thymine has been researched along with Cataract, Membranous in 7 studies
| 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, Membranous
| 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 |