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- BookClaus Cursiefen, Albert S. Jun, editors.Contents:
Epidemiology and genetic basis of Fuchs Endothelial Corneal Dystrophy
MicroRNAs in FED: New therapeutic option?
Clinical phenotypes of Fuchs Endothelial Corneal Dystrophy (FECD), disease progression, differential diagnosis, and medical therapy
Optical and anatomic changes in Fuchs Endothelial Dystrophy corneas
Evolution of posterior lamellar keratoplasty: PK-DLEK-DSEK/DSAEK-DMEK-DMET
DMEK Graft Preparation: eye bank perspective and risk factors for preparation failure
Donor-tissue splitting and tissue storage for DALK and DMEK surgery
DSAEK and UT-DSAEK in FED: Step-by-step approach
DSAEK (not only) in Asian eyes: What glide to use? Optimized insertion techniques
Intra- and postoperative complications and their management in DMEK
DMEK: step-by-step surgical approach
Complications of Descemet Stripping Automated Endothelial Keratoplasty (DSAEK) surgery
Revision for failed penetrating keratoplasty in FED
Long-term clear graft survival and chronic endothelial cell loss following posterior lamellar keratoplasty
Immune reactions and dry eye after posterior lamellar keratoplasty
Tissue engineering of a healthy corneal endothelium for FECD patients.Digital Access Springer 2017 - ArticleJones EW.Genetics. 1977 Feb;85(2):209-23.Forty ade3 mutants were examined with respect to their growth requirements, levels of the tetrahydrofolate interconversion enzymes, and/or map positions. Four deletions were detected. Mutations that result in a requirement for adenine and histidine map in one region of the locus; those which result in a requirement for adenine only map in a quite separate region of the locus, a region not disclosed in previous studies. No correlation was observed between growth properties of the strains and enzyme levels.