| P50 | author | Michael Kobor | Q42112272 |
| | Carolyn J. Brown | Q48078009 |
| | Allison M Cotton | Q55149604 |
| | Chih-Yu Chen | Q57230889 |
| P2093 | author name string | Wyeth W Wasserman | |
| | Lucia L Lam | |
| P2860 | cites work | A user's guide to the encyclopedia of DNA elements (ENCODE) | Q21092716 |
| | The DNA sequence of the human X chromosome | Q21735931 |
| | X-inactivation profile reveals extensive variability in X-linked gene expression in females | Q22122481 |
| | The UCSC Genome Browser Database: update 2006 | Q24538714 |
| | DNA methylation is the primary silencing mechanism for a set of germ line- and tumor-specific genes with a CpG-rich promoter | Q24554402 |
| | Escape from X inactivation in mice and humans | Q24601765 |
| | High-resolution analysis of DNA replication domain organization across an R/G-band boundary | Q24644428 |
| | A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced | Q24672840 |
| | Statistical significance for genomewide studies | Q24681264 |
| | A comparison of normalization methods for high density oligonucleotide array data based on variance and bias | Q27860710 |
| | Topological domains in mammalian genomes identified by analysis of chromatin interactions | Q28264221 |
| | The UCSC genome browser and associated tools | Q28273417 |
| | Boundaries between chromosomal domains of X inactivation and escape bind CTCF and lack CpG methylation during early development | Q28304098 |
| | Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis | Q28776573 |
| | Spatial partitioning of the regulatory landscape of the X-inactivation centre | Q29614999 |
| | Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome | Q29616819 |
| | An evaluation of new criteria for CpG islands in the human genome as gene markers | Q33197495 |
| | Evidence of influence of genomic DNA sequence on human X chromosome inactivation | Q33256101 |
| | Genomic environment predicts expression patterns on the human inactive X chromosome | Q33258823 |
| | CTdatabase: a knowledge-base of high-throughput and curated data on cancer-testis antigens | Q33374216 |
| | X chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophils | Q33734823 |
| | ENCODE whole-genome data in the UCSC Genome Browser: update 2012. | Q34072582 |
| | Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation | Q34206865 |
| | Mammalian X-chromosome inactivation | Q34257279 |
| | The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA | Q34386196 |
| | Analysis of active and inactive X chromosome architecture reveals the independent organization of 30 nm and large-scale chromatin structures | Q34571021 |
| | Word frequency analysis reveals enrichment of dinucleotide repeats on the human X chromosome and [GATA]n in the X escape region | Q34590995 |
| | A DNA insulator prevents repression of a targeted X-linked transgene but not its random or imprinted X inactivation | Q34682997 |
| | DNA methylation in transcriptional repression of two differentially expressed X-linked genes, GPC3 and SYBL1. | Q34828632 |
| | Chromosome-wide DNA methylation analysis predicts human tissue-specific X inactivation | Q35094123 |
| | Mapping identifiers for the integration of genomic datasets with the R/Bioconductor package biomaRt | Q35174434 |
| | Genetic evidence for the inactivation of a human autosomal locus attached to an inactive X chromosome. | Q35202468 |
| | DNA methylation profiles of human active and inactive X chromosomes | Q35451694 |
| | Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation | Q35570635 |
| | Epigenetic profiling of somatic tissues from human autopsy specimens identifies tissue- and individual-specific DNA methylation patterns | Q35784479 |
| | Escapees on the X chromosome | Q36087148 |
| | Spreading of X chromosome inactivation via a hierarchy of defined Polycomb stations | Q36285384 |
| | Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others | Q36395394 |
| | Targeting of >1.5 Mb of human DNA into the mouse X chromosome reveals presence of cis-acting regulators of epigenetic silencing | Q36439781 |
| | Number of CpG islands and genes in human and mouse | Q36738077 |
| | The ins and outs of gene regulation and chromosome territory organisation | Q36805999 |
| | Chromatin insulators: linking genome organization to cellular function | Q36895023 |
| | Transcription forms and remodels supercoiling domains unfolding large-scale chromatin structures | Q36946305 |
| | Escape from X chromosome inactivation is an intrinsic property of the Jarid1c locus | Q36964324 |
| | Normal human fibroblasts are resistant to RAS-induced senescence | Q37012141 |
| | Additional annotation enhances potential for biologically-relevant analysis of the Illumina Infinium HumanMethylation450 BeadChip array | Q37088466 |
| | High-resolution analysis of epigenetic changes associated with X inactivation. | Q37287380 |
| | Inactive X chromosome-specific histone H3 modifications and CpG hypomethylation flank a chromatin boundary between an X-inactivated and an escape gene | Q37477610 |
| | Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome | Q37694528 |
| | X-chromosome inactivation: molecular mechanisms from the human perspective | Q37873373 |
| | Unbalanced X;autosome translocations provide evidence for sequence specificity in the association of XIST RNA with chromatin | Q38486666 |
| | Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocation | Q38491467 |
| | Chromosome bands--flavours to savour | Q40830908 |
| | Investigation of the "variable spreading" of X inactivation into a translocated autosome | Q41312220 |
| | Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1). | Q41939345 |
| | Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome | Q47694131 |
| | X-chromosome inactivation: a repeat hypothesis | Q47790328 |
| | X-autosome translocation in normal mother and effectively 21-monosomic daughter. | Q54719929 |
| | The distribution of CpG islands in mammalian chromosomes | Q57185094 |
| | Analysis of spreading of inactivation in eight X autosome translocations utilizing the high resolution RBG technique | Q70030391 |
| | Late replication studies in a human X/13 translocation: correlation with autosomal gene expression | Q70663287 |
| | X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes | Q71274653 |
| | Xist RNA exhibits a banded localization on the inactive X chromosome and is excluded from autosomal material in cis | Q77946272 |
| | Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation | Q82522139 |
| P4510 | describes a project that uses | limma | Q112236343 |
| P433 | issue | 5 | |
| P304 | page(s) | 1211-1223 | |
| P577 | publication date | 2013-10-24 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Spread of X-chromosome inactivation into autosomal sequences: role for DNA elements, chromatin features and chromosomal domains | |
| P478 | volume | 23 | |