X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny. - Wikidata - wikimedia - TriplyDB

X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

http://www.wikidata.org/entity/Q34409822

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A mammal-specific Doublesex homolog associates with male sex chromatin and is required for male meiosis HORMAD2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activity The opossum genome: insights and opportunities from an alternative mammal Environmental epigenomics and disease susceptibility Two-step imprinted X inactivation: repeat versus genic silencing in the mouse Locus-specific ribosomal RNA gene silencing in nucleolar dominance Chromosomal gene movements reflect the recent origin and biology of therian sex chromosomes The status of dosage compensation in the multiple X chromosomes of the platypus Genome-wide views of chromatin structure Meiotic silencing and the epigenetics of sex ATRX marks the inactive X chromosome (Xi) in somatic cells and during imprinted X chromosome inactivation in trophoblast stem cells.Sex, sex chromosomes and gene expression Nucleolar dominance and ribosomal RNA gene silencing Paternally biased X inactivation in mouse neonatal brain Promoter analysis reveals globally differential regulation of human long non-coding RNA and protein-coding genes.Differential methylation of Xite and CTCF sites in Tsix mirrors the pattern of X-inactivation choice in mice.Sex-specific gene expression in preimplantation mouse embryos Activity map of the tammar X chromosome shows that marsupial X inactivation is incomplete and escape is stochastic.Modification of the FoxP3 transcription factor principally affects inducible T regulatory cells in a model of experimental autoimmune encephalomyelitis.The rhox homeobox gene cluster is imprinted and selectively targeted for regulation by histone h1 and DNA methylation.MDC1 directs chromosome-wide silencing of the sex chromosomes in male germ cells Loss of DNMT1o disrupts imprinted X chromosome inactivation and accentuates placental defects in females.Poly(ADP-ribose) polymerase-2 contributes to the fidelity of male meiosis I and spermiogenesis Detection of nascent RNA, single-copy DNA and protein localization by immunoFISH in mouse germ cells and preimplantation embryos.A survey for novel imprinted genes in the mouse placenta by mRNA-seq Painting of fourth and chromosome-wide regulation of the 4th chromosome in Drosophila melanogaster Sex chromosome silencing in the marsupial male germ line.A tapetal-like fundus reflex in a healthy male: evidence against a role in the pathophysiology of retinal degeneration?Random X inactivation in the mule and horse placenta.Molecular features and functional constraints in the evolution of the mammalian X chromosome.How imprinting centres work.Lessons from comparative analysis of species-specific imprinted genes.Regulatory RNAs and chromatin modification in dosage compensation: a continuous path from flies to humans?Impaired imprinted X chromosome inactivation is responsible for the skewed sex ratio following in vitro fertilization.X-inactivation and X-reactivation: epigenetic hallmarks of mammalian reproduction and pluripotent stem cells.Genomic imprinting mechanisms in mammals.Requirement for balanced Ca/NFAT signaling in hematopoietic and embryonic development.Multimegabase silencing in nucleolar dominance involves siRNA-directed DNA methylation and specific methylcytosine-binding proteins.Sex differences in response of the bovine embryo to colony-stimulating factor 2.Chromosome-wide profiling of X-chromosome inactivation and epigenetic states in fetal brain and placenta of the opossum, Monodelphis domestica.

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X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

http://www.wikidata.org/entity/Q34409822

description

2005 nî lūn-bûn

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2005 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2005年の論文

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2005年論文

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2005年論文

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X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

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X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

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X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

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X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

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X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

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X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

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X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

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Nature Reviews Genetics

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X-chromosome inactivation: a hypothesis linking ontogeny and phylogeny.

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Jeannie T Lee

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Khanh D Huynh

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P2860

Human testis-specific PGK gene lacks introns and possesses characteristics of a processed gene

Functional coherence of the human Y chromosome

XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure

A testis-specific form of the human pyruvate dehydrogenase E1 alpha subunit is coded for by an intronless gene on chromosome 4

In the platypus a meiotic chain of ten sex chromosomes shares genes with the bird Z and mammal X chromosomes

Expression of alpha-galactosidase in preimplantation mouse embryos

Silencing of unpaired chromatin and histone H2A ubiquitination in mammalian meiosis

An X-to-autosome retrogene is required for spermatogenesis in mice

Testis-specific expression of a functional retroposon encoding glucose-6-phosphate dehydrogenase in the mouse

The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus

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