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Nature Genetics, ISSN 1061-4036, 10/2000, Volume 26, Issue 2, pp. 237 - 241
Journal Article
国际眼科杂志:英文版, ISSN 2222-3959, 2012, Volume 5, Issue 3, pp. 301 - 306
AIM:To investigate whether mutations in TGFBI gene or CHST6 gene correlated with stromal corneal dystrophies(CD) in 8 Chinese probands.· METHODS:Eight... 
sulfotransferse | dystrophies | screening | CHST6 | corneal | gene | protein | Mutation | TGFBI | carbohydrate | Corneal dystrophies | Sulfotransferse CHST6 | TGFBI protein | Mutation screening | TGFBI gene | Carbohy drate
Journal Article
Oncotarget, ISSN 1949-2553, 2017, Volume 8, Issue 56, pp. 96301 - 96312
Macular corneal dystrophy (MCD) is an autosomal recessive disorder mainly caused by gene mutations of carbohydrate sulfotransferase (CHST6) leading to... 
CHST6 | Macular corneal dystrophy | Keratocytes | Apoptosis | Endoplasmic reticulum stress | CELLS | macular corneal dystrophy | ER STRESS | BIM | apoptosis | keratocytes | endoplasmic reticulum stress | SULFOTRANSFERASE | FAMILY | CELL BIOLOGY | GENE | BAX | TYPE-1 | KERATAN SULFATE
Journal Article
by Zhang, J and Wu, D and Li, Y and Fan, YD and Dai, YQ and Xu, JJ
AGING-US, ISSN 1945-4589, 02/2019, Volume 11, Issue 3, pp. 1019 - 1029
Macular corneal dystrophy (MCD) is an autosomal recessive disease featured by bilateral progressive stromal clouding and loss of vision, consequently... 
VIETNAMESE | CHST6 | PROTEOGLYCANS | SULFATION | macular corneal dystrophy | IMMUNOHISTOCHEMICAL EVIDENCE | CARBOHYDRATE-SULFOTRANSFERASE-6 | DISTINCT MUTATIONS | IDENTIFICATION | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | genetic variants | HETEROGENEITY | CARBOHYDRATE SULFOTRANSFERASE GENE | CHINESE PATIENTS
Journal Article
International Journal of Clinical and Experimental Medicine, ISSN 1940-5901, 08/2016, Volume 9, Issue 8, pp. 15073 - 15078
Corneal dystrophies (CDs), with lesions mainly appearing in the stroma, are defined to be stromal CDs. In recent years, growing knowledge about stromal CDs is... 
Pathology | Histology | Gene mutation | Pathogenesis | Stromal corneal dystrophies | MEDICINE, RESEARCH & EXPERIMENTAL | CHST6 | pathology | CROCODILE SHAGREEN | VIVO CONFOCAL MICROSCOPY | gene mutation | FRANCOIS | IDENTIFICATION | APOLIPOPROTEIN-E | FAMILY | pathogenesis | histology | LEUCINE-RICH PROTEOGLYCANS | UBIAD1 GENE | MUTATIONS
Journal Article
Iranian Journal of Child Neurology, ISSN 1735-4668, 09/2010, Volume 4, Issue 2, pp. 55 - 58
Objective Macuiar Corneal Dystrophy (MCD) is a rare autosomal recessive disorder affecting the stroma of cornea. Most cases of MCD are caused by mutations in... 
Iranian patients | Carbohydrate sulfotransferase 6 gene (CHST6) | Macular Corneal Dystrophy (MCD)
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 09/2006, Volume 103, Issue 36, pp. 13333 - 13338
Journal Article
International Journal of Human Genetics, ISSN 0972-3757, 03/2011, Volume 11, Issue 1, pp. 1 - 14
Corneal dystrophies are defined as a group of inherited corneal disorders characterized by opacification of the cornea. Initial classification of corneal... 
Corneal Dystrophy | Genetics | Histology | Molecular Analysis | Genes | GENOTYPE-PHENOTYPE CORRELATION | HELIX TERMINATION MOTIF | TGFBI BIGH3 GENE | M1S1 GENE | CHST6 GENE | SUPERFICIAL VARIANT | CARBOHYDRATE SULFOTRANSFERASE GENE | HEREDITARY ENDOTHELIAL DYSTROPHY | GENETICS & HEREDITY | COMPOUND HETEROZYGOUS MUTATIONS | GRANULAR DYSTROPHY
Journal Article
Journal Article
Experimental Eye Research, ISSN 0014-4835, 2010, Volume 91, Issue 2, pp. 293 - 299
Journal Article