(Q34446311)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

title

Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

Françoise Muscatelli

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

author name string

Elodie Le Meur

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

Miguel Landers

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

Rachel Sturny

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

Marc Lalande

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

language of work or name

English

0 references

publication date

29 August 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

number of pages

14

1 reference

based on heuristic

inferred from page(s)

published in

Developmental Biology

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

volume

286

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

page(s)

587-600

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

6 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16126194%20AND%20SRC:MED&resulttype=core&format=json

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

6 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Epigenetic gene regulation by noncoding RNAs

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Specific interference with gene expression induced by long, double-stranded RNA in mouse embryonal teratocarcinoma cell lines.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Calbindin D-28k and parvalbumin in the rat nervous system

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Angelman syndrome: a review of the clinical and genetic aspects

7 January 2021

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Epigenetic regulation of mammalian genomic imprinting

7 January 2021

1 reference

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Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

An imprinted, mammalian bicistronic transcript encodes two independent proteins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Intergenic transcription and developmental remodeling of chromatin subdomains in the human beta-globin locus.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11- q13 duplications

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Control elements within the PWS/AS imprinting box and their function in the imprinting process

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

UBE3A/E6-AP mutations cause Angelman syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Cytoplasmic and nuclear retained DMPK mRNAs are targets for RNA interference in myotonic dystrophy cells.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Molecular links between X-inactivation and autosomal imprinting: X-inactivation as a driving force for the evolution of imprinting?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Gene-specific timing and epigenetic memory in oocyte imprinting.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

RNA regulation: a new genetics?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

RNAi-mediated pathways in the nucleus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

The Angelman syndrome-associated protein, E6-AP, is a coactivator for the nuclear hormone receptor superfamily

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Specific and potent RNAi in the nucleus of human cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Promoter-restricted H3 Lys 4 di-methylation is an epigenetic mark for monoallelic expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Promoter-restricted histone code, not the differentially methylated DNA regions or antisense transcripts, marks the imprinting status of IGF2R in human and mouse.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

Neurons but not glial cells show reciprocal imprinting of sense and antisense transcripts of Ube3a

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2005.07.030