knock-out Mice in the Investigation of Ocular Surface Cell Biology
inferred← citeshttps://doi.org/10.1016/s1542-0124(12)70197-0openalex-snapshot
Genetics of Corneal Disease for the Ocular Surface Clinician
inferred← citeshttps://doi.org/10.1023/a:1025396316169openalex-snapshot
Roles of lumican and keratocan on corneal transparency
inferred← citeshttps://doi.org/10.1038/81619openalex-snapshot
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
inferred← citeshttps://doi.org/10.1038/eye.2016.198openalex-snapshot
The zebrafish eye—a paradigm for investigating human ocular genetics
inferred← citeshttps://doi.org/10.1038/npg.els.0005821openalex-snapshot
Chromosome 12
inferred← citeshttps://doi.org/10.1038/s41467-018-03646-6openalex-snapshot
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
inferred← citeshttps://doi.org/10.1038/s41536-026-00453-2openalex-snapshot
Activated Hedgehog signaling in keratocytes leads to stromal stiffness and impairs corneal regeneration
inferred← citeshttps://doi.org/10.1038/s41598-019-56529-1openalex-snapshot
Collagen fibrils and proteoglycans of peripheral and central stroma of the keratoconus cornea - Ultrastructure and 3D transmission electron tomography
inferred← citeshttps://doi.org/10.1055/a-2646-3744openalex-snapshot
Bilateral Excimer Laser-Assisted Penetrating Keratoplasty for Genetically Verified Autosomal Recessive Cornea Plana (CNA2) – Ultrastructural and Immunohistochemical Findings
inferred← citeshttps://doi.org/10.1073/pnas.111150598openalex-snapshot
Corneal collagen fibril structure in three dimensions: Structural insights into fibril assembly, mechanical properties, and tissue organization
inferred← citeshttps://doi.org/10.1074/jbc.m011290200openalex-snapshot
Expression Pattern and Gene Characterization ofAsporin
inferred← citeshttps://doi.org/10.1074/jbc.m103227200openalex-snapshot
Altered Fine Structures of Corneal and Skeletal Keratan Sulfate and Chondroitin/Dermatan Sulfate in Macular Corneal Dystrophy
inferred← citeshttps://doi.org/10.1074/jbc.m114.572941openalex-snapshot
Increased C-telopeptide Cross-linking of Tendon Type I Collagen in Fibromodulin-deficient Mice
inferred← citeshttps://doi.org/10.1074/jbc.m301169200openalex-snapshot
Keratocan-deficient Mice Display Alterations in Corneal Structure
inferred← citeshttps://doi.org/10.1074/jbc.m504724200openalex-snapshot
Maintenance of the Keratocyte Phenotype during Cell Proliferation Stimulated by Insulin
inferred← citeshttps://doi.org/10.1074/jbc.m707656200openalex-snapshot
Molecular Analysis and Characterization of Zebrafish Keratocan (zKera) Gene
inferred← citeshttps://doi.org/10.1074/jbc.r800020200openalex-snapshot
Biological Functions of the Small Leucine-rich Proteoglycans: From Genetics to Signal Transduction
inferred← citeshttps://doi.org/10.1080/02713680590959376openalex-snapshot
Expression of a Chondroitin Sulfate Proteoglycan, Versican (PG-M), During Development of Rat Cornea
inferred← citeshttps://doi.org/10.1080/02713680701795026openalex-snapshot
Morphological Differences between the Trabecular Meshworks of Zebrafish and Mammals
inferred← citeshttps://doi.org/10.1080/02713683.2025.2598813openalex-snapshot
Macromolecular Differences in the Extracellular Matrix Between Normal and Keratoconus Human Corneas: An Ex Vivo Study
inferred← citeshttps://doi.org/10.1080/13816810.2017.1350724openalex-snapshot
Corneal ectasia in a boy with homozygous KERA mutation
inferred← citeshttps://doi.org/10.1080/13816810.2018.1502792openalex-snapshot
Posterior amorphous corneal dystrophy in a patient with 12q21.33 deletion
inferred← citeshttps://doi.org/10.1080/13816810.2020.1804944openalex-snapshot
Corneal endothelial alterations in Recessive Cornea Plana: a report of 4 patients and review of literature
inferred← citeshttps://doi.org/10.1080/13816810490514397openalex-snapshot
A novelKERAmutation associated with autosomal recessive cornea plana
inferred← citeshttps://doi.org/10.1080/13816810600862469openalex-snapshot
Corneal Ectasia and Hydrops in a Patient with Autosomal Recessive Cornea Plana
inferred← citeshttps://doi.org/10.1080/13816810701351321openalex-snapshot
Autosomal Dominant Cornea Plana is not Associated with Pathogenic Mutations inDCN, DSPG3, FOXC1, KERA, LUM,orPITX2
inferred← citeshttps://doi.org/10.1080/13816810902937084openalex-snapshot
Corneal Decompensation in Recessive Cornea Plana
inferred← citeshttps://doi.org/10.1093/glycob/cwae014openalex-snapshot
Keratan sulfate, an electrosensory neurosentient bioresponsive cell instructive glycosaminoglycan
inferred← citeshttps://doi.org/10.1093/glycob/cwf065openalex-snapshot
Mice deficient in small leucine-rich proteoglycans: novel in vivo models for osteoporosis, osteoarthritis, Ehlers-Danlos syndrome, muscular dystrophy, and corneal diseases
inferred← citeshttps://doi.org/10.1093/hmg/11.11.1333openalex-snapshot
Protein localization in the human eye and genetic screen of opticin
inferred← citeshttps://doi.org/10.1093/med/9780195326147.003.0006openalex-snapshot
Cornea Plana
inferred← citeshttps://doi.org/10.1093/med/9780197659403.003.0009openalex-snapshot
Cornea Plana
inferred← citeshttps://doi.org/10.1096/fj.04-3019comopenalex-snapshot
Targeted disruption of Col8a1 and Col8a2 genes in mice leads to anterior segment abnormalities in the eye
inferred← citeshttps://doi.org/10.1097/01.ico.0000247207.55520.a4openalex-snapshot
Ocular Surface Tissue Morphogenesis in Normal and Disease States Revealed by Genetically Modified Mice
inferred← citeshttps://doi.org/10.1097/ico.0b013e3181c29744openalex-snapshot
Expression of Small Leucine-Rich Proteoglycans During Experimental Fungal Keratitis
inferred← citeshttps://doi.org/10.1097/icu.0b013e3283638374openalex-snapshot
Ocular genetic disease in the Middle East
inferred← citeshttps://doi.org/10.1097/ijg.0000000000000258openalex-snapshot
A Novel KERA Mutation in a Case of Autosomal Recessive Cornea Plana With Primary Angle-Closure Glaucoma
inferred← citeshttps://doi.org/10.1101/2020.08.06.240036openalex-snapshot
Single-cell analyses of the corneal epithelium: Unique cell types and gene expression profiles
inferred← citeshttps://doi.org/10.1101/2024.01.24.577150openalex-snapshot
Zebrafish carbohydrate sulfotransferase 6 ( chst6 ) mutants provide a preclinical model for macular corneal dystrophy
inferred← citeshttps://doi.org/10.1101/2025.07.16.664929openalex-snapshot
ndufs2 -/- zebrafish have impaired survival, neuromuscular activity, morphology, and one-carbon metabolism treatable with folic acid
inferred← citeshttps://doi.org/10.1111/acel.12324openalex-snapshot
Modifications in stromal extracellular matrix of aged corneas can be induced by ultraviolet A irradiation
inferred← citeshttps://doi.org/10.1111/aos.12533openalex-snapshot
Anterior segment optical coherence tomography in autosomal recessive cornea plana
inferred← citeshttps://doi.org/10.1111/aos.13484openalex-snapshot
Analysis of KERA in four families with cornea plana identifies two novel mutations
inferred← citeshttps://doi.org/10.1111/febs.12136openalex-snapshot
The regulatory roles of small leucine‐rich proteoglycans in extracellular matrix assembly
inferred← citeshttps://doi.org/10.1111/febs.17337openalex-snapshot
Loss of carbohydrate sulfotransferase 6 function leads to macular corneal dystrophy phenotypes and skeletal defects in zebrafish
inferred← citeshttps://doi.org/10.1111/j.1399-0004.2010.01455.xopenalex-snapshot
Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees
inferred← citeshttps://doi.org/10.1111/j.1440-169x.2012.01339.xopenalex-snapshot
Small leucine rich proteoglycan family regulates multiple signalling pathways in neural development and maintenance
inferred← citeshttps://doi.org/10.1111/j.1442-9071.2005.01011.xopenalex-snapshot
Inherited corneal disease: the evolving molecular, genetic and imaging revolution
inferred← citeshttps://doi.org/10.1124/pr.109.001289openalex-snapshot
Extracellular Matrix Molecules: Potential Targets in Pharmacotherapy
inferred← citeshttps://doi.org/10.1136/bjo.2004.058941openalex-snapshot
En face optical coherence tomography: a new method to analyse structural changes of the optic nerve head in rat glaucoma
inferred← citeshttps://doi.org/10.1136/bjo.2004.58941corr1openalex-snapshot
CORRECTIONS
inferred← citeshttps://doi.org/10.1136/bjo.2005.069021openalex-snapshot
Alteration of cyclic frequency by botulinum toxin injection in adult onset cyclic esotropia
inferred← citeshttps://doi.org/10.1136/bjo.2005.069567openalex-snapshot
Pneumosinus dilatans in a 13 year old female
inferred← citeshttps://doi.org/10.1136/bjo.2005.070839openalex-snapshot
Bilateral naevus of Ota with choroidal melanoma and diffuse retinal pigmentation in a dark skinned person
inferred← citeshttps://doi.org/10.1136/bjo.2005.071993openalex-snapshot
Temporal pterygium: benign or not?
inferred← citeshttps://doi.org/10.1136/bjo.2005.072538openalex-snapshot
Hand hygiene in routine glaucoma clinics
inferred← citeshttps://doi.org/10.1136/bjo.2005.073114openalex-snapshot
Treatment of neurotrophic keratopathy with nasal dilator strips
inferred← citeshttps://doi.org/10.1136/bjo.2005.073510openalex-snapshot
Pellucid marginal degeneration coexistent with cornea plana in one member of a family exhibiting a novel KERA mutation
inferred← citeshttps://doi.org/10.1136/bjo.2005.073866openalex-snapshot
Normal tension glaucoma
inferred← citeshttps://doi.org/10.1136/bjo.2005.073874openalex-snapshot
Cataract surgery and IOP
inferred← citeshttps://doi.org/10.1136/bjo.2005.074195openalex-snapshot
Total parenteral nutrition, vitamin E, and reversible macular dysfunction morphologically mimicking age related macular degeneration
inferred← citeshttps://doi.org/10.1136/bjo.2005.074427openalex-snapshot
Simultaneous intraosseous and intradural capillary haemangioma of orbit
inferred← citeshttps://doi.org/10.1136/bjo.2005.074468openalex-snapshot
Confocal microscopy of the cornea in nephropathic cystinosis
inferred← citeshttps://doi.org/10.1136/bjo.2005.075184openalex-snapshot
Two novel mutations of connexin genes in Chinese families with autosomal dominant congenital nuclear cataract
inferred← citeshttps://doi.org/10.1136/bjo.2005.075689openalex-snapshot
Successful treatment of Wegener's granulomatosis associated scleritis with rituximab
inferred← citeshttps://doi.org/10.1136/bjo.2005.075895openalex-snapshot
Patient satisfaction with anaesthesia comparing sub-Tenon's block and topical anaesthesia
inferred← citeshttps://doi.org/10.1136/bjo.2005.076935openalex-snapshot
Spontaneous involution of autologous lenses and phacoanaphylaxis reaction in Stickler syndrome
inferred← citeshttps://doi.org/10.1136/bjo.2005.077537openalex-snapshot
Retinopathy is not the only ocular symptom: myasthenia gravis in association with interferon therapy
inferred← citeshttps://doi.org/10.1136/bjo.2005.079137openalex-snapshot
Tobacco-alcohol amblyopia: a maculopathy?
inferred← citeshttps://doi.org/10.1136/bjo.2005.082453openalex-snapshot
TTT: local light absorption and heat convection versus heat conduction
inferred← citeshttps://doi.org/10.1136/bjo.2005.75895corr1openalex-snapshot
CORRECTIONS
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.22.010605.093433openalex-snapshot
The Molecular Diversity of Glycosaminoglycans Shapes Animal Development
inferred← citeshttps://doi.org/10.1159/000072038openalex-snapshot
A Molecular Perspective on Corneal Dystrophies
inferred← citeshttps://doi.org/10.1167/iovs.02-0783openalex-snapshot
Ocular and Scleral Alterations in Gene-Targeted Lumican-Fibromodulin Double-Null Mice
inferred← citeshttps://doi.org/10.1167/iovs.03-0484openalex-snapshot
Human Keratocytes Cultured on Amniotic Membrane Stroma Preserve Morphology and Express Keratocan
inferred← citeshttps://doi.org/10.1167/iovs.06-0581openalex-snapshot
Cell Surface Glycoconjugate Abnormalities and Corneal Epithelial Wound Healing in the Pax6 +/ − Mouse Model of Aniridia-Related Keratopathy
inferred← citeshttps://doi.org/10.1167/iovs.09-3550openalex-snapshot
Reduced Corneal Thickness and Enlarged Anterior Chamber in a Novel ColVIIIa2 G257D Mutant Mouse
inferred← citeshttps://doi.org/10.1167/iovs.09-4067openalex-snapshot
Linkage of Posterior Amorphous Corneal Dystrophy to Chromosome 12q21.33 and Exclusion of Coding Region Mutations in KERA , LUM , DCN , and EPYC
inferred← citeshttps://doi.org/10.1186/1479-7364-3-4-381openalex-snapshot
Animal Models in Eye Research
inferred← citeshttps://doi.org/10.1186/s12864-018-5417-zopenalex-snapshot
The transcriptome landscape of the carcinogenic treatment response in the blind mole rat: insights into cancer resistance mechanisms
inferred← citeshttps://doi.org/10.1186/s12864-025-12305-2openalex-snapshot
A comparative transcriptomic analysis provides new insights into the ecological adaptations in Ichthyophis bannanicus
inferred← citeshttps://doi.org/10.1186/s12881-015-0179-9openalex-snapshot
Case report: a novel KERA mutation associated with cornea plana and its predicted effect on protein function
inferred← citeshttps://doi.org/10.1371/journal.pone.0095037openalex-snapshot
Posterior Amorphous Corneal Dystrophy Is Associated with a Deletion of Small Leucine-rich Proteoglycans on Chromosome 12
inferred← citeshttps://doi.org/10.1371/journal.pone.0184028openalex-snapshot
Asporin-deficient mice have tougher skin and altered skin glycosaminoglycan content and structure
inferred← citeshttps://doi.org/10.1387/ijdb.041854jgopenalex-snapshot
Congenital hereditary cataracts
inferred← citeshttps://doi.org/10.1556/650.2016.30475openalex-snapshot
A cornealis sebgyógyulás és az extracelluláris mátrix
inferred← citeshttps://doi.org/10.1590/s0100-879x2003000800009openalex-snapshot
Collagens and proteoglycans of the corneal extracellular matrix
inferred← citeshttps://doi.org/10.19070/2332-290x-150006eopenalex-snapshot
Current Status and Future Directions on Corneal Genetics
inferred← citeshttps://doi.org/10.2174/0929866526666181208170027openalex-snapshot
Leucine Rich Repeat Proteins: Sequences, Mutations, Structures and Diseases
inferred← citeshttps://doi.org/10.30564/jim.v10i2.3382openalex-snapshot
An Association of Vitamins A and E with Hyaluronic and Lactobionic Acids may Prevent Molecular Changes Associated with Keratocyte to Myofibroblast Transition
inferred← citeshttps://doi.org/10.3109/13816810.2013.811272openalex-snapshot
Corneal Endothelial Findings in a Czech Patient with Compound Heterozygous Mutations inKERA
inferred← citeshttps://doi.org/10.3109/13816810.2013.851249openalex-snapshot
Axial Lengths in Children with Recessive Cornea Plana
inferred← citeshttps://doi.org/10.3109/13816810.2015.1059462openalex-snapshot
Regarding corneal decompensation in recessive cornea plana
inferred← citeshttps://doi.org/10.3109/13816810.2016.1164194openalex-snapshot
Posterior amorphous corneal dystrophy caused by a de novo deletion
inferred← citeshttps://doi.org/10.3233/pge-14102openalex-snapshot
Pediatric genetic disease of the cornea
inferred← citeshttps://doi.org/10.3389/fcell.2020.00731openalex-snapshot
Distribution and Function of Glycosaminoglycans and Proteoglycans in the Development, Homeostasis and Pathology of the Ocular Surface
inferred← citeshttps://doi.org/10.3389/fcell.2021.654397openalex-snapshot
The Scleraxis Transcription Factor Directly Regulates Multiple Distinct Molecular and Cellular Processes During Early Tendon Cell Differentiation
inferred← citeshttps://doi.org/10.3389/fgene.2021.717535openalex-snapshot
Congenital Disorders of Deficiency in Glycosaminoglycan Biosynthesis
inferred← citeshttps://doi.org/10.3390/ph18091352openalex-snapshot
Genetic Basis of Non-Syndromic Childhood Glaucoma Associated with Anterior Segment Dysgenesis: A Narrative Review
inferred← citeshttps://doi.org/10.3892/mmr.2019.10153openalex-snapshot
Novel variants in the KERA gene cause autosomal recessive cornea plana in a Chinese family: A case report
inferred← citeshttps://doi.org/10.4103/ijo.ijo_26_21openalex-snapshot
Multimodal imaging of autosomal recessive cornea plana associated with hard mature and polar cataract
inferred← citeshttps://doi.org/10.4103/ojo.ojo_12_2015openalex-snapshot
Two brothers with reduced vision
inferred← citeshttps://doi.org/10.4103/ojo.ojo_139_22openalex-snapshot
Cornea plana in a family from Pakistan: Case series and literature review on the principles of management
inferred← citeshttps://doi.org/10.4236/ojoph.2013.32009openalex-snapshot
Spinocerebellar Ataxia with Oculomotor Apraxia and Severe Corneal Astigmatism
inferred← citeshttps://doi.org/10.5812/jjm.58351openalex-snapshot
Toll-Like Receptors are Associated with Helicobacter pylori Infection and Gastric Mucosa Pathology
inferred← citeshttps://doi.org/10.63500/mv_v32_70openalex-snapshot
Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndrome
inferred← citeshttps://doi.org/10.70675/52dd9d84z6ca5z4eb3z96d8z449666a11714openalex-snapshot
Effet du lumicanne et de ses peptides dérivés sur le mélanome et les cellules souches : analyse de son mécanisme d'action
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