Page last updated: 2024-08-24

5-methylcytosine and Embryopathies

5-methylcytosine has been researched along with Embryopathies in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	1 (50.00)	2.80

Authors

Authors	Studies
Gibas, P; Gordevičius, J; Kriukienė, E; Krjutškov, K; Kvederavičiūtė, K; Narmontė, M; Paluoja, P; Salumets, A; Tomkutė, V	1
Camerino, G; Goodfellow, P	1

Reviews

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

Article	Year
A fragile understanding. Trends in genetics : TIG, 1991, Volume: 7, Issue:8 Topics: 5-Methylcytosine; Brain; Cytosine; Female; Fetal Diseases; Fragile X Syndrome; Gene Expression Regulation; Genetic Carrier Screening; Humans; Intellectual Disability; Male; Meiosis; Methylation; Models, Genetic; Organ Specificity; Prenatal Diagnosis; Repetitive Sequences, Nucleic Acid; X Chromosome	1991

Other Studies

1 other study(ies) available for 5-methylcytosine and Embryopathies

Article	Year
Identification of fetal unmodified and 5-hydroxymethylated CG sites in maternal cell-free DNA for non-invasive prenatal testing. Clinical epigenetics, 2020, 10-20, Volume: 12, Issue:1 Topics: 5-Methylcytosine; Adult; Cell-Free Nucleic Acids; DNA Methylation; Down Syndrome; Epigenomics; Female; Fetal Diseases; Fetus; Genetic Testing; High-Throughput Nucleotide Sequencing; Humans; Male; Placenta; Pregnancy; Prenatal Diagnosis; Sensitivity and Specificity; Sequence Analysis, DNA; Trisomy	2020

Article

Year

Identification of fetal unmodified and 5-hydroxymethylated CG sites in maternal cell-free DNA for non-invasive prenatal testing.

Clinical epigenetics, 2020, 10-20, Volume: 12, Issue:1

Topics: 5-Methylcytosine; Adult; Cell-Free Nucleic Acids; DNA Methylation; Down Syndrome; Epigenomics; Female; Fetal Diseases; Fetus; Genetic Testing; High-Throughput Nucleotide Sequencing; Humans; Male; Placenta; Pregnancy; Prenatal Diagnosis; Sensitivity and Specificity; Sequence Analysis, DNA; Trisomy

2020