proline has been researched along with Rett Syndrome in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Sheen, V; Torres, AR; Valencia, IM | 1 |
Kato, Y; Kurita, J; Miyakawa, T; Tanokura, M | 1 |
Barlow, PN; Bird, AP; Dryden, DT; Free, A; Smith, BO; Wakefield, RI | 1 |
3 other study(ies) available for proline and Rett Syndrome
Article | Year |
---|---|
Atypical features in MECP2 P152R-associated Rett syndrome.
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.
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.
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 |