Human corneal epithelium and endothelium synthesize beta IG-H3 in Fuchs' dystrophy

被引：0
|
作者：
Hirano, K
Klintworth, G
Bennett, K
Cintron, C
机构：
[1] HARVARD UNIV,SCH MED,SCHEPENS EYE RES INST,BOSTON,MA
[2] DUKE UNIV,CTR EYE,DURHAM,NC
[3] BRISTOL MYERS SQUIBB,SEATTLE,WA
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 1996年 / 37卷 / 03期
关键词：
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
引用
收藏
页码：4685 / 4685
页数：1
相关论文
共 50 条
  • [41] Integrative analysis of gene expression datasets in corneal endothelium samples of Fuchs endothelial corneal dystrophy
    Zhang, Jing
    Dai, Yiqin
    Li, Yue
    Xu, Jianjiang
    EXPERIMENTAL EYE RESEARCH, 2023, 237
  • [42] FUCHS ENDOTHELIAL DYSTROPHY - APPEARANCE OF CORNEAL ENDOTHELIUM UNDER ELECTRON-MICROSCOPE
    OFFRET, G
    POULIQUEN, Y
    RENARD, G
    KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 1977, 170 (06) : 796 - 803
  • [43] Identification of Circulating Fibrocytes and Dendritic Derivatives in Corneal Endothelium of Patients With Fuchs' Dystrophy
    De Roo, An-Katrien
    Wouters, Jasper
    Govaere, Olivier
    Foets, Beatrijs
    van den Oord, Joost J.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2017, 58 (01) : 670 - 681
  • [44] βIG-H3 antagonizes the formation of multicellular spheroids
    LeBaron, RG
    Thoma, BS
    MOLECULAR BIOLOGY OF THE CELL, 2001, 12 : 66A - 66A
  • [45] An unusual clinical phenotype of avellino corneal dystrophy associated with an Arg124His βig-H3 mutation in an African-American woman
    Meallet, MA
    Affeldt, JA
    McFarland, TJ
    Appukuttan, B
    Read, R
    Stout, JT
    Rao, NA
    AMERICAN JOURNAL OF OPHTHALMOLOGY, 2004, 137 (04) : 765 - 767
  • [46] New evidence suggesting that the central endothelium presents features of peripheral endothelium in Fuchs endothelial corneal dystrophy
    He, Zhiguo
    Gain, Philippe
    Jun, Albert S.
    Forest, Fabien
    Kallay, Laura
    Dumollard, Jean Marc
    Bergandi, Florian
    Peoc'h, Michel
    Thuret, Gilles
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2016, 57 (12)
  • [47] Transforming growth factor-β induced protein, βIG-H3, is present in degraded form and altered localization in lattice corneal dystrophy type I
    Takács, L
    Boross, P
    Tözsér, J
    Modis, L
    Tóth, G
    Berta, A
    EXPERIMENTAL EYE RESEARCH, 1998, 66 (06) : 739 - 745
  • [48] A new mutation (Leu569Arg) within exon 13 of the βig-h3 gene causes lattice corneal dystrophy type I
    Warren, JF
    Abbott, RL
    Crawford, JB
    Spencer, WH
    Margolis, TP
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 : U333 - U333
  • [49] beta ig-h3, a transforming growth factor beta-inducible gene, is overexpressed in atherosclerotic and restenotic human vascular lesions
    OBrien, ER
    Bennett, KL
    Garvin, MR
    Zderic, TW
    Hinohara, T
    Simpson, JB
    Kimura, T
    Nobuyoshi, M
    Mizgala, H
    Purchio, A
    Schwartz, SM
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1996, 16 (04) : 576 - 584
  • [50] Analysis of the OXPHOS complex in the corneal endothelium suggests impaired mitochondria! respiration in Fuchs Endothelial Corneal Dystrophy
    Halilovic, Adna
    Jurkunas, Ula V.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2016, 57 (12)
12345