thymine has been researched along with Cataract in 7 studies
Cataract: Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 6 (85.71) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zhou, G | 1 |
| Zhou, N | 1 |
| Hu, S | 1 |
| Zhao, L | 2 |
| Zhang, C | 1 |
| Qi, Y | 1 |
| De Becker, I | 1 |
| Walter, M | 1 |
| Noël, LP | 1 |
| Wong, K | 1 |
| Barbin, Y | 1 |
| Chakrabarti, S | 1 |
| Adams, P | 1 |
| Vanita, V | 2 |
| Singh, JR | 2 |
| Hejtmancik, JF | 1 |
| Nuernberg, P | 1 |
| Hennies, HC | 1 |
| Singh, D | 2 |
| Sperling, K | 2 |
| Addison, PK | 1 |
| Berry, V | 1 |
| Holden, KR | 1 |
| Espinal, D | 1 |
| Rivera, B | 1 |
| Su, H | 1 |
| Srivastava, AK | 1 |
| Bhattacharya, SS | 1 |
| Gu, F | 1 |
| Zhai, H | 1 |
| Li, D | 1 |
| Li, C | 1 |
| Huang, S | 1 |
| Ma, X | 1 |
| Guleria, K | 1 |
| Varon, R | 1 |
7 other studies available for thymine and Cataract
| Article | Year |
|---|---|
A missense mutation in CRYBA4 associated with congenital cataract and microcornea.
Topics: Adolescent; Adult; Amino Acid Substitution; Base Sequence; beta-Crystallin A Chain; Cataract; Child; | 2010 |
Phenotypic variations in patients with a 1630 A>T point mutation in the PAX6 gene.
Topics: Adenine; Adult; Aniridia; Cataract; Child, Preschool; Corneal Diseases; Eye Proteins; Female; Geneti | 2004 |
A point mutation in the iron-responsive element of the L-ferritin in a family with hereditary hyperferritinemia cataract syndrome.
Topics: Adult; Cataract; Female; Ferritins; Genes, Dominant; Guanine; Heterozygote; Humans; Iron-Regulatory | 2005 |
A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.
Topics: Asian People; Base Sequence; Cataract; Child; Chromosome Mapping; Chromosomes, Human, Pair 21; Corne | 2006 |
A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family.
Topics: Aspartic Acid; Cataract; Chromosome Mapping; Connexins; Female; Genes, Dominant; Genetic Linkage; Gu | 2006 |
A novel mutation in major intrinsic protein of the lens gene (MIP) underlies autosomal dominant cataract in a Chinese family.
Topics: Adult; Amino Acid Substitution; Aquaporins; Arginine; Asian People; Cataract; Cysteine; Cytosine; DN | 2007 |
A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.
Topics: Amino Acid Substitution; Arginine; Asian People; Cataract; Chromosome Mapping; Chromosomes, Human, P | 2007 |