X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse.

No abstract is available for this paper.

• Publication year

  1996

• Venue

  Human Molecular Genetics

• Publication date

  1996-03-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1093/HMG/5.3.391PMID 8852665
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• Mapping and expression of the ubiquitin-activating enzyme E1 (Ube1) gene in the mouse

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• Chromatin structure and gene expression.

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• A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status.

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  1995cited by this paper
• The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation.

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• Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals.

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• Escape from X inactivation in human and mouse.

  1995cited by this paper
• Cloning and characterization of a novel zinc finger gene in Xp11.2.

  1995cited by this paper
• Physical linkage of the cdc2-related gene (PCTK1) and the ubiquitin-activating enzyme E1 gene (UBE1) on human Xp11.3.

  1995cited by this paper
• Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22.

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  1995cited by this paper
• Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

  1995cited by this paper
• The DXS423E gene in Xp11.21 escapes X chromosome inactivation.

  1995cited by this paper
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  1995cited by this paper
• CpG islands in human ZFX and ZFY and mouse Zfx genes: sequence similarities and methylation differences.

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• Imprinting and X chromosome counting mechanisms determine Xist expression in early mouse development.

  1994cited by this paper
• New insights reveal complex mechanisms involved in genomic imprinting.

  1994cited by this paper
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  1994cited by this paper
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• B cell-specific demethylation: a novel role for the intronic kappa chain enhancer sequence.

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• Isolation and characterization of XE169, a novel human gene that escapes X-inactivation.

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• Molecular and Genetic Studies of Human X Chromosome Inactivation

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• A human pseudoautosomal gene encodes the ANT3 ADP/ATP translocase and escapes X-inactivation.

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• Isolation of a new gene from the distal short arm of the human X chromosome that escapes X-inactivation.

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• A family of human cdc2‐related protein kinases.

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• Marsupial Y chromosome encodes a homologue of the mouse Y-linked candidate spermatogenesis gene Ube1y

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• PCTAIRE-1 and PCTAIRE-3, two members of a novel cdc2/CDC28-related protein kinase gene family.

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• The silence of the X

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• 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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• Genome Analysis. Volume 1. Genetic and Physical Mapping

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• A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

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• A candidate spermatogenesis gene on the mouse Y chromosome is homologous to ubiquitin-activating enzyme E1

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• X-chromosome inactivation may explain the difference in viability of XO humans and mice

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• A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

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• Inactivation of the Rps4 gene on the mouse X chromosome.

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• Molecular cloning, sequence, and tissue distribution of the human ubiquitin-activating enzyme E1.

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• Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.

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• Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome

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• X chromosome inactivation of the human TIMP gene.

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• Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation.

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• Localization of the human A1S9 gene complementing the ts A1S9 mouse L-cell defect in DNA replication and cell cycle progression to Xp11.2----p11.4.

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• In vivo footprint and methylation analysis by PCR-aided genomic sequencing: comparison of active and inactive X chromosomal DNA at the CpG island and promoter of human PGK-1.

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