Mechanisms of X-chromosome inactivation.
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[1] A. C. Chinault,et al. Reduced levels of histone H3 acetylation on the inactive X chromosome in human females , 1996, Chromosoma.
[2] H. Willard,et al. X-inactivation profile reveals extensive variability in X-linked gene expression in females , 2005, Nature.
[3] Shridar Ganesan,et al. Dicer-deficient mouse embryonic stem cells are defective in differentiation and centromeric silencing. , 2005, Genes & development.
[4] B. Turner,et al. Differential underacetylation of histones H2A, H3 and H4 on the inactive X chromosome in human female cells , 1996, Human Genetics.
[5] C. Disteche,et al. Boundaries between chromosomal domains of X inactivation and escape bind CTCF and lack CpG methylation during early development. , 2005, Developmental cell.
[6] R. Jaenisch,et al. Developmentally regulated alterations in Polycomb repressive complex 1 proteins on the inactive X chromosome , 2004, The Journal of cell biology.
[7] Huntington F Willard,et al. Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[8] M. Schartl. Sex chromosome evolution in non-mammalian vertebrates. , 2004, Current opinion in genetics & development.
[9] J. Lawrence,et al. Ubiquitinated proteins including uH2A on the human and mouse inactive X chromosome: enrichment in gene rich bands , 2004, Chromosoma.
[10] Haruhiko Koseki,et al. Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation. , 2004, Developmental cell.
[11] T. Ohhata,et al. X‐inactivation is stably maintained in mouse embryos deficient for histone methyl transferase G9a , 2004, Genesis.
[12] Jeannie T. Lee,et al. Tsix Transcription- versus RNA-Based Mechanisms in Xist Repression and Epigenetic Choice , 2004, Current Biology.
[13] T. Canfield,et al. Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins , 2004, BMC Biology.
[14] G. Hannon,et al. Unlocking the potential of the human genome with RNA interference , 2004, Nature.
[15] I. Craig,et al. Application of microarrays to the analysis of the inactivation status of human X-linked genes expressed in lymphocytes , 2004, European Journal of Human Genetics.
[16] Steven Henikoff,et al. Histone variants, nucleosome assembly and epigenetic inheritance. , 2004, Trends in genetics : TIG.
[17] Anton Wutz,et al. A Chromosomal Memory Triggered by Xist Regulates Histone Methylation in X Inactivation , 2004, PLoS biology.
[18] Edith Heard,et al. Differential Histone H3 Lys-9 and Lys-27 Methylation Profiles on the X Chromosome , 2004, Molecular and Cellular Biology.
[19] S. Robertson,et al. Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[20] R. Adams,et al. Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome. , 2004, American journal of human genetics.
[21] N. Brockdorff,et al. Heterochromatin on the inactive X chromosome delays replication timing without affecting origin usage. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[22] E. Li,et al. De novo DNA methylation is dispensable for the initiation and propagation of X chromosome inactivation , 2004, Development.
[23] B. Meyer,et al. Recruitment and Spreading of the C. elegans Dosage Compensation Complex Along X Chromosomes , 2004, Science.
[24] N. Brockdorff,et al. Reactivation of the Paternal X Chromosome in Early Mouse Embryos , 2004, Science.
[25] D. Reinberg,et al. Epigenetic Dynamics of Imprinted X Inactivation During Early Mouse Development , 2004, Science.
[26] M. Young,et al. The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous gene , 1995, Human Genetics.
[27] P. Avner,et al. Mapping the murine Xce locus with (CA)n repeats , 1993, Mammalian Genome.
[28] H. Willard. Tissue-specific heterogeneity in DNA replication patterns of human X chromosomes , 1977, Chromosoma.
[29] A. Farazmand,et al. Expression of XIST sense and antisense in bovine fetal organs and cell cultures , 2004, Chromosome Research.
[30] N. Benvenisty,et al. Gene trap as a tool for genome annotation and analysis of X chromosome inactivation in human embryonic stem cells. , 2004, Nucleic acids research.
[31] P. Avner,et al. Controlling X-inactivation in mammals: what does the centre hold? , 2003, Seminars in cell & developmental biology.
[32] Carolyn J. Brown,et al. Forming facultative heterochromatin: silencing of an X chromosome in mammalian females , 2003, Cellular and Molecular Life Sciences CMLS.
[33] Karl J. Friston,et al. Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans. , 2003, Brain : a journal of neurology.
[34] R. Hansen,et al. X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis. , 2003, Human molecular genetics.
[35] Andrew J. Bannister,et al. Consequences of the depletion of zygotic and embryonic enhancer of zeste 2 during preimplantation mouse development , 2003, Development.
[36] Carolyn J. Brown,et al. Characterization of expression at the human XIST locus in somatic, embryonal carcinoma, and transgenic cell lines. , 2003, Genomics.
[37] N. Brockdorff,et al. Skewing X chromosome choice by modulating sense transcription across the Xist locus. , 2003, Genes & development.
[38] H. Willard,et al. Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome. , 2003, Human molecular genetics.
[39] Peter Kraft,et al. High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[40] Jeannie T. Lee,et al. X-linked genes in female embryonic stem cells carry an epigenetic mark prior to the onset of X inactivation. , 2003, Human molecular genetics.
[41] M. Bycroft,et al. The crystal structure of AF1521 a protein from Archaeoglobus fulgidus with homology to the non-histone domain of macroH2A. , 2003, Journal of molecular biology.
[42] A. Ladurner. Inactivating chromosomes: a macro domain that minimizes transcription. , 2003, Molecular cell.
[43] V. Meller. Initiation of dosage compensation in Drosophila embryos depends on expression of the roX RNAs , 2003, Mechanisms of Development.
[44] En Li,et al. Suv 39 h-Mediated Histone H 3 Lysine 9 Methylation Directs DNA Methylation to Major Satellite Repeats at Pericentric Heterochromatin , 2003 .
[45] T. Kouzarides,et al. The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase. , 2003, Nucleic acids research.
[46] D. Angelov,et al. The histone variant macroH2A interferes with transcription factor binding and SWI/SNF nucleosome remodeling. , 2003, Molecular cell.
[47] N. Brockdorff,et al. Establishment of histone h3 methylation on the inactive X chromosome requires transient recruitment of Eed-Enx1 polycomb group complexes. , 2003, Developmental cell.
[48] Hengbin Wang,et al. Role of Histone H3 Lysine 27 Methylation in X Inactivation , 2003, Science.
[49] Jeannie T. Lee,et al. Xite, X-inactivation intergenic transcription elements that regulate the probability of choice. , 2003, Molecular cell.
[50] B. Migeon. Is Tsix repression of Xist specific to mouse? , 2003, Nature Genetics.
[51] Tony Kouzarides,et al. The Methyl-CpG-binding Protein MeCP2 Links DNA Methylation to Histone Methylation* , 2003, The Journal of Biological Chemistry.
[52] Jeannie T. Lee,et al. Characterization and quantitation of differential Tsix transcripts: implications for Tsix function. , 2003, Human molecular genetics.
[53] E. Heard,et al. Integrated kinetics of X chromosome inactivation in differentiating embryonic stem cells , 2003, Cytogenetic and Genome Research.
[54] J. Lawrence,et al. Unbalanced X;autosome translocations provide evidence for sequence specificity in the association of XIST RNA with chromatin. , 2002, Human molecular genetics.
[55] A. Sharp,et al. Molecular and cytogenetic analysis of the spreading of X inactivation in X;autosome translocations. , 2002, Human molecular genetics.
[56] R. Jaenisch,et al. Meiotic sex chromosome inactivation in male mice with targeted disruptions of Xist , 2002, Journal of Cell Science.
[57] B. Turner,et al. Cellular Memory and the Histone Code , 2002, Cell.
[58] C. Deng,et al. BRCA1 Supports XIST RNA Concentration on the Inactive X Chromosome , 2002, Cell.
[59] Robin Lovell-Badge,et al. A Model System for Study of Sex Chromosome Effects on Sexually Dimorphic Neural and Behavioral Traits , 2002, The Journal of Neuroscience.
[60] E. Li. Chromatin modification and epigenetic reprogramming in mammalian development , 2002, Nature Reviews Genetics.
[61] Christos Sotiriou,et al. Gene expression profiles of BRCA1-linked, BRCA2-linked, and sporadic ovarian cancers. , 2002, Journal of the National Cancer Institute.
[62] N. Brockdorff,et al. Mitotically Stable Association of Polycomb Group Proteins Eed and Enx1 with the Inactive X Chromosome in Trophoblast Stem Cells , 2002, Current Biology.
[63] J. Lawrence,et al. An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[64] H. Willard,et al. Autosomal Dominant Mutations Affecting X Inactivation Choice in the Mouse , 2002, Science.
[65] Tony Kouzarides,et al. Histone H3 Lysine 4 Methylation Disrupts Binding of Nucleosome Remodeling and Deacetylase (NuRD) Repressor Complex* , 2002, The Journal of Biological Chemistry.
[66] T. Kouzarides. Histone methylation in transcriptional control. , 2002, Current opinion in genetics & development.
[67] S. Berger,et al. Histone modifications in transcriptional regulation. , 2002, Current opinion in genetics & development.
[68] S. Jacobs,et al. Structure of HP1 Chromodomain Bound to a Lysine 9-Methylated Histone H3 Tail , 2002, Science.
[69] D. Reinberg,et al. Set9, a novel histone H3 methyltransferase that facilitates transcription by precluding histone tail modifications required for heterochromatin formation. , 2002, Genes & development.
[70] A. West,et al. Insulators: many functions, many mechanisms. , 2002, Genes & development.
[71] Rudolf Jaenisch,et al. Chromosomal silencing and localization are mediated by different domains of Xist RNA , 2002, Nature Genetics.
[72] A. Børresen-Dale,et al. High frequency of skewed X inactivation in young breast cancer patients , 2002, Journal of medical genetics.
[73] Laurent Duret,et al. Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine. , 2000, Genome research.
[74] A. C. Chinault,et al. Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes , 2002, Nature Genetics.
[75] A. Bird. DNA methylation patterns and epigenetic memory. , 2002, Genes & development.
[76] R. Jaenisch,et al. Antisense Transcription through theXist Locus Mediates Tsix Function in Embryonic Stem Cells , 2001, Molecular and Cellular Biology.
[77] C. Allis,et al. Methylation of Histone H3 at Lys-9 Is an Early Mark on the X Chromosome during X Inactivation , 2001, Cell.
[78] Jeannie T. Lee,et al. CTCF, a Candidate Trans-Acting Factor for X-Inactivation Choice , 2001, Science.
[79] B. Migeon,et al. Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivation. , 2001, American journal of human genetics.
[80] N. Brockdorff,et al. Centrosomal association of histone macroH2A1.2 in embryonic stem cells and somatic cells. , 2001, Experimental cell research.
[81] C. Allis,et al. Translating the Histone Code , 2001, Science.
[82] Huntington F. Willard,et al. Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome , 2001, Nucleic Acids Res..
[83] C. Costanzi,et al. MACROH2A2, a New Member of the MACROH2A Core Histone Family* , 2001, The Journal of Biological Chemistry.
[84] K. Johansen,et al. The JIL-1 Tandem Kinase Mediates Histone H3 Phosphorylation and Is Required for Maintenance of Chromatin Structure in Drosophila , 2001, Cell.
[85] V. Rakyan,et al. The marks, mechanisms and memory of epigenetic states in mammals. , 2001, The Biochemical journal.
[86] Rudolf Jaenisch,et al. Synergism of Xist Rna, DNA Methylation, and Histone Hypoacetylation in Maintaining X Chromosome Inactivation , 2001, The Journal of cell biology.
[87] H. Willard,et al. Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant. , 2001, Human molecular genetics.
[88] K. Zhao,et al. MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome. , 2001, Human molecular genetics.
[89] E. Li,et al. Regulation of imprinted X-chromosome inactivation in mice by Tsix. , 2001, Development.
[90] Carolyn J. Brown,et al. X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications. , 2001, Human molecular genetics.
[91] P. Sharp,et al. XIST RNA Associates with Specific Regions of the Inactive X Chromatin* , 2000, The Journal of Biological Chemistry.
[92] C. Wijmenga,et al. Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant. , 2000, Human molecular genetics.
[93] R. Jaenisch,et al. Dynamic Relocalization of Histone Macroh2a1 from Centrosomes to Inactive X Chromosomes during X Inactivation , 2000, The Journal of cell biology.
[94] C. Ponting,et al. Regulation of chromatin structure by site-specific histone H3 methyltransferases , 2000, Nature.
[95] L. Wilkinson,et al. Imprinted genes, cognition and behaviour , 2000, Trends in Cognitive Sciences.
[96] J A Bailey,et al. Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[97] R. Schultz,et al. Histone macroH2A1 is concentrated in the inactive X chromosome of female preimplantation mouse embryos. , 2000, Development.
[98] K. Johansen,et al. Jil-1, a Chromosomal Kinase Implicated in Regulation of Chromatin Structure, Associates with the Male Specific Lethal (Msl) Dosage Compensation Complex , 2000, The Journal of cell biology.
[99] R. Kelley,et al. Ordered assembly of roX RNAs into MSL complexes on the dosage-compensated X chromosome in Drosophila , 2000, Current Biology.
[100] N. Brockdorff,et al. Histone Macroh2a1.2 Relocates to the Inactive X Chromosome after Initiation and Propagation of X-Inactivation , 1999, The Journal of cell biology.
[101] H. Willard,et al. A first-generation X-inactivation profile of the human X chromosome. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[102] C. Disteche,et al. Escapees on the X chromosome. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[103] P. Avner,et al. Functional Analysis of the DXPas34Locus, a 3′ Regulator of Xist Expression , 1999, Molecular and Cellular Biology.
[104] P. Sharp,et al. Promoter-specific hypoacetylation of X-inactivated genes. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[105] D. Haber,et al. DNA Methyltransferases Dnmt3a and Dnmt3b Are Essential for De Novo Methylation and Mammalian Development , 1999, Cell.
[106] Jeannie T. Lee,et al. Targeted Mutagenesis of Tsix Leads to Nonrandom X Inactivation , 1999, Cell.
[107] R. Jaenisch,et al. Messenger RNAs encoding mouse histone macroH2A1 isoforms are expressed at similar levels in male and female cells and result from alternative splicing. , 1999, Nucleic acids research.
[108] A. West,et al. The Protein CTCF Is Required for the Enhancer Blocking Activity of Vertebrate Insulators , 1999, Cell.
[109] R. Jaenisch,et al. Conditional deletion of Xist disrupts histone macroH2A localization but not maintenance of X inactivation , 1999, Nature Genetics.
[110] Lei Zeng,et al. Structure and ligand of a histone acetyltransferase bromodomain , 1999, Nature.
[111] N. Mise,et al. Molecular cloning of antisense transcripts of the mouse Xist gene. , 1999, Biochemical and biophysical research communications.
[112] L. Looijenga,et al. Heterogeneous X inactivation in trophoblastic cells of human full-term female placentas. , 1999, American journal of human genetics.
[113] Jeannie T. Lee,et al. Tsix, a gene antisense to Xist at the X-inactivation centre , 1999, Nature Genetics.
[114] J. Lee,et al. Genetic analysis of the mouse X inactivation center defines an 80-kb multifunction domain. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[115] A. Sood,et al. Association between nonrandom X-chromosome inactivation and BRCA1 mutation in germline DNA of patients with ovarian cancer. , 1999, Journal of the National Cancer Institute.
[116] N. Brockdorff,et al. Xist RNA exhibits a banded localization on the inactive X chromosome and is excluded from autosomal material in cis. , 1999, Human molecular genetics.
[117] D. Page,et al. A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated , 1998, Nature.
[118] Carolyn J. Brown,et al. Stabilization and Localization of Xist RNA are Controlled by Separate Mechanisms and are Not Sufficient for X Inactivation , 1998, The Journal of cell biology.
[119] M. Lyon,et al. X-Chromosome inactivation: a repeat hypothesis , 1998, Cytogenetic and Genome Research.
[120] H. Willard,et al. The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA. , 1998, American journal of human genetics.
[121] C. Costanzi,et al. Histone macroH2A1 is concentrated in the inactive X chromosome of female mammals , 1998, Nature.
[122] J. Strouboulis,et al. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription , 1998, Nature Genetics.
[123] C. Brown,et al. Induction of XIST expression from the human active X chromosome in mouse/human somatic cell hybrids by DNA demethylation. , 1998, Nucleic acids research.
[124] J. Pehrson,et al. Evolutionary conservation of histone macroH2A subtypes and domains. , 1998, Nucleic acids research.
[125] T. Canfield,et al. Reactivation of XIST in normal fibroblasts and a somatic cell hybrid: abnormal localization of XIST RNA in hybrid cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[126] S. Rastan,et al. Regulatory elements in the minimal promoter region of the mouse Xist gene. , 1997, Gene.
[127] L. Looijenga,et al. X inactivation in human testicular tumors. XIST expression and androgen receptor methylation status. , 1997, The American journal of pathology.
[128] Brian D. Hendrich,et al. Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation , 1997, Nucleic Acids Res..
[129] Y. Sakaki,et al. Identification of critical CpG sites for repression of L1 transcription by DNA methylation. , 1997, Gene.
[130] N. Brockdorff,et al. The mouse Smcx gene exhibits developmental and tissue specific variation in degree of escape from X inactivation. , 1996, Human molecular genetics.
[131] H. Willard,et al. Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene. , 1996, Human molecular genetics.
[132] R. Jaenisch,et al. DNA hypomethylation can activate Xist expression and silence X-linked genes. , 1996, Genes & development.
[133] R. Jaenisch,et al. A 450 kb Transgene Displays Properties of the Mammalian X-Inactivation Center , 1996, Cell.
[134] M. Leppert,et al. Heritability of X chromosome--inactivation phenotype in a large family. , 1996, American journal of human genetics.
[135] D. Schorderet,et al. Characterization of the promoter region of the mouse Xist gene. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[136] R. Jaenisch,et al. Loss of methylation activates Xist in somatic but not in embryonic cells. , 1995, Genes & development.
[137] S. Rastan,et al. Evidence that random and imprinted Xist expression is controlled by preemptive methylation , 1994, Cell.
[138] B. Turner,et al. The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression , 1993, Cell.
[139] S. Bressler,et al. Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST. , 1993, Human molecular genetics.
[140] Carolyn J. Brown,et al. Evolutionary conservation of possible functional domains of the human and murine XIST genes. , 1993, Human molecular genetics.
[141] H. Willard,et al. Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation. , 1993, Cold Spring Harbor symposia on quantitative biology.
[142] A. Razin,et al. Gene methylation patterns and expression. , 1993, EXS.
[143] H. Leonhardt,et al. A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei , 1992, Cell.
[144] Rudolf Jaenisch,et al. Targeted mutation of the DNA methyltransferase gene results in embryonic lethality , 1992, Cell.
[145] J. Spencer,et al. Sex chromosome evolution: platypus gene mapping suggests that part of the human X chromosome was originally autosomal. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[146] V. Chapman,et al. Use of a HpaII-polymerase chain reaction assay to study DNA methylation in the Pgk-1 CpG island of mouse embryos at the time of X-chromosome inactivation , 1990, Molecular and cellular biology.
[147] A. Riggs,et al. DNA methylation and late replication probably aid cell memory, and type I DNA reeling could aid chromosome folding and enhancer function. , 1990, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[148] B. Migeon,et al. Studies of X-chromosome inactivation in trisomies. , 1989, Cytogenetics and cell genetics.
[149] H. Willard,et al. Clonal analysis using recombinant DNA probes from the X-chromosome. , 1987, Cancer research.
[150] G. Martin,et al. Methylation of the Hprt gene on the inactive X occurs after chromosome inactivation , 1987, Cell.
[151] T. Mohandas,et al. Reactivation of an inactive human X chromosome: evidence for X inactivation by DNA methylation. , 1981, Science.
[152] B. Migeon,et al. Stability of the “two active X” phenotype in triploid somatic cells , 1979, Cell.
[153] T. Mohandas,et al. Non-inactivation of an x-chromosome locus in man. , 1979, Science.
[154] H. Willard,et al. Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. , 1976, American journal of human genetics.
[155] M. Sasaki,et al. Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse , 1975, Nature.
[156] S. Gartler,et al. Ontogeny of X-chromosome inactivation in the female germ line. , 1975, Experimental cell research.
[157] B. Migeon. Stability of X Chromosomal Inactivation in Human Somatic Cells , 1972, Nature.
[158] W. E. Poole,et al. Phosphoglycerate kinase polymorphism in kangaroos provides further evidence for paternal X inactivation. , 1971, Nature: New biology.
[159] L. B. Russell. Mammalian X-Chromosome Action: Inactivation Limited in Spread and in Region of Origin , 1963, Science.
[160] M. Lyon. Sex chromatin and gene action in the mammalian X-chromosome. , 1962, American journal of human genetics.
[161] M. Lyon. Gene Action in the X-chromosome of the Mouse (Mus musculus L.) , 1961, Nature.