lysine has been researched along with Congenital Foot Deformities in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Calabrò, V; De Simone, M; Guerrini, L; La Mantia, G; Pollice, A; Rossi, M; Santoro, R | 1 |
| Frey, HJ; Frey, ML; Riekkinen, PJ; Tuomola, HO | 1 |
| Fischer, MH; Gerritsen, T; Opitz, JM | 1 |
3 other study(ies) available for lysine and Congenital Foot Deformities
| Article | Year |
|---|---|
Itch/AIP4 associates with and promotes p63 protein degradation.
Topics: Amino Acid Sequence; Cell Line, Tumor; Cyclin-Dependent Kinase Inhibitor p57; DNA-Binding Proteins; Foot Deformities, Congenital; Genes, Reporter; Hand Deformities, Congenital; Humans; Luciferases; Lysine; Lysosomes; Mutation; Promoter Regions, Genetic; Proteasome Endopeptidase Complex; Protein Binding; Proto-Oncogene Proteins c-mdm2; Repressor Proteins; Trans-Activators; Transcription Factors; Transcriptional Activation; Transfection; Tumor Suppressor Proteins; Ubiquitin; Ubiquitin-Protein Ligases | 2006 |
A family with autosomal dominant spinocerebellar ataxia, with electrophysiological findings.
Topics: Action Potentials; Adult; Aged; Ataxia; Beta-Globulins; Cerebellar Ataxia; Electromyography; Female; Foot Deformities, Congenital; Histidine; Humans; Lysine; Male; Methods; Middle Aged; Neural Conduction; Nystagmus, Pathologic; Optic Atrophy; Pedigree | 1973 |
Alpha-aminoadipic aciduria, a non-deleterious inborn metabolic defect.
Topics: Adipates; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids, Dicarboxylic; Child; Female; Foot Deformities, Congenital; Humans; Intellectual Disability; Lysine; Male; Pedigree; Phenotype; Tuberous Sclerosis | 1974 |