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SCIENCE, ISSN 0036-8075, 06/2012, Volume 336, Issue 6086, pp. 1306 - 1310
Human UBIAD1 localizes to mitochondria and converts vitamin K-1 to vitamin K-2. Vitamin K-2 is best known as a cofactor in blood coagulation, but in bacteria... 
MENAQUINONE-4 | MULTIDISCIPLINARY SCIENCES | SCHNYDER | UBIAD1 GENE | MUTATIONS | DYSFUNCTION | IDENTIFICATION | DROSOPHILA-PINK1 | CRYSTALLINE CORNEAL-DYSTROPHY | PARKINSONS-DISEASE
Journal Article
Theoretical Computer Science, ISSN 0304-3975, 07/2019
Journal Article
CORNEA, ISSN 0277-3740, 12/2008, Volume 27, Issue 10, pp. S1 - S42
Background: The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification.... 
Grayson-Wilbrandt corneal dystrophy | Meesmann corneal dystrophy | TGFBI BIGH3 GENE | pre-Descemet corneal dystrophy | GROENOUW TYPE-I | corneal histopathology | GELSOLIN-RELATED AMYLOIDOSIS | Thiel-Behnke corneal dystrophy | posterior polymorphous corneal dystrophy | epithelial basement membrane dystrophy | POSTERIOR POLYMORPHOUS DYSTROPHY | granular corneal dystrophy 2 | COMPOUND HETEROZYGOUS MUTATIONS | granular corneal dystrophy 1 | genetic corneal disease | Schnyder corneal dystrophy | inherited corneal disease | WHORLED MICROCYSTIC DYSTROPHY | congenital hereditary endothelial dystrophy 1 | congenital hereditary endothelial dystrophy 2 | posterior amorphous corneal dystrophy | central cloudy dystrophy of Francois | macular corneal dystrophy | Schnyder crystalline corneal dystrophy | congenital stromal corneal dystrophy | gene | subepithelial mucinous corneal dystrophy | VIVO CONFOCAL MICROSCOPY | CENTRAL CLOUDY DYSTROPHY | Lisch epithelial corneal dystrophy | corneal dystrophy | eponym | X-linked endothelial corneal dystrophy | mutation | key reference | CARBOHYDRATE SULFOTRANSFERASE GENE | fleck corneal dystrophy | HEREDITARY ENDOTHELIAL DYSTROPHY | epithelial recurrent erosion dystrophy | gelatinous drop-like corneal dystrophy | OPHTHALMOLOGY | Avellino corneal dystrophy | lattice gelsolin type dystrophy | Fuchs endothelial corneal dystrophy | lattice corneal dystrophy | Reis-Bucklers corneal dystrophy
Journal Article
Leibniz International Proceedings in Informatics, LIPIcs, ISSN 1868-8969, 06/2019, Volume 129
Conference Proceeding
Electronic Notes in Discrete Mathematics, ISSN 1571-0653, 08/2017, Volume 61, pp. 421 - 427
Representations of planar triangulations as contact graphs of geometric shapes have received quite some attention in recent years. The most prominent example... 
Contact representation | Schnyder wood | α-orientation | pentagon
Journal Article
Electronic Journal of Combinatorics, ISSN 1077-8926, 09/2018, Volume 25, Issue 3
Representations of planar triangulations as contact graphs of a set of internally disjoint homothetic triangles or of a set of internally disjoint homothetic... 
Pentagon | Contact representation | Planar triangulation | Schnyder wood | MATHEMATICS | MATHEMATICS, APPLIED
Journal Article
POSTEPY HIGIENY I MEDYCYNY DOSWIADCZALNEJ, ISSN 0032-5449, 03/2018, Volume 72, pp. 116 - 130
UbiA prenyltransferase domain-containing protein 1 (UBIAD1) is a transmembrane enzyme that plays an essential physiological role in the human body. The most... 
MEDICINE, RESEARCH & EXPERIMENTAL | UBIAD1 | coenzyme Q10 | MATRIX GLA PROTEIN | PHENOTYPE | MEMBRANES | HMGCR | vitamin K | TERE1 | CELL CARCINOMA | METABOLISM | GENE | BIOLOGY | cholesterol | SCHNYDER | Schnyder corneal dystrophy | MUTATIONS
Journal Article
Klinische Monatsblatter fur Augenheilkunde, ISSN 0023-2165, 06/2016, Volume 233, Issue 6, pp. 708 - 712
Purpose: The first Oskar Fehr lecture is given in honour of Professor Fehr, a well respected ophthalmologist, who was head physician of the Department of Eye... 
genetic diseases | corneal dystrophy | genetic mutations | Schnyder corneal dystrophy | Schnyder crystalline corneal dystrophy | lipid | IC3D CLASSIFICATION | PRENYLTRANSFERASE | CORNEAL | DYSTROPHY | OPHTHALMOLOGY | UBIAD1 GENE | MUTATIONS
Journal Article
Journal Francais d'Ophtalmologie, ISSN 0181-5512, 12/2018, Volume 41, Issue 10, pp. 920 - 925
Introduction: The objective of this article is to describe the evolution of Schnyder dystrophy in 3 related patients of different ages and to highlight the... 
Cornea | UBIAD1 | Schnyder dystrophy | Cornea dystrophy | OPHTHALMOLOGY | UBIAD1 GENE | Humans | Middle Aged | Corneal Dystrophies, Hereditary - genetics | Male | Corneal Dystrophies, Hereditary - diagnosis | Mutation, Missense | Dimethylallyltranstransferase - genetics | DNA Mutational Analysis | Pedigree | Adult | Family | Female | France
Journal Article
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
Discrete & Computational Geometry, ISSN 0179-5376, 1/2019, Volume 61, Issue 1, pp. 161 - 184
We consider the problem of morphing between two planar drawings of the same triangulated graph, maintaining straight-line planarity. In “How to morph planar... 
05C10 | Computational geometry | Computational Mathematics and Numerical Analysis | Planar graphs | Graph drawing | Mathematics | Schnyder woods | Morphing | 68U05 | Combinatorics | 68R10 | MATHEMATICS | COMPUTER SCIENCE, THEORY & METHODS | Computer science | Drawings
Journal Article
Graefe's Archive for Clinical and Experimental Ophthalmology, ISSN 0721-832X, 11/2018, Volume 256, Issue 11, pp. 2127 - 2134
Schnyder corneal dystrophy (SCD) is a rare inherited disease that leads to gradual vision loss by the deposition of lipids in the corneal stroma. The aim of... 
Pathogenic variant | UBIAD1 | Medicine & Public Health | Confocal microscopy | Ophthalmology | Schnyder corneal dystrophy | Optical coherent tomography | CHOLESTEROL | PHENOTYPE | FAMILY | METABOLISM | GENE | MUTATION | VITAMIN-K | OPHTHALMOLOGY | Medicine, Experimental | Medical research | Family | Lipids | Cornea | Corneal dystrophy | Stroma | Dystrophy | Localization | Age | Genetic screening | Index Medicus
Journal Article
Electronic Notes in Discrete Mathematics, ISSN 1571-0653, 08/2017, Volume 61, pp. 301 - 307
In the study of lattice walks there are several examples of enumerative equivalences which amount to a trade-off between domain and endpoint constraints. We... 
Weyl chambers | Young tableaux | Dyck paths | excursions | lattice paths | open arc diagrams | Schnyder woods
Journal Article
Biomedical and Pharmacology Journal, ISSN 0974-6242, 06/2013, Volume 6, Issue 1, pp. 49 - 50
Journal Article
Information Processing Letters, ISSN 0020-0190, 04/2017, Volume 120, pp. 16 - 22
A monotone drawing of a graph is a straight-line planar drawing of such that every pair of vertices is connected by a path that is monotone with respect to... 
Schnyder woods | Monotone drawings | Graph algorithms | Hamiltonian graphs | Maximal planar graphs | CONVEX DRAWINGS | DIMENSION | PLANAR GRAPHS | COMPUTER SCIENCE, INFORMATION SYSTEMS | Algorithms
Journal Article
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