cytosine has been researched along with Prader-Willi Syndrome in 3 studies
Prader-Willi Syndrome: An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 from the mother (UNIPARENTAL DISOMY) which are imprinted (GENETIC IMPRINTING) and hence silenced. Clinical manifestations include MENTAL RETARDATION; MUSCULAR HYPOTONIA; HYPERPHAGIA; OBESITY; short stature; HYPOGONADISM; STRABISMUS; and HYPERSOMNOLENCE. (Menkes, Textbook of Child Neurology, 5th ed, p229)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Matin, MM | 1 |
| Baumer, A | 1 |
| Hornby, DP | 1 |
| Zeschnigk, M | 1 |
| Schmitz, B | 1 |
| Dittrich, B | 1 |
| Buiting, K | 1 |
| Horsthemke, B | 1 |
| Doerfler, W | 1 |
| Schweizer, J | 1 |
| Zynger, D | 1 |
| Francke, U | 1 |
3 other studies available for cytosine and Prader-Willi Syndrome
| Article | Year |
|---|---|
An analytical method for the detection of methylation differences at specific chromosomal loci using primer extension and ion pair reverse phase HPLC.
Topics: Ampicillin Resistance; Angelman Syndrome; Base Sequence; Chromatography, High Pressure Liquid; Chrom | 2002 |
Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
Topics: 5-Methylcytosine; Angelman Syndrome; Autoantigens; Chromosomes, Human, Pair 15; Cloning, Molecular; | 1997 |
In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit.
Topics: Alleles; Angelman Syndrome; Autoantigens; Binding Sites; Cell Line, Transformed; Chromatin; Chromoso | 1999 |