lysine has been researched along with DiGeorge Syndrome 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 |
|---|---|
| Arai, M; Arinami, T; Ichikawa, T; Itokawa, M; Iwayama, Y; Maekawa, M; Miyashita, M; Toyosima, M; Toyota, T; Yoshikawa, T | 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 DiGeorge Syndrome
| Article | Year |
|---|---|
Schizophrenia with the 22q11.2 deletion and additional genetic defects: case history.
Topics: Adult; Arginine; Chromosome Deletion; Chromosomes, Human, Pair 22; DiGeorge Syndrome; Exotropia; Female; Frameshift Mutation; Genetic Predisposition to Disease; Homeodomain Proteins; Humans; Lactoylglutathione Lyase; Lysine; Polymerase Chain Reaction; Schizophrenia; Transcription Factors | 2011 |
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 |