adenine has been researched along with Retinal Degeneration in 5 studies
Retinal Degeneration: A retrogressive pathological change in the retina, focal or generalized, caused by genetic defects, inflammation, trauma, vascular disease, or aging. Degeneration affecting predominantly the macula lutea of the retina is MACULAR DEGENERATION. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p304)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (20.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (60.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
---|---|
Bellingrath, JS | 1 |
McClements, ME | 1 |
Shanks, M | 1 |
Clouston, P | 1 |
Fischer, MD | 1 |
MacLaren, RE | 1 |
ARAS, AJ | 1 |
BECKER, M | 1 |
BROWN, AL | 1 |
HASS, GM | 1 |
Kloeckener-Gruissem, B | 1 |
Bartholdi, D | 1 |
Abdou, MT | 1 |
Zimmermann, DR | 1 |
Berger, W | 1 |
Gao, YQ | 1 |
Danciger, M | 1 |
Ozgul, RK | 1 |
Gribanova, Y | 1 |
Jacobson, S | 1 |
Farber, DB | 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 |
5 other studies available for adenine and Retinal Degeneration
Article | Year |
---|---|
Envisioning the development of a CRISPR-Cas mediated base editing strategy for a patient with a novel pathogenic
Topics: Adenine; Adolescent; Amino Acid Sequence; Codon, Nonsense; CRISPR-Cas Systems; Eye Proteins; Humans; | 2022 |
Separation of adenine, hypoxanthine, and the 5'-(mono-,di-,and tri-)-phosphates of adenosine and inosine by one-dimensional paper chromatography.
Topics: Adenine; Adenine Nucleotides; Adenosine; Chromatography; Chromatography, Paper; Hypoxanthine; Inosin | 1962 |
Identification of the genetic defect in the original Wagner syndrome family.
Topics: Adenine; Case-Control Studies; Chondroitin Sulfate Proteoglycans; Chromosome Segregation; DNA, Recom | 2006 |
Association of the Asn306Ser variant of the SP4 transcription factor and an intronic variant in the beta-subunit of transducin with digenic disease.
Topics: Adenine; Asparagine; Blindness; Cohort Studies; Exons; Genetic Variation; GTP-Binding Protein beta S | 2007 |
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 |