| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/NG0293-170 |
| P698 | PubMed publication ID | 8499950 |
| P2093 | author name string | Williams EA | |
| Tam PP | |||
| Tan SS | |||
| P2860 | cites work | Expression of alpha-galactosidase in preimplantation mouse embryos | Q28511003 |
| Control of chromosome inactivation | Q34087576 | ||
| Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse | Q34088761 | ||
| Mammalian X-chromosome inactivation | Q34257279 | ||
| Mechanisms of X-chromosome regulation | Q39569909 | ||
| HGPRT activity changes in preimplantation mouse embryos | Q44554534 | ||
| Methylation of CpG sites of two X-linked genes coincides with X-inactivation in the female mouse embryo but not in the germ line | Q45266088 | ||
| Sequential X chromosome inactivation coupled with cellular differentiation in early mouse embryos | Q59054723 | ||
| Derivation of mouse intestinal crypts from single progenitor cells | Q59060822 | ||
| Differential expression of α-fetoprotein genes on the inactive X chromosome in extraembryonic and somatic tissues of a transgenic mouse line | Q59086853 | ||
| Both X chromosomes function before visible X-chromosome inactivation in female mouse embryos | Q59094665 | ||
| Preferential expression of the maternally derived X chromosome in the mouse yolk sac | Q62555376 | ||
| Variation for X chromosome expression in mice detected by electrophoresis of phosphoglycerate kinase | Q67404030 | ||
| Demonstration of somatic mutation and colonic crypt clonality by X-linked enzyme histochemistry | Q68376417 | ||
| A chicken transferrin gene in transgenic mice escapes X-chromosome inactivation | Q68992792 | ||
| Methylation of the Hprt gene on the inactive X occurs after chromosome inactivation | Q69687603 | ||
| Differentiation of X chromosomes in early female mouse embryos | Q70016583 | ||
| A stem-line model for cellular and chromosomal differentiation in early mouse-development | Q70907332 | ||
| X-chromosome inactivation in extra-embryonic membranes of diploid parthenogenetic mouse embryos demonstrated by differential staining | Q71373424 | ||
| Regional and temporal changes in the pattern of X-chromosome replication during the early post-implantation development of the female mouse | Q72675838 | ||
| A MOUSE TRANSLOCATION SUPPRESSING SEX-LINKED VARIEGATION | Q77161988 | ||
| CYTOLOGICAL STUDY OF SEARLE'S X-AUTOSOME TRANSLOCATION IN MUS MUSCULUS | Q78317408 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 170-174 | |
| P577 | publication date | 1993-02-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | X-chromosome inactivation occurs at different times in different tissues of the post-implantation mouse embryo | |
| P478 | volume | 3 |
| Q37489046 | A change of ploidy can modify epigenetic silencing |
| Q36919163 | A history of the discovery of random x chromosome inactivation in the human female and its significance |
| Q36336288 | A rapid passage through a two-active-X-chromosome state accompanies the switch of imprinted X-inactivation patterns in mouse trophoblast stem cells |
| Q37153299 | Abnormal corneal epithelial maintenance in mice heterozygous for the micropinna microphthalmia mutation Mp |
| Q51033226 | An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrid. |
| Q49044208 | An X-linked GFP transgene reveals unexpected paternal X-chromosome activity in trophoblastic giant cells of the mouse placenta |
| Q52142100 | An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta. |
| Q44012248 | Analysis of cell lineage relationships in taste buds. |
| Q52042657 | Analysis of the Xist RNA isoforms suggests two distinctly different forms of regulation. |
| Q82711913 | Application of lacZ transgenic mice to cell lineage studies |
| Q59504115 | Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies |
| Q36374698 | Buccal swab as a reliable predictor for X inactivation ratio in inaccessible tissues |
| Q37632384 | Cellular resolution maps of X chromosome inactivation: implications for neural development, function, and disease |
| Q37306058 | Chromosome-wide mechanisms to decouple gene expression from gene dose during sex-chromosome evolution. |
| Q28589675 | Cited1 is required in trophoblasts for placental development and for embryo growth and survival |
| Q42525357 | Clonal analysis of patterns of growth, stem cell activity, and cell movement during the development and maintenance of the murine corneal epithelium |
| Q43972738 | Clonal architecture of the mouse hippocampus. |
| Q33820421 | Clonality markers in polycythaemia and primary thrombocythaemia |
| Q77747080 | Comparative methylation analysis of murine transgenes that undergo or escape X-chromosome inactivation |
| Q36057344 | Constitutive activation of MEK1 in chondrocytes causes Stat1-independent achondroplasia-like dwarfism and rescues the Fgfr3-deficient mouse phenotype |
| Q44728760 | Control of cortical neuron migration and layering: cell and non cell-autonomous effects of p35. |
| Q37124190 | Control of patterns of corneal innervation by Pax6. |
| Q38353039 | CpG dinucleotide methylation patterns in the human androgen receptor gene and X-chromosome inactivation in peripheral blood leukocytes of phenotypically normal women |
| Q36048943 | Developmental interneuron subtype deficits after targeted loss of Arx |
| Q35846168 | Developmental timing and tissue specificity of heterochromatin-mediated silencing |
| Q34119060 | Effects of aberrant Pax6 gene dosage on mouse corneal pathophysiology and corneal epithelial homeostasis |
| Q46880086 | Emergence of cellular markers and functional ionotropic glutamate receptors on tangentially dispersed cells in the developing mouse retina |
| Q28757092 | Environmental exposures and gene regulation in disease etiology |
| Q38626695 | Epigenesis and plasticity of mouse trophoblast stem cells |
| Q40701215 | Evolution of mammalian sex chromosomes and sex-determining genes. |
| Q51855866 | Exceptional LINE density at V1R loci: the Lyon repeat hypothesis revisited on autosomes. |
| Q49122808 | Expression of an X-linked HMG-lacZ transgene in mouse embryos: implication of chromosomal imprinting and lineage-specific X-chromosome activity |
| Q28513526 | FGFR1 is required for the development of the auditory sensory epithelium |
| Q79802062 | Fission of pancreatic islets during postnatal growth of the mouse |
| Q34611680 | Genetic and developmental analysis of X-inactivation in interspecific hybrid mice suggests a role for the Y chromosome in placental dysplasia. |
| Q35543807 | Heterochromatin, position effects, and the genetic dissection of chromatin. |
| Q33178120 | Heterogeneous X inactivation in trophoblastic cells of human full-term female placentas |
| Q34963442 | Increased corneal epithelial turnover contributes to abnormal homeostasis in the Pax6(+/-) mouse model of aniridia |
| Q35691966 | Interaction between hedgehog signalling and PAX6 dosage mediates maintenance and regeneration of the corneal epithelium |
| Q35882389 | Lack of X inactivation associated with maternal X isodisomy: evidence for a counting mechanism prior to X inactivation during human embryogenesis |
| Q33816529 | Lineage specification of neuronal precursors in the mouse spinal cord |
| Q33929594 | Lineage-specific regulation of imprinted X inactivation in extraembryonic endoderm stem cells |
| Q34090494 | Maternally transmitted severe glucose 6-phosphate dehydrogenase deficiency is an embryonic lethal |
| Q35974470 | Mechanisms controlling the formation of retinal mosaics |
| Q33679308 | Monozygotic twins discordant for Aicardi syndrome |
| Q48021691 | Mosaic analysis of small intestinal development using the spf(ash)-heterozygous female mouse |
| Q21284134 | Mosaic analysis of stem cell function and wound healing in the mouse corneal epithelium |
| Q48620961 | Mosaics of islet-1-expressing amacrine cells assembled by short-range cellular interactions. |
| Q71890842 | Mouse endogenous X-linked genes do not show lineage-specific delayed inactivation during development |
| Q36973379 | Multicolor lineage tracing methods and intestinal tumors |
| Q33910551 | Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation. |
| Q52540121 | NEMO/IKK gamma-deficient mice model incontinentia pigmenti. |
| Q36110131 | Neural crest contribution to lingual mesenchyme, epithelium and developing taste papillae and taste buds |
| Q74562756 | Non-cell-autonomous photoreceptor degeneration in rds mutant mice mosaic for expression of a rescue transgene |
| Q34173783 | Normal X-inactivation mosaicism in corneas of heterozygous FlnaDilp2/+ female mice--a model of human filamin A (FLNA) diseases |
| Q97640439 | OFCD syndrome and extraembryonic defects are revealed by conditional mutation of the polycomb-group repressive complex 1.1 (PRC1.1) gene BCOR |
| Q22065590 | Offspring from Oocytes Derived from in Vitro Primordial Germ Cell-like Cells in Mice |
| Q35080583 | Pancreatic cell lineage analyses in mice |
| Q41711767 | Pathogenesis of polycythaemia vera |
| Q42637029 | Quantitative analysis of patch patterns in mosaic tissues with ClonalTools software |
| Q34472888 | Radial and tangential dispersion patterns in the mouse retina are cell-class specific |
| Q48303382 | Radial mosaicism and tangential cell dispersion both contribute to mouse neocortical development |
| Q36285380 | Random X inactivation in the mule and horse placenta. |
| Q52212199 | Regionalisation of cell fate and morphogenetic movement of the mesoderm during mouse gastrulation. |
| Q47966300 | Relative transgene expression frequencies in homozygous versus hemizygous transgenic mice. |
| Q48400512 | Separate progenitors for radial and tangential cell dispersion during development of the cerebral neocortex |
| Q34383242 | Sex-specific parent-of-origin allelic expression in the mouse brain |
| Q72533488 | Simultaneous detection of beta-galactosidase activity and surface antigen expression in viable haematopoietic cells |
| Q35250287 | Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism |
| Q34551007 | Taste receptor cells arise from local epithelium, not neurogenic ectoderm |
| Q79357525 | Tetraploid embryos rescue the early defects of tw5/tw5 mouse embryos |
| Q33890376 | The clonal origin and clonal evolution of epithelial tumours |
| Q28596243 | The core planar cell polarity gene, Vangl2, directs adult corneal epithelial cell alignment and migration |
| Q43104654 | The great escape |
| Q34683156 | The role of tangential dispersion in retinal mosaic formation |
| Q39738331 | Three inhibitors of FGF receptor, ERK, and GSK3 establishes germline-competent embryonic stem cells of C57BL/6N mouse strain with high efficiency and stability |
| Q47340635 | Transgenic mice over-expressing endothelin-1 in testis transactivated by a Cre/loxP system showed decreased testicular capillary blood flow |
| Q34228130 | Twinning |
| Q41099938 | Twinning: mechanisms and genetic implications |
| Q37536110 | Variegated transgene expression in mouse mammary gland is determined by the transgene integration locus. |
| Q46300721 | When the Lyon(ized chromosome) roars: ongoing expression from an inactive X chromosome |
| Q40672454 | X chromosome inactivation and the Xist gene |
| Q36437452 | X chromosome inactivation patterns correlate with fetal-placental anatomy in monozygotic twin pairs: implications for immune relatedness and concordance for autoimmunity |
| Q36397379 | X inactivation and somatic cell selection rescue female mice carrying a Piga-null mutation |
| Q33675242 | X inactivation patterns in female monozygotic twins and their families |
| Q71864623 | X-chromosome activity of the mouse primordial germ cells revealed by the expression of an X-linked lacZ transgene |
| Q71958937 | X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes |
| Q77609113 | X-inactivation pattern in the liver of a manifesting female with ornithine transcarbamylase (OTC) deficiency |
| Q36568885 | X-tra! X-tra! News from the mouse X chromosome |
| Q43105065 | XIST expression and X-chromosome inactivation in human preimplantation embryos |
| Q49074365 | XIST expression is repressed when X inactivation is reversed in human placental cells: A model for study ofXIST regulation |
| Q34064288 | Xist has properties of the X-chromosome inactivation centre |
| Q43792424 | disabled-1 functions cell autonomously during radial migration and cortical layering of pyramidal neurons. |
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