Page last updated: 2024-08-18

isomethyleugenol and Abnormalities, Autosome

isomethyleugenol has been researched along with Abnormalities, Autosome in 73 studies

Research

Studies (73)

Timeframe	Studies, this research(%)	All Research%
pre-1990	13 (17.81)	18.7374
1990's	33 (45.21)	18.2507
2000's	17 (23.29)	29.6817
2010's	10 (13.70)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Carmalt, H; Chan, B; Cooper, CL; Karim, RZ; Lee, CS; Mak, C; O'Toole, SA; Putti, TC; Scolyer, RA; Selinger, C; Tan, PH; Tse, GM; Yu, B	1
Cocco, L; Duprez, E; Ford, KG; Maciejewski, JP; Melnick, A; Mufti, G; Nervi, C; Santini, V	1
Ishida, T	1
Suzuki, R	1
Dopp, E; Hartmann, LM; Hippler, J; Hirner, AV; Rabieh, S; Rettenmeier, AW; von Recklinghausen, U	1
Banerjee, S; Myung, K; Sikdar, N; Smith, S; Zhang, H	1
Celec, P; Minárik, G; Szemes, T; Turna, J; Vlková, B	1
Friebe, B; Gill, BS; Jiang, J; Zhang, W	1
Allday, MJ; Paschos, K	1
Groth, A; Jasencakova, Z	1
Altman, JK; Khan, I; Licht, JD	1
Arai, Y; Ariga, T; Furukawa, S; Haruta, M; Ichikawa, M; Kajii, T; Kaneko, Y	1
Akria, L; Arad, A; Aviv, A; Braester, A; Dally, N; Filanovsky, K; Gafter-Gvili, A; Gatt, ME; Hellmann, I; Herishanu, Y; Herzog-Tzarfati, K; Leiba, R; Merkel, D; Mittelman, M; Nagler, A; Nemets, A; Ofran, Y; Ronson, A; Rouvio, O; Silbershatz, I; Tadmor, T; Vidal, L; Yeganeh, S	1
Allen, JW; DeMarini, DM; Doerr, CL; Funasaka, K; Harrington-Brock, K; Kligerman, AD; Kundu, B; Mass, MJ; Poorman-Allen, P; Roop, BC; Tennant, AH; Winkfield, E	1
Afshari, CA; Crawford, YG; Gauthier, ML; Joubel, A; Kozakiewicz, K; Mantei, K; Tlsty, TD	1
Kaina, B	1
Angelucci, E; Attarbaschi, A; Biondi, A; Brady, HJ; Burmeister, T; Delabesse, E; den Boer, ML; Dingermann, T; Eckert, C; Ennas, MG; Greil, J; Griesinger, F; Haas, OA; Jakob, S; Jansen, MW; Kempski, H; Klingebiel, T; Koehl, U; Macintyre, E; Marschalek, R; Meyer, C; Niggli, FK; Nigro, LL; Pieters, R; Schäfer, BW; Schneider, B; Schnittger, S; Schoch, C; Schrappe, M; Stanulla, M; Strehl, S; Szczepański, T; Trka, J; van Dongen, JJ; Zuna, J; Zur Stadt, U	1
Agosti, M; Bonati, MT; Cogliati, F; Dalla Bernardina, B; Ferraiuolo, S; Finelli, P; Larizza, L; Recalcati, MP; Russo, S; Sala, M; Tibiletti, MG	1
Baty, DU; Carey, FA; Judson, H; Leslie, A; Pratt, NR; Steele, RJ; Stewart, A	1
Chen, CY; Chen, YC; Chou, WC; Huang, SY; Ko, BS; Shen, MC; Tang, JL; Tien, HF; Tsay, W; Wang, CH; Wu, SJ; Yao, M; Yeh, YC	1
Sakaguchi, A; Steward, R	1
Bongiorni, S; Pasqualini, B; Prantera, G; Singh, PB; Taranta, M	1
Fujita, H; Harada, K; Hiraoka, S; Horii, J; Kato, J; Sakaguchi, K; Shiratori, Y	1
Fukuhara, K; Hayashi, M; Honda, S; Ikota, N; Matsumura, T; Matsuoka, A; Miyata, N; Nakanishi, I; Okuda, H; Ozawa, T; Saito, S	1
Bezard, E; Brotchie, JM; Fox, SH; Hallett, PJ; Lubin, FD; Nicholas, AP; Ravenscroft, P; Standaert, DG; Sweatt, JD; Vattem, P; Zhou, S	1
Anisowicz, A; Gadi, IK; Harrison, JJ; Raffeld, M; Sager, R	1
Romanov, GA; Vaniushin, BF	1
Nicolson, GL	1
Benson, MC; Coffey, DS	1
Allfrey, VG; Boffa, LC; Gruss, RJ	1
Connell, JR; Medcalf, AS	1
Campos, A; Fernández, JL; Gosálvez, J; Goyanes, V; Pereira, S	1
Bourgeois, CA; Delattre, JY; Dutrillaux, AM; Dutrillaux, B; Kokalj-Vokac, N; Malfoy, B; Poisson, M; Vega, F	1
Bickmore, WA; Carothers, AD	1
Anttila, P; Heiskanen, M; Ihalainen, J; Juvonen, E; Palotie, A; Salo, A	1
Almeida, A; Dutrillaux, B; Jeanpierre, M; Kokalj-Vokac, N; Malfoy, B; Viegas-Péquignot, E	1
Bean, CL; Bradt, CI; Galloway, SM; Greenwood, SK; Hill, RB	1
Gillessen-Kaesbach, G; Gross, S; Horsthemke, B; Kaya-Westerloh, S; Passarge, E	1
Blanquet, V; Bonneau, D; Fischer, A; Herbelin, C; Jeanpierre, M; Miniou, P; Niveleau, A; Sibella, V; Viegas-Péquignot, E	1
Bliek, J; Boavida, M; Coad, N; Feinberg, AP; Hoovers, JM; Little, P; Mannens, M; Redeker, E; Steenman, M; Verjaal, M	1
Feduchi, E; Gallego, MI; Lazo, PA	1
Duan, DS; Gnarra, JR; Herman, JG; Latif, F; Lerman, MI; Linehan, WM; Liu, S; Samid, D; Weng, Y; Zbar, B	1
Bakker, PL; de Graaff, E; de Vries, BB; Deelen, WH; Halley, DJ; Niermeijer, MF; Oostra, BA; van den Ouweland, AM; van Hemel, JO	1
Aurias, A; Fischer, A; Jeanpierre, M; Ledeist, F; Prieur, M; Turleau, C; Viegas-Pequignot, E	1
D'Adamo, F; Diverio, D; Lo Coco, F; Pelicci, PG; Saglio, G	1
Buchhagen, DL; Etkind, P; Qiu, L	1
Pourcel, C	1
Almeida, A; Dutrillaux, B; Jeanpierre, M; Kokalj-Vokac, N; Lefrancois, D; Malfoy, B; Viegas-Pequignot, E	1
Cao, Y; Gu, JR; He, L; Li, D; Wang, NJ	1
Schwab, M	1
Beck, BD; Rudel, R; Slayton, TM	1
Alley, MR; Shapiro, L; Stephens, C; Wright, R; Zweiger, G	1
Butler, MG	1
Dimitrova, A; Gecheff, KI; Mirkova, VN; Stoilov, LM; Uzunova, V	1
Doerr, CL; Harrington-Brock, K; Moore, MM	1
Buiting, K; Dittrich, B; Färber, C; Horsthemke, B	1
Greally, JM	1
Forgacs, E; Minna, JD; Oláh, E; Zöchbauer-Müller, S	1
Chakraborty, S; Nucifora, G; Senyuk, V	1
Kihlman, BA; Sturelid, S	1
Crowther, P; Davidson, S; Radley, J; Woodcock, D	1
Park, JG; Reddy, EP	1
Lutze, LH; Morgan, WF; Phillips, JW; Winegar, RA	1
Du Sart, D; Kalitsis, P; Schmidt, M	1
Hall, JG	1
Dale, S; Du Sart, D; Kalitsis, P; Leversha, M; Schmidt, M; Sheffield, L; Toniolo, D	1
Gardiner, K; Horisberger, M; Korenberg, J; Kraus, J; Patterson, D; Rao, V; Reddy, S; Tantravahi, U	1
Alaoui-Jamali, MA; Castonguay, A; Rossignol, G; Schuller, HM	1
Castro, CE	1
Frost, P; Kendal, WS	1
Roberts, JJ; Sturrock, JE	1
Brogger, A	1
Bhuyan, BK	1

Reviews

16 review(s) available for isomethyleugenol and Abnormalities, Autosome

Article	Year
Recent insights into the molecular pathogenesis of mammary phyllodes tumours. Journal of clinical pathology, 2013, Volume: 66, Issue:6 Topics: Breast Neoplasms; Chromosome Aberrations; Comparative Genomic Hybridization; Female; Humans; Immunohistochemistry; Loss of Heterozygosity; Methylation; Mutation; Phyllodes Tumor; Transcriptome	2013
Epigenetics in focus: pathogenesis of myelodysplastic syndromes and the role of hypomethylating agents. Critical reviews in oncology/hematology, 2013, Volume: 88, Issue:2 Topics: Chromosome Aberrations; DNA Methylation; Epigenesis, Genetic; Epigenomics; Histone Deacetylase Inhibitors; Histones; Humans; Leukemia, Myeloid; Methylation; Myelodysplastic Syndromes	2013
[Chromosomal abnormalities and clonal evolution in multiple myeloma]. [Rinsho ketsueki] The Japanese journal of clinical hematology, 2014, Volume: 55, Issue:10 Topics: B-Lymphocytes; Cell Differentiation; Chromosome Aberrations; Clonal Evolution; Epigenesis, Genetic; Gene Dosage; GTP Phosphohydrolases; Humans; Immunoglobulin Heavy Chains; MAP Kinase Signaling System; Membrane Proteins; Methylation; Monoclonal Gammopathy of Undetermined Significance; Multiple Myeloma; Mutation; Plasma Cells; Proto-Oncogene Proteins; Proto-Oncogene Proteins B-raf; Proto-Oncogene Proteins p21(ras); ras Proteins; Risk Factors	2014
[Future perspectives of research and clinical studies for NK-cell malignancy in Asia]. [Rinsho ketsueki] The Japanese journal of clinical hematology, 2008, Volume: 49, Issue:8 Topics: Antineoplastic Combined Chemotherapy Protocols; Asia; ATP Binding Cassette Transporter, Subfamily B, Member 1; Chromosome Aberrations; DNA-Binding Proteins; Drug Design; Herpesvirus 4, Human; Humans; Killer Cells, Natural; Leukemia; Lymphoma; Methylation; Nuclear Proteins; Point Mutation; Proto-Oncogene Proteins c-kit; Tumor Protein p73; Tumor Suppressor Proteins	2008
Advances in the research of fetal DNA in maternal plasma for noninvasive prenatal diagnostics. Medical science monitor : international medical journal of experimental and clinical research, 2010, Volume: 16, Issue:4 Topics: Alleles; Chromosome Aberrations; DNA; Female; Fetus; Genotype; Humans; Male; Methylation; Nucleic Acids; Polymerase Chain Reaction; Pregnancy; Prenatal Diagnosis; Sequence Analysis, DNA; Sex Determination Analysis; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization	2010
Epigenetic reprogramming of host genes in viral and microbial pathogenesis. Trends in microbiology, 2010, Volume: 18, Issue:10 Topics: Animals; Bacteria; Bacterial Infections; Chromatin; Chromosome Aberrations; DNA Methylation; Epigenesis, Genetic; Gene Regulatory Networks; Gene Silencing; Histones; Humans; Methylation; Virus Diseases; Viruses	2010
Mechanisms and consequences of methylating agent-induced SCEs and chromosomal aberrations: a long road traveled and still a far way to go. Cytogenetic and genome research, 2004, Volume: 104, Issue:1-4 Topics: Alkylating Agents; Animals; Animals, Genetically Modified; Apoptosis; Base Pair Mismatch; Cell Cycle; Cell Transformation, Neoplastic; Chromosome Aberrations; Cricetinae; Cricetulus; DNA; DNA Damage; DNA Repair; DNA Replication; Fibroblasts; Guanine; Guanosine; Humans; Methylation; Mice; Models, Genetic; Mutagens; O(6)-Methylguanine-DNA Methyltransferase; Point Mutation; Recombination, Genetic; Sister Chromatid Exchange	2004
[Methylation of eukaryote DNA. II. Biological significance]. Nauchnye doklady vysshei shkoly. Biologicheskie nauki, 1981, Issue:1 Topics: Animals; Base Sequence; Cell Differentiation; Cell Transformation, Neoplastic; Chemical Phenomena; Chemistry; Chromosome Aberrations; Cricetinae; DNA; DNA (Cytosine-5-)-Methyltransferases; DNA Replication; DNA Restriction Enzymes; DNA-Directed RNA Polymerases; Gene Expression Regulation; Genes, Regulator; Histones; Methylation; Organoids; Transcription, Genetic	1981
Generation of phenotypic diversity and progression in metastatic tumor cells. Cancer metastasis reviews, 1984, Volume: 3, Issue:1 Topics: Animals; Cell Transformation, Neoplastic; Chromosome Aberrations; Clone Cells; DNA; Humans; Methylation; Mutation; Neoplasm Metastasis; Neoplasms; Phenotype	1984
Implications of arsenic genotoxicity for dose response of carcinogenic effects. Regulatory toxicology and pharmacology : RTP, 1996, Volume: 23, Issue:2 Topics: Animals; Arsenic; Carcinogens; Chromosome Aberrations; DNA Damage; DNA Ligases; Dose-Response Relationship, Drug; Humans; Mammals; Methylation; Sister Chromatid Exchange; Ultraviolet Rays	1996
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
Molecular genetic abnormalities in the pathogenesis of human lung cancer. Pathology oncology research : POR, 2001, Volume: 7, Issue:1 Topics: Apoptosis; Carcinoma, Non-Small-Cell Lung; Carcinoma, Small Cell; Chromosome Aberrations; Disease Susceptibility; Genes, Tumor Suppressor; Growth Substances; Humans; Lung Neoplasms; Methylation; Molecular Biology; Neoplasm Proteins; Oncogenes; Promoter Regions, Genetic; Stem Cells; Tobacco Smoke Pollution	2001
Genetic lesions and perturbation of chromatin architecture: a road to cell transformation. Journal of cellular biochemistry, 2001, Volume: 82, Issue:2 Topics: Acetylation; Amino Acid Motifs; Animals; Cell Transformation, Neoplastic; Chromatin; Chromosome Aberrations; CREB-Binding Protein; Dimerization; Gene Expression Regulation; Gene Targeting; Histones; Humans; Leukemia, Promyelocytic, Acute; Macromolecular Substances; Methylation; Mice; Models, Genetic; Multigene Family; Neoplasm Proteins; Nuclear Proteins; Nuclear Receptor Coactivator 2; Nucleosomes; Oncogene Proteins, Fusion; Phosphorylation; Protein Processing, Post-Translational; Receptors, Retinoic Acid; Trans-Activators; Transcription Factors; Transcription, Genetic; Translocation, Genetic	2001
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
Nutrient effects on DNA and chromatin structure. Annual review of nutrition, 1987, Volume: 7 Topics: Animals; Cell Nucleus; Chromatin; Chromosomal Proteins, Non-Histone; Chromosome Aberrations; DNA; Gene Expression Regulation; Histones; Humans; Interphase; Metaphase; Methylation; Nutritional Physiological Phenomena	1987
Genetic instability and tumor progression. Pathology and immunopathology research, 1986, Volume: 5, Issue:6 Topics: Aneuploidy; Animals; Chromosome Aberrations; Clone Cells; DNA, Neoplasm; Gene Expression Regulation; Humans; Methylation; Models, Biological; Mutation; Neoplasm Invasiveness; Neoplasm Metastasis; Neoplasms; Neoplasms, Experimental; Oncogenes; Precancerous Conditions	1986

Other Studies

57 other study(ies) available for isomethyleugenol and Abnormalities, Autosome

Article	Year
Methylated bismuth, but not bismuth citrate or bismuth glutathione, induces cyto- and genotoxic effects in human cells in vitro. Chemical research in toxicology, 2008, Volume: 21, Issue:6 Topics: Bismuth; Cell Survival; Cells, Cultured; Chromatography, Gas; Chromosome Aberrations; Citrates; Cytotoxins; DNA Damage; Erythrocytes; Glutathione; Hepatocytes; Humans; Lymphocytes; Methylation; Molecular Structure; Mutagens; Reactive Oxygen Species; Sister Chromatid Exchange	2008
Spt2p defines a new transcription-dependent gross chromosomal rearrangement pathway. PLoS genetics, 2008, Volume: 4, Issue:12 Topics: Cell Cycle; Chromosomal Proteins, Non-Histone; Chromosome Aberrations; Chromosomes, Fungal; DNA-Binding Proteins; Gene Expression; Histones; Methylation; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Transcription, Genetic	2008
Centromere inactivation and epigenetic modifications of a plant chromosome with three functional centromeres. Chromosoma, 2010, Volume: 119, Issue:5 Topics: Centromere; Chromatin; Chromosome Aberrations; Chromosomes, Plant; Epigenesis, Genetic; Gene Silencing; Histones; In Situ Hybridization, Fluorescence; Meiosis; Methylation; Triticum	2010
Replication stress, a source of epigenetic aberrations in cancer? BioEssays : news and reviews in molecular, cellular and developmental biology, 2010, Volume: 32, Issue:10 Topics: Chromatin; Chromosome Aberrations; DNA Replication; Epigenesis, Genetic; Epigenomics; Histones; Methylation; Neoplasms; Nuclear Proteins	2010
New strategies in acute myeloid leukemia: redefining prognostic markers to guide therapy. Clinical cancer research : an official journal of the American Association for Cancer Research, 2012, Oct-01, Volume: 18, Issue:19 Topics: Apoptosis; Chromosome Aberrations; fms-Like Tyrosine Kinase 3; Gene Expression Regulation, Neoplastic; Histone Deacetylase Inhibitors; Humans; Leukemia, Myeloid, Acute; Methylation; Mutation; Pathology, Molecular; Prognosis; Signal Transduction	2012
Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor. Genes, chromosomes & cancer, 2013, Volume: 52, Issue:3 Topics: Adolescent; Cell Transformation, Neoplastic; Child; Child, Preschool; Chromosome Aberrations; Core Binding Factor Alpha 3 Subunit; DNA Methylation; Epigenesis, Genetic; Female; Genomic Imprinting; Histones; Humans; Infant; Infant, Newborn; Male; Meiosis; Methylation; Mutation; Neoplasms, Germ Cell and Embryonal; Polymorphism, Single Nucleotide; snRNP Core Proteins; Uniparental Disomy	2013
Predicting infections in high-risk patients with myelodysplastic syndrome/acute myeloid leukemia treated with azacitidine: a retrospective multicenter study. American journal of hematology, 2013, Volume: 88, Issue:2 Topics: Adult; Aged; Aged, 80 and over; Antimetabolites, Antineoplastic; Azacitidine; Chromosome Aberrations; Disease Susceptibility; Female; Humans; Incidence; Infections; Israel; Leukemia, Myeloid, Acute; Male; Methylation; Middle Aged; Myelodysplastic Syndromes; Neutropenia; Retrospective Studies; Risk Factors; Severity of Illness Index; Thrombocytopenia	2013
Methylated trivalent arsenicals as candidate ultimate genotoxic forms of arsenic: induction of chromosomal mutations but not gene mutations. Environmental and molecular mutagenesis, 2003, Volume: 42, Issue:3 Topics: Arsenicals; Chromosome Aberrations; DNA Damage; Humans; Lymphocytes; Methylation; Mutagens; Mutation; Salmonella	2003
Histologically normal human mammary epithelia with silenced p16(INK4a) overexpress COX-2, promoting a premalignant program. Cancer cell, 2004, Volume: 5, Issue:3 Topics: Apoptosis; Breast; Chromosome Aberrations; Cyclin-Dependent Kinase Inhibitor p16; Cyclooxygenase 2; DNA Damage; Epithelial Cells; Female; Gene Expression Regulation, Neoplastic; Humans; Immunohistochemistry; Isoenzymes; Membrane Proteins; Methylation; Neovascularization, Pathologic; Precancerous Conditions; Prostaglandin-Endoperoxide Synthases; Prostaglandins; Telomerase	2004
The MLL recombinome of acute leukemias. Leukemia, 2006, Volume: 20, Issue:5 Topics: Acute Disease; Adult; Child; Chromosome Aberrations; Chromosome Mapping; DNA; Histone-Lysine N-Methyltransferase; Histones; Humans; Leukemia; Methylation; Myeloid-Lymphoid Leukemia Protein; Oncogene Proteins, Fusion; Translocation, Genetic	2006
Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region. Journal of medical genetics, 2006, Volume: 43, Issue:8 Topics: Beckwith-Wiedemann Syndrome; Child; Chromosome Aberrations; Chromosome Segregation; Chromosomes, Human, Pair 11; Female; Gene Duplication; Genome, Human; Histones; Humans; In Situ Hybridization, Fluorescence; Infant; Infant, Newborn; Male; Membrane Proteins; Methylation; Microsatellite Repeats; Pedigree; Physical Chromosome Mapping; Potassium Channels, Voltage-Gated	2006
Relationship between point gene mutation, chromosomal abnormality, and tumour suppressor gene methylation status in colorectal adenomas. The Journal of pathology, 2006, Volume: 210, Issue:3 Topics: Adaptor Proteins, Signal Transducing; Adenoma; Carrier Proteins; Chromosome Aberrations; Colorectal Neoplasms; DNA Modification Methylases; DNA Repair Enzymes; Genes, APC; Genes, p16; Genes, p53; Genes, Tumor Suppressor; Humans; Methylation; MutL Protein Homolog 1; Neoplasm Proteins; Nuclear Proteins; Nucleic Acid Hybridization; Phenotype; Point Mutation; Promoter Regions, Genetic; Tumor Suppressor Protein p14ARF; Tumor Suppressor Proteins	2006
Clinical implications of SOCS1 methylation in myelodysplastic syndrome. British journal of haematology, 2006, Volume: 135, Issue:3 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Child; Chromosome Aberrations; Disease Progression; Female; Genes, ras; Humans; Karyotyping; Leukemia; Male; Methylation; Middle Aged; Mutation; Myelodysplastic Syndromes; Polymerase Chain Reaction; Prognosis; Risk Factors; Suppressor of Cytokine Signaling 1 Protein; Suppressor of Cytokine Signaling Proteins	2006
Aberrant monomethylation of histone H4 lysine 20 activates the DNA damage checkpoint in Drosophila melanogaster. The Journal of cell biology, 2007, Jan-15, Volume: 176, Issue:2 Topics: Anaphase-Promoting Complex-Cyclosome; Animals; Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome; Brain; Cell Cycle; Cell Cycle Proteins; Checkpoint Kinase 1; Chromosome Aberrations; Cyclin B; DNA Breaks, Double-Stranded; DNA Damage; Down-Regulation; Drosophila melanogaster; Drosophila Proteins; Histone-Lysine N-Methyltransferase; Histones; Lysine; Methylation; Mitosis; Mutation; Neurons; Protein Kinases; Protein Serine-Threonine Kinases; Ubiquitin-Protein Ligase Complexes	2007
Epigenetic regulation of facultative heterochromatinisation in Planococcus citri via the Me(3)K9H3-HP1-Me(3)K20H4 pathway. Journal of cell science, 2007, Mar-15, Volume: 120, Issue:Pt 6 Topics: Animals; Chromosome Aberrations; Embryo, Nonmammalian; Epigenesis, Genetic; Genomic Imprinting; Hemiptera; Heterochromatin; Histones; Insect Proteins; Lysine; Male; Metaphase; Methylation; Nuclear Proteins; RNA, Double-Stranded; Signal Transduction	2007
Genetic and epigenetic alterations of Ras signalling pathway in colorectal neoplasia: analysis based on tumour clinicopathological features. British journal of cancer, 2007, Nov-19, Volume: 97, Issue:10 Topics: Adenoma; Adult; Aged; Aged, 80 and over; Chromosome Aberrations; Colorectal Neoplasms; DNA Mutational Analysis; Female; Genes, ras; Humans; Male; Methylation; Middle Aged; Multivariate Analysis; Mutation; Proteins; Proto-Oncogene Proteins B-raf; Proto-Oncogene Proteins p21(ras); Signal Transduction; Tumor Suppressor Proteins	2007
Effect of methyl substitution on the antioxidative property and genotoxicity of resveratrol. Chemical research in toxicology, 2008, Volume: 21, Issue:2 Topics: Animals; Antioxidants; Cell Line; Chromosome Aberrations; Cricetinae; Cricetulus; Dose-Response Relationship, Drug; Methylation; Mutagens; Resveratrol; Stilbenes; Structure-Activity Relationship	2008
Striatal histone modifications in models of levodopa-induced dyskinesia. Journal of neurochemistry, 2008, Volume: 106, Issue:1 Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Acetylation; Animals; Chromatin; Chromosome Aberrations; Corpus Striatum; Disease Models, Animal; Dopamine Agents; Dyskinesia, Drug-Induced; Extracellular Signal-Regulated MAP Kinases; Female; Histones; Levodopa; Macaca mulatta; Male; Methylation; Mice; Mice, Inbred C57BL; Parkinsonian Disorders; Phosphorylation; Protein Processing, Post-Translational; Species Specificity	2008
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
Prostate cancer research: current concepts and controversies. Seminars in urology, 1983, Volume: 1, Issue:4 Topics: Antibodies, Monoclonal; Chromosome Aberrations; Diethylstilbestrol; DNA; Flow Cytometry; Gonadotropin-Releasing Hormone; Humans; Male; Methylation; Oncogenes; Prostatic Neoplasms	1983
Aberrant and nonrandom methylation of chromosomal DNA-binding proteins of colonic epithelial cells by 1,2-dimethylhydrazine. Cancer research, 1982, Volume: 42, Issue:2 Topics: 1,2-Dimethylhydrazine; Amino Acids; Animals; Carrier Proteins; Cell Fractionation; Cell Nucleus; Chromatin; Chromosomal Proteins, Non-Histone; Chromosome Aberrations; Colon; Dimethylhydrazines; DNA-Binding Proteins; Epithelium; Histones; Male; Methylation; Methylhydrazines; Rats; Templates, Genetic	1982
The induction of SCE and chromosomal aberrations with relation to specific base methylation of DNA in Chinese hamster cells by N-methyl-N-nitrosourea and dimethyl sulphate. Carcinogenesis, 1982, Volume: 3, Issue:4 Topics: Animals; Cells, Cultured; Chromosome Aberrations; Cricetinae; Cricetulus; Crossing Over, Genetic; DNA; Ethylnitrosourea; Methylation; Mutagens; Nitrosourea Compounds; Sister Chromatid Exchange; Sulfuric Acid Esters; Sulfuric Acids	1982
An extra band within the human 9qh+ region that behaves like the surrounding constitutive heterochromatin. Journal of medical genetics, 1994, Volume: 31, Issue:8 Topics: 5-Methylcytosine; Adult; Azacitidine; Chromosome Aberrations; Chromosome Banding; Chromosomes, Human; Chromosomes, Human, Pair 9; Cytosine; Heterochromatin; Humans; In Situ Hybridization, Fluorescence; Lymphocytes; Male; Methylation; Microscopy, Electron	1994
[Characterization of chromosomal rearrangements by in situ hybridization in glioblastoma]. Bulletin du cancer, 1994, Volume: 81, Issue:5 Topics: Azacitidine; Chromosome Aberrations; Chromosome Mapping; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; Chromosomes, Human, Pair 9; DNA, Neoplasm; DNA, Satellite; Glioblastoma; Heterochromatin; Humans; In Situ Hybridization, Fluorescence; Karyotyping; Male; Methylation; Middle Aged; Tumor Cells, Cultured	1994
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
Idiopathic macrocytic anaemia in the aged: molecular and cytogenetic findings. British journal of haematology, 1995, Volume: 90, Issue:4 Topics: Aged; Aged, 80 and over; Anemia, Macrocytic; Calcitonin; Chromosome Aberrations; Chromosomes, Human, Pair 11; DNA; Female; Hematopoietic Stem Cells; Humans; Karyotyping; Male; Methylation; Myelodysplastic Syndromes; Point Mutation	1995
Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin. Cytogenetics and cell genetics, 1993, Volume: 63, Issue:1 Topics: Azacitidine; Cell Transformation, Neoplastic; Cells, Cultured; Chromosome Aberrations; Chromosome Banding; Chromosomes, Human, Pair 1; Chromosomes, Human, Pair 16; DNA; DNA Damage; DNA, Satellite; Heterochromatin; Humans; In Situ Hybridization, Fluorescence; Lymphocytes; Methylation; Nucleic Acid Denaturation	1993
A role for mismatch repair in production of chromosome aberrations by methylating agents in human cells. Mutation research, 1995, Volume: 346, Issue:4 Topics: Alkylating Agents; B-Lymphocytes; Cell Line; Chromosome Aberrations; Dimethylnitrosamine; DNA Repair; Dose-Response Relationship, Drug; Drug Resistance; Erythroid Precursor Cells; Guanine; Humans; Methylation; Methylnitronitrosoguanidine; Methylnitrosourea	1995
DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome. Journal of medical genetics, 1995, Volume: 32, Issue:2 Topics: Adolescent; Adult; Child; Child, Preschool; Chromosome Aberrations; Diagnosis, Differential; DNA; DNA Probes; Female; Genetic Markers; Humans; Infant; Male; Methylation; Muscle Hypotonia; Polymorphism, Restriction Fragment Length; Prader-Willi Syndrome	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
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia. European journal of human genetics : EJHG, 1994, Volume: 2, Issue:1 Topics: Beckwith-Wiedemann Syndrome; Child; Chromosome Aberrations; Chromosome Mapping; Chromosomes, Human, Pair 11; DNA; Female; Gene Expression; Genes, Tumor Suppressor; Humans; In Situ Hybridization, Fluorescence; Insulin; Insulin-Like Growth Factor II; Karyotyping; Male; Methylation; Neoplastic Syndromes, Hereditary; Parents; Pedigree; Polymorphism, Restriction Fragment Length; Sex Factors; Translocation, Genetic; Trisomy; Wilms Tumor	1994
The human zinc-finger protein-7 gene is located 90 kb 3' of MYC and is not expressed in Burkitt lymphoma cell lines. International journal of cancer, 1994, Sep-15, Volume: 58, Issue:6 Topics: Burkitt Lymphoma; Chromosome Aberrations; Chromosomes, Human, Pair 8; DNA, Neoplasm; Gene Amplification; Gene Expression; Genes, myc; Humans; Methylation; Tumor Cells, Cultured; Zinc Fingers	1994
Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma. Proceedings of the National Academy of Sciences of the United States of America, 1994, Oct-11, Volume: 91, Issue:21 Topics: Adenocarcinoma, Clear Cell; Base Sequence; Carcinoma, Renal Cell; Chromosome Aberrations; Dinucleoside Phosphates; DNA Primers; DNA, Neoplasm; Exons; Genes, Tumor Suppressor; Humans; Kidney Neoplasms; Methylation; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Restriction Mapping	1994
DNA diagnosis of the fragile X syndrome in a series of 236 mentally retarded subjects and evidence for a reversal of mutation in the FMR-1 gene. American journal of medical genetics, 1994, Jul-15, Volume: 51, Issue:4 Topics: Blotting, Southern; Child, Preschool; Chromosome Aberrations; Cloning, Molecular; Dinucleoside Phosphates; DNA Mutational Analysis; DNA Probes; Female; Fragile X Syndrome; Gene Dosage; Humans; Intellectual Disability; Male; Methylation; Polymerase Chain Reaction; Repetitive Sequences, Nucleic Acid; Suppression, Genetic	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
Polyclonal hemopoiesis in leukemia patients following molecularly documented remission. Leukemia, 1994, Volume: 8 Suppl 1 Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Chromosome Aberrations; Female; Gene Rearrangement; Hematopoiesis; Humans; Leukemia; Methylation; Middle Aged; X Chromosome	1994
Homozygous deletion, rearrangement and hypermethylation implicate chromosome region 3p14.3-3p21.3 in sporadic breast-cancer development. International journal of cancer, 1994, May-15, Volume: 57, Issue:4 Topics: Breast Neoplasms; Chromosome Aberrations; Chromosome Deletion; Chromosomes, Human, Pair 3; DNA Probes; DNA Restriction Enzymes; DNA, Neoplasm; Female; Fibroadenoma; Gene Amplification; Gene Rearrangement; Genetic Variation; Humans; Methylation; Nucleic Acid Hybridization; Polymerase Chain Reaction	1994
[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
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
Aberrations of p53 gene in human hepatocellular carcinoma from China. Carcinogenesis, 1993, Volume: 14, Issue:2 Topics: Aflatoxin B1; Base Sequence; Blotting, Southern; Carcinoma, Hepatocellular; China; Chromosome Aberrations; DNA, Neoplasm; DNA, Single-Stranded; Environmental Exposure; Genes, p53; Hepatitis B; Humans; Liver Neoplasms; Methylation; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Risk Factors	1993
Genes, chromosomes and cancer. First meeting of the "Arbeitsgemeinschaft Molekular- und Zytogenetik (AEK)" of the Deutsche Krebsgesellschaft. Journal of cancer research and clinical oncology, 1993, Volume: 119, Issue:7 Topics: Animals; Chromosome Aberrations; Humans; Methylation; Neoplasm Metastasis; Neoplasms; Oncogenes; Recombination, Genetic; Virus Integration	1993
Caulobacter Lon protease has a critical role in cell-cycle control of DNA methylation. Genes & development, 1996, Jun-15, Volume: 10, Issue:12 Topics: Amino Acid Sequence; ATP-Dependent Proteases; Base Sequence; Caulobacter crescentus; Cell Cycle; Chromosome Aberrations; DNA Replication; DNA, Bacterial; Gene Expression Regulation, Bacterial; Heat-Shock Proteins; Methylation; Molecular Sequence Data; Mutation; Sequence Homology, Amino Acid; Serine Endopeptidases; Site-Specific DNA-Methyltransferase (Adenine-Specific); Transcription, Genetic	1996
Molecular diagnosis of Prader-Willi syndrome: comparison of cytogenetic and molecular genetic data including parent of origin dependent methylation DNA patterns. American journal of medical genetics, 1996, Jan-11, Volume: 61, Issue:2 Topics: Adolescent; Adult; Blotting, Southern; Child; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, Pair 15; DNA; DNA Probes; Female; Humans; In Situ Hybridization, Fluorescence; Infant; Karyotyping; Male; Methylation; Polymerase Chain Reaction; Prader-Willi Syndrome; Sequence Deletion	1996
Restriction endonucleases induce chromosomal aberrations in barley. Mutagenesis, 1996, Volume: 11, Issue:1 Topics: Base Sequence; Cell Cycle; Chromosome Aberrations; Chromosomes; Deoxyribonuclease HpaII; Deoxyribonucleases, Type II Site-Specific; DNA Damage; DNA Restriction Enzymes; DNA, Plant; Hordeum; Methylation; Mutagens	1996
Relative genotoxic potency of arsenic and its methylated metabolites. Mutation research, 1997, Volume: 386, Issue:3 Topics: Animals; Arsenic; Chromosome Aberrations; Humans; Lymphoma; Methylation; Mice; Poisons; Tumor Cells, Cultured	1997
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
Enhancement by methylated oxypurines of the frequency of induced chromosomal aberrations. Hereditas, 1975, Volume: 79, Issue:1 Topics: Animals; Caffeine; Cell Line; Cells, Cultured; Chromosome Aberrations; Chromosomes; Cricetinae; Drug Synergism; Methylation; Mutation; Plants; Purines; Theobromine; Theophylline; Thiotepa; Uric Acid	1975
Cytotoxicity of 5-aza-2'-deoxycytidine in a mammalian cell system. European journal of cancer (Oxford, England : 1990), 1992, Volume: 28, Issue:2-3 Topics: Animals; Antineoplastic Agents; Azacitidine; Cell Cycle; Cells, Cultured; Chromosome Aberrations; Cricetinae; Cricetulus; Decitabine; DNA; Female; Methylation; Ovary	1992
Large-scale molecular mapping of human c-myb locus: c-myb proto-oncogene is not involved in 6q- abnormalities of lymphoid tumors. Oncogene, 1992, Volume: 7, Issue:8 Topics: Blotting, Southern; Chromosome Aberrations; Chromosomes, Human, Pair 6; Electrophoresis, Gel, Pulsed-Field; Humans; Leukemia-Lymphoma, Adult T-Cell; Leukemia, Myelomonocytic, Acute; Lymphoma, Non-Hodgkin; Methylation; Oncogenes; Proto-Oncogene Mas; Restriction Mapping; Tumor Cells, Cultured	1992
Chromosome aberration induction in Chinese hamster ovary cells by restriction enzymes with different methylation sensitivity. Somatic cell and molecular genetics, 1990, Volume: 16, Issue:3 Topics: Animals; Azacitidine; Cell Line; Chromosome Aberrations; Cricetinae; Cytosine; Decitabine; Deoxyribonuclease HpaII; Deoxyribonucleases, Type II Site-Specific; DNA; Methylation; Substrate Specificity	1990
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
Duplications of the X chromosome in males: evidence that most parts of the X chromosome can be active in two copies. Human genetics, 1991, Volume: 86, Issue:5 Topics: Blotting, Southern; Chromosome Aberrations; Chromosome Banding; DNA; Female; Gene Expression; Humans; Male; Methylation; Multigene Family; Restriction Mapping; X Chromosome	1991
Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions. The EMBO journal, 1990, Volume: 9, Issue:1 Topics: Base Composition; Chromosome Aberrations; Chromosome Mapping; Chromosomes, Human, Pair 21; DNA Probes; Electrophoresis; Humans; Hybrid Cells; Methylation; Nucleic Acid Hybridization; Phenotype; Restriction Mapping	1990
Metabolism and DNA damage induced by 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone in fetal tissues of the Syrian golden hamster. Cancer research, 1989, Oct-15, Volume: 49, Issue:20 Topics: Alkylating Agents; Animals; Chromosome Aberrations; Cricetinae; Culture Techniques; DNA Damage; Female; Fetus; Guanine; Lung; Maternal-Fetal Exchange; Methylation; Nitrosamines; Placenta; Pregnancy; Trachea	1989
Enhancement by caffeine of N-methyl-N-nitrosourea-induced mutations and chromosome aberrations in Chinese hamster cells. Mutation research, 1973, Volume: 20, Issue:2 Topics: Animals; Azaguanine; Caffeine; Cells, Cultured; Chromosome Aberrations; Cricetinae; DNA; Dose-Response Relationship, Drug; Drug Synergism; Female; Mesylates; Methylation; Mutation; Nitrosoguanidines; Nitrosourea Compounds; Ovary; Time Factors	1973
Caffeine-induced enhancement of chromosome damage in human lymphocytes treated with methyl-methanesulphonate, mitomycin C and X-rays. Mutation research, 1974, Volume: 23, Issue:3 Topics: Autoradiography; Binding Sites; Caffeine; Carbon Radioisotopes; Chromatids; Chromosome Aberrations; Chromosomes; DNA; DNA Repair; DNA Replication; Drug Synergism; Humans; In Vitro Techniques; Lymphocytes; Mesylates; Methylation; Mitomycins; Mutagens; Nucleic Acid Hybridization; Radiation Genetics; Tritium	1974
The action of streptozotocin on mammalian cells. Cancer research, 1970, Volume: 30, Issue:7 Topics: Animals; Antibiotics, Antineoplastic; Autoradiography; Cell Division; Chromosome Aberrations; Culture Techniques; Cytogenetics; DNA Nucleotidyltransferases; DNA, Neoplasm; Glucose; Leukemia L1210; Methylation; Mice; Phosphotransferases; RNA, Neoplasm; Thymidine Kinase; Transferases; Uracil Nucleotides	1970