(Q48084685)

8 February 2018

title

Mosaic and polymorphic imprinting of the WT1 gene in humans (English)

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8 February 2018

Reeve AE

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8 February 2018

author name string

Jinno Y

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8 February 2018

Yun K

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8 February 2018

Nishiwaki K

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8 February 2018

Kubota T

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8 February 2018

Ogawa O

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8 February 2018

Niikawa N

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8 February 2018

language of work or name

English

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publication date

1 March 1994

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8 February 2018

published in

Nature Genetics

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8 February 2018

volume

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8 February 2018

issue

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8 February 2018

page(s)

305-309

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8 February 2018

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

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Relaxation of imprinted genes in human cancer.

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Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression

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Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

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

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7 January 2021

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

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https://api.crossref.org/works/10.1038%2FNG0394-305

7 January 2021

Parental genomic imprinting of the human IGF2 gene

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https://api.crossref.org/works/10.1038%2FNG0394-305

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FNG0394-305

7 January 2021

Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1

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https://api.crossref.org/works/10.1038%2FNG0394-305

7 January 2021

Genomic imprinting and the strange case of the insulin-like growth factor II receptor

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https://api.crossref.org/works/10.1038%2FNG0394-305

7 January 2021

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

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https://api.crossref.org/works/10.1038%2FNG0394-305

7 January 2021

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

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https://api.crossref.org/works/10.1038%2FNG0394-305

7 January 2021

Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion

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7 January 2021

Wilms' tumour: reconciling genetics and biology

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7 January 2021

Wilms tumor with aniridia/iris dysplasia and apparently normal chromosomes

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7 January 2021

Clinicopathologic review of twelve children with nephropathy, Wilms tumor, and genital abnormalities (Drash syndrome).

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7 January 2021

Monoallelic expression of the human H19 gene

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7 January 2021

The genomic organization and expression of the WT1 gene

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7 January 2021

Hinfl polymorphism within the 3′ untranslated region of the candidate Wilms tumour gene

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7 January 2021

Methylation and imprinting: from host defense to gene regulation?

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7 January 2021

Genome imprinting, cellular mosaicism and carcinogenesis.

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7 January 2021

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

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7 January 2021

Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-305

7 January 2021

WT-1 is required for early kidney development

1 reference

https://api.crossref.org/works/10.1038%2FNG0394-305

7 January 2021

Mouse small eye results from mutations in a paired-like homeobox-containing gene

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7 January 2021

Identifiers

DOI

10.1038/NG0394-305

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8 February 2018

1 reference

8 February 2018