isomethyleugenol has been researched along with Chromosomal Fragility in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (29.41) | 18.7374 |
| 1990's | 12 (70.59) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Howard-Peebles, PN; Krumdieck, CL | 1 |
| Baker, E; Jones, C; Langdon, WY; Mattina, T; Penny, L; Richards, RI; Sutherland, GR; Tunnacliffe, A; Voullaire, L; Yu, S | 1 |
| Fan, Y; Fu, SD; Shen, Y | 1 |
| Willems, PJ | 1 |
| Nelson, DL; Oostra, BA; Parrish, JE; Reynolds, J; Richards, CS; Shaffer, LG; Spikes, AS; Verkerk, AJ | 1 |
| Bobrow, M; Cross, GS; Davies, KE; Grewal, PK; Hirst, MC; Knight, SJ; Ritchie, RJ | 1 |
| Carter, M; Ding, X; Dobkin, CS; Genovese, M; Henderson, J; Houck, GE; Jenkins, EC; Li, SY; Morys, I; Stark-Houck, SL | 1 |
| Fernandes, JG; Mingroni-Netto, RC; Vianna-Morgante, AM | 1 |
| Gahmberg, N; Peippo, M; Salo, A; Salonen, R; von Koskull, H | 1 |
| Callen, DF; Doggett, NA; Eyre, H; Holman, K; Kremer, E; Le Paslier, D; Nancarrow, JK; Richards, RI; Sutherland, GR | 1 |
| Carrasco, M; de Diego, Y; Hmadcha, A; Lucas, M; Pintado, E; Sierra, J | 1 |
| Briscioli, V; Cogliati, F; Lalatta, F; Larizza, L; Macchi, M; Russo, S | 1 |
| Secker-Walker, LM; Yamada, T | 1 |
| Berger, C; Coyle-Morris, J; Gemmill, RM; Glover, TW; Pearce-Birge, L | 1 |
| Abruzzo, MA; Jacobs, PA; Mayer, M | 1 |
| Neri, G; Zollino, M | 1 |
| Burgoyne, PS; Hunt, PA | 1 |
17 other study(ies) available for isomethyleugenol and Chromosomal Fragility
| Article | Year |
|---|---|
On the nature of folic-acid-sensitive fragile sites in human chromosomes: an hypothesis.
Topics: Base Composition; Chromatin; Chromosome Fragile Sites; Chromosome Fragility; Chromosomes, Human; DNA; Folic Acid; Humans; Methylation; Models, Biological; Nucleoproteins; Thymine; Uracil | 1983 |
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2.
Topics: Base Sequence; Blotting, Southern; Chromosome Deletion; Chromosome Fragile Sites; Chromosome Fragility; Chromosomes, Human, Pair 11; Female; Humans; Male; Methylation; Molecular Sequence Data; Pedigree; Proto-Oncogene Mas; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-cbl; Repetitive Sequences, Nucleic Acid; Restriction Mapping; Syndrome; Ubiquitin-Protein Ligases | 1995 |
[Unstable DNA sequence and methylation in fragile X syndrome].
Topics: Base Sequence; Chromosome Fragility; DNA; Female; Fragile X Syndrome; Humans; Male; Methylation; Molecular Sequence Data; Repetitive Sequences, Nucleic Acid; Sequence Analysis, DNA | 1994 |
Dynamic mutations hit double figures.
Topics: Chromosome Fragility; Chromosome Mapping; Chromosomes, Human, Pair 14; Female; Fragile X Mental Retardation Protein; Fragile X Syndrome; Gene Expression Regulation; Genetic Diseases, Inborn; Humans; Machado-Joseph Disease; Male; Methylation; Minisatellite Repeats; Mutation; Nerve Tissue Proteins; RNA-Binding Proteins; X Chromosome | 1994 |
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.
Topics: Alleles; Animals; Base Sequence; Chromosome Fragile Sites; Chromosome Fragility; Cricetinae; Female; Fragile X Syndrome; Genetic Markers; Humans; Male; Methylation; Mice; Minisatellite Repeats; Molecular Sequence Data; Pedigree; X Chromosome | 1994 |
The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.
Topics: Base Sequence; Case-Control Studies; Chromosome Fragile Sites; Chromosome Fragility; Cloning, Molecular; Female; Fragile X Syndrome; Humans; Male; Methylation; Molecular Sequence Data; Oligodeoxyribonucleotides; Repetitive Sequences, Nucleic Acid; Restriction Mapping; X Chromosome | 1994 |
Fragile X induction systems in CVS cultures: effect on cytogenetic, PCR, and genomic Southern Blot DNA analyses of the FMR-1 gene.
Topics: Blotting, Southern; Cells, Cultured; Chorionic Villi; Chorionic Villi Sampling; Chromosome Banding; Chromosome Fragility; Culture Techniques; Dinucleoside Phosphates; DNA; DNA Probes; False Negative Reactions; Female; Fetus; Floxuridine; Fragile X Syndrome; Gene Expression Regulation; Gene Frequency; Humans; Male; Methylation; Mutation; Polymerase Chain Reaction; Predictive Value of Tests; Pregnancy; Repetitive Sequences, Nucleic Acid; Thymidine; X Chromosome | 1994 |
Relationship of expansion of CGG repeats and X-inactivation with expression of fra(X)(q27.3) in heterozygotes.
Topics: Chromosome Fragile Sites; Chromosome Fragility; Dinucleoside Phosphates; DNA; DNA Probes; Dosage Compensation, Genetic; Female; Fragile X Syndrome; Gene Dosage; Gene Expression; Heterozygote; Humans; Methylation; Phenotype; Repetitive Sequences, Nucleic Acid; Statistics, Nonparametric | 1994 |
FRAXA locus in fragile X diagnosis: family studies, prenatal diagnosis, and diagnosis of sporadic cases of mental retardation.
Topics: Amniocentesis; Chorionic Villi Sampling; Chromosome Fragility; Diagnosis, Differential; Dinucleoside Phosphates; DNA Mutational Analysis; DNA Probes; Female; Fragile X Syndrome; Genetic Carrier Screening; Humans; Intellectual Disability; Male; Methylation; Mosaicism; Predictive Value of Tests; Prenatal Diagnosis; X Chromosome | 1994 |
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.
Topics: Alleles; Base Sequence; Chromosome Fragile Sites; Chromosome Fragility; Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 16; Dinucleoside Phosphates; Female; Fragile X Syndrome; Humans; Male; Methylation; Molecular Sequence Data; Pedigree; Polymerase Chain Reaction; Repetitive Sequences, Nucleic Acid | 1994 |
Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigree.
Topics: Alleles; Chromosome Fragility; DNA Mutational Analysis; Female; Fragile X Mental Retardation Protein; Fragile X Syndrome; Humans; Male; Methylation; Minisatellite Repeats; Nerve Tissue Proteins; Pedigree; Phenotype; Polymerase Chain Reaction; RNA-Binding Proteins; Trinucleotide Repeats; X Chromosome | 1995 |
An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutation.
Topics: Chromosome Fragility; Cytogenetics; DNA; Female; Fragile X Mental Retardation Protein; Fragile X Syndrome; Heterozygote; Humans; Intelligence; Intelligence Tests; Male; Methylation; Mutation; Nerve Tissue Proteins; Neuropsychological Tests; Nuclear Family; Pedigree; RNA-Binding Proteins; Sex Factors; Trinucleotide Repeat Expansion; X Chromosome | 1998 |
Possible evidence for acquired genetic activity at both chromosomal breakpoints of the Philadelphia translocation in chronic myeloid leukemia.
Topics: Bone Marrow; Chromatin; Chromosome Fragility; Chromosomes, Human, Pair 22; Chromosomes, Human, Pair 9; Chronic Disease; Deoxyribonuclease I; Gene Expression; Humans; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Male; Metaphase; Methylation; Middle Aged; Oncogenes; Philadelphia Chromosome; Translocation, Genetic | 1990 |
DNA demethylation induced by 5-azacytidine does not affect fragile X expression.
Topics: Azacitidine; Cell Line; Chromosome Fragility; DNA; DNA Restriction Enzymes; Fragile X Syndrome; Gene Expression Regulation; Genetic Markers; Humans; Lymphocytes; Male; Methylation; X Chromosome | 1986 |
The effect of methionine and 5-azacytidine on fragile X expression.
Topics: Azacitidine; Cells, Cultured; Chromosome Fragile Sites; Chromosome Fragility; Culture Media; DNA; Dose-Response Relationship, Drug; Female; Humans; Lymphocytes; Male; Methionine; Methylation; X Chromosome | 1985 |
Protective effect of S-adenosylmethionine against the induction of chromosome fragile sites.
Topics: Caffeine; Chromosome Fragile Sites; Chromosome Fragility; DNA Damage; Floxuridine; Humans; Lymphocytes; Methylation; S-Adenosylmethionine | 1987 |
A tissue-specific fragile site associated with the sex reversed (Sxr) mutation in the mouse.
Topics: Animals; Chromosome Fragile Sites; Chromosome Fragility; Disorders of Sex Development; DNA; Female; Genetic Markers; Male; Methylation; Mice; Mice, Mutant Strains; Mutation; Pregnancy; Tissue Distribution; X Chromosome; Y Chromosome | 1987 |