Page last updated: 2024-08-24

5-methylcytosine and Syndrome

5-methylcytosine has been researched along with Syndrome in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (33.33)	18.2507
2000's	2 (66.67)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-Péquignot, E	1
Ehrlich, M; Fiala, ES; Narayan, A; Sawyer, J; Smeets, DF; Sohn, OS; Tsien, F; Tuck-Muller, CM	1
Costello, JF; Plass, C	1

Reviews

1 review(s) available for 5-methylcytosine and Syndrome

Article	Year
Methylation matters. Journal of medical genetics, 2001, Volume: 38, Issue:5 Topics: 5-Methylcytosine; Chromosome Aberrations; CpG Islands; Cytosine; DNA Methylation; DNA Transposable Elements; Gene Expression Regulation, Neoplastic; Genomics; Humans; Neoplasms; Oncogenes; Syndrome	2001

Other Studies

2 other study(ies) available for 5-methylcytosine and Syndrome

Article	Year
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients. Human molecular genetics, 1994, Volume: 3, Issue:12 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
DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients. Cytogenetics and cell genetics, 2000, Volume: 89, Issue:1-2 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

Article

Year

Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.

Human molecular genetics, 1994, Volume: 3, Issue:12

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

DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.

Cytogenetics and cell genetics, 2000, Volume: 89, Issue:1-2

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