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5-methylcytosine and Abnormalities, Autosome

5-methylcytosine has been researched along with Abnormalities, Autosome in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	3 (42.86)	18.2507
2000's	2 (28.57)	29.6817
2010's	2 (28.57)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baranov, VS; Efimova, OA; Glotov, OS; Kopat, VV; Krapivin, MI; Navodnikova, PM; Pendina, AA; Petrovskaia-Kaminskaia, AV; Talantova, OE; Tikhonov, AV	1
Arakawa, T; Hori, M; Kimura, T; Nakamura, T; Nakano, T; Nakashima, H; Nakatani, T; Oda, M; Sekita, Y; Yamagata, K	1
Campos, A; Fernández, JL; Gosálvez, J; Goyanes, V; Pereira, S	1
Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-Péquignot, 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
Costello, JF; Plass, C	1

Reviews

1 review(s) available for 5-methylcytosine and Abnormalities, Autosome

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

6 other study(ies) available for 5-methylcytosine and Abnormalities, Autosome

Article	Year
Inter-Cell and Inter-Chromosome Variability of 5-Hydroxymethylcytosine Patterns in Noncultured Human Embryonic and Extraembryonic Cells. Cytogenetic and genome research, 2018, Volume: 156, Issue:3 Topics: 5-Methylcytosine; Cell Communication; Chromosome Aberrations; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; Chromosomes, Human, Pair 9; DNA Methylation; Embryo, Mammalian; Epigenesis, Genetic; Female; Fluorescent Antibody Technique; Humans; Pregnancy; Pregnancy Trimester, First	2018
Stella preserves maternal chromosome integrity by inhibiting 5hmC-induced γH2AX accumulation. EMBO reports, 2015, Volume: 16, Issue:5 Topics: 5-Methylcytosine; Animals; Cell Division; Cell Line; Cells, Cultured; Chromosomal Instability; Chromosomal Proteins, Non-Histone; Chromosome Aberrations; Chromosome Segregation; Cytosine; Dioxygenases; DNA Methylation; DNA Replication; DNA-Binding Proteins; Embryo, Mammalian; Epigenesis, Genetic; Female; Gene Knockout Techniques; Histones; Male; Mice; Protein Transport; Proto-Oncogene Proteins; Repressor Proteins; Zygote	2015
An extra band within the human 9qh+ region that behaves like the surrounding constitutive heterochromatin. Journal of medical genetics, 1994, Volume: 31, Issue:8 Topics: 5-Methylcytosine; Adult; Azacitidine; Chromosome Aberrations; Chromosome Banding; Chromosomes, Human; Chromosomes, Human, Pair 9; Cytosine; Heterochromatin; Humans; In Situ Hybridization, Fluorescence; Lymphocytes; Male; Methylation; Microscopy, Electron	1994
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