(Q58061470)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8220428%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

title

The insulin-like growth factor type-2 receptor gene is imprinted in the mouse but not in humans (English)

1 reference

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27 October 2019

1 reference

1

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27 October 2019

author name string

Mariman EC

2

1 reference

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27 October 2019

Schepens MT

3

1 reference

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27 October 2019

Rehder H

4

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27 October 2019

Ropers HH

5

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27 October 2019

language of work or name

English

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publication date

1 September 1993

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27 October 2019

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27 October 2019

volume

5

1 reference

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27 October 2019

page(s)

74-78

1 reference

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27 October 2019

issue

1

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https://scigraph.springernature.com/pub.10.1038/ng0993-74

27 October 2019

exact match

0 references

cites work

Differential expression of the human insulin-like growth factor II gene. Characterization of the IGF-II mRNAs and an mRNA encoding a putative IGF-II-associated protein

1 reference

Identification and initial characterization of a fourth leader exon and promoter of the human IGF-II gene.

21 January 2018

1 reference

Structural analysis of the human insulin-like growth factor-II P3 promoter

21 January 2018

1 reference

Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation.

21 January 2018

1 reference

7 January 2021

Genomic imprinting determines methylation of parental alleles in transgenic mice

1 reference

7 January 2021

Degree of methylation of transgenes is dependent on gamete of origin

1 reference

7 January 2021

Parental legacy determines methylation and expression of an autosomal transgene: a molecular mechanism for parental imprinting

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Parental imprinting of the mouse H19 gene

1 reference

7 January 2021

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

1 reference

7 January 2021

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

1 reference

7 January 2021

Monoallelic expression of the human H19 gene

1 reference

7 January 2021

Relaxation of imprinted genes in human cancer.

1 reference

7 January 2021

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

1 reference

7 January 2021

Parental genomic imprinting of the human IGF2 gene

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Parental imprinting of the human H19 gene

1 reference

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

7 January 2021

Rat insulin-like growth factor II gene. A single gene with two promoters expressing a multitranscript family.

1 reference

7 January 2021

Genetic analysis of genomic imprinting: An Imprintor-1 gene controls inactivation of the paternal copy of the mouse Tme locus

1 reference

7 January 2021

An evaluation of the inactive mouse X chromosome in somatic cell hybrids

1 reference

7 January 2021

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

1 reference

7 January 2021

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

1 reference

7 January 2021

Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q

1 reference

7 January 2021

A novel cyclin encoded by a bcl1-linked candidate oncogene

1 reference

7 January 2021

Tight linkage of apolipoprotein C2 to myotonic dystrophy on chromosome 19

1 reference

7 January 2021

Parental origin of chromosomes involved in the translocation t(9;22).

1 reference

7 January 2021

Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory

1 reference

7 January 2021

PCR amplification of long DNA fragments

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0993-74

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8220428%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

27 October 2019

0 references

1 reference