Parent-of-Origin DNA Methylation Dynamics during Mouse Development.
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R. Jaenisch | Hao Wu | S. Markoulaki | C. Shivalila | Yonatan Stelzer | Yuelin Song | Y. Stelzer | Hao Wu
[1] Arjun Raj,et al. Visualizing allele-specific expression in single cells reveals epigenetic mosaicism in an H19 loss-of-imprinting mutant , 2016, Genes & development.
[2] Xi C. He,et al. The Dlk1-Gtl2 Locus Preserves LT-HSC Function by Inhibiting the PI3K-mTOR Pathway to Restrict Mitochondrial Metabolism. , 2016, Cell stem cell.
[3] N. Benvenisty,et al. Pluripotent stem cells in disease modelling and drug discovery , 2016, Nature Reviews Molecular Cell Biology.
[4] I. Sandovici,et al. Differential genomic imprinting regulates paracrine and autocrine roles of IGF2 in mouse adult neurogenesis , 2015, Nature Communications.
[5] R. Jaenisch,et al. Tracing Dynamic Changes of DNA Methylation at Single-Cell Resolution , 2015, Cell.
[6] Jun S. Liu,et al. Quantitative and functional interrogation of parent-of-origin allelic expression biases in the brain , 2015, eLife.
[7] Michael Q. Zhang,et al. Integrative analysis of 111 reference human epigenomes , 2015, Nature.
[8] J. Cavaille,et al. The miR‐379/miR‐410 cluster at the imprinted Dlk1‐Dio3 domain controls neonatal metabolic adaptation , 2014, The EMBO journal.
[9] Matthew D. Schultz,et al. The developmental potential of iPSCs is greatly influenced by reprogramming factor selection. , 2014, Cell stem cell.
[10] O. Stegle,et al. Single-Cell Genome-Wide Bisulfite Sequencing for Assessing Epigenetic Heterogeneity , 2014, Nature Methods.
[11] J. Peters. The role of genomic imprinting in biology and disease: an expanding view , 2014, Nature Reviews Genetics.
[12] W. Reik,et al. Reprogramming the Methylome: Erasing Memory and Creating Diversity , 2014, Cell stem cell.
[13] Julie V. Harness,et al. Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment , 2014, Genome research.
[14] J. Nathans,et al. Cellular Resolution Maps of X Chromosome Inactivation: Implications for Neural Development, Function, and Disease , 2014, Neuron.
[15] V. Baladrón,et al. Dual role of delta-like 1 homolog (DLK1) in skeletal muscle development and adult muscle regeneration , 2013, Development.
[16] M. Gut,et al. Whole-genome bisulfite sequencing of two distinct interconvertible DNA methylomes of mouse embryonic stem cells. , 2013, Cell stem cell.
[17] G. Hon,et al. Adult tissue methylomes harbor epigenetic memory at embryonic enhancers , 2013, Nature Genetics.
[18] A. van Oudenaarden,et al. Allele-specific detection of single mRNA molecules in situ , 2013, Nature Methods.
[19] A. Gnirke,et al. Charting a dynamic DNA methylation landscape of the human genome , 2013, Nature.
[20] W. Reik,et al. FGF Signaling Inhibition in ESCs Drives Rapid Genome-wide Demethylation to the Epigenetic Ground State of Pluripotency , 2013, Clinical Epigenetics.
[21] N. Benvenisty,et al. Identification of Novel Imprinted Differentially Methylated Regions by Global Analysis of Human-Parthenogenetic-Induced Pluripotent Stem Cells , 2013, Stem cell reports.
[22] B. Ren,et al. Base-Resolution Analyses of Sequence and Parent-of-Origin Dependent DNA Methylation in the Mouse Genome , 2012, Cell.
[23] A. Ferguson-Smith. Genomic imprinting: the emergence of an epigenetic paradigm , 2011, Nature Reviews Genetics.
[24] Kirsten R. McEwen,et al. Postnatal loss of Dlk1 imprinting in stem cells and niche-astrocytes regulates neurogenesis , 2011, Nature.
[25] A. Ferguson-Smith,et al. Uniparental disomy and human disease: An overview , 2010, American journal of medical genetics. Part C, Seminars in medical genetics.
[26] G. Moore,et al. The Importance of Imprinting in the Human Placenta , 2010, PLoS genetics.
[27] Tomohiro Kono,et al. Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells , 2010, Nature.
[28] Y. Sotomaru,et al. Deletion of Gtl2, imprinted non-coding RNA, with its differentially methylated region induces lethal parent-origin-dependent defects in mice. , 2009, Human molecular genetics.
[29] R. Jaenisch,et al. Somatic cell nuclear transfer and derivation of embryonic stem cells in the mouse. , 2008, Methods.
[30] A. Ferguson-Smith,et al. Genomic imprinting at the mammalian Dlk1-Dio3 domain. , 2008, Trends in genetics : TIG.
[31] J. Cavaille,et al. Non‐coding RNAs in imprinted gene clusters , 2008, Biology of the cell.
[32] Kenji Nakamura,et al. Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta , 2008, Nature Genetics.
[33] William Davies,et al. Genomic imprinting effects on brain development and function , 2007, Nature Reviews Neuroscience.
[34] W. Reik. Stability and flexibility of epigenetic gene regulation in mammalian development , 2007, Nature.
[35] J. Cavaille,et al. Differential regulation of imprinting in the murine embryo and placenta by the Dlk1-Dio3 imprinting control region , 2007, Development.
[36] A. Ferguson-Smith,et al. Analysis of mouse conceptuses with uniparental duplication/deficiency for distal chromosome 12: comparison with chromosome 12 uniparental disomy and implications for genomic imprinting , 2006, Cytogenetic and Genome Research.
[37] N. Brockdorff,et al. Global hypomethylation of the genome in XX embryonic stem cells , 2005, Nature Genetics.
[38] K. Robertson. DNA methylation and human disease , 2005, Nature Reviews Genetics.
[39] L. Wilkinson,et al. Imprinted gene expression in the brain , 2005, Neuroscience & Biobehavioral Reviews.
[40] J. Rossant,et al. Mouse embryonic chimeras: tools for studying mammalian development , 2003, Development.
[41] J. Cavaille,et al. Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12 , 2003, Nature Genetics.
[42] Martina Paulsen,et al. Imprinted microRNA genes transcribed antisense to a reciprocally imprinted retrotransposon-like gene , 2003, Nature Genetics.
[43] H. Sul,et al. Mice Lacking Paternally Expressed Pref-1/Dlk1 Display Growth Retardation and Accelerated Adiposity , 2002, Molecular and Cellular Biology.
[44] M. Surani,et al. Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12. , 2000, Development.
[45] N. Cockett,et al. Polar Overdominance at the Ovine callipyge Locus , 1996, Science.
[46] R. Jaenisch,et al. Germ-line passage is required for establishment of methylation and expression patterns of imprinted but not of nonimprinted genes. , 1996, Genes & development.
[47] Rudolf Jaenisch,et al. Role for DNA methylation in genomic imprinting , 1993, Nature.
[48] M. Surani,et al. Influence of paternally imprinted genes on development. , 1991, Development.
[49] D. Solter,et al. The developmental fate of androgenetic, parthenogenetic, and gynogenetic cells in chimeric gastrulating mouse embryos. , 1988, Genes & development.
[50] D. Solter,et al. Completion of mouse embryogenesis requires both the maternal and paternal genomes , 1984, Cell.
[51] M. Surani,et al. Development of gynogenetic eggs in the mouse: implications for parthenogenetic embryos. , 1983, Science.
[52] R. Jaenisch,et al. Monitoring Dynamics of DNA Methylation at Single-Cell Resolution during Development and Disease. , 2015, Cold Spring Harbor symposia on quantitative biology.
[53] E. Redei,et al. Fine-tuning notes in the behavioral symphony: parent-of-origin allelic gene expression in the brain. , 2014, Advances in genetics.
[54] W. Reik,et al. Genomic imprinting: parental influence on the genome , 2001, Nature Reviews Genetics.
[55] M. Bartolomei,et al. Genomic imprinting in mammals. , 1997, Annual review of genetics.