(Q41523994)

2 October 2017

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

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2 October 2017

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5

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2 October 2017

Weksberg R

1

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2 October 2017

Shen DR

series ordinal

2

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2 October 2017

Fei YL

series ordinal

3

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2 October 2017

Song QL

series ordinal

4

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2 October 2017

language of work or name

English

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publication date

1 October 1993

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2 October 2017

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2 October 2017

5

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2 October 2017

143-150

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2 October 2017

2

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https://scigraph.springernature.com/pub.10.1038/ng1093-143

2 October 2017

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cites work

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Chromosome 11 and Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

The Wiedemann-Beckwith syndrome: pedigree studies on five families with evidence for autosomal dominant inheritance with variable expressivity

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Beckwith-Wiedemann syndrome: a demonstration of the mechanisms responsible for the excess of transmitting females

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Wiedemann-Beckwith syndrome: autosomal-dominant inheritance in a family

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Uniparental paternal disomy in a genetic cancer-predisposing syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Insulin-like growth factors I and II.

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Tissue-specific and developmentally regulated transcription of the insulin-like growth factor 2 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Isolation of the human insulin-like growth factor genes: insulin-like growth factor II and insulin genes are contiguous

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Expression of insulin-like growth factor-II transcripts in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues.

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Parental genomic imprinting of the human IGF2 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Dads and disomy and disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Polymerase chain reaction (PCR) for detection of APal polymorphism at the insulin like growth factor II gene (IGF2)

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Monoallelic expression of the human H19 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Maternal allele loss in Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

The myc oncogene: its role in transformation and differentiation

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Genetic mosaicism in normal tissues of Wilms' tumour patients

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Parental-origin-specific epigenetic modification of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

PstI polymorphism within the 3' untranslated region of the insulin gene detectable by the polymerase chain reaction (INS)

1 reference

https://api.crossref.org/works/10.1038%2FNG1093-143

7 January 2021

Identifiers

DOI

10.1038/NG1093-143

1 reference

Dimensions Publication ID

2 October 2017

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1 reference