cytosine has been researched along with Rett Syndrome in 9 studies
Rett Syndrome: An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 6 (66.67) | 24.3611 |
| 2020's | 3 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Buchmuller, BC | 1 |
| Kosel, B | 1 |
| Summerer, D | 1 |
| Chhatbar, K | 1 |
| Cholewa-Waclaw, J | 1 |
| Shah, R | 1 |
| Bird, A | 3 |
| Sanguinetti, G | 2 |
| Ibrahim, A | 1 |
| Papin, C | 1 |
| Mohideen-Abdul, K | 1 |
| Le Gras, S | 1 |
| Stoll, I | 1 |
| Bronner, C | 1 |
| Dimitrov, S | 1 |
| Klaholz, BP | 1 |
| Hamiche, A | 1 |
| Lagger, S | 1 |
| Connelly, JC | 1 |
| Schweikert, G | 1 |
| Webb, S | 1 |
| Selfridge, J | 1 |
| Ramsahoye, BH | 1 |
| Yu, M | 1 |
| He, C | 2 |
| Sowers, LC | 1 |
| Walkinshaw, MD | 1 |
| Rudenko, A | 1 |
| Tsai, LH | 1 |
| Lyst, MJ | 1 |
| Connelly, J | 1 |
| Merusi, C | 1 |
| Chia, JY | 1 |
| Tan, WS | 1 |
| Ng, CL | 1 |
| Hu, NJ | 1 |
| Foo, HL | 1 |
| Ho, KL | 1 |
| Szulwach, KE | 1 |
| Li, X | 1 |
| Li, Y | 1 |
| Song, CX | 1 |
| Wu, H | 1 |
| Dai, Q | 1 |
| Irier, H | 1 |
| Upadhyay, AK | 1 |
| Gearing, M | 1 |
| Levey, AI | 1 |
| Vasanthakumar, A | 1 |
| Godley, LA | 1 |
| Chang, Q | 1 |
| Cheng, X | 1 |
| Jin, P | 1 |
| Mellén, M | 1 |
| Ayata, P | 1 |
| Dewell, S | 1 |
| Kriaucionis, S | 1 |
| Heintz, N | 1 |
1 review available for cytosine and Rett Syndrome
| Article | Year |
|---|---|
Epigenetic modifications in the nervous system and their impact upon cognitive impairments.
Topics: 5-Methylcytosine; Acetylation; Animals; Central Nervous System; Cognition; Cognition Disorders; Cyto | 2014 |
8 other studies available for cytosine and Rett Syndrome
| Article | Year |
|---|---|
Complete Profiling of Methyl-CpG-Binding Domains for Combinations of Cytosine Modifications at CpG Dinucleotides Reveals Differential Read-out in Normal and Rett-Associated States.
Topics: CpG Islands; Cytosine; Dinucleotide Repeats; Humans; Methyl-CpG-Binding Protein 2; Rett Syndrome | 2020 |
Quantitative analysis questions the role of MeCP2 as a global regulator of alternative splicing.
Topics: Alternative Splicing; Animals; Brain; Cytosine; Disease Models, Animal; DNA (Cytosine-5-)-Methyltran | 2020 |
MeCP2 is a microsatellite binding protein that protects CA repeats from nucleosome invasion.
Topics: 5-Methylcytosine; Animals; Cells, Cultured; Chromatin; Cytosine; Dinucleotide Repeats; DNA Methylati | 2021 |
MeCP2 recognizes cytosine methylated tri-nucleotide and di-nucleotide sequences to tune transcription in the mammalian brain.
Topics: Animals; Brain; CpG Islands; Cytosine; Dinucleotide Repeats; DNA Methylation; Epigenesis, Genetic; M | 2017 |
Sequence-specific DNA binding by AT-hook motifs in MeCP2.
Topics: AT-Hook Motifs; Base Sequence; Chromatin; Cytosine; DNA Methylation; DNA-Binding Proteins; Humans; M | 2016 |
A/T Run Geometry of B-form DNA Is Independent of Bound Methyl-CpG Binding Domain, Cytosine Methylation and Flanking Sequence.
Topics: Animals; Calorimetry, Differential Scanning; Circular Dichroism; CpG Islands; Cytosine; DNA; DNA Met | 2016 |
5-hmC-mediated epigenetic dynamics during postnatal neurodevelopment and aging.
Topics: 5-Methylcytosine; Aging; Analysis of Variance; Animals; Animals, Newborn; Cerebellum; Chromosome Del | 2011 |
MeCP2 binds to 5hmC enriched within active genes and accessible chromatin in the nervous system.
Topics: 5-Methylcytosine; Animals; Cerebellum; Chromatin; Cytosine; Epigenesis, Genetic; Humans; Methyl-CpG- | 2012 |