Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY009052-04
Application #
2162662
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1993-01-01
Project End
2000-12-31
Budget Start
1996-01-26
Budget End
1996-12-31
Support Year
4
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Cedars-Sinai Medical Center
Department
Type
DUNS #
075307785
City
Los Angeles
State
CA
Country
United States
Zip Code
90048
Perez-Straziota, Claudia; Gaster, Ronald N; Rabinowitz, Yaron S (2018) Corneal Cross-Linking for Pediatric Keratcoconus Review. Cornea 37:802-809
Khaled, Mariam Lofty; Bykhovskaya, Yelena; Yablonski, Sarah E R et al. (2018) Differential Expression of Coding and Long Noncoding RNAs in Keratoconus-Affected Corneas. Invest Ophthalmol Vis Sci 59:2717-2728
Bykhovskaya, Yelena; Fardaei, Majid; Khaled, Mariam Lotfy et al. (2017) TSC1 Mutations in Keratoconus Patients With or Without Tuberous Sclerosis. Invest Ophthalmol Vis Sci 58:6462-6469
Bykhovskaya, Yelena; Li, Xiaohui; Taylor, Kent D et al. (2016) Linkage Analysis of High-density SNPs Confirms Keratoconus Locus at 5q Chromosomal Region. Ophthalmic Genet 37:109-10
Bykhovskaya, Yelena; Gromova, Anastasia; Makarenkova, Helen P et al. (2016) Abnormal regulation of extracellular matrix and adhesion molecules in corneas of patients with keratoconus. Int J Keratoconus Ectatic Corneal Dis 5:63-70
Bykhovskaya, Yelena; Margines, Benjamin; Rabinowitz, Yaron S (2016) Genetics in Keratoconus: where are we? Eye Vis (Lond) 3:16
Bykhovskaya, Yelena; Caiado Canedo, Ana L; Wright, Kenneth W et al. (2015) C.57 C > T Mutation in MIR 184 is Responsible for Congenital Cataracts and Corneal Abnormalities in a Five-generation Family from Galicia, Spain. Ophthalmic Genet 36:244-7
Kramerov, Andrei A; Saghizadeh, Mehrnoosh; Maguen, Ezra et al. (2015) Persistence of reduced expression of putative stem cell markers and slow wound healing in cultured diabetic limbal epithelial cells. Mol Vis 21:1357-67
Bykhovskaya, Yelena; Seldin, Michael F; Liu, Yutao et al. (2015) Independent origin of c.57 C?>?T mutation in MIR184 associated with inherited corneal and lens abnormalities. Ophthalmic Genet 36:95-7
Rabinowitz, Yaron S; Li, Xiaohui; Canedo, Ana Laura Caiado et al. (2014) Optical coherence tomography combined with videokeratography to differentiate mild keratoconus subtypes. J Refract Surg 30:80-7

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