PLX099194
GSE142636: Transcriptome of Human Primary Corneal Endothelial Cells with SLC4A11 deficiency
- Organsim human
- Type RNASEQ
- Target gene
- Project ARCHS4
Mutations in the solute-linked carrier family 4 member 11 (SLC4A11) gene are associated with several corneal endothelial dystrophies, in all of which visually significant cornea edema may require corneal transplantation. To elucidate the pathogenesis of SLC4A11 associated corneal endothelial dystrophies, we analyzed the transcriptome of SLC4A11 knock-down primary human corneal endothelium (SLC4A11 KD pHCEnC) and scrambled RNA treated pHCEnC as controls. SOURCE: Wenlin Zhang (w.zhang@jsei.ucla.edu) - UCLA, Jules Stein Eye Institute
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