Page last updated: 2024-08-18

isomethyleugenol and 4p Deletion Syndrome

isomethyleugenol has been researched along with 4p Deletion Syndrome in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's2 (40.00)24.3611
2020's2 (40.00)2.80

Authors

AuthorsStudies
Cueto-González, AM; Fernández-Álvarez, P; Lasa-Aranzasti, A; Palafoll, IV; Tizzano, EF; Vendrell Bayona, T1
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, M1
Ikawa, M; Kaneda, Y; Nimura, K; Okabe, M; Schwartz, RJ; Shiratori, H; Ura, K1
Ciccia, A; Elledge, SJ; Hajdu, I; Lewis, SM1
Jelinek, DF; Liu, T; Lou, Z; Pei, H; Wu, X; Yu, K1

Other Studies

5 other study(ies) available for isomethyleugenol and 4p Deletion Syndrome

ArticleYear
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.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2022, Volume: 24, Issue:3

    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.
    Genetics in medicine : official journal of the American College of Medical Genetics, 2021, Volume: 23, Issue:8

    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.
    Nature, 2009, Jul-09, Volume: 460, Issue:7252

    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.
    Proceedings of the National Academy of Sciences of the United States of America, 2011, Aug-09, Volume: 108, Issue:32

    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.
    Journal of immunology (Baltimore, Md. : 1950), 2013, Jan-15, Volume: 190, Issue:2

    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
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