adenine has been researched along with Neurofibromatosis 2 in 1 studies
Neurofibromatosis 2: An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| De Klein, A | 1 |
| Riegman, PH | 1 |
| Bijlsma, EK | 1 |
| Heldoorn, A | 1 |
| Muijtjens, M | 1 |
| den Bakker, MA | 1 |
| Avezaat, CJ | 1 |
| Zwarthoff, EC | 1 |
1 other study available for adenine and Neurofibromatosis 2
| Article | Year |
|---|---|
A G-->A transition creates a branch point sequence and activation of a cryptic exon, resulting in the hereditary disorder neurofibromatosis 2.
Topics: Adenine; Adult; Aged; Alternative Splicing; Amino Acid Sequence; Base Sequence; Cloning, Molecular; | 1998 |