(Q41759014)

8 October 2017

1 reference

title

Insulin-like growth factor 2 and overgrowth: molecular biology and clinical implications (English)

1 reference

8 October 2017

1 reference

1

1 reference

8 October 2017

Reeve AE

2

1 reference

8 October 2017

1 March 1998

1 reference

Trends in Molecular Medicine

8 October 2017

1 reference

8 October 2017

4

1 reference

8 October 2017

110-115

1 reference

8 October 2017

3

1 reference

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

8 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Role of insulin-like growth factors in embryonic and postnatal growth

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

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%2FS1357-4310%2897%2901197-0

7 January 2021

Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Intrauterine growth retardation and postnatal growth failure associated with deletion of the insulin-like growth factor I gene

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Hemizygosity at the insulin-like growth factor I receptor (IGF1R) locus and growth failure in the ring chromosome 15 syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

c-Myc-induced apoptosis in fibroblasts is inhibited by specific cytokines.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Insulin-like growth factor II stimulates cell proliferation through the insulin receptor

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

A comprehensive and critical assessment of overgrowth and overgrowth syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Somatic overgrowth associated with overexpression of insulin-like growth factor II.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Wiedemann-Beckwith syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Tight linkage between the Beckwith-Wiedemann syndrome and a microsatellite marker for the TH locus.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13----pter.: correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Human p57(KIP2) defines a new imprinted domain on chromosome 11p but is not a tumour suppressor gene in Wilms tumour

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Genetic mosaicism in normal tissues of Wilms' tumour patients

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

OCI-5/rat glypican-3 binds to fibroblast growth factor-2 but not to insulin-like growth factor-2.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Activation of an imprinted allele of the insulin-like growth factor II gene implicated in rhabdomyosarcoma

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1357-4310%2897%2901197-0

7 January 2021

10.1016/S1357-4310(97)01197-0

Identifiers

DOI

1 reference

8 October 2017

1 reference

PubMed ID

9575493