thymine has been researched along with Aqueductal Stenosis in 3 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Congenital hydrocephalus (CH) is caused by genetic mutations, but whether factors impacting human genetic mutations are disease-specific remains elusive." | 2.72 | Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions. ( Hart, C; McKnight, I; Park, IH; Shim, JW, 2021) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 2 (66.67) | 2.80 |
| Authors | Studies |
|---|---|
| Hart, M | 1 |
| Conrad, J | 1 |
| Barrett, E | 1 |
| Legg, K | 1 |
| Ivey, G | 1 |
| Lee, PHU | 1 |
| Yung, YC | 1 |
| Shim, JW | 2 |
| McKnight, I | 1 |
| Hart, C | 1 |
| Park, IH | 1 |
| Sztriha, L | 1 |
| Frossard, P | 1 |
| Hofstra, RM | 1 |
| Verlind, E | 1 |
| Nork, M | 1 |
2 reviews available for thymine and Aqueductal Stenosis
| Article | Year |
|---|---|
X-linked hydrocephalus genes: Their proximity to telomeres and high A + T content compared to Parkinson's disease.
Topics: Animals; Genes, X-Linked; Humans; Hydrocephalus; Mice; Mutation; Parkinson Disease; Rats; Telomere; | 2023 |
Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions.
Topics: Adenine; Alzheimer Disease; Animals; Carrier Proteins; Chromosome Mapping; Chromosomes; Databases, G | 2021 |
1 other study available for thymine and Aqueductal Stenosis
| Article | Year |
|---|---|
Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus.
Topics: Agenesis of Corpus Callosum; Child; Guanine; Humans; Hydrocephalus; Intellectual Disability; Leukocy | 2000 |