The influence of non-coding RNAs on allele-specific gene expression in mammals (Q36088917)

12 August 2017

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title

The influence of non-coding RNAs on allele-specific gene expression in mammals (English)

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12 August 2017

Michael J O'Neill

1

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12 August 2017

language of work or name

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1 April 2005

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12 August 2017

published in

Human Molecular Genetics

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12 August 2017

volume

14 Spec No 1

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12 August 2017

page(s)

R113-20

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Genomic imprinting: intricacies of epigenetic regulation in clusters.

12 August 2017

cites work

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Identification and characterisation of imprinted genes in the mouse

21 January 2018

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Xist RNA and the mechanism of X chromosome inactivation

21 January 2018

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Recent advances in X-chromosome inactivation

21 January 2018

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The role of RNA interference in heterochromatic silencing

21 January 2018

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21 January 2018

In search of antisense

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Parental imprinting of the mouse insulin-like growth factor II gene.

21 January 2018

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The product of the H19 gene may function as an RNA

21 January 2018

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Parental imprinting of the mouse H19 gene

21 January 2018

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Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

21 January 2018

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Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

21 January 2018

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Igf2 imprinting does not require its own DNA methylation or H19 RNA.

21 January 2018

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Chromatin conformation of the H19 epigenetic mark

21 January 2018

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Characterization of novel parent-specific epigenetic modifications upstream of the imprinted mouse H19 gene.

21 January 2018

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Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

21 January 2018

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Transgenic RNAi reveals essential function for CTCF in H19 gene imprinting

21 January 2018

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CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease

21 January 2018

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Mechanisms of insulator function in gene regulation and genomic imprinting

21 January 2018

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Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.

21 January 2018

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M6P/IGF2R imprinting evolution in mammals

21 January 2018

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The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

21 January 2018

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Divergent evolution in M6P/IGF2R imprinting from the Jurassic to the Quaternary

21 January 2018

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Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes

21 January 2018

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The non-coding Air RNA is required for silencing autosomal imprinted genes

21 January 2018

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Imprinted silencing of Slc22a2 and Slc22a3 does not need transcriptional overlap between Igf2r and Air.

21 January 2018

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Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

21 January 2018

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Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting

21 January 2018

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A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

21 January 2018

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Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1

21 January 2018

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Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome

21 January 2018

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Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation.

21 January 2018

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An antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control region

21 January 2018

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Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.

21 January 2018

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Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12.

21 January 2018

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Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region.

21 January 2018

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Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region

21 January 2018

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Imprinted microRNA genes transcribed antisense to a reciprocally imprinted retrotransposon-like gene

21 January 2018

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Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12.

21 January 2018

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The callipyge locus: evidence for the trans interaction of reciprocally imprinted genes

21 January 2018

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Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

21 January 2018

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Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

21 January 2018

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Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

21 January 2018

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‘Puppet’ Children A Report on Three Cases

21 January 2018

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UBE3A/E6-AP mutations cause Angelman syndrome

21 January 2018

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Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

21 January 2018

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The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain

21 January 2018

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Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

21 January 2018

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Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

21 January 2018

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The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a

21 January 2018

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Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

21 January 2018

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The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice

21 January 2018

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Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

21 January 2018

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Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome

21 January 2018

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Disruption of the mouse necdin gene results in early post-natal lethality

21 January 2018

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Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

21 January 2018

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A mouse model for Prader-Willi syndrome imprinting-centre mutations

21 January 2018

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Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome

21 January 2018

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Minireview: GNAS: normal and abnormal functions.

21 January 2018

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Activating mutations of the stimulatory G protein in the McCune-Albright syndrome

21 January 2018

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Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome

21 January 2018

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Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene

21 January 2018

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The gsalpha gene: predominant maternal origin of transcription in human thyroid gland and gonads

21 January 2018

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Neuroendocrine secretory protein 55 (NESP55): alternative splicing onto transcripts of the GNAS gene and posttranslational processing of a maternally expressed protein

21 January 2018

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The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins

21 January 2018

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Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins

21 January 2018

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Identification of a methylation imprint mark within the mouse Gnas locus

21 January 2018

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Epigenetic properties and identification of an imprint mark in the Nesp-Gnasxl domain of the mouse Gnas imprinted locus.

21 January 2018

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Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy

21 January 2018

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Mutations of the Gs alpha-subunit gene in Albright hereditary osteodystrophy detected by denaturing gradient gel electrophoresis

21 January 2018

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Imprinting in Albright's hereditary osteodystrophy

21 January 2018

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Paternal imprinting of Galpha(s) in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a.

21 January 2018

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The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding.

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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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

21 January 2018

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The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus

21 January 2018

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Evolutionary conservation of possible functional domains of the human and murine XIST genes

21 January 2018

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Inheritance of a pre-inactivated paternal X chromosome in early mouse embryos.

21 January 2018

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Epigenetic dynamics of imprinted X inactivation during early mouse development

21 January 2018

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Reactivation of the paternal X chromosome in early mouse embryos

21 January 2018

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X-chromosome inactivation: closing in on proteins that bind Xist RNA.

21 January 2018

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Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse

21 January 2018

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Non-random X chromosome inactivation in mammalian cells.

21 January 2018

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Tsix, a gene antisense to Xist at the X-inactivation centre

21 January 2018

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Targeted mutagenesis of Tsix leads to nonrandom X inactivation.

21 January 2018

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CTCF, a candidate trans-acting factor for X-inactivation choice

21 January 2018

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Methylation profiles of DXPas34 during the onset of X-inactivation

21 January 2018

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De novo DNA methylation is dispensable for the initiation and propagation of X chromosome inactivation.

21 January 2018

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X inactivation: pre- or post-fertilisation turn-off?

21 January 2018

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Tsix transcription- versus RNA-based mechanisms in Xist repression and epigenetic choice.

21 January 2018

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Genomic imprinting at the WT1 gene involves a novel coding transcript (AWT1) that shows deregulation in Wilms' tumours.

21 January 2018

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The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 gene.

21 January 2018

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Lack of reciprocal genomic imprinting of sense and antisense RNA of mouse insulin-like growth factor II receptor in the central nervous system

21 January 2018

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Genomic imprinting and kinship: how good is the evidence?

21 January 2018

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Ectopic Expression of DLK1 Protein in Skeletal Muscle of Padumnal Heterozygotes Causes the Callipyge Phenotype

21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/HMG/DDI108

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12 August 2017

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