cytosine has been researched along with Autosomal Chromosome Disorders in 3 studies
Excerpt | Relevance | Reference |
---|---|---|
"We have investigated the distribution of DNA methylation in chromosomes and nuclei of normal individuals and ICF (Immunodeficiency, Centromeric instability and Facial abnormalities) syndrome patients, using 5-methylcytosine monoclonal antibody." | 3.69 | Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients. ( Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-Péquignot, E, 1994) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (66.67) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Grömminger, S | 1 |
Erkan, S | 1 |
Schöck, U | 1 |
Stangier, K | 1 |
Bonnet, J | 1 |
Schloo, R | 1 |
Schubert, A | 1 |
Prott, EC | 1 |
Knoll, U | 1 |
Stumm, M | 1 |
von Kalle, C | 1 |
Hofmann, W | 1 |
Miniou, P | 1 |
Jeanpierre, M | 2 |
Blanquet, V | 1 |
Sibella, V | 1 |
Bonneau, D | 1 |
Herbelin, C | 1 |
Fischer, A | 2 |
Niveleau, A | 1 |
Viegas-Péquignot, E | 2 |
Turleau, C | 1 |
Aurias, A | 1 |
Prieur, M | 1 |
Ledeist, F | 1 |
3 other studies available for cytosine and Autosomal Chromosome Disorders
Article | Year |
---|---|
The influence of low molecular weight heparin medication on plasma DNA in pregnant women.
Topics: Anticoagulants; Blood Specimen Collection; Chromosome Disorders; Chromosomes, Human, Pair 13; Chromo | 2015 |
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.
Topics: 5-Methylcytosine; Abnormalities, Multiple; Base Sequence; Case-Control Studies; Centromere; Child; C | 1994 |
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.
Topics: 5-Methylcytosine; Adult; Centromere; Child; Child, Preschool; Chromosome Aberrations; Chromosome Dis | 1993 |