thymine has been researched along with Retinitis Pigmentosa in 5 studies
Retinitis Pigmentosa: Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 4 (80.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chakarova, CF | 1 |
| Cherninkova, S | 1 |
| Tournev, I | 1 |
| Waseem, N | 1 |
| Kaneva, R | 1 |
| Jordanova, A | 1 |
| Veraitch, BK | 1 |
| Gill, B | 1 |
| Colclough, T | 1 |
| Nakova, A | 1 |
| Oscar, A | 1 |
| Mihaylova, V | 1 |
| Nikolova-Hill, A | 1 |
| Wright, AF | 1 |
| Black, GC | 1 |
| Ramsden, S | 1 |
| Kremensky, I | 1 |
| Bhattacharya, SS | 1 |
| Riazuddin, SA | 1 |
| Zulfiqar, F | 1 |
| Zhang, Q | 1 |
| Yao, W | 1 |
| Li, S | 1 |
| Jiao, X | 1 |
| Shahzadi, A | 1 |
| Amer, M | 1 |
| Iqbal, M | 1 |
| Hussnain, T | 1 |
| Sieving, PA | 1 |
| Riazuddin, S | 1 |
| Hejtmancik, JF | 1 |
| Yzer, S | 1 |
| van den Born, LI | 1 |
| Zonneveld, MN | 1 |
| Lopez, I | 1 |
| Ayyagari, R | 1 |
| Teye-Botchway, L | 1 |
| Mota-Vieira, L | 1 |
| Cremers, FP | 1 |
| Koenekoop, RK | 1 |
| Köhn, L | 1 |
| Burstedt, MS | 1 |
| Jonsson, F | 1 |
| Kadzhaev, K | 1 |
| Haamer, E | 1 |
| Sandgren, O | 1 |
| Golovleva, I | 1 |
| Trujillo, MJ | 1 |
| Millán, JM | 1 |
| Nájera, C | 1 |
| Beneyto, M | 1 |
| García-Sandoval, B | 1 |
| Rodriguez de Alba, M | 1 |
| Sanz, R | 1 |
| Ayuso, C | 1 |
5 other studies available for thymine and Retinitis Pigmentosa
| Article | Year |
|---|---|
Molecular genetics of retinitis pigmentosa in two Romani (Gypsy) families.
Topics: Adolescent; Adult; Base Sequence; Chromosomes, Human, X; Eye Proteins; Female; Genes, Dominant; Gene | 2006 |
Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families.
Topics: Asian People; Base Sequence; Chromosomes, Human, Pair 5; Consanguinity; Cytosine; DNA Transposable E | 2006 |
Molecular and phenotypic analysis of a family with autosomal recessive cone-rod dystrophy and Stargardt disease.
Topics: Adenine; Adult; ATP-Binding Cassette Transporters; Cytosine; Female; Fundus Oculi; Genes, Recessive; | 2007 |
Carrier of R14W in carbonic anhydrase IV presents Bothnia dystrophy phenotype caused by two allelic mutations in RLBP1.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Substitution; Arginine; Carbonic Anh | 2008 |
Identification of two rare variants (G-->A at nucleotide 721; C-->T at nucleotide 5200) in the rhodopsin gene. Mutations in brief no. 187. Online.
Topics: Adenine; Cytosine; Guanine; Humans; Point Mutation; Retinitis Pigmentosa; Rhodopsin; Thymine | 1998 |