lysine has been researched along with Deafness-Retinitis Pigmentosa Syndrome in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alagramam, KN; Askew, C; Chen, DH; Furness, DN; Geng, R; Holt, JR; Horwitz, G; Imanishi, Y; Melki, S; Moser, T; Neef, J; Oshima-Takago, T; Tian, G | 1 |
| Aittakorpi, A; Isosomppi, J; Sankila, EM; Vastinsalo, H | 1 |
2 other study(ies) available for lysine and Deafness-Retinitis Pigmentosa Syndrome
| Article | Year |
|---|---|
The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene.
Topics: Acoustic Stimulation; Age Factors; Alcohol Oxidoreductases; Animals; Animals, Newborn; Asparagine; Barium; Biophysical Phenomena; Cadherins; Cell Line, Transformed; Cochlea; Disease Models, Animal; DNA-Binding Proteins; Evoked Potentials, Auditory, Brain Stem; Green Fluorescent Proteins; Hair Cells, Auditory; Humans; Lysine; Mechanoreceptors; Membrane Potentials; Membrane Proteins; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microscopy, Electron, Scanning; Mutation; Nerve Fibers; Organ Culture Techniques; Patch-Clamp Techniques; Physical Stimulation; Psychoacoustics; Pyridinium Compounds; Quaternary Ammonium Compounds; Receptors, AMPA; Synapses; Transfection; Usher Syndromes | 2012 |
Two Finnish USH1B patients with three novel mutations in myosin VIIA.
Topics: Amino Acid Substitution; Codon, Nonsense; Dyneins; Female; Finland; Frameshift Mutation; Gene Deletion; Glutamic Acid; Glutamine; Heterozygote; Humans; Lysine; Male; Mutation; Myosin VIIa; Myosins; Pedigree; Usher Syndromes | 2006 |