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Accession: PRJNA369763 ID: 369763

Homo sapiens (human)

Comprehensive characterization of DNA methylation changes in Fuchs Endothelial Corneal Dystrophy

See Genome Information for Homo sapiens
Transparency of the human cornea is necessary for vision. Fuchs Endothelial Corneal Dystrophy (FECD) is a bilateral, heritable degeneration of the corneal endothelium, and a leading indication for corneal transplantation in developed countries. More...
AccessionPRJNA369763; GEO: GSE94462
Data TypeEpigenomics
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsPan P et al., "Aberrant DNA methylation of miRNAs in Fuchs endothelial corneal dystrophy.", Sci Rep, 2019 Nov 8;9(1):16385
SubmissionRegistration date: 3-Feb-2017
Matilda Chan, Ophthalmology, University of California, San Francisco
Project Data:
Resource NameNumber
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GEO DataSets1
GEO Data Details
Data volume, Supplementary Mbytes172

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