Compounds > isomethyleugenol
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isomethyleugenol and Infant, Small for Gestational Age

isomethyleugenol has been researched along with Infant, Small for Gestational Age in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's1 (25.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Chen, P; Deng, J; Deng, X; Huang, Y; Lin, X; Liu, H; Xie, L; Xu, A; Yang, J; Zhang, Y1
Kenny, LC; O'Keeffe, GW1
Amor, DJ1
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, N1

Other Studies

4 other study(ies) available for isomethyleugenol and Infant, Small for Gestational Age

ArticleYear
Promoter methylation changes in the placenta involved in the relationship between prenatal depression and small for gestational age.
    BMC pregnancy and childbirth, 2022, Oct-02, Volume: 22, Issue:1

    Topics: Female; Fetal Growth Retardation; Gestational Age; Humans; Infant, Newborn; Infant, Small for Gestational Age; Methylation; Placenta; Pregnancy; Promoter Regions, Genetic; Prospective Studies; Vitamins

2022
Predicting infant neurodevelopmental outcomes using the placenta?
    Trends in molecular medicine, 2014, Volume: 20, Issue:6

    Topics: Autistic Disorder; Child Development; Developmental Disabilities; Female; Humans; Infant; Infant, Small for Gestational Age; Leptin; Methylation; Placenta; Pregnancy

2014
Genomic imprinting, small babies and assisted reproduction.
    European journal of human genetics : EJHG, 2009, Volume: 17, Issue:1

    Topics: Embryo, Mammalian; Female; Fetal Growth Retardation; Genetic Diseases, Inborn; Genomic Imprinting; Humans; Infant; Infant, Newborn; Infant, Small for Gestational Age; Methylation; Placentation; Potassium Channels, Voltage-Gated; Pregnancy; Reproduction; Reproductive Techniques, Assisted

2009
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.
    The Journal of clinical endocrinology and metabolism, 2007, Volume: 92, Issue:8

    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