Page last updated: 2024-08-18

isomethyleugenol and Craniofacial Abnormalities

isomethyleugenol has been researched along with Craniofacial Abnormalities in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's7 (77.78)24.3611
2020's2 (22.22)2.80

Authors

AuthorsStudies
Artinger, KB; Goyama, S; Kurokawa, M; Menzel, J; Sen, R; Shull, LC1
Bonefas, KM; Collette, KM; Dou, Y; Garay, PM; Iwase, S; Keegan, CE; Porter, RS; Raines, B; Seo, YA; Tronson, NC; Vallianatos, CN; Wu, MC1
Shimura, C; Shinkai, Y; Yamada, A1
Benevento, M; Dubos, A; Feil, R; Habibi, E; Herault, Y; Iacono, G; Kasri, NN; Kleefstra, T; Mandoli, A; Méziane, H; Riet, F; Selloum, M; Stunnenberg, HG; van Bokhoven, H; Zhou, H1
Cai, T; Chen, S; Gao, S; Jiang, Y; Li, H; Li, J; Liu, N; Meng, L; Wu, H; Xiong, J; Zhang, Z; Zhao, Z; Zheng, Y; Zhou, X; Zhu, B1
Ba, W; Benevento, M; Frega, M; Iacono, G; Keller, J; Kleefstra, T; Lewerissa, E; Mancini, R; Nadif Kasri, N; Oudakker, A; Selten, M; Stunnenberg, HG; van Bokhoven, H; Zhou, H1
Higashimoto, K; Ihara, K; Imagawa, E; Matsumoto, N; Matsunaga, S; Miyake, N; Miyatake, S; Mizuguchi, T; Nakashima, M; Nishimura, G; Numakura, C; Okamoto, N; Ryo, A; Saitsu, H; Sakai, Y; Sanefuji, M; Sato, Y; Soejima, H; Takada, Y1
Cambi, F; Haziza, S; Hershkovitz, E; Houtz, R; Magen, S; Magnani, R; Parvari, R1
Billington, CJ; Georgieff, MK; Gopalakrishnan, R; Hodges, JS; Petryk, A; Schmidt, B; Schotta, G; Zhang, L1

Other Studies

9 other study(ies) available for isomethyleugenol and Craniofacial Abnormalities

ArticleYear
The conserved and divergent roles of Prdm3 and Prdm16 in zebrafish and mouse craniofacial development.
    Developmental biology, 2020, 05-15, Volume: 461, Issue:2

    Topics: Animals; Chromatin; Craniofacial Abnormalities; DNA-Binding Proteins; Ear, Middle; Facial Bones; Female; Genes, Lethal; Histone Code; Histone Methyltransferases; Histones; Jaw; Male; MDS1 and EVI1 Complex Locus Protein; Methylation; Mice, Inbred C57BL; Protein Processing, Post-Translational; Skull; Species Specificity; Transcription Factors; Zebrafish; Zebrafish Proteins

2020
Mutually suppressive roles of KMT2A and KDM5C in behaviour, neuronal structure, and histone H3K4 methylation.
    Communications biology, 2020, 06-01, Volume: 3, Issue:1

    Topics: Abnormalities, Multiple; Aggression; Animals; Craniofacial Abnormalities; Dendritic Spines; Disease Models, Animal; Growth Disorders; Histone Demethylases; Histone-Lysine N-Methyltransferase; Histones; Hypertrichosis; Intellectual Disability; Male; Mental Retardation, X-Linked; Methylation; Mice; Myeloid-Lymphoid Leukemia Protein

2020
Biochemical validation of EHMT1 missense mutations in Kleefstra syndrome.
    Journal of human genetics, 2018, Volume: 63, Issue:5

    Topics: Amino Acid Substitution; Animals; Chromosome Deletion; Chromosomes, Human, Pair 9; Craniofacial Abnormalities; Disease Models, Animal; Embryonic Stem Cells; Female; Heart Defects, Congenital; Histocompatibility Antigens; Histone-Lysine N-Methyltransferase; Histones; Humans; Intellectual Disability; Methylation; Mice; Mice, Knockout; Models, Molecular; Mutation, Missense; Protein Binding; Protein Conformation; Protein Multimerization; Structure-Activity Relationship

2018
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome.
    Nucleic acids research, 2018, 06-01, Volume: 46, Issue:10

    Topics: Animals; Animals, Newborn; Cadherins; Chromosome Deletion; Chromosomes, Human, Pair 9; Cognitive Dysfunction; Craniofacial Abnormalities; Disease Models, Animal; Gene Expression Regulation; Heart Defects, Congenital; Hippocampus; Histone-Lysine N-Methyltransferase; Histones; Intellectual Disability; Lysine; Male; Methylation; Mice, Knockout

2018
Recognition of H3K9 methylation by GLP is required for efficient establishment of H3K9 methylation, rapid target gene repression, and mouse viability.
    Genes & development, 2015, Feb-15, Volume: 29, Issue:4

    Topics: Animals; Cell Differentiation; Craniofacial Abnormalities; Embryonic Stem Cells; Female; Fetal Growth Retardation; Gene Expression Regulation, Developmental; Gene Silencing; Histone-Lysine N-Methyltransferase; Histones; Homeodomain Proteins; Male; Methylation; Mice; Mice, Inbred C57BL; Mutation; Nanog Homeobox Protein; Nucleosomes; Octamer Transcription Factor-3; Protein Binding

2015
Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling.
    Neuron, 2016, 07-20, Volume: 91, Issue:2

    Topics: Animals; Brain-Derived Neurotrophic Factor; Chromosome Deletion; Chromosomes, Human, Pair 9; Craniofacial Abnormalities; Heart Defects, Congenital; Hippocampus; Histone-Lysine N-Methyltransferase; Histones; Homeostasis; Intellectual Disability; Methylation; Mice, Transgenic; Neuronal Plasticity; Patch-Clamp Techniques; Synapses

2016
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome.
    Human mutation, 2017, Volume: 38, Issue:6

    Topics: Abnormalities, Multiple; Adult; Child; Child, Preschool; Congenital Hypothyroidism; Craniofacial Abnormalities; Cullin Proteins; DNA-Binding Proteins; Enhancer of Zeste Homolog 2 Protein; Female; Hand Deformities, Congenital; Heterozygote; Histones; Humans; Male; Methylation; Mutation; Neoplasm Proteins; Pedigree; Polycomb Repressive Complex 2; Protein Interaction Maps; Transcription Factors

2017
Human calmodulin methyltransferase: expression, activity on calmodulin, and Hsp90 dependence.
    PloS one, 2012, Volume: 7, Issue:12

    Topics: Amino Acid Sequence; Animals; Base Sequence; Benzoquinones; Calmodulin; Cell Line; Chromosome Deletion; Chromosomes, Human, Pair 21; Craniofacial Abnormalities; Cystinuria; Green Fluorescent Proteins; HSP90 Heat-Shock Proteins; Humans; Intellectual Disability; Lactams, Macrocyclic; Methylation; Methyltransferases; Mice; Mice, Inbred ICR; Mitochondrial Diseases; Molecular Sequence Data; Muscle Hypotonia; Protein Binding; Protein Stability; Protein Structure, Tertiary; Protein Transport; Proteolysis; Recombinant Fusion Proteins; Subcellular Fractions; Transcription, Genetic

2012
Maternal diet supplementation with methyl donors and increased parity affect the incidence of craniofacial defects in the offspring of twisted gastrulation mutant mice.
    The Journal of nutrition, 2013, Volume: 143, Issue:3

    Topics: Animals; Betaine; Choline; Craniofacial Abnormalities; Dietary Supplements; Disease Models, Animal; Face; Female; Folic Acid; Gastrulation; Jaw; Male; Methylation; Mice; Mice, Inbred C57BL; Mice, Knockout; Mutation; Parity; Pregnancy; Proteins; Risk Factors; Vitamin B 12; Vitamin B Complex

2013
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