5-methylcytosine has been researched along with Immunologic Deficiency Syndromes in 3 studies
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 |
---|---|
Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-PĂ©quignot, E | 1 |
Aurias, A; Fischer, A; Jeanpierre, M; Ledeist, F; Prieur, M; Turleau, C; Viegas-Pequignot, E | 1 |
Ehrlich, M; Fiala, ES; Narayan, A; Sawyer, J; Smeets, DF; Sohn, OS; Tsien, F; Tuck-Muller, CM | 1 |
3 other study(ies) available for 5-methylcytosine and Immunologic Deficiency Syndromes
Article | Year |
---|---|
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; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; Cytosine; DNA, Satellite; Face; Female; Heterochromatin; Humans; Immunologic Deficiency Syndromes; Infant; Male; Methylation; Molecular Sequence Data; Syndrome; X Chromosome | 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 Disorders; Cytosine; DNA, Satellite; Embryo, Mammalian; Face; Female; Genetic Markers; Humans; Immunologic Deficiency Syndromes; Infant; Leukocytes; Male; Methylation; Placenta; Polymorphism, Restriction Fragment Length; Pregnancy; Repetitive Sequences, Nucleic Acid; Testis | 1993 |
DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.
Topics: 5-Methylcytosine; Abnormalities, Multiple; Brain; Cell Line; Centromere; Chromosome Aberrations; Chromosome Fragility; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; Cytosine; DNA Methylation; DNA, Satellite; Face; Female; Heterochromatin; Humans; Immunologic Deficiency Syndromes; Infant; Karyotyping; Male; Syndrome; Telomere | 2000 |