Literature DB >> 26310150

Corneal Dystrophies: Overview and Summary.

Daniel Schorderet1.   

Abstract

In this chapter, I shall discuss the genetics, mode of inheritance and molecular origin of several corneal dystrophies.
© 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  AGBL; BIGH3; CHST6; COL8A1; Corneal dystrophy; KRT12; KRT3; PIP5K3; SLC4A11; TACSTD2; TGFBI; UBAID1; ZEB1

Mesh：

Year:  2015        PMID： 26310150     DOI： 10.1016/bs.pmbts.2015.04.004

Source DB:  PubMed          Journal:  Prog Mol Biol Transl Sci        ISSN： 1877-1173            Impact factor:   3.622


  4 in total

1.  Transforming growth factor β induced mutation-associated phenotype in a Chinese family exhibiting lattice corneal dystrophy.

Authors:  Chao Qu; Man Yu; Xiaoxin Guo; Jing Li; Xiaoqi Liu; Yi Shi; Bo Gong
Journal:  Biomed Rep       Date:  2017-08-30

2.  Vps35-deficiency impairs SLC4A11 trafficking and promotes corneal dystrophy.

Authors:  Wei Liu; Fu-Lei Tang; Sen Lin; Kai Zhao; Lin Mei; Jian Ye; Wen-Cheng Xiong
Journal:  PLoS One       Date:  2017-09-21       Impact factor: 3.240

Review 3.  CRISPR-Cas Genome Surgery in Ophthalmology.

Authors:  James E DiCarlo; Jesse D Sengillo; Sally Justus; Thiago Cabral; Stephen H Tsang; Vinit B Mahajan
Journal:  Transl Vis Sci Technol       Date:  2017-05-31       Impact factor: 3.283

4.  Analysis of TGFBI Gene Mutations in Three Chinese Families with Corneal Dystrophy.

Authors:  Feng Zhao; Yuan Liu; Tao Guan
Journal:  J Ophthalmol       Date:  2019-01-22       Impact factor: 1.909
  4 in total

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