transferrin has been researched along with Keratoconus in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Blasiak, J; Jiménez-García, MP; Kaminska, A; Polakowski, P; Synowiec, E; Szaflik, J; Szaflik, JP; Wójcik, KA | 1 |
Bassi, M; Chakravarti, S; Daoud, Y; Foster, J; Jun, AS; Mohan, D; Scott, SG; Stark, WJ; Wu, WH | 1 |
2 other study(ies) available for transferrin and Keratoconus
Article | Year |
---|---|
Polymorphism of the transferrin gene in eye diseases: keratoconus and Fuchs endothelial corneal dystrophy.
Topics: Adult; Aged; Aged, 80 and over; Alleles; Eye Diseases; Female; Fuchs' Endothelial Dystrophy; Genotype; Humans; Keratoconus; Male; Middle Aged; Oxidative Stress; Polymorphism, Single Nucleotide; Risk Factors; Transferrin; Young Adult | 2013 |
Transforming growth factor β and insulin signal changes in stromal fibroblasts of individual keratoconus patients.
Topics: Cell Culture Techniques; Cell Proliferation; Cell Survival; Cells, Cultured; Corneal Stroma; Extracellular Matrix Proteins; Fibroblasts; Gene Expression Regulation; Humans; Insulin; Keratoconus; Mass Spectrometry; Selenium; Signal Transduction; Tissue Donors; Transferrin; Transforming Growth Factor beta | 2014 |