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Cornea, ISSN 0277-3740, 02/2015, Volume 34, Issue 2, pp. 117 - 159
PURPOSE:To update the 2008 International Classification of Corneal Dystrophies (IC3D) incorporating new clinical, histopathologic, and genetic information.... 
Fleck corneal dystrophy | Cornea | Epithelial and subepithelial dystrophies | Descemetmembrane | Posterior amorphous corneal dystrophy | Confocal microscopy | Cornea pathology | Thiel-Behnke corneal dystrophy | Lattice corneal dystrophy | Macular corneal dystrophy | Stromal dystrophies | Hereditary disease | Epithelial basement membranedystrophy | Pre-Descemet corneal dystrophy | Histopathology | Keratoconus | Congenital corneal endothelial dystrophy and X-linked endothelialdystrophy | Bowman membrane | Subepithelialmucinous corneal dystrophy | Endothelial dystrophies | Genetics | Schnyder corneal dystrophy | Gelatinousdrop-like corneal dystrophy | Fuchsendothelial corneal dystrophy | Epithelial-stromal TGFBI dystrophies | Lisch epithelial corneal dystrophy | Stroma | Histology | Meesmann dystrophy | Epithelium | Endothelium | Genetic disease | Epithelial recurrent erosion dystrophies | Posteror polymorphous corneal dystrophy | Centralcloudy dystrophy of François | Granular corneal dystrophy type 1 | Granular corneal dystrophy type 2 | TGFBI | Reis-Bücklers corneal dystrophy | Congenital stromal corneal dystrophy | Cornea dystrophy | cornea | endothelial dystrophies | histology | epithelial basement membrane dystrophy | genetic disease | epithelial and subepithelial dystrophies | central cloudy dystrophy of Francois | macular corneal dystrophy | subepithelial mucinous corneal dystrophy | cornea pathology | stroma | FRANCOIS | congenital corneal endothelial dystrophy and X-linked endothelial dystrophy | posteror polymorphous corneal dystrophy | DISEASE | epithelium | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy | pre-Descemet corneal dystrophy | histopathology | INDIVIDUAL PHENOTYPIC VARIANCES | FAMILY | epithelial recurrent erosion dystrophies | granular corneal dystrophy type 1 | granular corneal dystrophy type 2 | genetics | cornea dystrophy | UBIAD1 GENE | MUTATIONS | Descemet membrane | endothelium | hereditary disease | epithelial-stromal TGFBI dystrophies | keratoconus | posterior amorphous corneal dystrophy | congenital stromal corneal dystrophy | stromal dystrophies | fleck corneal dystrophy | confocal microscopy | gelatinous drop-like corneal dystrophy | EDEMA | OPHTHALMOLOGY | LINKAGE | Corneal Dystrophies, Hereditary - genetics | Terminology as Topic | International Classification of Diseases | Corneal Dystrophies, Hereditary - classification | Corneal Dystrophies, Hereditary - pathology | Humans | Index Medicus
Journal Article
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 08/2014, Volume 450, Issue 4, pp. 1505 - 1511
Journal Article
Cornea, ISSN 0277-3740, 05/2018, Volume 37, Issue 5, pp. 542 - 547
PURPOSE:In granular corneal dystrophy type 2 (GCD2), corneal deposits containing fragments of transforming growth factor-β–induced protein appear in sequence... 
BETA-INDUCED PROTEIN | visual acuity | AUTOPHAGY | corneal opacity | FIBROBLASTS | KERATO-EPITHELIN | granular corneal dystrophy type 2 | DEPOSITS | GENE | OPHTHALMOLOGY | MUTATIONS | TGFBI | diffuse haze | Care and treatment | Corneal diseases | Development and progression | Visual acuity | Genetic aspects | Transforming growth factors | Health aspects | Index Medicus
Journal Article
Journal Article
PROTEOMICS, ISSN 1615-9853, 02/2016, Volume 16, Issue 3, pp. 539 - 543
More than 60 mutations in transforming growth factor beta‐induced protein (TGFBIp) have been reported in humans causing a variety of phenotypic protein... 
2DE immunoblotting | Cornea | Biomedicine | Granular corneal dystrophy type 2 | TGFBIp | XIC label‐free quantification | XIC label-free quantification | DEPOSITS | GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | MUTATIONS | LATTICE | Cornea - surgery | Proteome - genetics | Molecular Weight | Humans | Protein Multimerization | Corneal Dystrophies, Hereditary - genetics | Male | Case-Control Studies | Tandem Mass Spectrometry | Corneal Dystrophies, Hereditary - pathology | Protein Aggregation, Pathological - pathology | Proteolysis | Chromatography, Liquid | Adult | Female | Cornea - pathology | Protein Aggregation, Pathological - genetics | Extracellular Matrix Proteins - metabolism | Protein Aggregation, Pathological - etiology | Gene Expression | Extracellular Matrix Proteins - genetics | Molecular Sequence Annotation | Corneal Dystrophies, Hereditary - metabolism | Cornea - metabolism | Homozygote | Transforming Growth Factor beta - genetics | Keratomileusis, Laser In Situ - adverse effects | Corneal Dystrophies, Hereditary - surgery | Mutation | Proteome - metabolism | Transforming Growth Factor beta - metabolism | Protein Aggregation, Pathological - metabolism | Eye | Proteins | Arginine | Surgery | Growth factors | Molecular weight | Transforming growth factor-b | Immunoblotting | Patients | Accumulation | Amino acid substitution | Histidine | Aggregates | Corneal dystrophy | Extracellular matrix | Dystrophy | Index Medicus
Journal Article
Journal of Pineal Research, ISSN 0742-3098, 08/2011, Volume 51, Issue 1, pp. 94 - 103
Journal Article
Journal Article
Experimental Eye Research, ISSN 0014-4835, 05/2019, Volume 182, pp. 167 - 174
Alzheimer's disease (AD) primarily affects the brain and is the most common form of dementia worldwide. Despite more than a century of research, there are... 
Cornea | Biomarker | Granular corneal dystrophy type 2 | Alzheimer's disease | Amyloid precursor protein | PROTEOGLYCANS | AUTOPHAGY | MESSENGER-RNAS | A-BETA | OPHTHALMOLOGY | TGFBI | MYOFIBROBLAST DIFFERENTIATION | EXPRESSION | SULFATED GLYCOSAMINOGLYCANS | KERATOCYTES | Physiological aspects | Epithelium | Amyloid beta-protein
Journal Article