isomethyleugenol and 4p Deletion Syndrome
isomethyleugenol has been researched along with 4p Deletion Syndrome in 5 studies
Research
Studies (5)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 2 (40.00) | 2.80 |
Authors
Authors | Studies |
---|---|
Cueto-González, AM; Fernández-Álvarez, P; Lasa-Aranzasti, A; Palafoll, IV; Tizzano, EF; Vendrell Bayona, T | 1 |
Andrews, M; Attie-Bitach, T; Bahr, A; Belnap, N; Benoit, V; Blok, LS; de Vries, BBA; Delplancq, G; Faivre, L; Gozani, O; Grotto, S; Joset, P; Lacombe, D; Lang-Muritano, M; Larson, A; Maystadt, I; Mourmans, J; Õunap, K; Petrilli, G; Pfundt, R; Ramsey, K; Rauch, A; Sengupta, D; Shinawi, M; Steindl, K; Sticht, H; Tsatsaris, V; van Ravenswaaij-Arts, CMA; Vitobello, A; Wevers, MR; Wheeler, PG; Wojcik, M; Zanoni, P; Zweier, M | 1 |
Ikawa, M; Kaneda, Y; Nimura, K; Okabe, M; Schwartz, RJ; Shiratori, H; Ura, K | 1 |
Ciccia, A; Elledge, SJ; Hajdu, I; Lewis, SM | 1 |
Jelinek, DF; Liu, T; Lou, Z; Pei, H; Wu, X; Yu, K | 1 |
Other Studies
5 other study(ies) available for isomethyleugenol and 4p Deletion Syndrome
Article | Year |
---|---|
Correspondence on "Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype" by Zanoni et al.
Topics: Histone-Lysine N-Methyltransferase; Humans; Methylation; Mutation, Missense; Phenotype; Wolf-Hirschhorn Syndrome | 2022 |
Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype.
Topics: Female; Histone-Lysine N-Methyltransferase; Humans; Methylation; Mutation, Missense; Phenotype; Pregnancy; Wolf-Hirschhorn Syndrome | 2021 |
A histone H3 lysine 36 trimethyltransferase links Nkx2-5 to Wolf-Hirschhorn syndrome.
Topics: Animals; DNA-Binding Proteins; Gene Expression Regulation; Histone-Lysine N-Methyltransferase; Histones; Homeobox Protein Nkx-2.5; Homeodomain Proteins; Lysine; Methylation; Mice; Mice, Inbred C57BL; Nanog Homeobox Protein; Protein Binding; Repressor Proteins; Transcription Factors; Transcription, Genetic; Wolf-Hirschhorn Syndrome | 2009 |
Wolf-Hirschhorn syndrome candidate 1 is involved in the cellular response to DNA damage.
Topics: Cell Line, Tumor; Checkpoint Kinase 2; DNA Damage; DNA Replication; Enzyme Activation; Gene Silencing; Histone-Lysine N-Methyltransferase; Histones; Humans; Hydroxyurea; Intracellular Signaling Peptides and Proteins; Lysine; Methylation; Phosphorylation; Protein Serine-Threonine Kinases; Protein Transport; Replication Protein A; Repressor Proteins; Stress, Physiological; Tumor Suppressor p53-Binding Protein 1; Wolf-Hirschhorn Syndrome | 2011 |
The histone methyltransferase MMSET regulates class switch recombination.
Topics: Cell Line; Gene Expression Regulation; Genetic Loci; Histone-Lysine N-Methyltransferase; Histones; Humans; Immunoglobulin Class Switching; Immunoglobulin Heavy Chains; Intracellular Signaling Peptides and Proteins; Methylation; Protein Binding; Repressor Proteins; Transcription, Genetic; Tumor Suppressor p53-Binding Protein 1; V(D)J Recombination; Wolf-Hirschhorn Syndrome | 2013 |