lysine has been researched along with Angioedemas, Hereditary in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 2 (40.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dickeson, SK; Feener, EP; Gailani, D; Kumar, S; Law, RHP; Mohammed, BM; Phillips, DR; Quek, AJ; Sun, MF; Whisstock, JC | 1 |
| Kaplan, AP | 1 |
| Cheng, Q; Dickeson, SK; Gailani, D; Gruber, A; Ivanov, I; Kundu, S; Matafonov, A; McCrae, K; Mohammed, BM; Sun, MF; Verhamme, IM | 1 |
| Caballero, T; Drouet, C; Favier, B; Gómez-Traseira, C; López-Lera, A; López-Trascasa, M; Pérez-Fernández, E; Prior, N | 1 |
| Fernández-Cruz, E; Prieto, A; Rodriguez-Sainz, C; Rubio, M; Tornero, P | 1 |
5 other study(ies) available for lysine and Angioedemas, Hereditary
| Article | Year |
|---|---|
A mechanism for hereditary angioedema caused by a lysine 311-to-glutamic acid substitution in plasminogen.
Topics: Angioedemas, Hereditary; Animals; Bradykinin; Factor XIIa; Fibrinolysin; Glutamic Acid; Humans; Kininogens; Lysine; Mammals; Mice; Plasma Kallikrein; Plasminogen; Tissue Plasminogen Activator | 2022 |
Bradykinin formation by mutant plasminogen.
Topics: Angioedemas, Hereditary; Bradykinin; Fibrinolysis; Glutamic Acid; Humans; Lysine; Plasminogen | 2022 |
A mechanism for hereditary angioedema with normal C1 inhibitor: an inhibitory regulatory role for the factor XII heavy chain.
Topics: Angioedemas, Hereditary; Animals; Arginine; Blood Coagulation; Bradykinin; Catalysis; Complement C1 Inhibitor Protein; Factor XIa; Factor XII; Factor XIIa; HEK293 Cells; Hereditary Angioedema Type III; Humans; Kininogens; Lysine; Mice; Mice, Inbred C57BL; Plasma Kallikrein; Prekallikrein; Protein Binding; Recombinant Proteins; Surface Properties; Thrombin | 2019 |
Hereditary angioedema caused by the p.Thr309Lys mutation in the F12 gene: a multifactorial disease.
Topics: Adolescent; Adult; Angioedemas, Hereditary; Factor XII; Family; Female; Hereditary Angioedema Type III; Humans; Lysine; Male; Mutation; Pedigree; Severity of Illness Index; Spain; Threonine; Young Adult | 2013 |
Missense mutation Thr309Lys in the coagulation factor XII gene in a Spanish family with hereditary angioedema type III.
Topics: Adult; Amino Acid Substitution; Angioedemas, Hereditary; Factor XII; Female; Humans; Lysine; Male; Mutation, Missense; Pedigree; Threonine | 2009 |