(Q35043723)

6 August 2017

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title

Imprinting and disease (English)

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6 August 2017

Jörn Walter

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6 August 2017

Martina Paulsen

series ordinal

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6 August 2017

language of work or name

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1 February 2003

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Seminars in Cell & Developmental Biology

6 August 2017

published in

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6 August 2017

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6 August 2017

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6 August 2017

page(s)

101-110

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A catalogue of imprinted genes and parent-of-origin effects in humans and animals.

6 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Genomic imprinting: implications for human disease

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

The impact of genomic imprinting for neurobehavioral and developmental disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Wiedemann-Beckwith syndrome: further prenatal characterization of the condition

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Parental genomic imprinting of the human IGF2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Placental-specific IGF-II is a major modulator of placental and fetal growth.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

p57(Kip2) regulates the proper development of labyrinthine and spongiotrophoblasts

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Placental overgrowth in mice lacking the imprinted gene Ipl

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Genomic imprinting of Mash2, a mouse gene required for trophoblast development

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

The human ASCL2 gene escaping genomic imprinting and its expression pattern

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Roles for genomic imprinting and the zygotic genome in placental development.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Urinary odour preferences in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Paternally inherited HLA alleles are associated with women's choice of male odor

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

DNA methylation in genomic imprinting, development, and disease

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Dnmt3L and the establishment of maternal genomic imprints

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

An enhancer deletion affects both H19 and Igf2 expression

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Disruption of imprinting caused by deletion of the H19 gene region in mice

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

The pre-implantation ontogeny of the H19 methylation imprint

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

An imprinting element from the mouse H19 locus functions as a silencer in Drosophila.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

A silencer element identified in Drosophila is required for imprinting of H19 reporter transgenes in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

An intragenic methylated region in the imprinted Igf2 gene augments transcription.

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

The mouse Gtl2 gene is differentially expressed during embryonic development, encodes multiple alternatively spliced transcripts, and may act as an RNA

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

Mouse parthenogenetic embryos with monoallelic H19 expression can develop to day 17.5 of gestation

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084-9521%2802%2900142-8

7 January 2021

10.1016/S1084-9521(02)00142-8

Identifiers

DOI

1 reference

6 August 2017

1 reference