lysine has been researched along with Autism-Dementia-Ataxia-Loss of Purposeful Hand Use 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 | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Doughty, ML; Stalker, L; Wynder, C | 1 |
Francke, U; Lee, SS; Wan, M; Zhao, K | 1 |
1 review(s) available for lysine and Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome
Article | Year |
---|---|
Role of H3K4 demethylases in complex neurodevelopmental diseases.
Topics: Autistic Disorder; DNA-Directed RNA Polymerases; Epigenesis, Genetic; Gene Expression Regulation, Developmental; Histone Demethylases; Histones; Humans; Jumonji Domain-Containing Histone Demethylases; Lysine; Minor Histocompatibility Antigens; Nervous System Diseases; Nuclear Proteins; Oxidoreductases, N-Demethylating; Repressor Proteins; Rett Syndrome | 2010 |
1 other study(ies) available for lysine and Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome
Article | Year |
---|---|
MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome.
Topics: Acetylation; Alleles; Blotting, Western; Cell Line; Chromosomal Proteins, Non-Histone; DNA Mutational Analysis; DNA-Binding Proteins; Female; Frameshift Mutation; Histones; Humans; Lysine; Male; Methyl-CpG-Binding Protein 2; Mutation; Polymerase Chain Reaction; Repressor Proteins; Rett Syndrome; RNA, Messenger; X Chromosome | 2001 |