lysine has been researched along with Cerebrovascular Moyamoya Disease in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Choi, J; Harada, KH; Kim, M; Kobayashi, H; Koizumi, A; Mizushima, T; Oichi, Y; Takeda, M; Taketani, S; Tezuka, T; Youssefian, S | 1 |
| Fujimura, M; Ito, A; Kanoke, A; Kure, S; Morita-Fujimura, Y; Niizuma, K; Sakata, H; Sato-Maeda, M; Tominaga, T | 1 |
| Jang, MA; Ki, CS; Shin, S; Yoon, JH | 1 |
3 other study(ies) available for lysine and Cerebrovascular Moyamoya Disease
| Article | Year |
|---|---|
Moyamoya disease patient mutations in the RING domain of RNF213 reduce its ubiquitin ligase activity and enhance NFκB activation and apoptosis in an AAA+ domain-dependent manner.
Topics: AAA Domain; Adenosine Triphosphatases; Amino Acid Sequence; Apoptosis; HEK293 Cells; Humans; Lysine; Moyamoya Disease; Mutant Proteins; Mutation; NF-kappa B; Polyubiquitin; RING Finger Domains; Transcription Factors; Ubiquitin-Conjugating Enzymes; Ubiquitin-Protein Ligases | 2020 |
Temporal profile of the vascular anatomy evaluated by 9.4-tesla magnetic resonance angiography and histological analysis in mice with the R4859K mutation of RNF213, the susceptibility gene for moyamoya disease.
Topics: Adenosine Triphosphatases; Analysis of Variance; Animals; Arginine; Blood Vessels; Brain; Disease Models, Animal; Humans; Hyperplasia; Image Processing, Computer-Assisted; Lysine; Magnetic Resonance Angiography; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Moyamoya Disease; Mutation; Time Factors; Ubiquitin-Protein Ligases | 2015 |
Frequency of the moyamoya-related RNF213 p.Arg4810Lys variant in 1,516 Korean individuals.
Topics: Adenosine Triphosphatases; Adult; Arginine; Humans; Lysine; Moyamoya Disease; Republic of Korea; Ubiquitin-Protein Ligases | 2015 |