Page last updated: 2024-10-17

cytosine and Cataract

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)

Research Excerpts

ExcerptRelevanceReference
"Cataracts are the most common cause of blindness worldwide."1.37A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract. ( Berry, V; Bhattacharya, SS; Francis, PJ; Moore, AT; Prescott, Q; Waseem, NH, 2011)

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (80.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Berry, V1
Francis, PJ1
Prescott, Q1
Waseem, NH1
Moore, AT1
Bhattacharya, SS1
Vanita, V2
Singh, JR2
Hejtmancik, JF1
Nuernberg, P1
Hennies, HC2
Singh, D2
Sperling, K2
Messina-Baas, OM1
Gonzalez-Huerta, LM1
Cuevas-Covarrubias, SA1
Nürnberg, P1
Gu, F1
Zhai, H1
Li, D1
Zhao, L1
Li, C1
Huang, S1
Ma, X1

Other Studies

5 other studies available for cytosine and Cataract

ArticleYear
A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract.
    Molecular vision, 2011, Volume: 17

    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.
    Molecular vision, 2006, May-22, Volume: 12

    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.
    Molecular vision, 2006, Aug-24, Volume: 12

    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.
    Molecular vision, 2006, Oct-18, Volume: 12

    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.
    Molecular vision, 2007, Sep-11, Volume: 13

    Topics: Adult; Amino Acid Substitution; Aquaporins; Arginine; Asian People; Cataract; Cysteine; Cytosine; DN

2007