Compounds > proline

proline and Rett Syndrome

proline has been researched along with Rett Syndrome in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Sheen, V; Torres, AR; Valencia, IM1
Kato, Y; Kurita, J; Miyakawa, T; Tanokura, M1
Barlow, PN; Bird, AP; Dryden, DT; Free, A; Smith, BO; Wakefield, RI1

Other Studies

3 other study(ies) available for proline and Rett Syndrome

ArticleYear
Atypical features in MECP2 P152R-associated Rett syndrome.
    Pediatric neurology, 2013, Volume: 49, Issue:2

    Topics: Arginine; Child; Female; Genotype; Humans; Methyl-CpG-Binding Protein 2; Phenotype; Proline; Rett Syndrome

2013
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
DNA recognition by the methyl-CpG binding domain of MeCP2.
    The Journal of biological chemistry, 2001, Feb-02, Volume: 276, Issue:5

    Topics: Alanine; Amino Acid Substitution; Arginine; Aspartic Acid; Chromosomal Proteins, Non-Histone; CpG Islands; DNA; DNA-Binding Proteins; Electrophoresis; Glycine; Humans; Methyl-CpG-Binding Protein 2; Mutagenesis, Site-Directed; Mutation, Missense; Proline; Protein Conformation; Protein Structure, Tertiary; Repressor Proteins; Rett Syndrome

2001