isomethyleugenol has been researched along with Abnormalities, Congenital in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (16.67) | 18.2507 |
| 2000's | 1 (16.67) | 29.6817 |
| 2010's | 2 (33.33) | 24.3611 |
| 2020's | 2 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Afenjar, A; Banka, S; Barish, S; Bellen, HJ; Blyth, M; Choufani, S; Costain, G; Cytrynbaum, C; Deshwar, AR; Haldeman-Englert, C; Hayes, I; Haynes, D; Huang, Y; Jobling, R; Kanca, O; Keren, B; Le Quesne Stabej, P; Mao, X; Mignot, C; Nil, Z; Prescott, T; Robin-Renaldo, F; Shinawi, M; Sisco, K; Tveten, K; Vøllo, A; Wangler, MF; Wegner, DJ; Weksberg, R; Wheeler, PG; Wilson, C; Yamamoto, S; Yap, P; Zhang, X; Zon, J | 1 |
| Elder, K; Ménézo, Y | 1 |
| Janga, SC; Kadumuri, RV | 1 |
| Cohen, T; Erkek, S; Godmann, M; Hallett, M; Kimmins, S; Lafleur, C; Lambrot, R; McGraw, S; Peters, AH; Siklenka, K; Suderman, M; Trasler, J; Xia, J | 1 |
| Paoloni-Giacobino, A | 1 |
| Christensen, B | 1 |
4 review(s) available for isomethyleugenol and Abnormalities, Congenital
| Article | Year |
|---|---|
Epigenetic remodeling of chromatin in human ART: addressing deficiencies in culture media.
Topics: Amino Acids; Blastocyst; Chromatin; Chromatin Assembly and Disassembly; Congenital Abnormalities; Culture Media; DNA Methylation; DNA Repair; Embryo Culture Techniques; Embryonic Development; Endocrine Disruptors; Female; Genomic Imprinting; Glucose; Humans; Infant, Newborn; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Oocytes; Oxidative Stress; Pregnancy; Reproductive Techniques, Assisted; S-Adenosylmethionine | 2020 |
Epitranscriptomic Code and Its Alterations in Human Disease.
Topics: Cardiovascular Diseases; Congenital Abnormalities; Epigenesis, Genetic; High-Throughput Nucleotide Sequencing; Humans; Metabolic Diseases; Methylation; Mitochondrial Diseases; Neoplasms; Nervous System Diseases; Purine Nucleotides; Pyrimidine Nucleotides; RNA; RNA Processing, Post-Transcriptional; Transcriptome | 2018 |
Implications of reproductive technologies for birth and developmental outcomes: imprinting defects and beyond.
Topics: Animals; Congenital Abnormalities; Epigenesis, Genetic; Female; Genetic Diseases, Inborn; Genomic Imprinting; Genomics; Humans; Male; Methylation; Models, Biological; Pregnancy; Pregnancy Outcome; Reproductive Techniques, Assisted | 2006 |
[Folate deficiency, cancer and congenital abnormalities. Is there a connection?].
Topics: Adult; Congenital Abnormalities; DNA; Female; Folic Acid; Folic Acid Deficiency; Hematinics; Humans; Methylation; Neoplasms; Pregnancy | 1996 |
2 other study(ies) available for isomethyleugenol and Abnormalities, Congenital
| Article | Year |
|---|---|
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies.
Topics: Congenital Abnormalities; Developmental Disabilities; Drosophila; Drosophila Proteins; Gain of Function Mutation; Histone-Lysine N-Methyltransferase; Histones; Humans; Lysine; Methylation; Methyltransferases; Neoplasms | 2023 |
Disruption of histone methylation in developing sperm impairs offspring health transgenerationally.
Topics: Animals; Congenital Abnormalities; CpG Islands; DNA Methylation; Epigenesis, Genetic; Female; Gene Expression Regulation, Developmental; Histone Demethylases; Histones; Male; Methylation; Mice; Mice, Transgenic; RNA, Messenger; Spermatogenesis; Spermatozoa | 2015 |