5-methylcytosine has been researched along with Fra(X) Syndrome in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (40.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Drongitis, D; Miano, MG; Poeta, L; Verrillo, L | 1 |
| Galloway, JN; Jin, P; Lin, L; Nelson, DL; Street, RC; Wu, H; Yao, B; Zalewski, ZA | 1 |
| Andrade, NS; Bennison, S; Esanov, R; Wahlestedt, C; Zeier, Z | 1 |
| Hornstra, IK; Nelson, DL; Warren, ST; Yang, TP | 1 |
| Camerino, G; Goodfellow, P | 1 |
2 review(s) available for 5-methylcytosine and Fra(X) Syndrome
| Article | Year |
|---|---|
DNA Hypermethylation and Unstable Repeat Diseases: A Paradigm of Transcriptional Silencing to Decipher the Basis of Pathogenic Mechanisms.
Topics: 5-Methylcytosine; DNA Methylation; Fragile X Mental Retardation Protein; Fragile X Syndrome; Gene Silencing; Humans; Trinucleotide Repeat Expansion; Trinucleotide Repeats | 2020 |
A fragile understanding.
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 |
3 other study(ies) available for 5-methylcytosine and Fra(X) Syndrome
| Article | Year |
|---|---|
Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome.
Topics: 5-Methylcytosine; Animals; Ataxia; Base Sequence; Cerebellum; Consensus Sequence; Cytosine; Disease Models, Animal; DNA Methylation; Fragile X Syndrome; Humans; Mice; Mice, Transgenic; Terminator Regions, Genetic; Transcription Initiation Site; Tremor | 2014 |
The FMR1 promoter is selectively hydroxymethylated in primary neurons of fragile X syndrome patients.
Topics: 5-Methylcytosine; Adolescent; Adult; Aged; Aged, 80 and over; DNA Methylation; Female; Fragile X Mental Retardation Protein; Fragile X Syndrome; Gene Silencing; Humans; Male; Middle Aged; Mutation; Neurons; Promoter Regions, Genetic; Trinucleotide Repeat Expansion | 2016 |
High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome.
Topics: 5-Methylcytosine; Base Sequence; Cytosine; Dosage Compensation, Genetic; Female; Fragile X Syndrome; Gene Expression Regulation; Humans; Male; Methylation; Molecular Sequence Data; Repetitive Sequences, Nucleic Acid; Sequence Alignment; X Chromosome | 1993 |