valine has been researched along with Corneal Dystrophies in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (66.67) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bisceglia, L; De Bonis, P; Laborante, A; Longo, C | 1 |
| FERRARO, A; GIVNER, I; ROIZIN, L | 1 |
| Ramirez-Miranda, A; Santacruz-Valdes, C; Suarez-Sanchez, R; Zenteno, JC | 1 |
| Bowling, BL; Jonasson, F; Klintworth, GK; Liu, NP; Smith, CF | 1 |
| Aldave, AJ; Bourla, N; Chen, MC; Gorin, MB; Khan, MA; Momi, RS; Rayner, SA; Sampat, KM; Sonmez, B; Yellore, VS | 1 |
| Afshari, NA; Bahadur, RP; Eifrig, DE; Enghild, JJ; Klintworth, GK; Thogersen, IB | 1 |
6 other study(ies) available for valine and Corneal Dystrophies
| Article | Year |
|---|---|
Lattice Corneal Dystrophy-Variant: a report of three new cases due to p.V631D mutation in the TGFBI gene.
Topics: Aspartic Acid; Biomarkers; Corneal Dystrophies, Hereditary; Early Diagnosis; Extracellular Matrix Proteins; Humans; Point Mutation; Prognosis; Transforming Growth Factor beta; Valine | 2013 |
Ocular changes in rats in diets deficient in amino acids; corneal dystrophy due to valine deficiency.
Topics: Amino Acids; Animals; Cornea; Corneal Dystrophies, Hereditary; Diet; Rats; Valine | 1947 |
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; Extracellular Matrix Proteins; Female; Guanine; Heterozygote; Humans; Isoleucine; Mutation, Missense; Transforming Growth Factor beta; Valine | 2006 |
Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland.
Topics: Alanine; Carbohydrate Sulfotransferases; Corneal Dystrophies, Hereditary; DNA Transposable Elements; Female; Frameshift Mutation; Heterozygote; Homozygote; Humans; Iceland; Immunohistochemistry; Immunophenotyping; Leucine; Male; Mutation; Pedigree; Polymerase Chain Reaction; Sulfotransferases; Valine | 2006 |
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
Topics: Amino Acid Substitution; Asparagine; Corneal Dystrophies, Hereditary; Dimethylallyltranstransferase; Female; Humans; Leucine; Male; Mutation; Mutation, Missense; Polymorphism, Single Nucleotide; Proteins; Serine; Valine | 2007 |
Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene.
Topics: Base Sequence; Corneal Dystrophies, Hereditary; Extracellular Matrix Proteins; Homozygote; Humans; Male; Methionine; Middle Aged; Mutation; Transforming Growth Factor beta; Valine | 2008 |