isomethyleugenol and Craniofacial Abnormalities
isomethyleugenol has been researched along with Craniofacial Abnormalities in 9 studies
Research
Studies (9)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 7 (77.78) | 24.3611 |
2020's | 2 (22.22) | 2.80 |
Authors
Authors | Studies |
---|---|
Artinger, KB; Goyama, S; Kurokawa, M; Menzel, J; Sen, R; Shull, LC | 1 |
Bonefas, KM; Collette, KM; Dou, Y; Garay, PM; Iwase, S; Keegan, CE; Porter, RS; Raines, B; Seo, YA; Tronson, NC; Vallianatos, CN; Wu, MC | 1 |
Shimura, C; Shinkai, Y; Yamada, A | 1 |
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, H | 1 |
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, B | 1 |
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, H | 1 |
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, Y | 1 |
Cambi, F; Haziza, S; Hershkovitz, E; Houtz, R; Magen, S; Magnani, R; Parvari, R | 1 |
Billington, CJ; Georgieff, MK; Gopalakrishnan, R; Hodges, JS; Petryk, A; Schmidt, B; Schotta, G; Zhang, L | 1 |
Other Studies
9 other study(ies) available for isomethyleugenol and Craniofacial Abnormalities
Article | Year |
---|---|
The conserved and divergent roles of Prdm3 and Prdm16 in zebrafish and mouse craniofacial development.
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.
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.
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.
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.
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.
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.
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.
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.
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 |