adenine has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 5 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "In spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD), the expanded cytosine adenine guanine (CAG) repeat in ATXN3 is the causal mutation, and its length is the main factor in determining the age at onset (AO) of clinical symptoms." | 4.02 | CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3. ( Brunt, ER; de Mattos, EP; de Vries, JJ; Jardim, LB; Kampinga, HH; Leotti, VB; Oliveira, CM; Te Meerman, GJ; Verbeek, DS, 2021) |
| "Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disease caused by the expansion of a polyglutamine (polyQ) tract in ataxin-1 (ATXN1)." | 1.43 | BIIB021, a synthetic Hsp90 inhibitor, induces mutant ataxin-1 degradation through the activation of heat shock factor 1. ( Adachi, H; Ding, Y; Iida, M; Katsuno, M; Kondo, N; Nakatsuji, H; Sahashi, K; Sobue, G; Tohnai, G, 2016) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (40.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Leotti, VB | 1 |
| de Vries, JJ | 1 |
| Oliveira, CM | 1 |
| de Mattos, EP | 1 |
| Te Meerman, GJ | 1 |
| Brunt, ER | 1 |
| Kampinga, HH | 1 |
| Jardim, LB | 1 |
| Verbeek, DS | 1 |
| Ding, Y | 1 |
| Adachi, H | 1 |
| Katsuno, M | 1 |
| Sahashi, K | 1 |
| Kondo, N | 1 |
| Iida, M | 1 |
| Tohnai, G | 1 |
| Nakatsuji, H | 1 |
| Sobue, G | 1 |
| Kasumu, AW | 1 |
| Hougaard, C | 1 |
| Rode, F | 1 |
| Jacobsen, TA | 1 |
| Sabatier, JM | 1 |
| Eriksen, BL | 1 |
| Strøbæk, D | 1 |
| Liang, X | 1 |
| Egorova, P | 1 |
| Vorontsova, D | 1 |
| Christophersen, P | 1 |
| Rønn, LC | 1 |
| Bezprozvanny, I | 1 |
| Klebe, S | 1 |
| Faivre, L | 1 |
| Forlani, S | 1 |
| Dussert, C | 1 |
| Tourbah, A | 1 |
| Brice, A | 1 |
| Stevanin, G | 1 |
| Durr, A | 1 |
| Silveira, I | 1 |
| Miranda, C | 1 |
| Guimarães, L | 1 |
| Moreira, MC | 1 |
| Alonso, I | 1 |
| Mendonça, P | 1 |
| Ferro, A | 1 |
| Pinto-Basto, J | 1 |
| Coelho, J | 1 |
| Ferreirinha, F | 1 |
| Poirier, J | 1 |
| Parreira, E | 1 |
| Vale, J | 1 |
| Januário, C | 1 |
| Barbot, C | 1 |
| Tuna, A | 1 |
| Barros, J | 1 |
| Koide, R | 1 |
| Tsuji, S | 1 |
| Holmes, SE | 1 |
| Margolis, RL | 1 |
| Jardim, L | 1 |
| Pandolfo, M | 1 |
| Coutinho, P | 1 |
| Sequeiros, J | 1 |
5 other studies available for adenine and Autosomal Dominant Cerebellar Ataxia, Type II
| Article | Year |
|---|---|
CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3.
Topics: Adenine; Adult; Ataxin-3; Cytosine; Disease Progression; Female; Guanine; Humans; Machado-Joseph Dis | 2021 |
BIIB021, a synthetic Hsp90 inhibitor, induces mutant ataxin-1 degradation through the activation of heat shock factor 1.
Topics: Adenine; Ataxin-1; Brain Stem; Cerebellum; DNA-Binding Proteins; Heat Shock Transcription Factors; H | 2016 |
Selective positive modulator of calcium-activated potassium channels exerts beneficial effects in a mouse model of spinocerebellar ataxia type 2.
Topics: Adenine; Animals; Calcium; Cerebellum; Disease Models, Animal; HEK293 Cells; Humans; In Vitro Techni | 2012 |
Another mutation in cysteine 131 in protein kinase C gamma as a cause of spinocerebellar ataxia type 14.
Topics: Adenine; Amino Acid Substitution; Cysteine; Guanine; Humans; Magnetic Resonance Imaging; Male; Mutat | 2007 |
Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.
Topics: Adenine; Adult; Aged; Alleles; Brazil; Cytosine; Female; Guanine; Heterozygote; Humans; Male; Middle | 2002 |