proline has been researched along with Corneal Dystrophies in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (28.57) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ji, YW; Kim, EK; Kim, TI; Lee, J; Park, SY; Seo, KY | 1 |
| Affeldt, JA; Aldave, AJ; Gutmark, JG; Klintworth, GK; Meallet, MA; Rao, NA; Small, KW; Udar, N; Yellore, VS | 1 |
| Chen, L; Ge, Z; Gu, Y; Guo, L; Qi, M; Si, J; Yan, X; Yang, Y; Yu, P | 1 |
| Aldave, AJ; Chen, MC; Rayner, SA; Sonmez, B; Thonar, EJ; Yellore, VS | 1 |
| Bhattacharya, SS; Bowling, BL; Ebenezer, ND; Filipec, M; Hardcastle, AJ; Jirsova, K; Klintworth, GK; Liskova, P; Tuft, SJ | 1 |
| Bennett, K; Dota, A; Kawasaki, S; Kinoshita, S; Nishida, K; Quantock, AJ | 1 |
| Endo, S; Fujiki, K; Hotta, Y; Ishida, N; Kanai, A; Nakayasu, K; Nguyen, TH; Yamaguchi, T | 1 |
7 other study(ies) available for proline and Corneal Dystrophies
| Article | Year |
|---|---|
Delayed Onset of Lattice Corneal Dystrophy Type IIIA Due to a Novel T621P Mutation in TGFBI.
Topics: Adult; Cornea; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Exons; Extracellular Matrix Proteins; Female; Humans; Male; Middle Aged; Pedigree; Point Mutation; Proline; Threonine; Tomography, Optical Coherence; Transforming Growth Factor beta; Visual Acuity | 2016 |
Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.
Topics: Adult; Alanine; Amyloid; Amyloidosis; Aspartic Acid; Cornea; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Exons; Extracellular Matrix Proteins; Female; Glutamine; Haplotypes; Humans; Mutation, Missense; Pedigree; Proline; Transforming Growth Factor beta | 2004 |
A clinical and molecular-genetic analysis of Chinese patients with lattice corneal dystrophy and novel Thr538Pro mutation in the TGFBI (BIGH3) gene.
Topics: China; Corneal Dystrophies, Hereditary; Female; Humans; Male; Mutation; Pedigree; Polymerase Chain Reaction; Proline; Threonine; Transforming Growth Factor beta; Transforming Growth Factor beta1 | 2006 |
An unusual presentation of macular corneal dystrophy associated with uniparental isodisomy and a novel Leu173Pro mutation.
Topics: Adult; Amino Acid Sequence; Carbohydrate Sulfotransferases; Conserved Sequence; Cornea; Corneal Dystrophies, Hereditary; Genotype; Homozygote; Humans; Keratan Sulfate; Leucine; Male; Mutation; Mutation, Missense; Pedigree; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Proline; Sulfotransferases; Uniparental Disomy | 2007 |
Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families.
Topics: Adult; Amyloid; Cataract; Cornea; Corneal Dystrophies, Hereditary; Czech Republic; Extracellular Matrix Proteins; Female; Histidine; Humans; Male; Middle Aged; Mutation; Phenotype; Proline; Transforming Growth Factor beta | 2008 |
Amyloid and Pro501 Thr-mutated (beta)ig-h3 gene product colocalize in lattice corneal dystrophy type IIIA.
Topics: Aged; Amyloid; Congo Red; Corneal Dystrophies, Hereditary; DNA; Exons; Extracellular Matrix Proteins; Humans; Immunoenzyme Techniques; Male; Neoplasm Proteins; Point Mutation; Polymerase Chain Reaction; Proline; Threonine; Transforming Growth Factor beta | 1999 |
Leu518Pro mutation of the beta ig-h3 gene causes lattice corneal dystrophy type I.
Topics: Adolescent; Adult; Base Sequence; Cornea; Corneal Dystrophies, Hereditary; DNA; Exons; Extracellular Matrix Proteins; Female; Humans; Keratoplasty, Penetrating; Leucine; Male; Middle Aged; Molecular Sequence Data; Neoplasm Proteins; Pedigree; Point Mutation; Proline; Transforming Growth Factor beta | 1999 |