cytosine has been researched along with Cataract in 5 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)
| Excerpt | Relevance | Reference |
|---|---|---|
| "Cataracts are the most common cause of blindness worldwide." | 1.37 | A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract. ( Berry, V; Bhattacharya, SS; Francis, PJ; Moore, AT; Prescott, Q; Waseem, NH, 2011) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (80.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Berry, V | 1 |
| Francis, PJ | 1 |
| Prescott, Q | 1 |
| Waseem, NH | 1 |
| Moore, AT | 1 |
| Bhattacharya, SS | 1 |
| Vanita, V | 2 |
| Singh, JR | 2 |
| Hejtmancik, JF | 1 |
| Nuernberg, P | 1 |
| Hennies, HC | 2 |
| Singh, D | 2 |
| Sperling, K | 2 |
| Messina-Baas, OM | 1 |
| Gonzalez-Huerta, LM | 1 |
| Cuevas-Covarrubias, SA | 1 |
| Nürnberg, P | 1 |
| Gu, F | 1 |
| Zhai, H | 1 |
| Li, D | 1 |
| Zhao, L | 1 |
| Li, C | 1 |
| Huang, S | 1 |
| Ma, X | 1 |
5 other studies available for cytosine and Cataract
| Article | Year |
|---|---|
A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract.
Topics: Cataract; Chromosomes, Human, Pair 10; Cytosine; Exons; Gene Deletion; Genes, Dominant; Genetic Link | 2011 |
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 |
Two affected siblings with nuclear cataract associated with a novel missense mutation in the CRYGD gene.
Topics: Adenosine; Adult; Alanine; Amino Acid Substitution; Case-Control Studies; Cataract; Cytosine; Female | 2006 |
A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.
Topics: Asian People; Base Sequence; Cataract; Child; Connexins; Cytosine; DNA Mutational Analysis; Eye Prot | 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 |