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Journal Article
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 06/2012, Volume 53, Issue 7, pp. 4130 - 4138
Journal Article
Experimental Eye Research, ISSN 0014-4835, 05/2016, Volume 146, pp. 26 - 34
Corneal epithelium is renewed by limbal epithelial stem cells (LESCs), a type of tissue-specific stem cells located in the limbal palisades of Vogt at the... 
Corneal epithelium | Serum-free culture conditions | Human pluripotent stem cells | Tissue engineering | Regenerative medicine | Limbal epithelial stem cells | OCULAR SURFACE | COMPRESSED COLLAGEN | REGENERATION | RAFT TISSUE EQUIVALENTS | AMNIOTIC MEMBRANE | DEFICIENCY | TRANSPLANTATION | IN-VITRO | OPHTHALMOLOGY | EXTRACELLULAR-MATRIX | DIFFERENTIATION | Biomarkers - metabolism | Microscopy, Electron, Scanning | Cell Proliferation | Tissue Engineering - methods | Limbus Corneae - ultrastructure | Pluripotent Stem Cells - ultrastructure | Corneal Transplantation - methods | Cell Count | Humans | Cells, Cultured | Culture Media, Serum-Free | Epithelium, Corneal - ultrastructure | Corneal Diseases - surgery | Epithelium, Corneal - transplantation | Pluripotent Stem Cells - metabolism | Stem Cell Transplantation | Limbus Corneae - metabolism | Epithelium, Corneal - metabolism | Cell Differentiation | Corneal Diseases - pathology | Keratin | Usage | Collagen | Stem cells | Transplantation | Ophthalmology | Albumin | Transforming growth factors | Embryonic stem cells | Index Medicus | Basic Medicine | Corneal epithelium;Limbal epithelial stem cells;Human pluripotent stem cells;Serum-free culture conditions;Tissue engineering;Regenerative medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Cell and Molecular Biology | Cell- och molekylärbiologi
Journal Article
Laboratory Investigation, ISSN 0023-6837, 11/2018, Volume 98, Issue 11, pp. 1375 - 1383
Journal Article
Laboratory Investigation, ISSN 0023-6837, 12/2016, Volume 96, Issue 12, pp. 1311 - 1326
Macular corneal dystrophy (MCD) is characterized by multiple punctate gray-white opacities in the corneal stromal region, due to the accumulation of abnormally... 
MEDICINE, RESEARCH & EXPERIMENTAL | SULFATION | GLYCOSAMINOGLYCANS | MATRIX-METALLOPROTEINASE | BIOSYNTHESIS | CHLORATE | ULTRASTRUCTURE | CELL-ADHESION | PATHOLOGY | EXPRESSION | CHONDROGENESIS | MORPHOLOGY | Cornea - ultrastructure | Matrix Metalloproteinases - genetics | Goats | Stromal Cells - pathology | Multienzyme Complexes - metabolism | Sulfate Adenylyltransferase - metabolism | Epithelium, Corneal - pathology | Cornea - drug effects | Corneal Dystrophies, Hereditary - pathology | Enzyme Inhibitors - toxicity | Stromal Cells - drug effects | Epithelium, Corneal - drug effects | Spectrum Analysis, Raman | Cornea - pathology | Eye Proteins - antagonists & inhibitors | Eye Proteins - genetics | Gene Ontology | Chlorates - toxicity | Microscopy, Electron, Scanning | Stromal Cells - metabolism | Cells, Cultured | Sulfate Adenylyltransferase - antagonists & inhibitors | Herbicides - toxicity | Corneal Dystrophies, Hereditary - metabolism | Epithelium, Corneal - ultrastructure | Multienzyme Complexes - antagonists & inhibitors | Gene Expression Regulation - drug effects | Cornea - metabolism | Stromal Cells - ultrastructure | Animals | Wnt Signaling Pathway - drug effects | Eye Proteins - metabolism | Image Processing, Computer-Assisted | Matrix Metalloproteinases - chemistry | Epithelium, Corneal - metabolism | Matrix Metalloproteinases - metabolism | Microtechnology | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2011, Volume 6, Issue 12, pp. e28895 - e28895
Background: Altered dosage of the transcription factor PAX6 causes multiple human eye pathophysiologies. PAX6(+/-) heterozygotes suffer from aniridia and... 
NASAL DEVELOPMENT | DEFECTS | HOMEOBOX-CONTAINING GENE | MUS-MUSCULUS | STEM-CELL FUNCTION | ABNORMALITIES | BIOLOGY | MUTATIONS | MODEL | ANIRIDIA-RELATED KERATOPATHY | EYE DEVELOPMENT | Paired Box Transcription Factors - genetics | X Chromosome Inactivation - genetics | Humans | Male | Epithelium, Corneal - pathology | Endothelial Cells - ultrastructure | Intercellular Junctions - pathology | beta-Galactosidase - metabolism | Female | Eye Proteins - genetics | Microvilli - pathology | Gene Dosage - genetics | Endothelial Cells - metabolism | Transgenes - genetics | Intercellular Junctions - metabolism | Repressor Proteins - genetics | Genotype | Mice, Transgenic | PAX6 Transcription Factor | Epithelium, Corneal - abnormalities | Epithelium, Corneal - ultrastructure | Homeodomain Proteins - genetics | Animals | Epithelium, Corneal - physiopathology | Microvilli - metabolism | Microvilli - ultrastructure | Corneal Stroma - pathology | Heterozygote | Mosaicism | Mice | Endothelial Cells - pathology | Intercellular Junctions - ultrastructure | Corneal Stroma - abnormalities | Homeostasis - genetics | Analysis | Stem cells | Cornea | Spermatogenesis | Homeostasis | Heterozygotes | Dosage | Inactivation | Defects | Eye | Missense mutation | Aniridia | Genetics | Life sciences | Localization | Drug dosages | Genotypes | Quantitative analysis | Gene dosage | Medical research | Mosaics | Deactivation | Cloning | Stroma | Electron microscopy | Mutants | Endothelium | Pax6 protein | Overexpression | Microscopy | Councils | Corneal dystrophy | Dystrophy | Mutation | Aberration | Cell migration | Index Medicus
Journal Article