azacitidine has been researched along with Rett Syndrome in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Carrette, LLG; Kelleher, RJ; Lee, JT; Ma, W; Press, W; Wang, CY; Wei, C | 1 |
| Czymmek, KJ; Kamboj, S; Kudo, S; Kumar, A; LaSalle, JM; Malone, BM; Schanen, NC; Twiss, JL | 1 |
| Kumar, A | 1 |
| Green, SH; Kormann-Bortolotto, MH; Webb, T; Woods, CG | 1 |
4 other study(ies) available for azacitidine and Rett Syndrome
| Article | Year |
|---|---|
A mixed modality approach towards Xi reactivation for Rett syndrome and other X-linked disorders.
Topics: Animals; Azacitidine; Brain; Cell Line; Decitabine; DNA Methylation; Female; Gene Expression Profiling; Genetic Therapy; Male; Methyl-CpG-Binding Protein 2; Mice; Oligonucleotides, Antisense; Rett Syndrome; X Chromosome Inactivation | 2018 |
Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo.
Topics: 3T3 Cells; Amino Acid Sequence; Animals; Azacitidine; Blotting, Western; Cell Nucleus; Chromatin; Decitabine; DNA Methylation; Epigenesis, Genetic; Fluorescent Antibody Technique; Kinetics; Methyl-CpG-Binding Protein 2; Mice; Molecular Sequence Data; Mutation; Protein Binding; Protein Isoforms; Protein Transport; Rett Syndrome | 2008 |
Rett and ICF syndromes: methylation moves into medicine.
Topics: Abnormalities, Multiple; Animals; Azacitidine; Chromosomal Proteins, Non-Histone; Craniofacial Abnormalities; DNA (Cytosine-5-)-Methyltransferases; DNA Methylation; DNA Methyltransferase 3A; DNA Methyltransferase 3B; DNA Mutational Analysis; DNA-Binding Proteins; Embryonic and Fetal Development; Female; Gene Expression Regulation, Developmental; Gene Silencing; Genes, Lethal; Genotype; Heterochromatin; Humans; Immunologic Deficiency Syndromes; Infant, Newborn; Male; Methyl-CpG-Binding Protein 2; Mice; Mutation, Missense; Phenotype; Repressor Proteins; Rett Syndrome; Sequence Deletion; Syndrome; X Chromosome | 2000 |
X-inactivation in girls with Rett syndrome.
Topics: Adolescent; Adult; Autoradiography; Azacitidine; Bromodeoxyuridine; Child; Chromosome Banding; DNA Replication; Dosage Compensation, Genetic; Female; Humans; Rett Syndrome; X Chromosome | 1992 |