cytosine has been researched along with Fra(X) Syndrome in 17 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder in which patients carry premutation alleles of 55-200 CGG repeats in the FMR1 gene." | 5.40 | Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome. ( Galloway, JN; Jin, P; Lin, L; Nelson, DL; Street, RC; Wu, H; Yao, B; Zalewski, ZA, 2014) |
| "Fragile X syndrome (FXS) and associated disorders are caused by expansion of the cytosine-guanine-guanine (CGG) trinucleotide repeat in the 5' untranslated region (UTR) of the Fragile X mental retardation-1 (FMR1) gene promoter." | 3.91 | A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene. ( Cheung, WC; Choy, KW; Gui, B; Kwok, KY; Lim, R; Pietilä, S; Shi, M; Wang, H; Yang, Z; Zhu, X; Zhu, Y, 2019) |
| "Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder in which patients carry premutation alleles of 55-200 CGG repeats in the FMR1 gene." | 1.40 | Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome. ( Galloway, JN; Jin, P; Lin, L; Nelson, DL; Street, RC; Wu, H; Yao, B; Zalewski, ZA, 2014) |
| "Fragile X syndrome is the most common form of inherited mental retardation in man." | 1.29 | High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome. ( Hornstra, IK; Nelson, DL; Warren, ST; Yang, TP, 1993) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 8 (47.06) | 18.2507 |
| 2000's | 5 (29.41) | 29.6817 |
| 2010's | 3 (17.65) | 24.3611 |
| 2020's | 1 (5.88) | 2.80 |
| Authors | Studies |
|---|---|
| Yang, H | 1 |
| Wang, Y | 1 |
| Xiang, Y | 1 |
| Yadav, T | 1 |
| Ouyang, J | 1 |
| Phoon, L | 1 |
| Zhu, X | 2 |
| Shi, Y | 1 |
| Zou, L | 1 |
| Lan, L | 1 |
| Wang, H | 1 |
| Gui, B | 1 |
| Cheung, WC | 1 |
| Shi, M | 1 |
| Yang, Z | 1 |
| Kwok, KY | 1 |
| Lim, R | 1 |
| Pietilä, S | 1 |
| Zhu, Y | 1 |
| Choy, KW | 1 |
| Yao, B | 1 |
| Lin, L | 1 |
| Street, RC | 1 |
| Zalewski, ZA | 1 |
| Galloway, JN | 1 |
| Wu, H | 1 |
| Nelson, DL | 2 |
| Jin, P | 1 |
| Lombroso, PJ | 1 |
| Ogren, MP | 1 |
| Rochette, PJ | 1 |
| Lacoste, S | 1 |
| Therrien, JP | 1 |
| Bastien, N | 1 |
| Brash, DE | 1 |
| Drouin, R | 1 |
| Stöger, R | 2 |
| Genereux, DP | 1 |
| Hagerman, RJ | 1 |
| Hagerman, PJ | 2 |
| Tassone, F | 2 |
| Laird, CD | 2 |
| Chandler, SP | 1 |
| Kansagra, P | 1 |
| Hirst, MC | 1 |
| Arocena, DG | 1 |
| Iwahashi, CK | 1 |
| Won, N | 1 |
| Beilina, A | 1 |
| Ludwig, AL | 1 |
| Schwartz, PH | 1 |
| Snow, K | 1 |
| Doud, LK | 1 |
| Hagerman, R | 1 |
| Pergolizzi, RG | 1 |
| Erster, SH | 1 |
| Thibodeau, SN | 1 |
| Hornstra, IK | 1 |
| Warren, ST | 1 |
| Yang, TP | 1 |
| Kajimura, TM | 1 |
| Brown, WT | 1 |
| Jara, L | 1 |
| Aspillaga, M | 1 |
| Avendaño, I | 1 |
| Obreque, V | 1 |
| Blanco, R | 1 |
| Valenzuela, CY | 1 |
| Oostra, BA | 1 |
| Hoogeveen, AT | 1 |
| Meyer, GA | 1 |
| Blum, NJ | 1 |
| Hitchcock, W | 1 |
| Fortina, P | 1 |
| Mariappan, SV | 1 |
| Silks, LA | 1 |
| Bradbury, EM | 1 |
| Gupta, G | 1 |
| Romero, RM | 1 |
| Rojsitthisak, P | 1 |
| Haworth, IS | 1 |
| Camerino, G | 1 |
| Goodfellow, P | 1 |
2 reviews available for cytosine and Fra(X) Syndrome
| Article | Year |
|---|---|
Animal model for fragile X syndrome.
Topics: Animals; Carrier Proteins; Codon; Cytosine; Disease Models, Animal; Fragile X Mental Retardation Pro | 1997 |
A fragile understanding.
Topics: 5-Methylcytosine; Brain; Cytosine; Female; Fetal Diseases; Fragile X Syndrome; Gene Expression Regul | 1991 |
15 other studies available for cytosine and Fra(X) Syndrome
| Article | Year |
|---|---|
FMRP promotes transcription-coupled homologous recombination via facilitating TET1-mediated m5C RNA modification demethylation.
Topics: Cytosine; Demethylation; Fragile X Mental Retardation Protein; Fragile X Syndrome; Homologous Recomb | 2022 |
A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene.
Topics: Blotting, Southern; Cytosine; Female; Fragile X Mental Retardation Protein; Fragile X Syndrome; Gene | 2019 |
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 | 2014 |
Fragile X syndrome: keys to the molecular genetics of synaptic plasticity.
Topics: Amino Acid Sequence; Child; Cytosine; Exons; Female; Fragile X Mental Retardation Protein; Fragile X | 2008 |
Influence of cytosine methylation on ultraviolet-induced cyclobutane pyrimidine dimer formation in genomic DNA.
Topics: Base Sequence; Cells, Cultured; Chromosomes, Human, X; Cytosine; DNA Damage; DNA Methylation; DNA Pr | 2009 |
Testing the FMR1 promoter for mosaicism in DNA methylation among CpG sites, strands, and cells in FMR1-expressing males with fragile X syndrome.
Topics: Alleles; Base Sequence; Case-Control Studies; CpG Islands; Cytosine; DNA; DNA Methylation; Female; F | 2011 |
Fragile X (CGG)n repeats induce a transcriptional repression in cis upon a linked promoter: evidence for a chromatin mediated effect.
Topics: Animals; Chromatin; Cytosine; Disease Models, Animal; Enzyme Inhibitors; Fragile X Syndrome; Gene Ex | 2003 |
Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells.
Topics: 5' Untranslated Regions; alpha-Crystallin B Chain; Apoptosis; Cell Nucleus; Cells, Cultured; Cytosin | 2005 |
Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.
Topics: Blotting, Southern; Cytosine; DNA; Evaluation Studies as Topic; Female; Fragile X Mental Retardation | 1993 |
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; | 1993 |
Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1.
Topics: Alleles; Base Sequence; Chromosome Aberrations; Cloning, Molecular; CpG Islands; Cytosine; DNA; DNA | 1997 |
Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population.
Topics: Alleles; Chile; Cytosine; Fragile X Mental Retardation Protein; Fragile X Syndrome; Genetic Markers; | 1998 |
Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder.
Topics: Autistic Disorder; Blotting, Southern; Child; Child, Preschool; Cohort Studies; Confidence Intervals | 1998 |
Fragile X DNA triplet repeats, (GCC)n, form hairpins with single hydrogen-bonded cytosine.cytosine mispairs at the CpG sites: isotope-edited nuclear magnetic resonance spectroscopy on (GCC)n with selective 15N4-labeled cytosine bases.
Topics: 5' Untranslated Regions; Base Pair Mismatch; Cytosine; DNA; Fragile X Mental Retardation Protein; Fr | 1998 |
DNA interstrand crosslink formation by mechlorethamine at a cytosine-cytosine mismatch pair: kinetics and sequence dependence.
Topics: Alkylating Agents; Base Composition; Base Pair Mismatch; Base Pairing; Base Sequence; Computer Simul | 2001 |