(Q48000452)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9618174%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. (English)

1 reference

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Beckwith-Wiedemann syndrome

12 November 2019

main subject

1 reference

12

1 reference

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12 November 2019

Wolf Reik

14

1 reference

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12 November 2019

Wendy Dean

7

1 reference

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12 November 2019

author name string

M Paulsen

1

1 reference

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12 November 2019

K R Davies

2

1 reference

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12 November 2019

L M Bowden

3

1 reference

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12 November 2019

A J Villar

4

1 reference

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12 November 2019

O Franck

5

1 reference

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12 November 2019

M Fuermann

6

1 reference

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12 November 2019

T F Moore

8

1 reference

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12 November 2019

N Rodrigues

9

1 reference

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12 November 2019

K E Davies

10

1 reference

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12 November 2019

R J Hu

11

1 reference

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12 November 2019

E R Maher

13

1 reference

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12 November 2019

J Walter

15

1 reference

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12 November 2019

publication date

1 July 1998

1 reference

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12 November 2019

published in

Human Molecular Genetics

1 reference

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12 November 2019

volume

7

1 reference

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12 November 2019

issue

7

1 reference

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12 November 2019

page(s)

1149-1159

1 reference

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Imprinting mechanisms in mammals.

12 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Imprinted genes and regulation of gene expression by epigenetic inheritance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Competition--a common motif for the imprinting mechanism?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Parental imprinting and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Genomic imprinting in mice: its function and mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

DNA methylation in genomic imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Allele-specific replication timing of imprinted gene regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Tissue- and developmental stage-specific imprinting of the mouse proinsulin gene, Ins2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Relaxation of imprinted genes in human cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Structure and expression of the mouse L23mrp gene downstream of the imprinted H19 gene: biallelic expression and lack of interaction with the H19 enhancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Imprinting of mouse Kvlqt1 is developmentally regulated.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

A member of the MAP kinase phosphatase gene family in mouse containing a complex trinucleotide repeat in the coding region

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Interpreting cDNA sequences: some insights from studies on translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Functional characterization of human nucleosome assembly protein-2 (NAP1L4) suggests a role as a histone chaperone

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Normal lymphocyte development but delayed humoral immune response in CD81-null mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Drosophila NAP-1 is a core histone chaperone that functions in ATP-facilitated assembly of regularly spaced nucleosomal arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Members of the NAP/SET family of proteins interact specifically with B-type cyclins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

NAP1 acts with Clb1 to perform mitotic functions and to suppress polar bud growth in budding yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

An enhancer deletion affects both H19 and Igf2 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Yeast artificial chromosome libraries containing large inserts from mouse and human DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Simplified mammalian DNA isolation procedure

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1149

21 January 2018

Identifiers

DOI

10.1093/HMG/7.7.1149

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9618174%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference