Compounds > isomethyleugenol
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isomethyleugenol and Autosomal Chromosome Disorders

isomethyleugenol has been researched along with Autosomal Chromosome Disorders in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19901 (10.00)18.7374
1990's8 (80.00)18.2507
2000's0 (0.00)29.6817
2010's1 (10.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Garay, PM; Iwase, S; Wallner, MA1
Anisowicz, A; Gadi, IK; Harrison, JJ; Raffeld, M; Sager, R1
Bickmore, WA; Carothers, AD1
Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-Péquignot, E1
Aurias, A; Fischer, A; Jeanpierre, M; Ledeist, F; Prieur, M; Turleau, C; Viegas-Pequignot, E1
Pourcel, C1
Buiting, K; Dittrich, B; Färber, C; Horsthemke, B1
Greally, JM1
Du Sart, D; Kalitsis, P; Schmidt, M1
Hall, JG1

Reviews

3 review(s) available for isomethyleugenol and Autosomal Chromosome Disorders

ArticleYear
Yin-yang actions of histone methylation regulatory complexes in the brain.
    Epigenomics, 2016, Volume: 8, Issue:12

    Topics: Abnormalities, Multiple; Animals; Brain; Chromosome Disorders; Chromosome Duplication; Circadian Rhythm; Co-Repressor Proteins; Gene Expression; High Mobility Group Proteins; Histone Demethylases; Histone-Lysine N-Methyltransferase; Histones; Humans; Methylation; Myeloid-Lymphoid Leukemia Protein; Nerve Tissue Proteins; Smith-Magenis Syndrome; Trans-Activators; Transcription Factors

2016
Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome.
    Molecular biotechnology, 1999, Volume: 11, Issue:2

    Topics: Beckwith-Wiedemann Syndrome; Chromatin; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Chromosomes, Human, Pair 11; CpG Islands; Genomic Imprinting; Heterochromatin; Humans; Insulin-Like Growth Factor II; Methylation; Models, Genetic; Muscle Proteins; RNA, Long Noncoding; RNA, Untranslated

1999
Genomic imprinting.
    Current opinion in genetics & development, 1991, Volume: 1, Issue:1

    Topics: Animals; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Dosage Compensation, Genetic; Gene Expression Regulation; Humans; Mammals; Methylation; Models, Genetic; Neoplasms; Parents; Phenotype; Ploidies; Syndrome

1991

Other Studies

7 other study(ies) available for isomethyleugenol and Autosomal Chromosome Disorders

ArticleYear
Azacytidine-induced tumorigenesis of CHEF/18 cells: correlated DNA methylation and chromosome changes.
    Proceedings of the National Academy of Sciences of the United States of America, 1983, Volume: 80, Issue:21

    Topics: Adipose Tissue; Animals; Azacitidine; Cell Line; Chromosome Aberrations; Chromosome Disorders; Cricetinae; DNA, Neoplasm; Karyotyping; Methylation; Mice; Mice, Nude; Neoplasms, Experimental; Trisomy

1983
Factors affecting the timing and imprinting of replication on a mammalian chromosome.
    Journal of cell science, 1995, Volume: 108 ( Pt 8)

    Topics: Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosome Mapping; Chromosomes, Human, Pair 11; Cosmids; DNA; DNA Replication; DNA-Binding Proteins; Fathers; Female; Genes, Wilms Tumor; Genomic Imprinting; Humans; In Situ Hybridization, Fluorescence; Insulin-Like Growth Factor II; Kinetics; Male; Methylation; Models, Genetic; Mothers; S Phase; Time Factors; Transcription Factors; WT1 Proteins

1995
Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients.
    Human molecular genetics, 1994, Volume: 3, Issue:12

    Topics: 5-Methylcytosine; Abnormalities, Multiple; Base Sequence; Case-Control Studies; Centromere; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; Cytosine; DNA, Satellite; Face; Female; Heterochromatin; Humans; Immunologic Deficiency Syndromes; Infant; Male; Methylation; Molecular Sequence Data; Syndrome; X Chromosome

1994
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.
    Human molecular genetics, 1993, Volume: 2, Issue:6

    Topics: 5-Methylcytosine; Adult; Centromere; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Cytosine; DNA, Satellite; Embryo, Mammalian; Face; Female; Genetic Markers; Humans; Immunologic Deficiency Syndromes; Infant; Leukocytes; Male; Methylation; Placenta; Polymorphism, Restriction Fragment Length; Pregnancy; Repetitive Sequences, Nucleic Acid; Testis

1993
[Parent imprinting: methylation-epigenetic heredity].
    Pathologie-biologie, 1993, Volume: 41, Issue:8

    Topics: Chromosome Aberrations; Chromosome Disorders; Female; Gene Expression Regulation; Genes; Genetic Diseases, Inborn; Humans; Male; Methylation; Neoplasms

1993
The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion.
    Human molecular genetics, 1999, Volume: 8, Issue:2

    Topics: Angelman Syndrome; Autoantigens; Base Sequence; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 15; DNA; Exons; Gene Expression; Genomic Imprinting; Humans; Methylation; Molecular Sequence Data; Prader-Willi Syndrome; Reverse Transcriptase Polymerase Chain Reaction; Ribonucleoproteins, Small Nuclear; RNA; Sequence Deletion; snRNP Core Proteins; Transcription, Genetic

1999
Noninactivation of a portion of Xq28 in a balanced X-autosome translocation.
    American journal of medical genetics, 1992, Jan-15, Volume: 42, Issue:2

    Topics: Child; Chromosome Aberrations; Chromosome Banding; Chromosome Disorders; Chromosome Mapping; Chromosomes, Human, Pair 9; DNA; Dosage Compensation, Genetic; Female; Humans; Karyotyping; Methylation; Phenotype; Translocation, Genetic; X Chromosome

1992