|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
4
|
|
pubmed:dateCreated |
2000-11-8
|
|
pubmed:abstractText |
Recently, mutations in the M1S1 gene have been identified as responsible for gelatinous drop-like corneal dystrophy (GDLD). How the abnormal M1S1 gene product causes GDLD is not known, although evidence suggests that it may compromise corneal epithelial function. This investigation attempted to determine the effect of the abnormal M1S1 gene product by assessing epithelial barrier function and epithelial ultrastructure in GDLD corneas.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Jul
|
|
pubmed:issn |
0277-3740
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
19
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
551-5
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:10928776-Adult,
pubmed-meshheading:10928776-Cell Membrane Permeability,
pubmed-meshheading:10928776-Contrast Media,
pubmed-meshheading:10928776-Corneal Dystrophies, Hereditary,
pubmed-meshheading:10928776-Epithelium, Corneal,
pubmed-meshheading:10928776-Fluorescein,
pubmed-meshheading:10928776-Fluorophotometry,
pubmed-meshheading:10928776-Humans,
pubmed-meshheading:10928776-Male,
pubmed-meshheading:10928776-Microscopy, Atomic Force,
pubmed-meshheading:10928776-Microscopy, Electron, Scanning,
pubmed-meshheading:10928776-Middle Aged,
pubmed-meshheading:10928776-Ophthalmic Solutions,
pubmed-meshheading:10928776-Severity of Illness Index
|
|
pubmed:year |
2000
|
|
pubmed:articleTitle |
Epithelial barrier function and ultrastructure of gelatinous drop-like corneal dystrophy.
|
|
pubmed:affiliation |
Department of Ophthalmology, Kyoto Prefectural University of Medicine, Japan.
|
|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|
