leucine and Rett Syndrome

leucine has been researched along with Rett Syndrome in 2 studies

Research

Studies (2)

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

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

Other Studies

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. 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

Article

Year

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