isomethyleugenol has been researched along with Disomy, Uniparental in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Bourdet, K; Burgevin, M; Coutant, R; Donadille, B; Faivre, L; Lacroix, A; Manouvrier-Hanu, S; Netchine, I; Odent, S; Ollivier, F; Petit, F; Thauvin-Robinet, C; Toutain, A | 1 |
| Bartsch, O; Beyer, V; Damatova, N; Haaf, T; Kohlschmidt, N; Rittner, G; Zechner, U | 1 |
| Arroyo, J; Bernal-Chico, A; Castaño, L; de Nanclares, GP; Fernández-Rebollo, E; Garin, I; Goñi, F; Lecumberri, B; Orduña, R | 1 |
| Arai, Y; Ariga, T; Furukawa, S; Haruta, M; Ichikawa, M; Kajii, T; Kaneko, Y | 1 |
| Bullman, H; Lever, M; Mackay, DJ; Shrubb, V; Temple, IK | 1 |
| Algar, E; Bennetts, B; McGillivray, G; Peters, G; Poon, C; Wilson, M; Wu, ZH | 1 |
6 other study(ies) available for isomethyleugenol and Disomy, Uniparental
| Article | Year |
|---|---|
Executive functioning in adolescents and adults with Silver-Russell syndrome.
Topics: Bayes Theorem; DNA Methylation; Executive Function; Female; Genomic Imprinting; Humans; Methylation; Phenotype; Pregnancy; Silver-Russell Syndrome; Uniparental Disomy | 2023 |
Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotype.
Topics: Abnormalities, Multiple; Adult; Base Sequence; Child; Chromosomes, Human, Pair 14; Epigenesis, Genetic; Female; Genomic Imprinting; Humans; Male; Methylation; Molecular Sequence Data; Mothers; Mutation; Phenotype; Polymorphism, Single Nucleotide; Uniparental Disomy | 2009 |
New mechanisms involved in paternal 20q disomy associated with pseudohypoparathyroidism.
Topics: Adult; Child, Preschool; Chromogranins; Chromosomes, Human, Pair 20; Female; GTP-Binding Protein alpha Subunits, Gs; Humans; Male; Methylation; Microsatellite Repeats; Middle Aged; Polymorphism, Single Nucleotide; Pseudohypoparathyroidism; Uniparental Disomy | 2010 |
Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor.
Topics: Adolescent; Cell Transformation, Neoplastic; Child; Child, Preschool; Chromosome Aberrations; Core Binding Factor Alpha 3 Subunit; DNA Methylation; Epigenesis, Genetic; Female; Genomic Imprinting; Histones; Humans; Infant; Infant, Newborn; Male; Meiosis; Methylation; Mutation; Neoplasms, Germ Cell and Embryonal; Polymorphism, Single Nucleotide; snRNP Core Proteins; Uniparental Disomy | 2013 |
Isolated imprinting mutation of the DLK1/GTL2 locus associated with a clinical presentation of maternal uniparental disomy of chromosome 14.
Topics: Animals; Calcium-Binding Proteins; Child; Chromosomes, Human, Pair 14; DNA Methylation; Drosophila; Genomic Imprinting; Humans; Intercellular Signaling Peptides and Proteins; Male; Membrane Proteins; Methylation; Microsatellite Repeats; Phenotype; Proteins; RNA, Long Noncoding; Uniparental Disomy | 2007 |
The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports.
Topics: Beckwith-Wiedemann Syndrome; Child; Child, Preschool; Female; Genome, Human; Genotype; Humans; Methylation; Microsatellite Repeats; Mosaicism; Phenotype; Polymorphism, Single Nucleotide; Uniparental Disomy | 2008 |