Page last updated: 2024-08-18

isomethyleugenol and Abnormalities, Congenital, Nervous System

isomethyleugenol has been researched along with Abnormalities, Congenital, Nervous System in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Agolini, E; Agrawal, PB; Alders, M; Bruel, AL; Collins, SC; Duncan, AR; Faivre, L; Genetti, CA; Goizet, C; Grant, PE; Guillen Sacoto, MJ; Lelliott, CJ; Maas, SM; Nizon, M; Novelli, A; Philippe, C; Prontera, P; Rodan, L; Santiago-Sim, T; Seman, AR; Shi, J; Sorlin, A; Stoler, J; Trimouille, A; van Dooren, MF; Vancollie, VE; Vitobello, A; Wojcik, MH; Yalcin, B; Yoon, G1
Cui, GS; Jiang, GB; Jiang, LY; Lai, WY; Li, A; Li, W; Liu, X; Sun, BF; Tong, WM; Wang, CX; Wang, HL; Wang, M; Wang, XJ; Xu, K; Yang, Y; Yang, YG; Zhang, XX; Zhou, Q1
Amores-Sánchez, MI; Medina, M; Urdiales, JL1

Reviews

1 review(s) available for isomethyleugenol and Abnormalities, Congenital, Nervous System

ArticleYear
Roles of homocysteine in cell metabolism: old and new functions.
    European journal of biochemistry, 2001, Volume: 268, Issue:14

    Topics: Cardiovascular Diseases; Cell Physiological Phenomena; Female; Homocysteine; Humans; Hyperhomocysteinemia; Methionine; Methylation; Nervous System Malformations; Pregnancy; Pregnancy Complications; RNA, Transfer, Amino Acyl; S-Adenosylmethionine

2001

Other Studies

2 other study(ies) available for isomethyleugenol and Abnormalities, Congenital, Nervous System

ArticleYear
Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects.
    American journal of human genetics, 2020, 12-03, Volume: 107, Issue:6

    Topics: Animals; Brain; Developmental Disabilities; Epigenesis, Genetic; Female; Genetic Variation; Heterozygote; Hippocampus; Histones; Humans; Jumonji Domain-Containing Histone Demethylases; Magnetic Resonance Imaging; Male; Methylation; Mice; Nervous System Malformations; Protein Processing, Post-Translational; Seizures; Signal Transduction

2020
METTL3-mediated m6A modification is required for cerebellar development.
    PLoS biology, 2018, Volume: 16, Issue:6

    Topics: Adenosine; Alternative Splicing; Animals; Apoptosis; Cells, Cultured; Cerebellum; Developmental Disabilities; Gene Expression Regulation; Methylation; Methyltransferases; Mice; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Knockout; Nervous System Malformations; RNA Stability; RNA, Messenger

2018