leucine and Rett Syndrome

leucine has been researched along with Rett Syndrome in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kato, Y; Kurita, J; Miyakawa, T; Tanokura, M1
Afenjar, A; Bahi-Buisson, N; Bienvenu, T; Chelly, J; Girard, B; Nectoux, J; Prieur, F; Rosas-Vargas, H1

Other Studies

2 other study(ies) available for leucine and Rett Syndrome

ArticleYear
Structure of FBP11 WW1-PL ligand complex reveals the mechanism of proline-rich ligand recognition by group II/III WW domains.
    The Journal of biological chemistry, 2006, Dec-29, Volume: 281, Issue:52

    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.
    Pediatric neurology, 2007, Volume: 37, Issue:4

    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