isomethyleugenol has been researched along with Syndrome in 18 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (22.22) | 18.7374 |
| 1990's | 6 (33.33) | 18.2507 |
| 2000's | 5 (27.78) | 29.6817 |
| 2010's | 1 (5.56) | 24.3611 |
| 2020's | 2 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Al Ojaimi, M; Almannai, M; Banimortada, BJ; El-Hattab, AW; Othman, A; Riedhammer, KM | 1 |
| Bankfalvi, A; Griewank, K; Hadaschik, E; Horn, S; Jansen, P; Kretz, J; Kutzner, H; Livingstone, E; Lutsik, P; Mayakonda, A; Möller, I; Müller, H; Murali, R; Paschen, A; Philip, M; Plass, C; Riedel, A; Rose, C; Schadendorf, D; Schaller, J; Stadtler, N; Sucker, A; Zaremba, A; Zimmer, L | 1 |
| Afenjar, A; Bienvenu, T; Billuart, P; Giurgea, I; Goldenberg, A; Hamroune, J; Lebrun, N; Mietton, L; Saintpierre, B | 1 |
| Fan, G; Fan, Z; Lee, JS; Shi, S; Wang, CY; Wang, S; Yamaza, T; Yu, J | 1 |
| Abdel-Rahman, WM; Butzow, R; Järvelä, I; Kariola, R; Lindroos, A; Moisio, AL; Ollikainen, M; Peltomäki, P; Pöyhönen, M | 1 |
| Bliek, J; Hamel, B; Kroes, H; Letteboer, T; Maas, S; Mannens, M; Salieb-Beugelaar, G; Simon, M; Terhal, P; van den Bogaard, MJ; van der Smagt, J | 1 |
| Azzi, S; Bertrand, AM; Cabrol, S; Carel, JC; Danton, F; Demay, MC; Dufourg, MN; Esteva, B; Gicquel, C; Heinrichs, C; Houang, M; Jacquemont, ML; Le Bouc, Y; Loeuille, GA; Netchine, I; Perin, L; Petriczko, E; Pinto, G; Rossignol, S; Rousseau, A; Steunou, V; Thibaud, N | 1 |
| Fontaine, B; Lyon-Caen, O; Saudubray, JM; Sedel, F | 1 |
| Baker, E; Jones, C; Langdon, WY; Mattina, T; Penny, L; Richards, RI; Sutherland, GR; Tunnacliffe, A; Voullaire, L; Yu, S | 1 |
| Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-Péquignot, E | 1 |
| Mys'ko, GN | 1 |
| Avidano, KM; Driscoll, DJ; Glenn, CC; Nicholls, RD; Waters, MF; Williams, CA; Zori, RT | 1 |
| Call, K; Glaser, T; Heckl-Ostreicher, B; Held, M; Housman, D; Loos, U; Ragg, S; Royer-Pokora, B; Saunders, G; Zabel, B | 1 |
| Kraakman, ME; Lambert, M; Schuurman, RK; van den Elsen, PJ; van Eggermond, MC | 1 |
| Hall, JG | 1 |
| Barker, DF; Ledbetter, DH; Ledbetter, SA; Nakamura, Y; Robinson, TJ; Summers, KM; vanTuinen, P; Wallace, MR; White, R; Wolff, R | 1 |
| Björkhem, I; Blomstrand, R; Boström, B; Kase, BF; Sisfontes, L | 1 |
| Häger, A; Hallgren, P; Hansson, G; Henriksson, KG; Lundblad, A; Svensson, S | 1 |
3 review(s) available for isomethyleugenol and Syndrome
| Article | Year |
|---|---|
Disorders of histone methylation: Molecular basis and clinical syndromes.
Topics: Histone Demethylases; Histone Methyltransferases; Histone-Lysine N-Methyltransferase; Histones; Humans; Lysine; Methylation; Syndrome | 2022 |
Hereditary spastic paraparesis in adults associated with inborn errors of metabolism: a diagnostic approach.
Topics: Age of Onset; Decision Trees; Female; Genetic Diseases, Inborn; Humans; Male; Metabolism, Inborn Errors; Methylation; Motor Neurons; Paraparesis, Spastic; Spinal Cord; Syndrome | 2007 |
Genomic imprinting.
Topics: Animals; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Dosage Compensation, Genetic; Gene Expression Regulation; Humans; Mammals; Methylation; Models, Genetic; Neoplasms; Parents; Phenotype; Ploidies; Syndrome | 1991 |
15 other study(ies) available for isomethyleugenol and Syndrome
| Article | Year |
|---|---|
Genetic and methylation profiles distinguish benign, malignant and spitzoid melanocytic tumors.
Topics: Diagnosis, Differential; DNA Copy Number Variations; Humans; Melanoma; Methylation; Nevus, Epithelioid and Spindle Cell; Paraganglioma; Skin Neoplasms; Syndrome | 2022 |
RNA Sequencing and Pathway Analysis Identify Important Pathways Involved in Hypertrichosis and Intellectual Disability in Patients with Wiedemann-Steiner Syndrome.
Topics: Adolescent; Adult; Child; Female; Fibroblasts; Gene Expression Regulation; Histone-Lysine N-Methyltransferase; Histones; Humans; Hypertrichosis; Intellectual Disability; Loss of Function Mutation; Lysine; Male; Methylation; Middle Aged; Myeloid-Lymphoid Leukemia Protein; Nitric Oxide Synthase Type III; Rare Diseases; Sequence Analysis, RNA; Signal Transduction; Syndrome; Transcription, Genetic; Young Adult | 2018 |
BCOR regulates mesenchymal stem cell function by epigenetic mechanisms.
Topics: Abnormalities, Multiple; Animals; Blotting, Western; Cell Transplantation; Cells, Cultured; Epigenesis, Genetic; Eye Abnormalities; Face; Female; Gene Expression Profiling; Heart Septal Defects, Atrial; Histones; Humans; Mesenchymal Stem Cells; Methylation; Mice; Mice, Nude; Mutation; Osteopontin; Proto-Oncogene Proteins; Repressor Proteins; Reverse Transcriptase Polymerase Chain Reaction; Syndrome; Tooth Abnormalities; Transcription Factor AP-2; Transplantation, Heterologous | 2009 |
Molecular analysis of familial endometrial carcinoma: a manifestation of hereditary nonpolyposis colorectal cancer or a separate syndrome?
Topics: Adaptor Proteins, Signal Transducing; Adult; Aged; Aged, 80 and over; Carrier Proteins; Colorectal Neoplasms, Hereditary Nonpolyposis; DNA-Binding Proteins; Endometrial Neoplasms; Female; Humans; Immunohistochemistry; Loss of Heterozygosity; Methylation; Middle Aged; Mutation, Missense; MutL Protein Homolog 1; MutS Homolog 2 Protein; MutS Homolog 3 Protein; Neoplasm Proteins; Nuclear Proteins; Proto-Oncogene Proteins; Syndrome | 2005 |
Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype.
Topics: Abnormalities, Multiple; Base Sequence; DNA Probes; Female; Humans; Male; Methylation; Phenotype; RNA, Long Noncoding; RNA, Untranslated; Syndrome | 2006 |
11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations.
Topics: Abnormalities, Multiple; Aging; Chromosomes, Human, Pair 7; DNA; Face; Female; Fetal Growth Retardation; Genomic Imprinting; Humans; Infant, Newborn; Infant, Small for Gestational Age; Insulin-Like Growth Factor II; Male; Methylation; Mutation; Phenotype; Syndrome | 2007 |
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 |
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.
Topics: 5-Methylcytosine; Abnormalities, Multiple; Base Sequence; Case-Control Studies; Centromere; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; Cytosine; DNA, Satellite; Face; Female; Heterochromatin; Humans; Immunologic Deficiency Syndromes; Infant; Male; Methylation; Molecular Sequence Data; Syndrome; X Chromosome | 1994 |
[Several indices of the methylation process in schizophrenic patients].
Topics: Adult; Antipsychotic Agents; Automatism; Catechol O-Methyltransferase; Depression; Female; Hallucinations; Humans; Isoproterenol; Male; Methylation; Middle Aged; Niacinamide; Schizophrenia; Schizophrenia, Catatonic; Schizophrenia, Paranoid; Syndrome | 1977 |
A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.
Topics: Blotting, Southern; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 15; DNA; DNA Probes; Female; Humans; Intellectual Disability; Male; Methylation; Movement Disorders; Parents; Prader-Willi Syndrome; Sex Factors; Syndrome | 1992 |
Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare.
Topics: Alleles; Aniridia; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; DNA Probes; DNA, Neoplasm; Electrophoresis, Agar Gel; Genes, Wilms Tumor; Humans; Kidney Neoplasms; Methylation; Restriction Mapping; Syndrome; Urogenital Abnormalities; Wilms Tumor | 1991 |
The MHC class II deficiency syndrome: heterogeneity at the level of the response to 5-azadeoxycytidine.
Topics: Azacitidine; Cell Line, Transformed; Decitabine; DNA; Gene Expression Regulation; Genes, MHC Class II; HLA-D Antigens; Humans; Immunologic Deficiency Syndromes; Lymphocytes; Methylation; Promoter Regions, Genetic; Syndrome; Transcription, Genetic | 1990 |
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.
Topics: Biological Evolution; Blotting, Southern; Brain; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 17; Face; Genes; Humans; Methylation; Restriction Mapping; Syndrome | 1989 |
Simple diagnosis of the Zellweger syndrome by gas-liquid chromatography of dimethylacetals.
Topics: Acetals; Amniotic Fluid; Bile Acids and Salts; Cells, Cultured; Child, Preschool; Chromatography, Gas; Chromatography, High Pressure Liquid; Clinical Laboratory Techniques; Erythrocytes; Fatty Acids, Nonesterified; Female; Fibroblasts; Humans; Infant; Lipid Metabolism, Inborn Errors; Methylation; Pregnancy; Prenatal Diagnosis; Reference Values; Syndrome | 1986 |
Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease).
Topics: Adult; Cardiomyopathies; Chemical Phenomena; Chemistry; Child; Chromatography, Gel; Chromatography, Paper; Electrophoresis; Fucose; Galactose; Glucose; Glucosidases; Glycogen Storage Disease; Humans; Male; Mannose; Methylation; Oligosaccharides; Optical Rotation; Syndrome; Ultrafiltration | 1974 |