Chromosome territory reorganization in a human disease with altered DNA methylation - Wikidata - awgldk - TriplyDB

Chromosome territory reorganization in a human disease with altered DNA methylation

Chromosome territory reorganization in a human disease with altered DNA methylation

http://www.wikidata.org/entity/Q36082296

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Spatial Genome Organization and Its Emerging Role as a Potential Diagnosis Tool DNA modifications: function and applications in normal and disease States DNA looping facilitates targeting of a chromatin remodeling enzyme.Germline genes hypomethylation and expression define a molecular signature in peripheral blood of ICF patients: implications for diagnosis and etiology.Altered intra-nuclear organisation of heterochromatin and genes in ICF syndrome.Coordinated expression domains in mammalian genomes ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing.Super-resolution structure of DNA significantly differs in buccal cells of controls and Alzheimer's patients Gene positioning.Alternative splicing of the human gene SYBL1 modulates protein domain architecture of Longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms Epigenetic control of hypoxia inducible factor-1α-dependent expression of placental growth factor in hypoxic conditions.Epigenetic regulatory mechanisms associated with infertility 3D-FISH analysis reveals chromatid cohesion defect during interphase in Roberts syndrome.Chromatin condensation via the condensin II complex is required for peripheral T-cell quiescence Mutations in ZBTB24 are associated with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2.Increased expression of P-glycoprotein and doxorubicin chemoresistance of metastatic breast cancer is regulated by miR-298.MeCP2 as a genome-wide modulator: the renewal of an old story.DNA methylation in development and human disease The dynamic DNA methylomes of double-stranded DNA viruses associated with human cancer.The dosage compensation complex shapes the conformation of the X chromosome in Drosophila.Spatial organization of genes as a component of regulated expression.Nuclear architecture as an epigenetic regulator of neural development and function.Genetic alterations of DNA methylation machinery in human diseases.A single day of 5-azacytidine exposure during development induces neurodegeneration in neonatal mice and neurobehavioral deficits in adult mice.Effects of methotrexate on the quality of oocyte maturation in vitro.The changes in chromosome 6 spatial organization during chromatin polytenization in the Calliphora erythrocephala Mg. (Diptera: Calliphoridae) nurse cells.

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P2860

Chromosome territory reorganization in a human disease with altered DNA methylation

http://www.wikidata.org/entity/Q36082296

description

2007 nî lūn-bûn

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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2007年论文

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name

Chromosome territory reorganization in a human disease with altered DNA methylation

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Chromosome territory reorganization in a human disease with altered DNA methylation

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type

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Chromosome territory reorganization in a human disease with altered DNA methylation

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Chromosome territory reorganization in a human disease with altered DNA methylation

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prefLabel

Chromosome territory reorganization in a human disease with altered DNA methylation

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Chromosome territory reorganization in a human disease with altered DNA methylation

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Proceedings of the National Academy of Sciences of the United States of America

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Chromosome territory reorganization in a human disease with altered DNA methylation

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Maria R Matarazzo

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Maurizio D'Esposito

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Shelagh Boyle

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P2860

Genetic variation in ICF syndrome: evidence for genetic heterogeneity

Chromatin decondensation and nuclear reorganization of the HoxB locus upon induction of transcription

A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced

Clustering of multiple specific genes and gene-rich R-bands around SC-35 domains: evidence for local euchromatic neighborhoods

Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region

Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes

The pseudoautosomal regions, SHOX and disease

A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation

Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications

The IL-9 receptor gene, located in the Xq/Yq pseudoautosomal region, has an autosomal origin, escapes X inactivation and is expressed from the Y

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104

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DNA methylation

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2034264

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