Page last updated: 2024-08-18

isomethyleugenol and Genetic Diseases, Inborn

isomethyleugenol has been researched along with Genetic Diseases, Inborn in 19 studies

Research

Studies (19)

Timeframe	Studies, this research(%)	All Research%
pre-1990	5 (26.32)	18.7374
1990's	10 (52.63)	18.2507
2000's	4 (21.05)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Amor, DJ	1
Pandita, TK; Richardson, C	1
Paoloni-Giacobino, A	1
Fontaine, B; Lyon-Caen, O; Saudubray, JM; Sedel, F	1
Willems, PJ	1
Bates, G; Lehrach, H	1
Gregersen, PK	1
Pourcel, C	1
Holliday, R	2
Sasaki, H	1
Malcolm, S	1
Monk, M	1
Jones, PA; Rideout, WM; Shen, JC; Spruck, CH; Tsai, YC	1
Sapienza, C	1
Shire, JG	1
Cattanach, BM	1
Cooper, DN; Youssoufian, H	1
Hamer, DH	1

Reviews

13 review(s) available for isomethyleugenol and Genetic Diseases, Inborn

Article	Year
Chromatin remodeling finds its place in the DNA double-strand break response. Nucleic acids research, 2009, Volume: 37, Issue:5 Topics: Adaptor Proteins, Signal Transducing; Chromatin; Chromatin Assembly and Disassembly; DNA Breaks, Double-Stranded; DNA Repair; Genetic Diseases, Inborn; Humans; Methylation; Protein Kinases; Signal Transduction; Ubiquitination	2009
Implications of reproductive technologies for birth and developmental outcomes: imprinting defects and beyond. Expert reviews in molecular medicine, 2006, Jun-05, Volume: 8, Issue:12 Topics: Animals; Congenital Abnormalities; Epigenesis, Genetic; Female; Genetic Diseases, Inborn; Genomic Imprinting; Genomics; Humans; Male; Methylation; Models, Biological; Pregnancy; Pregnancy Outcome; Reproductive Techniques, Assisted	2006
Hereditary spastic paraparesis in adults associated with inborn errors of metabolism: a diagnostic approach. Journal of inherited metabolic disease, 2007, Volume: 30, Issue:6 Topics: Age of Onset; Decision Trees; Female; Genetic Diseases, Inborn; Humans; Male; Metabolism, Inborn Errors; Methylation; Motor Neurons; Paraparesis, Spastic; Spinal Cord; Syndrome	2007
Trinucleotide repeat expansions and human genetic disease. BioEssays : news and reviews in molecular, cellular and developmental biology, 1994, Volume: 16, Issue:4 Topics: Adult; Age of Onset; Base Sequence; Child; Embryonic and Fetal Development; Fragile X Syndrome; Genetic Diseases, Inborn; Humans; Huntington Disease; Infant, Newborn; Intellectual Disability; Male; Methylation; Middle Aged; Molecular Sequence Data; Muscular Atrophy, Spinal; Myotonic Dystrophy; Repetitive Sequences, Nucleic Acid; Spermatozoa; Spinocerebellar Degenerations	1994
Discordance for autoimmunity in monozygotic twins. Are "identical" twins really identical? Arthritis and rheumatism, 1993, Volume: 36, Issue:9 Topics: Autoimmunity; DNA; Gene Expression; Genes; Genetic Diseases, Inborn; Genetic Linkage; Genetic Variation; Genome; Humans; Methylation; Phenotype; Twins, Monozygotic; X Chromosome	1993
Epigenetic inheritance based on DNA methylation. EXS, 1993, Volume: 64 Topics: Aging; Animals; Base Sequence; Cell Line; DNA; Fragile X Syndrome; Genetic Diseases, Inborn; Humans; Mammals; Methylation; Neoplasms; Repetitive Sequences, Nucleic Acid; Sex Chromosome Aberrations; X Chromosome; Zea mays	1993
[Parental imprinting of mammalian genomes]. Seikagaku. The Journal of Japanese Biochemical Society, 1992, Volume: 64, Issue:10 Topics: Alleles; Animals; Cell Differentiation; Chromatin; Chromosomes; DNA; Genetic Diseases, Inborn; Genome; Humans; Methylation; Mice; Mice, Inbred BALB C; Neoplasms	1992
Molecular detection of altered X-inactivation patterns in the diagnosis of genetic disease. Journal of inherited metabolic disease, 1992, Volume: 15, Issue:4 Topics: Diseases in Twins; Dosage Compensation, Genetic; Female; Genetic Diseases, Inborn; Heterozygote; Humans; Methylation; Twins, Monozygotic; X Chromosome	1992
The X chromosome in development in mouse and man. Journal of inherited metabolic disease, 1992, Volume: 15, Issue:4 Topics: Animals; Disease Models, Animal; Dosage Compensation, Genetic; Embryonic and Fetal Development; Female; Genetic Diseases, Inborn; Humans; Male; Methylation; Mice; Mosaicism; Sequence Homology, Nucleic Acid; X Chromosome	1992
Methylation, mutation and cancer. BioEssays : news and reviews in molecular, cellular and developmental biology, 1992, Volume: 14, Issue:1 Topics: 5-Methylcytosine; Animals; Cell Transformation, Neoplastic; Cytosine; Deamination; DNA; DNA, Neoplasm; Female; Genes, p53; Genetic Diseases, Inborn; Humans; Male; Methylation; Mutation; Neoplasms; Neoplasms, Experimental; Vertebrates	1992
Unequal parental contributions: genomic imprinting in mammals. The New biologist, 1989, Volume: 1, Issue:2 Topics: Animals; Disease Susceptibility; DNA; Dosage Compensation, Genetic; Embryonic and Fetal Development; Female; Gene Expression Regulation; Genetic Diseases, Inborn; Humans; Male; Methylation; Mice; Mice, Inbred Strains; Mice, Transgenic; Neoplasms; Nuclear Transfer Techniques; Sex Determination Analysis; X Chromosome; Zygote	1989
The inheritance of epigenetic defects. Science (New York, N.Y.), 1987, Oct-09, Volume: 238, Issue:4824 Topics: Aging; Animals; DNA; DNA Repair; Genetic Diseases, Inborn; Humans; Meiosis; Methylation; Mutation	1987
Metallothionein. Annual review of biochemistry, 1986, Volume: 55 Topics: Animals; Biological Evolution; Cloning, Molecular; Gene Amplification; Gene Expression Regulation; Genetic Diseases, Inborn; Genetic Engineering; Hormones; Humans; Metallothionein; Metals; Methylation; Models, Biological; Protein Conformation; Saccharomyces cerevisiae; Transcription, Genetic	1986

Other Studies

6 other study(ies) available for isomethyleugenol and Genetic Diseases, Inborn

Article	Year
Genomic imprinting, small babies and assisted reproduction. European journal of human genetics : EJHG, 2009, Volume: 17, Issue:1 Topics: Embryo, Mammalian; Female; Fetal Growth Retardation; Genetic Diseases, Inborn; Genomic Imprinting; Humans; Infant; Infant, Newborn; Infant, Small for Gestational Age; Methylation; Placentation; Potassium Channels, Voltage-Gated; Pregnancy; Reproduction; Reproductive Techniques, Assisted	2009
Dynamic mutations hit double figures. Nature genetics, 1994, Volume: 8, Issue:3 Topics: Chromosome Fragility; Chromosome Mapping; Chromosomes, Human, Pair 14; Female; Fragile X Mental Retardation Protein; Fragile X Syndrome; Gene Expression Regulation; Genetic Diseases, Inborn; Humans; Machado-Joseph Disease; Male; Methylation; Minisatellite Repeats; Mutation; Nerve Tissue Proteins; RNA-Binding Proteins; X Chromosome	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
Parental imprinting of genes. Scientific American, 1990, Volume: 263, Issue:4 Topics: Animals; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 15; DNA; Female; Genetic Diseases, Inborn; Genetics; Humans; Huntington Disease; Male; Methylation; Mice; Ovum; Rhabdomyosarcoma; Sex Chromosomes; Spermatozoa	1990
Mammalian chromosome imprinting. Genome, 1989, Volume: 31, Issue:2 Topics: Animals; Chromosomes; DNA; Female; Gene Expression Regulation; Genetic Diseases, Inborn; Humans; Male; Methylation; Mice; Phenotype; Sex Factors	1989
The CpG dinucleotide and human genetic disease. Human genetics, 1988, Volume: 78, Issue:2 Topics: 5-Methylcytosine; Codon; Cytidine Monophosphate; Cytosine; Cytosine Nucleotides; Dinucleoside Phosphates; DNA; Genetic Diseases, Inborn; Guanosine; Humans; Methylation; Mutation	1988