azacitidine has been researched along with Beckwith-Wiedemann 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 | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Beischlag, TV; Hollebakken, R; Kolybaba, AM; Labrecque, MP; Massah, S; Prefontaine, GG | 1 |
| Amin, R; Blake, T; Choufani, S; Evans, SR; Finegold, M; Jogunoori, W; Kreishman, P; Kumar, R; Mishra, B; Mishra, L; Rashid, A; Reddy, EP; Sidawy, AA; Weksberg, R; Yao, W; Yao, ZX | 1 |
| Eliyahu, E; McGovern, MM; Park, JH; Schuchman, EH; Shtraizent, N; Simonaro, CM | 1 |
3 other study(ies) available for azacitidine and Beckwith-Wiedemann Syndrome
| Article | Year |
|---|---|
Epigenetic characterization of the growth hormone gene identifies SmcHD1 as a regulator of autosomal gene clusters.
Topics: Amino Acid Sequence; Animals; Azacitidine; Base Sequence; Beckwith-Wiedemann Syndrome; Cadherins; Cell Line; Chromosomal Proteins, Non-Histone; Chromosomes, Mammalian; DNA Methylation; Epigenesis, Genetic; Growth Hormone; Humans; Mice; Molecular Sequence Data; Multigene Family; Promoter Regions, Genetic; Silver-Russell Syndrome; Up-Regulation | 2014 |
Epigenetic silencing of beta-spectrin, a TGF-beta signaling/scaffolding protein in a human cancer stem cell disorder: Beckwith-Wiedemann syndrome.
Topics: Animals; Azacitidine; Base Sequence; Beckwith-Wiedemann Syndrome; Blotting, Western; Decitabine; DNA Methylation; Enzyme Inhibitors; Epigenesis, Genetic; Epigenomics; Gene Expression Profiling; Hep G2 Cells; Heterozygote; Humans; Insulin-Like Growth Factor II; Mice; Mice, Knockout; Neoplastic Stem Cells; Oligonucleotide Array Sequence Analysis; Phenotype; Promoter Regions, Genetic; Spectrin; Tumor Cells, Cultured | 2010 |
Imprinting at the SMPD1 locus: implications for acid sphingomyelinase-deficient Niemann-Pick disease.
Topics: Adult; Animals; Azacitidine; Beckwith-Wiedemann Syndrome; Cells, Cultured; Chlorocebus aethiops; Chromosomes, Human, Pair 11; COS Cells; Decitabine; DNA Methylation; Genomic Imprinting; Heterozygote; Humans; Male; Mutation; Niemann-Pick Diseases; Pedigree; Polymorphism, Single Nucleotide; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Sphingomyelin Phosphodiesterase; Transfection | 2006 |