Compounds > isomethyleugenol
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isomethyleugenol and Chromosome Deletion

isomethyleugenol has been researched along with Chromosome Deletion in 99 studies

Research

Studies (99)

TimeframeStudies, this research(%)All Research%
pre-199031 (31.31)18.7374
1990's54 (54.55)18.2507
2000's3 (3.03)29.6817
2010's10 (10.10)24.3611
2020's1 (1.01)2.80

Authors

AuthorsStudies
Billia, F; Brown, KR; Burston, HE; Chen, S; Cowen, J; Coyaud, E; Dadson, K; De Carvalho, DD; He, HH; Ishak, C; Kannu, P; Kent, OA; Laurent, EM; Law, N; Matsumoto, Y; Montgomery-Song, A; Raught, B; Rose, J; Rottapel, R; Saha, M; St-Germain, J; Sun, RX1
Shimura, C; Shinkai, Y; Yamada, A1
Bender, B; Bier, G; Brendle, C; Castaneda Vega, S; Ernemann, U; Hempel, JM; Klose, U; Schittenhelm, J; Skardelly, M; Tabatabai, G1
Benevento, M; Dubos, A; Feil, R; Habibi, E; Herault, Y; Iacono, G; Kasri, NN; Kleefstra, T; Mandoli, A; Méziane, H; Riet, F; Selloum, M; Stunnenberg, HG; van Bokhoven, H; Zhou, H1
Cao, Q; Chen, GJ; Cheng, J; Lin, L; Liu, A; Ma, K; Matas, E; Wang, W; Wang, X; Wang, ZJ; Wei, J; Yan, Z; Zhang, F; Zheng, Y1
Chapet, S; Lévy, S; Mazeron, JJ1
Cohen, Y; Golan, H; Haziza, S; Hershkovitz, E; Houtz, RL; Keinan, O; Lan, D; Magnani, R; Nevo, Y; Parvari, R; Saada, A; Sheffield, VC; Yanay, N1
Ba, W; Benevento, M; Frega, M; Iacono, G; Keller, J; Kleefstra, T; Lewerissa, E; Mancini, R; Nadif Kasri, N; Oudakker, A; Selten, M; Stunnenberg, HG; van Bokhoven, H; Zhou, H1
Bauer, T; Berthold, F; Brors, B; Ehrich, M; Eils, R; Fischer, M; Hero, B; König, R; Oberthür, A; Spitz, R; Theissen, J; Westermann, F1
Farina, A; Gurvich, N; Hurwitz, J; Menendez, S; Nimer, SD; Perna, F; Voza, F1
Cambi, F; Haziza, S; Hershkovitz, E; Houtz, R; Magen, S; Magnani, R; Parvari, R1
Bench, AJ; Delabesse, E; Deloukas, P; Fourouclas, N; Green, AR; Hunt, AR; Huntly, BJ; Li, J1
Chan, C; Dent, SY; Hawke, DH; Kobayashi, R; Latham, JA; Lin, W; Riefler, GM; Schumacher, JM; Tatchell, K; Zhang, K1
Dackowski, W; Morrison, SL1
Arya, SK1
Adley, CC; Bukhari, AI1
Collins, FS; Weissman, SM1
Nathans, D; Peden, KW1
Caron, H; Cheng, NC; Delattre, O; Laureys, G; Slater, R; van der Drift, P; Van Roy, N; Versteeg, R; Voûte, PA; Westerveld, A1
Bickmore, WA; Carothers, AD1
Baker, E; Jones, C; Langdon, WY; Mattina, T; Penny, L; Richards, RI; Sutherland, GR; Tunnacliffe, A; Voullaire, L; Yu, S1
Bova, GS; Brooks, JD; Bussemakers, MJ; Ewing, CM; Isaacs, WB; Morton, RA1
Beggs, AH; Black, PM; Busque, L; Dashner, K; Frosch, MP; Gilliland, DG; Zhu, J1
Halley, DJ; Hennekam, RC; Los, FJ; Meijers-Heijboer, HJ; Niermeijer, MF; Tijmensen, TS; van den Ouweland, AM; van der Est, MN; Van Hemel, JO; Wesby-van Swaay, E1
Young, ID1
Dante, R; Frappart, L; Lointier, P; Martin, V; Ribieras, S; Song-Wang, XG1
Cassidy, SB; Erickson, RP; Lai, LW1
Abeliovich, D; Buiting, K; Dittrich, B; Guitart, M; Horsthemke, B; Lerer, I; Robinson, WP1
Buchhagen, DL; Etkind, P; Qiu, L1
Carcangiu, ML; Han, H; Li, S; Resnik, E; Schwartz, PE; Yang-Feng, TL1
Andrews, T; Clayton-Smith, J; Driscoll, DJ; Malcolm, S; Nicholls, RD; Pembrey, ME; Waters, MF; Webb, T1
Bergsagel, PL; Eckhardt, LA; Hines, MD; Kuehl, WM; Lieberman, SA1
Baylin, SB; Brodeur, GM; Cavenee, WK; Chazin, VR; Makos, M; Nelkin, BD1
Artifoni, L; Aviv, H; Baccichetti, C; Bernasconi, F; Franzoni, E; Robinson, WP; Schinzel, AA; Shih, LY; Suslak, L; Wagstaff, J1
Cattanach, BM; Ferguson-Smith, AC; Sasaki, H; Surani, MA1
Nivard, MJ; Vogel, EW; Zijlstra, JA1
Baylin, SB; Brooks, J; Gnarra, JR; Isaacs, W; Linehan, M; Makos, M; Nelkin, BD; Reiter, RE1
Abatecola, M; Cozzi, R; de Capoa, A; Giancotti, P; Grappelli, C; Perticone, P; Poggesi, I1
Lee, NK; Nisen, PD; Waber, PG1
Ahomadegbe, JC; Barrois, M; Coll, J; Douc-Rasy, S; Fogel, S; Riou, G; Stéhelin, D1
Bova, GS; Isaacs, WB; Jarrard, DF1
Brøndum-Nielsen, K; Hansen, C; Ledbeter, DH; Schulze, A; Skakkebaek, NE; Tommerup, N1
Baylin, SB; Herman, JG; Jen, J; Merlo, A1
Barth-Witte, U; Buchholz, B; Duba, HC; Erdel, M; Köchl, S; Schuffenhauer, S; Utermann, B; Utermann, G1
Burke, LW; Driscoll, DJ; Glenn, CC; Kushnick, T; Loud, KM; Smith, AJ; Wiley, JE1
Beitsma, MM; Chan, AJ; Cheng, NC; Speleman, F; Versteeg, R; Westerveld, A1
Chadwick, D; Chitayat, D; Kobayashi, J; Ray, P; Shuman, C; Siegel-Bartelt, J; Strasberg, P; Teshima, I; Weksberg, R1
Beitsma, M; Chan, A; Cheng, NC; Op den Camp, I; Pronk, J; Versteeg, R; Westerveld, A1
Christianson, AL; de la Rey, M; van Rensburg, EJ; Viljoen, DL; Winship, WS1
Baens, M; Corveleyn, A; Hagemeijer, A; Hoornaert, I; Marynen, P; Wlodarska, I1
Croteau, S; Naumova, AK; Polychronakos, C1
De Greve, H; Hernalsteens, JP; Renckens, S; Van Montagu, M1
Goldgaber, D; Quitschke, WW1
Avidano, KM; Driscoll, DJ; Glenn, CC; Nicholls, RD; Waters, MF; Williams, CA; Zori, RT1
Heidmann, I; Linn, F; Meyer, H; Meyer, P; Niedenhof, I; Saedler, H1
Bassing, CH; Chandrasegaran, S; Kim, YG; Li, L1
Marguerie, G; Martin, F; Prandini, MH; Thevenon, D; Uzan, G1
Call, K; Glaser, T; Heckl-Ostreicher, B; Held, M; Housman, D; Loos, U; Ragg, S; Royer-Pokora, B; Saunders, G; Zabel, B1
Kohler, SW; Kretz, PL; Short, JM1
Levy, AA; Walbot, V1
Giese, S; Jemiolo, DK; Taurence, JS1
Goto, H; Ogasawara, N; Yamada, Y1
Howe, CC; Lamb, BT; Li, L; Satyamoorthy, K; Solter, D1
Hall, JG1
Asakura, H; Kamimura, T; Ogata, N1
Crowther, PJ; Doherty, JP; Graham, MW; Linsenmeyer, ME; Williamson, M; Woodcock, DM1
Cogswell, JP; Ting, JP; Vilen, BJ1
Bourbonnière, M; Nalbantoglu, J1
Bianchini, E; degli Uberti, E; del Senno, L; Maestri, I; Piva, R; Rossi, R1
Cox, DW; Hofker, MH; Surti, U; Walter, MA1
Brindle, PK; Holland, JP; Holland, MJ1
Barr, FG; Lieberman, MW; Rajagopalan, S1
Glimcher, LH; Ivashkiv, LB; Kara, CJ; Liou, HC1
Karlsson, S; Nienhuis, AW1
Cotner, T; Dixon, L; Johnson, R; Levine, F; Pious, D1
Anagnou, NP; Karlsson, S; Keller, G; Moulton, AD; Nienhuis, AW; Papayannopoulou, T; Stamatoyannopoulos, G1
Cole, JL; Collins, FS; Iannuzzi, MC; Lockwood, WK1
Feingold, EA; Forget, BG1
Ferluga, J1
Jones, JE; Nebert, DW; Neuhold, LA; Ozato, K; Shirayoshi, Y1
Grafstrom, RH; Learn, BA1
Barker, DF; Ledbetter, DH; Ledbetter, SA; Nakamura, Y; Robinson, TJ; Summers, KM; vanTuinen, P; Wallace, MR; White, R; Wolff, R1
Prat, S; Sánchez-Serrano, JJ; Willmitzer, L1
Arnemann, J; Beato, M; Brüller, HJ; Chalepakis, G; Gross, B; Slater, E1
Reik, W; Surani, MA1
Maniloff, J; Nowak, JA; Sladek, TL1
Derbyshire, KM; Grindley, ND1
Gilman, MZ; Weinberg, RA; Wilson, RN1
Gerbi, SA1
Harris, M; Wise, TL1
Arlett, CF; Burke, JF; Drevon, C; Gebara, MM; Harcourt, SA; James, MR; Lehmann, AR; Steingrimsdottir, H1
Grosschedl, R; Marx, M1
Chambon, P; Kumar, V1
Morisawa, H; Mukai, S; Shibahara, S1
Abou-Zamzam, AM; Demple, B; Shevell, DE; Walker, GC1
Affara, NA; Burmeister, M; Ferguson-Smith, MA; Gillard, EF; Kunkel, LM; Lehrach, H; Monaco, AP; van Ommen, GJ1
Blöcker, H; Frank, R; Kahmann, R; Seiler, A1
Lerner, RA; Levy, DE; Wilson, MC1
Feinberg, AP1

Reviews

9 review(s) available for isomethyleugenol and Chromosome Deletion

ArticleYear
[Management of gliomas].
    Cancer radiotherapie : journal de la Societe francaise de radiotherapie oncologique, 2014, Volume: 18, Issue:5-6

    Topics: Age Factors; Antibodies, Monoclonal, Humanized; Antineoplastic Agents, Alkylating; Antineoplastic Combined Chemotherapy Protocols; Bevacizumab; Brain Neoplasms; Chemoradiotherapy; Chromosome Deletion; Chromosomes, Human, Pair 1; Clinical Trials as Topic; Combined Modality Therapy; Dacarbazine; Dose Fractionation, Radiation; Drug Resistance, Neoplasm; Glioma; Humans; Lomustine; Methylation; Multicenter Studies as Topic; Neoplasm Proteins; Neurosurgical Procedures; O(6)-Methylguanine-DNA Methyltransferase; Procarbazine; Radiotherapy Dosage; Radiotherapy, Intensity-Modulated; Temozolomide; Treatment Outcome; Vincristine

2014
The molecular genetics of human hemoglobin.
    Progress in nucleic acid research and molecular biology, 1984, Volume: 31

    Topics: Biological Evolution; Chromosome Deletion; Codon; Deoxyribonuclease I; Gene Conversion; Gene Expression Regulation; Genes; Genetic Linkage; Globins; Hemoglobins; Humans; Methylation; Mutation; Polymorphism, Genetic; Promoter Regions, Genetic; Protein Biosynthesis; RNA Splicing; RNA, Messenger; Thalassemia; Transcription, Genetic

1984
1p36: every subband a suppressor?
    European journal of cancer (Oxford, England : 1990), 1995, Volume: 31A, Issue:4

    Topics: Antigens, Neoplasm; Chromosome Deletion; Chromosomes, Human, Pair 1; Genes, myc; Genes, Tumor Suppressor; Histocompatibility Antigens Class I; Humans; Methylation; Neuroblastoma; Translocation, Genetic

1995
Molecular biology of prostate cancer progression.
    Cancer surveys, 1995, Volume: 23

    Topics: Cadherins; Chromosome Deletion; DNA; Genes, Retinoblastoma; Humans; Male; Methylation; Oncogenes; Prostatic Neoplasms

1995
DNA methylation, molecular genetic, and linkage studies in prostate cancer.
    The Prostate. Supplement, 1996, Volume: 6

    Topics: Chromosome Deletion; DNA; Genes, Tumor Suppressor; Genetic Linkage; Humans; Male; Methylation; Prostatic Neoplasms

1996
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
Developmental regulation of human globin genes.
    Annual review of biochemistry, 1985, Volume: 54

    Topics: Azacitidine; Chromatin; Chromosome Deletion; Chromosomes, Human, 16-18; Chromosomes, Human, 6-12 and X; Enhancer Elements, Genetic; Fetal Hemoglobin; Gene Expression Regulation; Genes; Globins; Hemoglobins; Humans; Methylation; Mutation; Poly A; Promoter Regions, Genetic; Protein Biosynthesis; Repetitive Sequences, Nucleic Acid; RNA Caps; RNA Processing, Post-Transcriptional; RNA, Messenger; Thalassemia; Transcription Factors

1985
Cis-acting sequences that affect the expression of the human fetal gamma-globin genes.
    Progress in clinical and biological research, 1985, Volume: 191

    Topics: Base Sequence; Chromosome Deletion; Cloning, Molecular; DNA Restriction Enzymes; Endonucleases; Female; Fetal Hemoglobin; Gene Expression Regulation; HeLa Cells; Humans; Male; Methylation; Mutation; Operon; Pedigree; Single-Strand Specific DNA and RNA Endonucleases

1985
Replicative and conservative transposition in bacteria.
    Cell, 1986, Nov-07, Volume: 47, Issue:3

    Topics: Bacteriophage mu; Chromosome Deletion; DNA Replication; DNA Transposable Elements; DNA, Bacterial; DNA, Viral; Methylation

1986

Other Studies

90 other study(ies) available for isomethyleugenol and Chromosome Deletion

ArticleYear
Haploinsufficiency of RREB1 causes a Noonan-like RASopathy via epigenetic reprogramming of RAS-MAPK pathway genes.
    Nature communications, 2020, 09-16, Volume: 11, Issue:1

    Topics: Abnormalities, Multiple; Animals; Chromosome Deletion; Chromosomes, Human, Pair 6; DNA-Binding Proteins; Epigenesis, Genetic; Female; Fibroblast Growth Factors; Haploinsufficiency; Histone Demethylases; Histones; Humans; Male; MAP Kinase Signaling System; Methylation; Mice, Inbred C57BL; Mice, Knockout; Noonan Syndrome; ras Proteins; Sin3 Histone Deacetylase and Corepressor Complex; Transcription Factors

2020
Biochemical validation of EHMT1 missense mutations in Kleefstra syndrome.
    Journal of human genetics, 2018, Volume: 63, Issue:5

    Topics: Amino Acid Substitution; Animals; Chromosome Deletion; Chromosomes, Human, Pair 9; Craniofacial Abnormalities; Disease Models, Animal; Embryonic Stem Cells; Female; Heart Defects, Congenital; Histocompatibility Antigens; Histone-Lysine N-Methyltransferase; Histones; Humans; Intellectual Disability; Methylation; Mice; Mice, Knockout; Models, Molecular; Mutation, Missense; Protein Binding; Protein Conformation; Protein Multimerization; Structure-Activity Relationship

2018
In Vivo Molecular Profiling of Human Glioma : Cross-Sectional Observational Study Using Dynamic Susceptibility Contrast Magnetic Resonance Perfusion Imaging.
    Clinical neuroradiology, 2019, Volume: 29, Issue:3

    Topics: Adult; Aged; Aged, 80 and over; Algorithms; Brain Neoplasms; Cerebral Blood Volume; Chromosome Deletion; Chromosomes, Human, 1-3; Contrast Media; Cross-Sectional Studies; DNA Modification Methylases; DNA Repair Enzymes; Gene Expression Profiling; Glioblastoma; Glioma; Humans; Isocitrate Dehydrogenase; Magnetic Resonance Angiography; Methylation; Middle Aged; Mutation; Retrospective Studies; Tumor Suppressor Proteins; X-linked Nuclear Protein; Young Adult

2019
Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome.
    Nucleic acids research, 2018, 06-01, Volume: 46, Issue:10

    Topics: Animals; Animals, Newborn; Cadherins; Chromosome Deletion; Chromosomes, Human, Pair 9; Cognitive Dysfunction; Craniofacial Abnormalities; Disease Models, Animal; Gene Expression Regulation; Heart Defects, Congenital; Hippocampus; Histone-Lysine N-Methyltransferase; Histones; Intellectual Disability; Lysine; Male; Methylation; Mice, Knockout

2018
Inhibition of EHMT1/2 rescues synaptic and cognitive functions for Alzheimer's disease.
    Brain : a journal of neurology, 2019, 03-01, Volume: 142, Issue:3

    Topics: Alzheimer Disease; Animals; Chromosome Deletion; Cognition; Cognition Disorders; Cognitive Dysfunction; Disease Models, Animal; DNA Methylation; Epigenesis, Genetic; Hippocampus; Histocompatibility Antigens; Histone-Lysine N-Methyltransferase; Histones; Humans; Lysine; Memory Disorders; Methylation; Mice; Mice, Transgenic; Prefrontal Cortex; Synapses

2019
Calmodulin Methyltransferase Is Required for Growth, Muscle Strength, Somatosensory Development and Brain Function.
    PLoS genetics, 2015, Volume: 11, Issue:8

    Topics: Animals; Brain; Chromosome Deletion; Feedback, Sensory; Female; Male; Methylation; Methyltransferases; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Knockout; Muscle Strength; Muscle, Skeletal; Protein Processing, Post-Translational

2015
Histone Methylation by the Kleefstra Syndrome Protein EHMT1 Mediates Homeostatic Synaptic Scaling.
    Neuron, 2016, 07-20, Volume: 91, Issue:2

    Topics: Animals; Brain-Derived Neurotrophic Factor; Chromosome Deletion; Chromosomes, Human, Pair 9; Craniofacial Abnormalities; Heart Defects, Congenital; Hippocampus; Histone-Lysine N-Methyltransferase; Histones; Homeostasis; Intellectual Disability; Methylation; Mice, Transgenic; Neuronal Plasticity; Patch-Clamp Techniques; Synapses

2016
Integrated genomic profiling identifies two distinct molecular subtypes with divergent outcome in neuroblastoma with loss of chromosome 11q.
    Oncogene, 2010, Feb-11, Volume: 29, Issue:6

    Topics: Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 11; Computational Biology; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Genomics; Humans; Methylation; Neuroblastoma; Prognosis; Promoter Regions, Genetic

2010
L3MBTL1 polycomb protein, a candidate tumor suppressor in del(20q12) myeloid disorders, is essential for genome stability.
    Proceedings of the National Academy of Sciences of the United States of America, 2010, Dec-28, Volume: 107, Issue:52

    Topics: Blotting, Western; Cell Cycle; Cell Line; Cell Line, Tumor; Cell Proliferation; Chromosomal Proteins, Non-Histone; Chromosome Deletion; Chromosomes, Human, Pair 20; DNA Damage; DNA Replication; Genomic Instability; HEK293 Cells; Histones; Humans; Immunoprecipitation; K562 Cells; Lysine; Methylation; Myeloproliferative Disorders; Neoplasm Proteins; Protein Binding; Repressor Proteins; Retinoblastoma Protein; RNA Interference; Tumor Suppressor Proteins

2010
Human calmodulin methyltransferase: expression, activity on calmodulin, and Hsp90 dependence.
    PloS one, 2012, Volume: 7, Issue:12

    Topics: Amino Acid Sequence; Animals; Base Sequence; Benzoquinones; Calmodulin; Cell Line; Chromosome Deletion; Chromosomes, Human, Pair 21; Craniofacial Abnormalities; Cystinuria; Green Fluorescent Proteins; HSP90 Heat-Shock Proteins; Humans; Intellectual Disability; Lactams, Macrocyclic; Methylation; Methyltransferases; Mice; Mice, Inbred ICR; Mitochondrial Diseases; Molecular Sequence Data; Muscle Hypotonia; Protein Binding; Protein Stability; Protein Structure, Tertiary; Protein Transport; Proteolysis; Recombinant Fusion Proteins; Subcellular Fractions; Transcription, Genetic

2012
Characterization of the imprinted polycomb gene L3MBTL, a candidate 20q tumour suppressor gene, in patients with myeloid malignancies.
    British journal of haematology, 2004, Volume: 127, Issue:5

    Topics: Alternative Splicing; Bone Marrow Diseases; Case-Control Studies; Chromosomal Proteins, Non-Histone; Chromosome Deletion; CpG Islands; DNA Mutational Analysis; Gene Expression; Genes, Tumor Suppressor; Humans; Methylation; Myelodysplastic Syndromes; Myeloproliferative Disorders; Neoplasm Proteins; Repressor Proteins; Reverse Transcriptase Polymerase Chain Reaction; Sequence Alignment; Tumor Suppressor Proteins

2004
The Set1 methyltransferase opposes Ipl1 aurora kinase functions in chromosome segregation.
    Cell, 2005, Sep-09, Volume: 122, Issue:5

    Topics: Amino Acid Sequence; Aurora Kinases; Cell Cycle Proteins; Chromosome Deletion; Chromosome Segregation; DNA-Binding Proteins; Gene Deletion; Histone-Lysine N-Methyltransferase; Intracellular Signaling Peptides and Proteins; Methylation; Methyltransferases; Microtubule-Associated Proteins; Mitosis; Molecular Sequence Data; Mutation; Phenotype; Phosphorylation; Protein Kinases; Protein Serine-Threonine Kinases; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Alignment; Transcription Factors

2005
Two alpha heavy chain disease proteins with different genomic deletions demonstrate that nonexpressed alpha heavy chain genes contain methylated bases.
    Proceedings of the National Academy of Sciences of the United States of America, 1981, Volume: 78, Issue:11

    Topics: Alleles; Animals; Base Sequence; Cell Line; Chromosome Deletion; DNA Restriction Enzymes; Genes; Heavy Chain Disease; Immunoglobulin Heavy Chains; Methylation; Mice; Nucleic Acid Hybridization; Peptide Fragments; Phenotype; Plasmacytoma; Trypsin

1981
Organization of polyoma virus DNA in mouse tumor cell lines.
    Archives of virology, 1984, Volume: 79, Issue:3-4

    Topics: Animals; Base Sequence; Cell Line; Cell Transformation, Neoplastic; Cell Transformation, Viral; Chromosome Deletion; DNA Restriction Enzymes; DNA, Viral; Genes, Viral; Methylation; Mice; Polyomavirus; Recombination, Genetic; Repetitive Sequences, Nucleic Acid

1984
Methylation dependent expression of the mom gene of bacteriophage Mu: deletions downstream from the methylation sites affect expression.
    Nucleic acids research, 1984, Apr-25, Volume: 12, Issue:8

    Topics: Base Sequence; Chromosome Deletion; Coliphages; DNA Restriction Enzymes; DNA, Bacterial; DNA, Viral; Escherichia coli; Genes, Viral; Methylation; Plasmids

1984
Local mutagenesis within deletion loops of DNA heteroduplexes.
    Proceedings of the National Academy of Sciences of the United States of America, 1982, Volume: 79, Issue:23

    Topics: Base Sequence; Chromosome Deletion; Chromosome Mapping; DNA, Bacterial; Escherichia coli; Genetic Engineering; Methylation; Mutation; Plasmids

1982
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
Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2.
    Nature, 1995, Jul-13, Volume: 376, Issue:6536

    Topics: Base Sequence; Blotting, Southern; Chromosome Deletion; Chromosome Fragile Sites; Chromosome Fragility; Chromosomes, Human, Pair 11; Female; Humans; Male; Methylation; Molecular Sequence Data; Pedigree; Proto-Oncogene Mas; Proto-Oncogene Proteins; Proto-Oncogene Proteins c-cbl; Repetitive Sequences, Nucleic Acid; Restriction Mapping; Syndrome; Ubiquitin-Protein Ligases

1995
Analysis of meningiomas by methylation- and transcription-based clonality assays.
    Cancer research, 1995, Sep-01, Volume: 55, Issue:17

    Topics: Adult; Aged; Brain Chemistry; Chromosome Deletion; Chromosomes, Human, Pair 22; Dosage Compensation, Genetic; Female; Humans; Kidney; Meningeal Neoplasms; Meningioma; Methylation; Middle Aged; Phosphoglycerate Kinase; Polymerase Chain Reaction; Receptors, Androgen

1995
DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63).
    Human genetics, 1995, Volume: 95, Issue:5

    Topics: Alleles; Angelman Syndrome; Blotting, Southern; Chromosome Deletion; Chromosomes, Human, Pair 15; DNA; DNA Probes; DNA, Satellite; Female; Genetic Markers; Humans; Male; Methylation; Polymorphism, Restriction Fragment Length; Prader-Willi Syndrome

1995
Diagnosing Prader-Willi syndrome.
    Lancet (London, England), 1995, Jun-24, Volume: 345, Issue:8965

    Topics: Chromosome Deletion; Chromosomes, Human, Pair 15; DNA; DNA Probes; Genomic Imprinting; Humans; In Situ Hybridization, Fluorescence; Methylation; Prader-Willi Syndrome

1995
Human breast and colon cancers exhibit alterations of DNA methylation patterns at several DNA segments on chromosomes 11p and 17p.
    Journal of cellular biochemistry, 1994, Volume: 56, Issue:1

    Topics: Adenocarcinoma; Base Sequence; Breast Neoplasms; Calcitonin; Carcinoma in Situ; Carcinoma, Lobular; Catalase; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 17; Colonic Neoplasms; DNA; DNA, Neoplasm; Genes, ras; Globins; Humans; Intestinal Mucosa; Methylation; Parathyroid Hormone; Restriction Mapping

1994
Clinical correlates of chromosome 15 deletions and maternal disomy in Prader-Willi syndrome.
    American journal of diseases of children (1960), 1993, Volume: 147, Issue:11

    Topics: Adolescent; Adult; Child; Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 15; DNA Probes; Female; Humans; Infant; Male; Methylation; Molecular Biology; Pedigree; Polymorphism, Restriction Fragment Length; Prader-Willi Syndrome

1993
Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implications.
    Human molecular genetics, 1994, Volume: 3, Issue:6

    Topics: Adolescent; Autoantigens; Blotting, Southern; Child, Preschool; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 15; DNA; DNA, Satellite; Female; Genotype; Humans; Male; Methylation; Prader-Willi Syndrome; Ribonucleoproteins, Small Nuclear; snRNP Core Proteins

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
Advanced ovarian carcinoma: molecular evidence of unifocal origin.
    Gynecologic oncology, 1993, Volume: 51, Issue:1

    Topics: Adult; Aged; Alleles; Chromosome Deletion; Cystadenocarcinoma, Papillary; DNA; Dosage Compensation, Genetic; Female; Heterozygote; Humans; Methylation; Middle Aged; Ovarian Neoplasms

1993
Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
    American journal of medical genetics, 1993, Oct-01, Volume: 47, Issue:5

    Topics: Angelman Syndrome; Child; Chromosome Deletion; Chromosomes, Human, Pair 15; DNA; DNA Probes; Humans; Male; Methylation; Pedigree; Prader-Willi Syndrome

1993
Coordinate silencing of myeloma-specific genes in myeloma x T lymphoma hybrids.
    Journal of immunology (Baltimore, Md. : 1950), 1993, Sep-01, Volume: 151, Issue:5

    Topics: Cell Fusion; Cell Line; Chromosome Deletion; Chromosomes, Human; Enhancer Elements, Genetic; Gene Expression Regulation; Genes, Immunoglobulin; Humans; Hybrid Cells; Immunoglobulin Heavy Chains; Lymphoma, T-Cell; Methylation; Multiple Myeloma

1993
DNA hypermethylation is associated with 17p allelic loss in neural tumors.
    Cancer research, 1993, Jun-15, Volume: 53, Issue:12

    Topics: Alleles; Astrocytoma; Brain Neoplasms; Chromosome Deletion; Chromosomes, Human, Pair 17; DNA, Neoplasm; Glioblastoma; Humans; Methylation; Neuroblastoma

1993
Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.
    Journal of medical genetics, 1993, Volume: 30, Issue:9

    Topics: Angelman Syndrome; Child; Child, Preschool; Chromosome Deletion; Chromosome Inversion; Chromosomes, Human, Pair 15; Fathers; Humans; Karyotyping; Male; Methylation; Mothers; Prader-Willi Syndrome; Trisomy

1993
Parental-origin-specific epigenetic modification of the mouse H19 gene.
    Nature, 1993, Apr-22, Volume: 362, Issue:6422

    Topics: Animals; Chromatin; Chromosome Deletion; Deoxyribonucleases; Dinucleoside Phosphates; Dosage Compensation, Genetic; Embryo, Mammalian; Fathers; Female; Gene Expression Regulation; Genes; Insulin-Like Growth Factor II; Male; Methylation; Mice; Mice, Inbred BALB C; Mice, Mutant Strains; Mothers; Promoter Regions, Genetic; Restriction Mapping; RNA, Messenger; Spermatozoa

1993
Genetic method for pre-classification of genotoxins into monofunctional or cross-linking agents.
    Environmental and molecular mutagenesis, 1993, Volume: 21, Issue:4

    Topics: Alkylating Agents; Animals; Chromosome Deletion; Cross-Linking Reagents; DNA; Drosophila; Female; Genes, Lethal; Genes, Recessive; Intercalating Agents; Male; Methylation; Mutagenesis; Mutagenicity Tests; Mutagens; Mutation; Reproducibility of Results

1993
Regional DNA hypermethylation at D17S5 precedes 17p structural changes in the progression of renal tumors.
    Cancer research, 1993, Jun-15, Volume: 53, Issue:12

    Topics: Alleles; Chromosome Deletion; Chromosomes, Human, Pair 17; DNA, Neoplasm; Genes, p53; Humans; Kidney Neoplasms; Methylation; Point Mutation

1993
Persistence of increased levels of ribosomal gene activity in CHO-K1 cells treated in vitro with demethylating agents.
    Mutation research, 1995, Volume: 348, Issue:4

    Topics: Animals; Antimetabolites; Azacitidine; CHO Cells; Chromosome Deletion; Clone Cells; Cricetinae; DNA, Ribosomal; Ethionine; Gene Expression Regulation, Neoplastic; Germ-Line Mutation; Methylation; Mitotic Index; Mutagens; Nucleolus Organizer Region; Silver Staining

1995
Frequent allelic loss at chromosome arm 3p is distinct from genetic alterations of the Von-Hippel Lindau tumor suppressor gene in head and neck cancer.
    Oncogene, 1996, Jan-18, Volume: 12, Issue:2

    Topics: Carcinoma, Squamous Cell; Chromosome Deletion; Chromosomes, Human, Pair 3; Genes, Tumor Suppressor; Head and Neck Neoplasms; Humans; Methylation; Mutation; Polymorphism, Restriction Fragment Length; von Hippel-Lindau Disease

1996
High incidence of loss of heterozygosity and abnormal imprinting of H19 and IGF2 genes in invasive cervical carcinomas. Uncoupling of H19 and IGF2 expression and biallelic hypomethylation of H19.
    Oncogene, 1996, Jan-18, Volume: 12, Issue:2

    Topics: Alleles; Chromosome Deletion; Female; Genomic Imprinting; Humans; Insulin-Like Growth Factor II; Methylation; Muscle Proteins; RNA, Long Noncoding; RNA, Untranslated; Uterine Cervical Neoplasms

1996
Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
    Nature genetics, 1996, Volume: 12, Issue:4

    Topics: Adolescent; Adult; Autoantigens; Base Sequence; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 15; Chromosomes, Human, Pair 9; DNA; DNA Primers; Female; Genomic Imprinting; Humans; In Situ Hybridization, Fluorescence; Male; Methylation; Molecular Sequence Data; Pedigree; Prader-Willi Syndrome; Ribonucleoproteins, Small Nuclear; snRNP Core Proteins; Translocation, Genetic

1996
Hypermethylation-associated inactivation indicates a tumor suppressor role for p15INK4B.
    Cancer research, 1996, Feb-15, Volume: 56, Issue:4

    Topics: Adult; Breast Neoplasms; Carrier Proteins; Cell Cycle Proteins; Cell Line; Child; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 9; Colonic Neoplasms; Cyclin-Dependent Kinase Inhibitor p15; Cyclin-Dependent Kinase Inhibitor p16; Dinucleoside Phosphates; DNA; DNA, Neoplasm; Female; Genes, Tumor Suppressor; Glioma; Homozygote; Humans; Leukemia; Leukemia, Myeloid, Acute; Lung Neoplasms; Lymphocytes; Male; Methylation; Polymerase Chain Reaction; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Prostatic Neoplasms; Reference Values; Restriction Mapping; Tumor Cells, Cultured; Tumor Suppressor Proteins

1996
Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).
    Human genetics, 1996, Volume: 97, Issue:6

    Topics: Adolescent; Adult; Angelman Syndrome; Child; Child, Preschool; Chromosome Banding; Chromosome Deletion; Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 15; DNA; Female; Humans; In Situ Hybridization, Fluorescence; Infant; Male; Methylation; Phenotype; Prader-Willi Syndrome; Sensitivity and Specificity

1996
Familial cryptic translocation resulting in Angelman syndrome:implications for imprinting or location of the Angelman gene?
    American journal of human genetics, 1996, Volume: 58, Issue:4

    Topics: Angelman Syndrome; Autoantigens; Child; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 14; Chromosomes, Human, Pair 15; DNA; DNA Probes; Female; Genomic Imprinting; Humans; Methylation; Ribonucleoproteins, Small Nuclear; snRNP Core Proteins; Translocation, Genetic

1996
A human modifier of methylation for class I HLA genes (MEMO-1) maps to chromosomal bands 1p35-36.1.
    Human molecular genetics, 1996, Volume: 5, Issue:3

    Topics: Alleles; Cell Fusion; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 1; Genes, MHC Class I; Humans; Methylation; Neuroblastoma; Tissue Distribution; Tumor Cells, Cultured

1996
FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.
    American journal of medical genetics, 1996, Mar-29, Volume: 62, Issue:3

    Topics: Angelman Syndrome; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 15; Dinucleotide Repeats; Female; Humans; In Situ Hybridization, Fluorescence; Male; Methylation; Prader-Willi Syndrome

1996
Lack of class I HLA expression in neuroblastoma is associated with high N-myc expression and hypomethylation due to loss of the MEMO-1 locus.
    Oncogene, 1996, Oct-17, Volume: 13, Issue:8

    Topics: Cell Fusion; Chromosome Deletion; Genes, MHC Class I; Genes, myc; HLA-A Antigens; HLA-C Antigens; Humans; Methylation; Neuroblastoma; RNA, Messenger; Tumor Cells, Cultured

1996
Prader-Willi syndrome in South African patients--clinical and molecular diagnosis.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1998, Volume: 88, Issue:6

    Topics: Blotting, Southern; Chromosome Deletion; Chromosomes, Human, Pair 15; DNA Probes; Female; Humans; Male; Methylation; Nucleic Acid Hybridization; Prader-Willi Syndrome; Prospective Studies; South Africa

1998
A physical, transcript, and deletion map of chromosome region 12p12.3 flanked by ETV6 and CDKN1B: hypermethylation of the LRP6 CpG island in two leukemia patients with hemizygous del(12p).
    Genomics, 1999, Feb-15, Volume: 56, Issue:1

    Topics: Cell Cycle Proteins; Chromosome Banding; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 12; CpG Islands; Cyclin-Dependent Kinase Inhibitor p27; DNA-Binding Proteins; DNA, Complementary; ETS Translocation Variant 6 Protein; Exons; Expressed Sequence Tags; Female; Humans; In Situ Hybridization, Fluorescence; Introns; Leukemia; Low Density Lipoprotein Receptor-Related Protein-6; Male; Methylation; Microsatellite Repeats; Microtubule-Associated Proteins; Physical Chromosome Mapping; Polymorphism, Genetic; Proto-Oncogene Proteins c-ets; Receptors, LDL; Repressor Proteins; Transcription Factors; Tumor Suppressor Proteins

1999
Imprinting defects in mouse embryos: stochastic errors or polymorphic phenotype?
    Genesis (New York, N.Y. : 2000), 2001, Volume: 31, Issue:1

    Topics: Alleles; Animals; Chromosome Deletion; Crosses, Genetic; DNA; DNA Primers; Embryo, Mammalian; Embryonic Development; Female; Gene Expression Regulation; Genomic Imprinting; Incidence; Insulin-Like Growth Factor II; Male; Methylation; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Inbred DBA; Phenotype; Polymorphism, Genetic; Pregnancy; Reverse Transcriptase Polymerase Chain Reaction; RNA, Long Noncoding; RNA, Untranslated

2001
Petunia plants escape from negative selection against a transgene by silencing the foreign DNA via methylation.
    Molecular & general genetics : MGG, 1992, Volume: 233, Issue:1-2

    Topics: Agrobacterium tumefaciens; Amidohydrolases; Azacitidine; Blotting, Southern; Cell Line; Chromosome Deletion; Cloning, Molecular; DNA Transposable Elements; DNA, Bacterial; Gene Expression Regulation, Enzymologic; Methylation; Nucleic Acid Hybridization; Phenotype; Plants, Genetically Modified; Restriction Mapping; Selection, Genetic; Transformation, Genetic

1992
The amyloid beta-protein precursor promoter. A region essential for transcriptional activity contains a nuclear factor binding domain.
    The Journal of biological chemistry, 1992, Aug-25, Volume: 267, Issue:24

    Topics: Actins; Amyloid beta-Protein Precursor; Animals; Base Sequence; Binding Sites; Blotting, Northern; Cell Line; Chickens; Chloramphenicol O-Acetyltransferase; Chromosome Deletion; DNA; Gene Expression; Humans; Methylation; Molecular Sequence Data; Mutagenesis; Nuclear Proteins; Oligodeoxyribonucleotides; Promoter Regions, Genetic; Restriction Mapping; RNA; Transcription, Genetic; Transfection

1992
A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.
    Genomics, 1992, Volume: 13, Issue:4

    Topics: Blotting, Southern; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 15; DNA; DNA Probes; Female; Humans; Intellectual Disability; Male; Methylation; Movement Disorders; Parents; Prader-Willi Syndrome; Sex Factors; Syndrome

1992
Endogenous and environmental factors influence 35S promoter methylation of a maize A1 gene construct in transgenic petunia and its colour phenotype.
    Molecular & general genetics : MGG, 1992, Volume: 231, Issue:3

    Topics: Alcohol Oxidoreductases; Base Sequence; Chromosome Deletion; Color; Environment; Genes, Plant; Methylation; Molecular Sequence Data; Phenotype; Plant Physiological Phenomena; Plants; Plants, Genetically Modified; Promoter Regions, Genetic; Restriction Mapping; Zea mays

1992
Overproduction, purification and characterization of M.HinfI methyltransferase and its deletion mutant.
    Gene, 1992, Apr-01, Volume: 113, Issue:1

    Topics: Amino Acid Sequence; Base Sequence; Chromosome Deletion; Cloning, Molecular; Escherichia coli; Genes, Bacterial; Haemophilus; Kinetics; Methylation; Molecular Sequence Data; Oligodeoxyribonucleotides; Plasmids; Polymerase Chain Reaction; Protein Biosynthesis; Recombinant Proteins; Regulatory Sequences, Nucleic Acid; Restriction Mapping; Site-Specific DNA-Methyltransferase (Adenine-Specific); Transcription, Genetic

1992
Characterization of a specific erythromegakaryocytic enhancer within the glycoprotein IIb promoter.
    The Journal of biological chemistry, 1992, May-25, Volume: 267, Issue:15

    Topics: Base Sequence; Cell Line; Chloramphenicol O-Acetyltransferase; Chromosome Deletion; Electrophoresis, Polyacrylamide Gel; Enhancer Elements, Genetic; Erythroid Precursor Cells; HeLa Cells; Humans; Luciferases; Megakaryocytes; Methylation; Molecular Sequence Data; Mutagenesis, Site-Directed; Plasmids; Platelet Membrane Glycoproteins; Promoter Regions, Genetic; Transcription, Genetic; Transfection

1992
Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare.
    Genes, chromosomes & cancer, 1991, Volume: 3, Issue:2

    Topics: Alleles; Aniridia; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 11; DNA Probes; DNA, Neoplasm; Electrophoresis, Agar Gel; Genes, Wilms Tumor; Humans; Kidney Neoplasms; Methylation; Restriction Mapping; Syndrome; Urogenital Abnormalities; Wilms Tumor

1991
Identification and characterization of a gene responsible for inhibiting propagation of methylated DNA sequences in mcrA mcrB1 Escherichia coli strains.
    Journal of bacteriology, 1991, Volume: 173, Issue:15

    Topics: Animals; Bacteriophage lambda; Chromosome Deletion; Chromosomes, Bacterial; Cloning, Molecular; Cosmids; DNA Transposable Elements; DNA-Cytosine Methylases; DNA, Bacterial; Escherichia coli; Gene Amplification; Genes, Bacterial; Methylation; Mice; Mice, Transgenic; Restriction Mapping

1991
Molecular analysis of the loss of somatic instability in the bz2::mu1 allele of maize.
    Molecular & general genetics : MGG, 1991, Volume: 229, Issue:1

    Topics: Alleles; Anthocyanins; Base Sequence; Blotting, Southern; Chromosome Deletion; Crosses, Genetic; DNA Transposable Elements; Methylation; Molecular Sequence Data; Mutagenesis; Restriction Mapping; Zea mays

1991
Mutations in 16S rRNA in Escherichia coli at methyl-modified sites: G966, C967, and G1207.
    Nucleic acids research, 1991, Aug-11, Volume: 19, Issue:15

    Topics: Base Sequence; Chromosome Deletion; Escherichia coli; Genes, Dominant; Genes, Lethal; Methylation; Molecular Sequence Data; Mutagenesis, Site-Directed; Nucleic Acid Conformation; Phenotype; Ribosomes; RNA Processing, Post-Transcriptional; RNA, Bacterial; RNA, Ribosomal, 16S

1991
HPRT gene mutations in a female Lesch-Nyhan patient.
    Advances in experimental medicine and biology, 1991, Volume: 309B

    Topics: Adolescent; Base Sequence; Chromosome Deletion; DNA; Dosage Compensation, Genetic; Female; Humans; Hypoxanthine Phosphoribosyltransferase; Lesch-Nyhan Syndrome; Methylation; Molecular Sequence Data; X Chromosome

1991
CpG methylation of an endogenous retroviral enhancer inhibits transcription factor binding and activity.
    Gene expression, 1991, Volume: 1, Issue:3

    Topics: Animals; Base Sequence; Cell Differentiation; Chromosome Deletion; Dinucleoside Phosphates; DNA Mutational Analysis; DNA-Binding Proteins; DNA-Cytosine Methylases; Enhancer Elements, Genetic; Gene Expression Regulation, Viral; Genes, Intracisternal A-Particle; HeLa Cells; Humans; Methylation; Mice; Molecular Sequence Data; Repetitive Sequences, Nucleic Acid; Retroviridae; Transcription Factors; Transcription, Genetic

1991
Point mutation, allelic loss and increased methylation of c-Ha-ras gene in human hepatocellular carcinoma.
    Hepatology (Baltimore, Md.), 1991, Volume: 13, Issue:1

    Topics: Adult; Alleles; Carcinoma, Hepatocellular; Chromosome Deletion; Codon; DNA, Neoplasm; DNA, Viral; Female; Genes, ras; Hepatitis B virus; Heterozygote; Humans; Liver Neoplasms; Male; Methylation; Middle Aged; Mutation

1991
Effects of mcr restriction of methylated CpG islands of the L1 transposons during packaging and plating stages of mammalian genomic library construction.
    Gene, 1991, Feb-01, Volume: 98, Issue:1

    Topics: Animals; Bacteriophages; Chromosome Deletion; Cloning, Molecular; Deoxyribonucleases; Dinucleoside Phosphates; DNA Transposable Elements; Escherichia coli; Genes, Bacterial; Genetic Vectors; Genomic Library; Genotype; Humans; Methylation; Rats; Repetitive Sequences, Nucleic Acid

1991
Stereospecific alignment of the X and Y elements is required for major histocompatibility complex class II DRA promoter function.
    Molecular and cellular biology, 1991, Volume: 11, Issue:5

    Topics: Animals; Base Sequence; Cell Line; Cell Nucleus; Chloramphenicol O-Acetyltransferase; Chromosome Deletion; DNA, Neoplasm; Genes, MHC Class II; Humans; Methylation; Mice; Models, Structural; Molecular Sequence Data; Nucleic Acid Conformation; Plasmids; Promoter Regions, Genetic; Recombinant Fusion Proteins; Stereoisomerism; Transfection

1991
The restriction enzyme AlwNI is blocked by overlapping methylation.
    Nucleic acids research, 1991, Sep-11, Volume: 19, Issue:17

    Topics: 5-Methylcytosine; Adenosine; Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Base Sequence; Chromosome Deletion; Cloning, Molecular; Cytosine; Deoxyribonucleases, Type II Site-Specific; DNA; DNA Mutational Analysis; Methylation; Molecular Sequence Data; Plasmids; Protein Precursors

1991
A c-myc gene variant without exon 1 and with an abnormal methylation pattern inherited in a woman with no evidence of malignancy.
    Oncogene, 1991, Volume: 6, Issue:10

    Topics: Chromosome Deletion; Chromosome Mapping; DNA; Exons; Female; Genes, myc; Humans; Introns; Italy; Methylation; Pedigree

1991
The physical organization of the human immunoglobulin heavy chain gene complex.
    The EMBO journal, 1990, Volume: 9, Issue:10

    Topics: Chromosome Deletion; DNA; DNA Probes; DNA Transposable Elements; Electrophoresis, Gel, Two-Dimensional; Genes, Immunoglobulin; Humans; Immunoglobulin Heavy Chains; Immunoglobulin Variable Region; Methylation; Multigene Family; Polymorphism, Genetic; Restriction Mapping

1990
Sequences within an upstream activation site in the yeast enolase gene ENO2 modulate repression of ENO2 expression in strains carrying a null mutation in the positive regulatory gene GCR1.
    Molecular and cellular biology, 1990, Volume: 10, Issue:9

    Topics: Base Sequence; Chromosome Deletion; DNA Probes; DNA-Binding Proteins; Enzyme Activation; Enzyme Repression; Genes, Fungal; Genes, Regulator; Methylation; Molecular Sequence Data; Mutation; Nucleotide Mapping; Phosphopyruvate Hydratase; Saccharomyces cerevisiae

1990
Analysis of the rearrangements associated with carcinogen-induced activation of the hamster thymidine kinase gene.
    Nucleic acids research, 1990, Jan-11, Volume: 18, Issue:1

    Topics: Animals; Blotting, Southern; Carcinogens; Cell Line; Chromatin; Chromosome Deletion; Cloning, Molecular; Cricetinae; DNA Damage; Gene Expression Regulation; Gene Rearrangement; Methylation; Restriction Mapping; Thymidine Kinase

1990
A cDNA for a human cyclic AMP response element-binding protein which is distinct from CREB and expressed preferentially in brain.
    Molecular and cellular biology, 1990, Volume: 10, Issue:4

    Topics: Activating Transcription Factor 2; Amino Acid Sequence; B-Lymphocytes; Base Sequence; Brain; Chromosome Deletion; Cloning, Molecular; Cyclic AMP Response Element-Binding Protein; DNA; DNA-Binding Proteins; Gene Expression; Gene Library; Humans; Methylation; Molecular Sequence Data; Mutation; Oligonucleotide Probes; Organ Specificity; Protein Biosynthesis; Sequence Homology, Nucleic Acid; Transcription Factors; Transcription, Genetic

1990
HLA class II regulation and structure. Analysis with HLA-DR3 and HLA-DP point mutants.
    The Journal of experimental medicine, 1985, Oct-01, Volume: 162, Issue:4

    Topics: Antibodies, Monoclonal; Chromosome Deletion; Epitopes; Histocompatibility Antigens Class II; HLA-DP Antigens; HLA-DR3 Antigen; Humans; Methylation; Mutation; RNA, Messenger

1985
The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases.
    Blood, 1987, Volume: 70, Issue:6

    Topics: Chromatin; Chromosome Deletion; Chromosome Mapping; DNA Restriction Enzymes; Electrophoresis, Agar Gel; Fetal Hemoglobin; Globins; Humans; Methylation; Multigene Family; Thalassemia

1987
The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster.
    Blood, 1989, Nov-01, Volume: 74, Issue:6

    Topics: Amino Acid Sequence; Base Sequence; Blotting, Southern; Chromosome Deletion; Enhancer Elements, Genetic; Erythroid Precursor Cells; Fetal Hemoglobin; Gene Expression Regulation; Globins; Hemoglobinopathies; Humans; Methylation; Molecular Sequence Data; Regulatory Sequences, Nucleic Acid; Restriction Mapping; Thalassemia; Transcription, Genetic

1989
Possible organ and age-related epigenetic factors in Huntington's disease and colorectal carcinoma.
    Medical hypotheses, 1989, Volume: 29, Issue:1

    Topics: Aging; Animals; Chromosome Deletion; Colorectal Neoplasms; Gene Expression Regulation; Genes, Switch; Humans; Huntington Disease; Methylation; Mutation

1989
Regulation of mouse CYP1A1 gene expression by dioxin: requirement of two cis-acting elements during induction.
    Molecular and cellular biology, 1989, Volume: 9, Issue:6

    Topics: Animals; Base Sequence; Binding, Competitive; Cell Line; Chloramphenicol O-Acetyltransferase; Chromosome Deletion; Cytochrome P-450 Enzyme System; Dioxins; DNA-Binding Proteins; Hot Temperature; Methylation; Mice; Molecular Sequence Data; Oligonucleotides; Plasmids; Polychlorinated Dibenzodioxins; Receptors, Drug; Regulatory Sequences, Nucleic Acid; Simian virus 40; Transfection

1989
Methyl-directed repair of frameshift heteroduplexes in cell extracts from Escherichia coli.
    Journal of bacteriology, 1989, Volume: 171, Issue:12

    Topics: Base Composition; Base Sequence; Chromosome Deletion; Cloning, Molecular; Coliphages; DNA Repair; DNA, Bacterial; DNA, Viral; Escherichia coli; Genes, Bacterial; Methylation; Molecular Sequence Data; Mutation; Nucleic Acid Heteroduplexes

1989
Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.
    Proceedings of the National Academy of Sciences of the United States of America, 1989, Volume: 86, Issue:13

    Topics: Biological Evolution; Blotting, Southern; Brain; Chromosome Deletion; Chromosome Mapping; Chromosomes, Human, Pair 17; Face; Genes; Humans; Methylation; Restriction Mapping; Syndrome

1989
Nuclear proteins binding to a cauliflower mosaic virus 35S truncated promoter.
    Molecular & general genetics : MGG, 1989, Volume: 217, Issue:2-3

    Topics: Base Sequence; Binding Sites; Chromosome Deletion; DNA, Viral; Methylation; Molecular Sequence Data; Mosaic Viruses; Nuclear Proteins; Promoter Regions, Genetic

1989
Differential gene activation by glucocorticoids and progestins through the hormone regulatory element of mouse mammary tumor virus.
    Cell, 1988, May-06, Volume: 53, Issue:3

    Topics: Animals; Base Sequence; Chromosome Deletion; Chromosome Inversion; Deoxyribonuclease I; DNA, Viral; Gene Expression Regulation; Genes, Viral; Glucocorticoids; Mammary Tumor Virus, Mouse; Methylation; Molecular Sequence Data; Mutation; Progestins; Promoter Regions, Genetic; Receptors, Glucocorticoid; Receptors, Progesterone; Regulatory Sequences, Nucleic Acid; Repetitive Sequences, Nucleic Acid; Transcriptional Activation

1988
Cancer genetics. Genomic imprinting and embryonal tumours.
    Nature, 1989, Mar-09, Volume: 338, Issue:6211

    Topics: Alleles; Chromosome Deletion; Methylation; Models, Genetic; Mutation; Neoplasms

1989
Mycoplasma restriction: identification of a new type of restriction specificity for DNA containing 5-methylcytosine.
    Journal of bacteriology, 1986, Volume: 165, Issue:1

    Topics: 5-Methylcytosine; Acholeplasma laidlawii; Bacteriophages; Base Sequence; Chromosome Deletion; Cytosine; DNA Restriction Enzymes; DNA, Bacterial; Methylation; Mutation; Transfection

1986
Multiple protein-binding sites in the 5'-flanking region regulate c-fos expression.
    Molecular and cellular biology, 1986, Volume: 6, Issue:12

    Topics: Animals; Base Sequence; Cell Line; Cells, Cultured; Chromosome Deletion; DNA Restriction Enzymes; DNA-Binding Proteins; Genes, Regulator; Lymphoma; Methylation; Mice; Mice, Inbred BALB C; Oncogenes; Transcription, Genetic

1986
The evolution of eukaryotic ribosomal DNA.
    Bio Systems, 1986, Volume: 19, Issue:4

    Topics: Animals; Base Sequence; Biological Evolution; Cells; Chromosome Deletion; DNA Transposable Elements; DNA, Ribosomal; Drosophila melanogaster; Escherichia coli; Eukaryotic Cells; Introns; Methylation; Mutation; Nucleic Acid Conformation; RNA, Ribosomal; Xenopus

1986
Deletion and hypermethylation of thymidine kinase gene in V79 Chinese hamster cells resistant to bromodeoxyuridine.
    Somatic cell and molecular genetics, 1988, Volume: 14, Issue:6

    Topics: Animals; Blotting, Northern; Blotting, Southern; Bromodeoxyuridine; Chromosome Deletion; Cricetinae; Cricetulus; DNA; Drug Resistance; Gene Expression Regulation; Genes; Methylation; Restriction Mapping; Thymidine Kinase; Time Factors

1988
Inactivation of a transfected gene in human fibroblasts can occur by deletion, amplification, phenotypic switching, or methylation.
    Molecular and cellular biology, 1987, Volume: 7, Issue:4

    Topics: Cell Line; Chromosome Deletion; Cloning, Molecular; Escherichia coli; Gene Amplification; Genes; Humans; Hypoxanthine Phosphoribosyltransferase; Methylation; Pentosyltransferases; Phenotype; Plasmids

1987
Stable propagation of the active transcriptional state of an immunoglobulin mu gene requires continuous enhancer function.
    Cell, 1988, Nov-18, Volume: 55, Issue:4

    Topics: Base Sequence; Chromosome Deletion; Enhancer Elements, Genetic; Genes, Immunoglobulin; Immunoglobulin Heavy Chains; Immunoglobulin mu-Chains; Methylation; Molecular Sequence Data; Recombination, Genetic; Transcription, Genetic; Transfection

1988
The estrogen receptor binds tightly to its responsive element as a ligand-induced homodimer.
    Cell, 1988, Oct-07, Volume: 55, Issue:1

    Topics: Binding Sites; Cell Line; Chromosome Deletion; DNA; DNA Probes; Estradiol; Humans; Ligands; Macromolecular Substances; Methylation; Receptors, Estrogen; Tamoxifen

1988
A new method for the unidirectional deletion of DNA with Bal 31 nuclease using 2'-O-MeRNA-DNA chimeric adaptors.
    Nucleic acids symposium series, 1988, Issue:19

    Topics: Chimera; Chromosome Deletion; DNA; Endodeoxyribonucleases; Genes; Genetic Engineering; Methylation; RNA, Double-Stranded

1988
Construction of an Escherichia coli K-12 ada deletion by gene replacement in a recD strain reveals a second methyltransferase that repairs alkylated DNA.
    Journal of bacteriology, 1988, Volume: 170, Issue:7

    Topics: Alkylation; Bacterial Proteins; Chromosome Deletion; DNA Repair; DNA, Bacterial; Escherichia coli; Escherichia coli Proteins; Genes, Bacterial; Methylation; Methyltransferases; Mutation; O(6)-Methylguanine-DNA Methyltransferase; Transcription Factors

1988
A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene.
    Genomics, 1988, Volume: 2, Issue:3

    Topics: Chromosome Deletion; Chromosome Mapping; Cloning, Molecular; Electrophoresis; Genetic Linkage; Humans; Methylation; Muscular Dystrophies; X Chromosome

1988
The mom gene of bacteriophage Mu: the mechanism of methylation-dependent expression.
    The EMBO journal, 1986, Volume: 5, Issue:10

    Topics: Base Sequence; Chromosome Deletion; Coliphages; DNA, Viral; Escherichia coli; Genes, Viral; Methylation; Mutation; Nucleic Acid Conformation; Promoter Regions, Genetic

1986
The Gv-1 locus coordinately regulates the expression of multiple endogenous murine retroviruses.
    Cell, 1985, Volume: 41, Issue:1

    Topics: Animals; Chromosome Deletion; Cloning, Molecular; DNA, Viral; Gene Expression Regulation; Genes, Regulator; Genes, Viral; Methylation; Mice; Nucleic Acid Hybridization; Repetitive Sequences, Nucleic Acid; Retroviridae; RNA, Viral; Transcription, Genetic

1985
The molecular biology of human cancer.
    Progress in clinical and biological research, 1985, Volume: 198

    Topics: Chromosome Deletion; DNA; DNA, Neoplasm; Gene Amplification; Humans; Methylation; Mutation; Neoplasms

1985