Compounds > isomethyleugenol

Page last updated: 2024-08-18

isomethyleugenol and Down Syndrome

isomethyleugenol has been researched along with Down Syndrome in 12 studies

Research

Studies (12)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (8.33)	18.7374
1990's	1 (8.33)	18.2507
2000's	4 (33.33)	29.6817
2010's	6 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Jankun, J; Matthews-Brzozowska, T; Matthews-Kozanecka, M; Skrzypczak-Jankun, E; Wyganowska-Świątkowska, M	1
Antonarakis, SE; Bonilla, X; Borel, C; Chevalier, C; Deutsch, S; Falconnet, E; Farinelli, L; Feki, A; Gagnebin, M; Garieri, M; Gehrig, C; Gonzalez, D; Guigo, R; Guipponi, M; Herault, Y; Hibaoui, Y; Kind, J; Letourneau, A; Migliavacca, E; Popadin, K; Robyr, D; Sailani, MR; Sandstrom, RS; Santoni, FA; Stamatoyannopoulos, JA; Thurman, R; van Steensel, B; Vannier, A	1
de Jonge, R; Helbing, WA; Ottenkamp, J; Steegers, EA; Steegers-Theunissen, RP; van Driel, LM; van Zelst, BD	1
Barbosa-Morais, NL; Conboy, CM; Fisher, EM; Odom, DT; Schmidt, D; Tavaré, S; Tybulewicz, VL; Vanes, L; Wilson, MD	1
de Jonge, R; Helbing, WA; Obermann-Borst, SA; Steegers, EA; Steegers-Theunissen, RP; van Driel, LM; Wildhagen, MF	1
Andria, G; Castegna, A; Iacobazzi, F; Iacobazzi, V; Infantino, V; Scala, I; Spera, I	1
Geisel, J; Gortner, L; Hartmuth, K; Herrmann, W; Nijhout, HF; Obeid, R; Reed, MC; Rohrer, TR	1
Duncan, TM; Nijhout, HF; Reed, MC	1
Kumar, A; Mehta, S; Pandey, LK; Rai, AK; Raman, R; Singh, S	1
Andria, G; D'Angelo, S; D'Aniello, A; De Bonis, ML; Galletti, P; Ingrosso, D; Raimo, M; Scala, I; Sorrentino, A; Zappia, V	1
Hara, J; Inoue, M; Ishihara, S; Kawa-Ha, K; Kurahashi, H; Murayama, N; Okada, S; Tawa, A; Yumura-Yagi, K	1
Candide, C; de Blois, MC; Lejeune, J; Mazière, C; Mazière, JC; Polonovski, J	1

Reviews

1 review(s) available for isomethyleugenol and Down Syndrome

Article	Year
Can EGCG Alleviate Symptoms of Down Syndrome by Altering Proteolytic Activity? International journal of molecular sciences, 2018, Jan-15, Volume: 19, Issue:1 Topics: Animals; Biomarkers; Catechin; Down Syndrome; Humans; Matrix Metalloproteinase Inhibitors; Metalloendopeptidases; Methylation; Proteolysis; Signal Transduction; Tissue Plasminogen Activator	2018

Other Studies

11 other study(ies) available for isomethyleugenol and Down Syndrome

Article	Year
Domains of genome-wide gene expression dysregulation in Down's syndrome. Nature, 2014, Apr-17, Volume: 508, Issue:7496 Topics: Animals; Cells, Cultured; Chromatin; Chromosomes, Human, Pair 21; Chromosomes, Mammalian; DNA Replication Timing; Down Syndrome; Female; Fetus; Fibroblasts; Gene Expression Regulation; Genome; Histones; Humans; Induced Pluripotent Stem Cells; Lysine; Male; Methylation; Mice; Transcriptome; Twins, Monozygotic	2014
Maternal global methylation status and risk of congenital heart diseases. Obstetrics and gynecology, 2008, Volume: 112, Issue:2 Pt 1 Topics: Adult; Biomarkers; Case-Control Studies; Child; Down Syndrome; Female; Heart; Heart Defects, Congenital; Humans; Hyperhomocysteinemia; Infant; Linear Models; Methylation; Pregnancy; Pregnancy Complications; Pregnancy Outcome; Prenatal Exposure Delayed Effects; Risk Factors; S-Adenosylhomocysteine; S-Adenosylmethionine	2008
Species-specific transcription in mice carrying human chromosome 21. Science (New York, N.Y.), 2008, Oct-17, Volume: 322, Issue:5900 Topics: Animals; Base Sequence; Cell Nucleus; Chromatin Assembly and Disassembly; Chromatin Immunoprecipitation; Chromosomes, Human, Pair 21; Disease Models, Animal; Down Syndrome; Gene Expression Regulation; Hepatocyte Nuclear Factors; Hepatocytes; Histones; Humans; Methylation; Mice; Oligonucleotide Array Sequence Analysis; Regulatory Sequences, Nucleic Acid; Species Specificity; Transcription Initiation Site; Transcription, Genetic	2008
Congenital heart defects and biomarkers of methylation in children: a case-control study. European journal of clinical investigation, 2011, Volume: 41, Issue:2 Topics: Biomarkers; Case-Control Studies; Child, Preschool; Down Syndrome; Female; Folic Acid; Heart Defects, Congenital; Humans; Hyperhomocysteinemia; Infant; Male; Methylation; Netherlands; Pregnancy; Prenatal Exposure Delayed Effects; Risk Factors; Vitamin B 12	2011
Impairment of methyl cycle affects mitochondrial methyl availability and glutathione level in Down's syndrome. Molecular genetics and metabolism, 2011, Volume: 102, Issue:3 Topics: Adolescent; Carrier Proteins; Cell Line, Transformed; Child; Child, Preschool; Cytosol; Down Syndrome; Glutathione; Humans; Infant; Methylation; Mitochondria; S-Adenosylmethionine	2011
Blood biomarkers of methylation in Down syndrome and metabolic simulations using a mathematical model. Molecular nutrition & food research, 2012, Volume: 56, Issue:10 Topics: Adolescent; Adult; Betaine; Biomarkers; Case-Control Studies; Child; Child, Preschool; Choline; Cystathionine; Cysteine; Down Syndrome; Female; Glutathione; Humans; Infant; Male; Methionine; Methylation; Models, Theoretical; S-Adenosylhomocysteine; S-Adenosylmethionine; Sarcosine; Young Adult	2012
The relationship between intracellular and plasma levels of folate and metabolites in the methionine cycle: a model. Molecular nutrition & food research, 2013, Volume: 57, Issue:4 Topics: Cystathionine beta-Synthase; Down Syndrome; Folic Acid; Folic Acid Deficiency; Half-Life; Homocysteine; Humans; Methionine; Methylation; Models, Theoretical; Nutrition Surveys; Nutritional Status; Oxidative Stress; S-Adenosylmethionine; Vitamin B 12 Deficiency; Vitamin B Complex; Vitamins	2013
MTHFR C677T and A1298C polymorphisms are risk factors for Down's syndrome in Indian mothers. Journal of human genetics, 2006, Volume: 51, Issue:4 Topics: 5,10-Methylenetetrahydrofolate Reductase (FADH2); Adolescent; Adult; Alleles; Case-Control Studies; Chi-Square Distribution; Confidence Intervals; Down Syndrome; Female; Folic Acid; Gene Frequency; Homozygote; Humans; India; Male; Maternal Age; Methylation; Middle Aged; Nondisjunction, Genetic; Odds Ratio; Pedigree; Polymorphism, Single Nucleotide; Pregnancy; Risk Factors	2006
Accumulation of altered aspartyl residues in erythrocyte proteins from patients with Down's syndrome. The FEBS journal, 2007, Volume: 274, Issue:20 Topics: Case-Control Studies; Child; Down Syndrome; Erythrocyte Aging; Erythrocyte Membrane; Herpesvirus 4, Human; Humans; Isoaspartic Acid; Lymphocytes; Membrane Proteins; Methemoglobin; Methionine; Methylation; Oxidative Stress; Protein D-Aspartate-L-Isoaspartate Methyltransferase; Recombinant Proteins; S-Adenosylhomocysteine	2007
Monoclonal nature of transient abnormal myelopoiesis in Down's syndrome. Blood, 1991, Mar-15, Volume: 77, Issue:6 Topics: Bone Marrow; Cell Differentiation; DNA; Down Syndrome; Female; Genes; Heterozygote; Humans; Hypoxanthine Phosphoribosyltransferase; Infant, Newborn; Infant, Newborn, Diseases; Male; Methylation; Myeloproliferative Disorders; Phosphoglycerate Kinase; Polymorphism, Restriction Fragment Length; Stem Cells; X Chromosome	1991
[Phospholipid methylation in fibroblasts of patients with trisomy 21]. Annales de genetique, 1987, Volume: 30, Issue:4 Topics: Cells, Cultured; Down Syndrome; Fibroblasts; Humans; Methylation; Phospholipids; Skin	1987