Compounds > isomethyleugenol
Page last updated: 2024-08-18

isomethyleugenol and Anemia, Fanconi

isomethyleugenol has been researched along with Anemia, Fanconi in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (60.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Gao, F; Li, D; Qin, Y; Xu, L; Xu, W; Yang, Y; Yu, X; Zhao, S1
Amarachintha, S; Du, W; Erden, O; Pang, Q; Wilson, A1
Almeida, A; Dutrillaux, B; Jeanpierre, M; Kokalj-Vokac, N; Lefrancois, D; Malfoy, B; Viegas-Pequignot, E1
Arwert, F; de Winter, JP; Gibson, RA; Hoatlin, ME; Ianzano, L; Joenje, H; Mathew, CG; Morgan, NV; Pronk, JC; Savino, M; Savoia, A; van Berkel, CG; Waisfisz, Q1
Dutrillaux, B; Kokalj-Vokac, N; Lefrançois, D; Lemieux, N; Malfoy, B; Saint-Ruf, C; Viegas-Péquignot, E1

Other Studies

5 other study(ies) available for isomethyleugenol and Anemia, Fanconi

ArticleYear
FANCI plays an essential role in spermatogenesis and regulates meiotic histone methylation.
    Cell death & disease, 2021, 08-09, Volume: 12, Issue:8

    Topics: Animals; Apoptosis; Cell Differentiation; Epigenesis, Genetic; Fanconi Anemia; Gene Deletion; Histones; Infertility, Male; Lysine; Male; Meiosis; Methylation; Mice; Organ Specificity; Prophase; Recombination, Genetic; RNA, Messenger; Sex Chromosomes; Spermatogenesis; Spermatogonia; Spermatozoa; Testis

2021
The Fanconi anemia pathway controls oncogenic response in hematopoietic stem and progenitor cells by regulating PRMT5-mediated p53 arginine methylation.
    Oncotarget, 2016, Sep-13, Volume: 7, Issue:37

    Topics: Animals; Antigens, Differentiation; Arginine; Carcinogenesis; Cell Cycle; DNA Damage; Fanconi Anemia; Fanconi Anemia Complementation Group Proteins; Hematopoietic Stem Cells; Humans; Luciferases; Methylation; Mice; Mice, Knockout; Mice, Transgenic; Protein-Arginine N-Methyltransferases; Signal Transduction; Tumor Suppressor Protein p53

2016
Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines.
    Human genetics, 1993, Volume: 91, Issue:6

    Topics: Ataxia Telangiectasia; Blotting, Southern; Cell Line; Chromosome Aberrations; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; DNA, Satellite; Fanconi Anemia; Heterochromatin; Humans; Karyotyping; Methylation

1993
Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.
    Nature genetics, 1999, Volume: 22, Issue:4

    Topics: Alleles; Base Sequence; Cell Cycle Proteins; DNA-Binding Proteins; Dose-Response Relationship, Drug; Fanconi Anemia; Fanconi Anemia Complementation Group A Protein; Fanconi Anemia Complementation Group C Protein; Fanconi Anemia Complementation Group Proteins; Female; Frameshift Mutation; Gene Deletion; Homozygote; Humans; Male; Methylation; Molecular Sequence Data; Mosaicism; Nuclear Proteins; Phenotype; Precipitin Tests; Proteins; Transfection

1999
A t(X;15)(q23;q25) with Xq reactivation in a lymphoblastoid cell line from Fanconi anemia.
    Cytogenetics and cell genetics, 1991, Volume: 57, Issue:1

    Topics: Cell Line; Chromosome Banding; Chromosomes, Human, Pair 15; DNA; Fanconi Anemia; Female; Humans; Hypoxanthine Phosphoribosyltransferase; Karyotyping; Lymphocytes; Male; Methylation; Nucleic Acid Hybridization; Phosphoglycerate Kinase; Sister Chromatid Exchange; Translocation, Genetic; X Chromosome

1991