lysine has been researched along with Tetralogy of Fallot in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gu, R; Huang, G; Lin, Y; Ma, D; Ma, X; Sheng, W; Xu, J | 1 |
| Andria, G; Borsani, G; Castaldo, P; Incerti, B; Rossi, E; Sebastio, G; Sperandeo, MP; Taglialatela, M; Zollo, M; Zuffardi, O | 1 |
2 other study(ies) available for lysine and Tetralogy of Fallot
| Article | Year |
|---|---|
The role of histone modification and a regulatory single-nucleotide polymorphism (rs2071166) in the Cx43 promoter in patients with TOF.
Topics: Acetylation; Alleles; Asian People; Biomarkers; Connexin 43; Genetic Predisposition to Disease; Genotype; Histone Code; Histones; Humans; Immunohistochemistry; Lysine; Phenotype; Polymorphism, Single Nucleotide; Promoter Regions, Genetic; Protein Binding; Retinoid X Receptor alpha; Risk Factors; RNA, Messenger; Sequence Analysis, DNA; Tetralogy of Fallot | 2017 |
The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome.
Topics: Abnormalities, Multiple; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acid Sequence; Amino Acid Transport Systems, Basic; Animals; Blotting, Northern; Carrier Proteins; Chromosome Deletion; Chromosome Mapping; Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Dinucleotide Repeats; Female; Humans; Lysine; Membrane Proteins; Molecular Sequence Data; Oocytes; Sequence Analysis, DNA; Syndrome; Tetralogy of Fallot; Velopharyngeal Insufficiency; Xenopus | 1998 |