lysine has been researched along with Deafness 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 | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Mammano, F; Polles, G; Zanotti, G; Zonta, F | 1 |
| Schröder, JM; Sindern, E; Vorgerd, M; Züchner, S | 1 |
| Cervin, C; Cilio, CM; Groop, L; Heikkinen, S; Liljeström, B; Tapanainen, JS; Tuomi, T | 1 |
3 other study(ies) available for lysine and Deafness
| Article | Year |
|---|---|
Permeation pathway of homomeric connexin 26 and connexin 30 channels investigated by molecular dynamics.
Topics: Amino Acid Sequence; Calcium; Cell Membrane; Connexin 26; Connexin 30; Connexins; Crystallography, X-Ray; Deafness; Humans; Lysine; Models, Molecular; Molecular Dynamics Simulation; Molecular Sequence Data; Phospholipids; Protein Conformation | 2012 |
The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathy.
Topics: Adult; Aged; Aged, 80 and over; Axons; Charcot-Marie-Tooth Disease; Deafness; DNA Mutational Analysis; Female; Genetic Testing; Glutamic Acid; Humans; Lysine; Male; Microscopy, Electron; Middle Aged; Muscle Weakness; Mutation; Neural Conduction; Neurofilament Proteins; Pedigree; Peripheral Nerves; Phenotype; Protein Structure, Tertiary; Sural Nerve | 2004 |
Cosegregation of MIDD and MODY in a pedigree: functional and clinical consequences.
Topics: Adolescent; Adult; Aged; Chromosome Segregation; Deafness; Diabetes Mellitus; Diabetes Mellitus, Type 2; DNA-Binding Proteins; DNA, Mitochondrial; Female; HeLa Cells; Hepatocyte Nuclear Factor 1; Hepatocyte Nuclear Factor 1-alpha; Humans; Lysine; Male; Methionine; Middle Aged; Mutation; Nuclear Proteins; Pedigree; Transcription Factors; Transcription, Genetic | 2004 |