Basic concepts of epigenetics.
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Sanaa Choufani | Rosanna Weksberg | R. Weksberg | S. Choufani | D. Butcher | M. Inbar‐Feigenberg | Darci T Butcher | Maian Roifman | Michal Inbar-Feigenberg | M. Roifman | Maian Roifman
[1] D. Shelton,et al. MicroRNA expression in the human blastocyst. , 2013, Fertility and sterility.
[2] Nadav S. Bar,et al. Landscape of transcription in human cells , 2012, Nature.
[3] T. Ogata,et al. Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies. , 2012, Human reproduction.
[4] F. Vermeylen,et al. Maternal choline intake alters the epigenetic state of fetal cortisol‐regulating genes in humans , 2012, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[5] T. Haaf,et al. Constitutive promoter methylation of BRCA1 and RAD51C in patients with familial ovarian cancer and early-onset sporadic breast cancer , 2012, Human Molecular Genetics.
[6] Howard Cedar,et al. Programming of DNA methylation patterns. , 2012, Annual review of biochemistry.
[7] H. Putter,et al. Prenatal Famine and Genetic Variation Are Independently and Additively Associated with DNA Methylation at Regulatory Loci within IGF2/H19 , 2012, PloS one.
[8] L. Layman,et al. Role of ART in Imprinting Disorders , 2012, Seminars in Reproductive Medicine.
[9] A. McLysaght,et al. Mammalian X chromosome inactivation evolved as a dosage-compensation mechanism for dosage-sensitive genes on the X chromosome , 2012, Proceedings of the National Academy of Sciences.
[10] K. Kurimoto,et al. Epigenetic reprogramming in mouse pre-implantation development and primordial germ cells , 2012, Development.
[11] Thomas Lengauer,et al. Genomic Distribution and Inter-Sample Variation of Non-CpG Methylation across Human Cell Types , 2011, PLoS genetics.
[12] M. Mann,et al. Embryonic imprinting perturbations do not originate from superovulation-induced defects in DNA methylation acquisition. , 2011, Fertility and sterility.
[13] B. Hales,et al. Epigenetic programming: from gametes to blastocyst. , 2011, Birth defects research. Part A, Clinical and molecular teratology.
[14] Shi-ling Chen,et al. Assisted reproductive technologies do not increase risk of abnormal methylation of PEG1/MEST in human early pregnancy loss. , 2011, Fertility and sterility.
[15] C. Glass,et al. Non-coding RNAs as regulators of gene expression and epigenetics. , 2011, Cardiovascular research.
[16] C. Allis,et al. Operating on chromatin, a colorful language where context matters. , 2011, Journal of molecular biology.
[17] W. Reik,et al. Dynamic regulation of 5-hydroxymethylcytosine in mouse ES cells and during differentiation , 2011, Nature.
[18] R. Weksberg,et al. WNT2 promoter methylation in human placenta is associated with low birthweight percentile in the neonate , 2011, Epigenetics.
[19] R. Stewart,et al. Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells , 2011, Nature.
[20] D. Pinto,et al. A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes. , 2011, Genome research.
[21] Riitta Lahesmaa,et al. Tet1 and Tet2 regulate 5-hydroxymethylcytosine production and cell lineage specification in mouse embryonic stem cells. , 2011, Cell stem cell.
[22] P. Avner,et al. Genetics and epigenetics of the X chromosome , 2010, Annals of the New York Academy of Sciences.
[23] W. Reik,et al. Epigenetic Reprogramming in Plant and Animal Development , 2010, Science.
[24] R. Martorell,et al. Early life exposure to the 1959-1961 Chinese famine has long-term health consequences. , 2010, The Journal of nutrition.
[25] B. Horsthemke. Mechanisms of imprint dysregulation , 2010, American journal of medical genetics. Part C, Seminars in medical genetics.
[26] T. Eggermann,et al. Russell-Silver syndrome , 1984, Indian journal of pediatrics.
[27] A. Ferguson-Smith,et al. Uniparental disomy and human disease: An overview , 2010, American journal of medical genetics. Part C, Seminars in medical genetics.
[28] K. Buiting. Prader–Willi syndrome and Angelman syndrome , 2010, American journal of medical genetics. Part C, Seminars in medical genetics.
[29] R. Weksberg. Imprinted genes and human disease , 2010, American journal of medical genetics. Part C, Seminars in medical genetics.
[30] D. Mackay,et al. Transient neonatal diabetes mellitus type 1 , 2010, American journal of medical genetics. Part C, Seminars in medical genetics.
[31] F. Hu,et al. Exposure to the Chinese Famine in Early Life and the Risk of Hyperglycemia and Type 2 Diabetes in Adulthood , 2010, Diabetes.
[32] M. Surani,et al. Genome-Wide Reprogramming in the Mouse Germ Line Entails the Base Excision Repair Pathway , 2010, Science.
[33] A. Gabory,et al. The H19 locus: Role of an imprinted non‐coding RNA in growth and development , 2010, BioEssays : news and reviews in molecular, cellular and developmental biology.
[34] S. Grewal. RNAi-dependent formation of heterochromatin and its diverse functions. , 2010, Current opinion in genetics & development.
[35] M. Pellegrini,et al. Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency , 2010, Nature.
[36] P. Robson,et al. Conserved long noncoding RNAs transcriptionally regulated by Oct4 and Nanog modulate pluripotency in mouse embryonic stem cells. , 2010, RNA.
[37] P. Slagboom,et al. The epigenome: Archive of the prenatal environment , 2009, Epigenetics.
[38] M. Shirakawa,et al. Structural basis for recognition of H3K4 methylation status by the DNA methyltransferase 3A ATRX–DNMT3–DNMT3L domain , 2009, EMBO reports.
[39] S. Scherer,et al. Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell–Silver syndrome , 2009, American journal of medical genetics. Part A.
[40] E. Heard,et al. Lessons from comparative analysis of X-chromosome inactivation in mammals , 2009, Chromosome Research.
[41] A. Harris,et al. Role of Hypoxia‐Inducible Factors in Epigenetic Regulation via Histone Demethylases , 2009, Annals of the New York Academy of Sciences.
[42] J. Rinn,et al. Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression , 2009, Proceedings of the National Academy of Sciences.
[43] P. Sham,et al. Prenatal malnutrition and adult schizophrenia: further evidence from the 1959-1961 Chinese famine. , 2009, Schizophrenia bulletin.
[44] Adam Z. Stein,et al. Transgenerational effects of prenatal exposure to the Dutch famine , 2009, BJOG : an international journal of obstetrics and gynaecology.
[45] G. Crawford,et al. Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns. , 2009, Genome research.
[46] W. Reik,et al. Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome) , 2009, PLoS genetics.
[47] C. Ponting,et al. Evolution and Functions of Long Noncoding RNAs , 2009, Cell.
[48] E. Sontheimer,et al. Origins and Mechanisms of miRNAs and siRNAs , 2009, Cell.
[49] Michael F. Lin,et al. Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals , 2009, Nature.
[50] A. Munshi,et al. Histone modifications dictate specific biological readouts. , 2009, Journal of genetics and genomics = Yi chuan xue bao.
[51] H. Kayserili,et al. Epigenetic mutations of the imprinted IGF2-H19 domain in Silver–Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes , 2008, Journal of Medical Genetics.
[52] Hein Putter,et al. Persistent epigenetic differences associated with prenatal exposure to famine in humans , 2008, Proceedings of the National Academy of Sciences.
[53] P. Leder,et al. A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints. , 2008, Developmental cell.
[54] K. Seeger,et al. Hypoxia upregulates the histone demethylase JMJD1A via HIF-1. , 2008, Biochemical and biophysical research communications.
[55] A. Hattersley,et al. Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57 , 2008, Nature Genetics.
[56] M. Skinner,et al. Transgenerational epigenetic effects of the endocrine disruptor vinclozolin on pregnancies and female adult onset disease. , 2008, Reproduction.
[57] Meredith Wilson,et al. The clinical phenotype of mosaicism for genome‐wide paternal uniparental disomy: Two new reports , 2008, American journal of medical genetics. Part A.
[58] N. Brockdorff,et al. Early Loss of Xist RNA Expression and Inactive X Chromosome Associated Chromatin Modification in Developing Primordial Germ Cells , 2007, PloS one.
[59] R. Waterland,et al. Epigenetic epidemiology of the developmental origins hypothesis. , 2007, Annual review of nutrition.
[60] G. Pinto,et al. 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations. , 2007, The Journal of clinical endocrinology and metabolism.
[61] K. Abe,et al. X Chromosome Reactivation Initiates in Nascent Primordial Germ Cells in Mice , 2007, PLoS genetics.
[62] Peter A. Jones,et al. Epigenetics and MicroRNAs , 2007, Pediatric Research.
[63] H. Cedar,et al. Role of DNA Methylation in Stable Gene Repression* , 2007, Journal of Biological Chemistry.
[64] Michael B. Stadler,et al. Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome , 2007, Nature Genetics.
[65] A. Stein,et al. Anthropometric measures in middle age after exposure to famine during gestation: evidence from the Dutch famine. , 2007, The American journal of clinical nutrition.
[66] V. P. Collins,et al. MMASS: an optimized array-based method for assessing CpG island methylation , 2006, Nucleic acids research.
[67] E. Li,et al. DNA methylation is a primary mechanism for silencing postmigratory primordial germ cell genes in both germ cell and somatic cell lineages , 2006, Development.
[68] Clive Osmond,et al. Early onset of coronary artery disease after prenatal exposure to the Dutch famine. , 2006, The American journal of clinical nutrition.
[69] C. Disteche,et al. Dosage compensation in mammals: fine-tuning the expression of the X chromosome. , 2006, Genes & development.
[70] W. Reik,et al. Epigenetic reprogramming in mammals. , 2005, Human molecular genetics.
[71] D. J. Driscoll,et al. Prader-Willi syndrome. , 1984, Current problems in pediatrics.
[72] J. Fulka,et al. DNA methylation pattern in human zygotes and developing embryos. , 2004, Reproduction.
[73] Paul T. Groth,et al. The ENCODE (ENCyclopedia Of DNA Elements) Project , 2004, Science.
[74] E. Li,et al. Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting , 2004, Nature.
[75] I. Wilmut,et al. Non-conservation of mammalian preimplantation methylation dynamics , 2004, Current Biology.
[76] A. Mclaren,et al. Primordial germ cells in the mouse. , 2003, Developmental biology.
[77] V. Kim,et al. The nuclear RNase III Drosha initiates microRNA processing , 2003, Nature.
[78] Wendy Dean,et al. Regulation of supply and demand for maternal nutrients in mammals by imprinted genes , 2003, The Journal of physiology.
[79] B. Tycko,et al. Physiological functions of imprinted genes , 2002, Journal of cellular physiology.
[80] W. Filipowicz. Faculty Opinions recommendation of A microRNA in a multiple-turnover RNAi enzyme complex. , 2002 .
[81] J. Clayton-Smith,et al. Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region. , 2002, Human Genetics.
[82] D. Bonthron,et al. A global disorder of imprinting in the human female germ line , 2002, Nature.
[83] T. Bestor,et al. Dnmt3L and the Establishment of Maternal Genomic Imprints , 2001, Science.
[84] W Dean,et al. Conservation of methylation reprogramming in mammalian development: Aberrant reprogramming in cloned embryos , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[85] W. Reik,et al. Epigenetic Reprogramming in Mammalian Development , 2001, Science.
[86] C. Plass,et al. Methylation matters , 2001, Journal of medical genetics.
[87] F. Ding,et al. Genomic Imprinting Disrupted by a Maternal Effect Mutation in the Dnmt1 Gene , 2001, Cell.
[88] L. Wilkinson,et al. Imprinted genes, cognition and behaviour , 2000, Trends in Cognitive Sciences.
[89] W P Robinson,et al. Mechanisms leading to uniparental disomy and their clinical consequences , 2000, BioEssays : news and reviews in molecular, cellular and developmental biology.
[90] J. Walter,et al. Embryogenesis: Demethylation of the zygotic paternal genome , 2000, Nature.
[91] R J Roberts,et al. Recombinant Human DNA (Cytosine-5) Methyltransferase , 1999, The Journal of Biological Chemistry.
[92] C Osmond,et al. Obesity at the age of 50 y in men and women exposed to famine prenatally. , 1999, The American journal of clinical nutrition.
[93] D. Haber,et al. DNA Methyltransferases Dnmt3a and Dnmt3b Are Essential for De Novo Methylation and Mammalian Development , 1999, Cell.
[94] H. Zoghbi,et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 , 1999, Nature Genetics.
[95] Alan S. Brown,et al. Prenatal Factors and Adult Mental and Physical Health , 1999, Canadian journal of psychiatry. Revue canadienne de psychiatrie.
[96] G. Mutter. Role of imprinting in abnormal human development. , 1997, Mutation research.
[97] J. Graham,et al. Longitudinal observations on 15 children with Wiedemann-Beckwith syndrome. , 1995, American journal of medical genetics.
[98] Rudolf Jaenisch,et al. Targeted mutation of the DNA methyltransferase gene results in embryonic lethality , 1992, Cell.
[99] V. Chapman,et al. Cell lineage-specific undermethylation of mouse repetitive DNA , 1984, Nature.
[100] R. Sahay,et al. IDIOPATHIC MALE INFERTILITY , 2013 .
[101] Martin Renqiang Min,et al. An integrated encyclopedia of DNA elements in the human genome , 2012 .
[102] Julia Arand,et al. DNA methylation reprogramming and DNA repair in the mouse zygote. , 2010, The International journal of developmental biology.
[103] J. Mathers. Early nutrition: impact on epigenetics. , 2007, Forum of nutrition.
[104] Wendy Dean,et al. Dynamic reprogramming of DNA methylation in the early mouse embryo. , 2002, Developmental biology.
[105] A. Bird. DNA methylation patterns and epigenetic memory. , 2002, Genes & development.
[106] W. Reik,et al. Genomic imprinting: parental influence on the genome , 2001, Nature Reviews Genetics.
[107] W. Watson,et al. Effect of hypoxia on hepatic DNA methylation and tRNA methyltransferase in rat: similarities to effects of methyl-deficient diets. , 1996, Journal of cellular biochemistry.
[108] T. Lyngbye,et al. [Beckwith-Wiedemann syndrome]. , 1985, Ugeskrift for laeger.
[109] B. Bruneau,et al. This Review Is Part of a Thematic Series on Epigenetics, Which Includes the following Articles: Epigenetic Regulation of the Cardiovascular System: Introduction to a Review Series Epigenome Mapping in Normal and Disease States Epigenetic Reprogramming for Cardiovascular Regeneration Chromatin Remode , 2022 .
[110] M. A. Rector,et al. References and Notes Materials and Methods Som Text Fig. S1 Table S1 References a Microrna in a Multiple- Turnover Rnai Enzyme Complex , 2022 .