Page last updated: 2024-08-24

5-methylcytosine and Immunologic Deficiency Syndromes

5-methylcytosine has been researched along with Immunologic Deficiency Syndromes in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-PĂ©quignot, E1
Aurias, A; Fischer, A; Jeanpierre, M; Ledeist, F; Prieur, M; Turleau, C; Viegas-Pequignot, E1
Ehrlich, M; Fiala, ES; Narayan, A; Sawyer, J; Smeets, DF; Sohn, OS; Tsien, F; Tuck-Muller, CM1

Other Studies

3 other study(ies) available for 5-methylcytosine and Immunologic Deficiency Syndromes

ArticleYear
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
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.
    Human molecular genetics, 1993, Volume: 2, Issue:6

    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.
    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