leucine has been researched along with Rett 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 | 2 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Kato, Y; Kurita, J; Miyakawa, T; Tanokura, M | 1 |
Afenjar, A; Bahi-Buisson, N; Bienvenu, T; Chelly, J; Girard, B; Nectoux, J; Prieur, F; Rosas-Vargas, H | 1 |
2 other study(ies) available for leucine and Rett Syndrome
Article | Year |
---|---|
Structure of FBP11 WW1-PL ligand complex reveals the mechanism of proline-rich ligand recognition by group II/III WW domains.
Topics: Amino Acid Motifs; Carrier Proteins; Humans; Huntington Disease; Leucine; Ligands; Magnetic Resonance Spectroscopy; Peptides; Proline; Proline-Rich Protein Domains; Protein Structure, Tertiary; Rett Syndrome; Ribonucleoprotein, U1 Small Nuclear; Saccharomyces cerevisiae Proteins; Sequence Homology, Amino Acid; Tryptophan | 2006 |
Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsy.
Topics: Adolescent; Adult; Amino Acid Substitution; Base Sequence; Brain Diseases; Child; Child, Preschool; Epilepsy; Female; Genetic Variation; Glycoproteins; GPI-Linked Proteins; Humans; Leucine; Mutation; Nerve Tissue Proteins; Netrins; Phenotype; Rett Syndrome; Valine | 2007 |