lysine has been researched along with Genetic Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ieko, M; Ishii, H; Kaneko, H; Mizukami, K; Mizuno, H; Murase, T; Naitoh, S; Nakabayashi, T; Nakagawa, T; Shikamoto, Y; Takeda, M; Tarumi, T | 1 |
| Baitei, EY; Raef, H; Shi, Y; Zou, M | 1 |
| Berg, K; Darin, N; Kyllerman, M; Martinsson, T; Oldfors, A; Tajsharghi, H; Wahlstrom, J | 1 |
| Benson, PF | 1 |
1 review(s) available for lysine and Genetic Diseases
| Article | Year |
|---|---|
Gene derepression: possible applications to diagnosis and management of genetic disease.
Topics: Animals; Biochemical Phenomena; Biochemistry; Carrier Proteins; Cell Differentiation; Cells, Cultured; Cricetinae; DNA; Enzyme Activation; Enzymes; Female; Fetal Diseases; Genetic Code; Genetic Diseases, Inborn; Histones; Humans; Lysine; Metabolism, Inborn Errors; Molecular Biology; Pregnancy; Prenatal Diagnosis; Proteins; RNA; Species Specificity; Subcellular Fractions | 1973 |
3 other study(ies) available for lysine and Genetic Diseases
| Article | Year |
|---|---|
Molecular dynamics calculations of wild type vs. mutant protein C: relationship between binding affinity to endothelial cell protein C receptor and hereditary disease.
Topics: 1-Carboxyglutamic Acid; Amino Acid Substitution; Antigens, CD; Computer Simulation; Endothelial Protein C Receptor; Endothelium, Vascular; Genetic Diseases, Inborn; Humans; Kinetics; Lysine; Models, Genetic; Models, Molecular; Protein Binding; Protein C; Protein Conformation; Receptors, Cell Surface | 2006 |
Genotype-phenotype correlation in a family with primary cortisol resistance: possible modulating effect of the ER22/23EK polymorphism.
Topics: Adrenal Gland Diseases; Adult; Amino Acid Substitution; Arginine; Family; Genetic Diseases, Inborn; Genotype; Glutamic Acid; Heterozygote; Homozygote; Humans; Hydrocortisone; Lysine; Male; Phenotype; Polymorphism, Genetic; Receptors, Glucocorticoid | 2008 |
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene.
Topics: Adult; Amino Acid Sequence; Animals; Child; Female; Genetic Diseases, Inborn; Glutamic Acid; Humans; Lysine; Male; Microscopy, Electron; Middle Aged; Molecular Sequence Data; Molecular Structure; Muscular Diseases; Mutation, Missense; Myosin Heavy Chains; Myosins; NADH Tetrazolium Reductase; Pedigree; Staining and Labeling | 2000 |