adenine has been researched along with Corneal Dystrophies in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 3 (60.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Szabó, DJ | 1 |
| Nagymihály, R | 1 |
| Veréb, Z | 1 |
| Josifovska, N | 1 |
| Noer, A | 1 |
| Liskova, P | 1 |
| Facskó, A | 1 |
| Moe, MC | 1 |
| Petrovski, G | 1 |
| Nie, D | 1 |
| Peng, Y | 1 |
| Li, M | 1 |
| Liu, X | 1 |
| Zhu, M | 1 |
| Ye, L | 1 |
| Clausen, I | 1 |
| Duncker, GI | 1 |
| Grünauer-Kloevekorn, C | 1 |
| Sullivan, LS | 1 |
| Zhao, X | 1 |
| Bowne, SJ | 1 |
| Xu, X | 1 |
| Daiger, SP | 1 |
| Yee, SB | 1 |
| Yee, RW | 1 |
| Zenteno, JC | 1 |
| Ramirez-Miranda, A | 1 |
| Santacruz-Valdes, C | 1 |
| Suarez-Sanchez, R | 1 |
5 other studies available for adenine and Corneal Dystrophies
| Article | Year |
|---|---|
Ex vivo 3D human corneal stroma model for Schnyder corneal dystrophy - role of autophagy in its pathogenesis and resolution.
Topics: Adenine; Adult; Aged; Autophagy; Cadaver; Cells, Cultured; Cornea; Corneal Dystrophies, Hereditary; | 2018 |
Lithium chloride (LiCl) induced autophagy and downregulated expression of transforming growth factor β-induced protein (TGFBI) in granular corneal dystrophy.
Topics: Adenine; Adjuvants, Immunologic; Autophagy; Blotting, Western; Cell Survival; Corneal Dystrophies, H | 2018 |
Identification of a novel mutation in the cornea specific keratin 12 gene causing Meesmann's corneal dystrophy in a German family.
Topics: Adenine; Aged, 80 and over; Codon; Cornea; Corneal Dystrophies, Hereditary; Exons; Female; Guanine; | 2010 |
Exclusion of the human collagen type XVII (COL17A1) gene as the cause of Thiel-Behnke corneal dystrophy (CDB2) on chromosome 10q23-q25.
Topics: Adenine; Autoantigens; Base Sequence; Carrier Proteins; Chromosomes, Human, Pair 10; Collagen; Colla | 2003 |
Expanding the mutational spectrum in TGFBI-linked corneal dystrophies: Identification of a novel and unusual mutation (Val113Ile) in a family with granular dystrophy.
Topics: Adenine; Adult; Base Sequence; Corneal Dystrophies, Hereditary; Corneal Opacity; Corneal Stroma; Ext | 2006 |