(Q52220644)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798299%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798299%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

2

1 reference

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26 October 2019

author name string

M Montagna

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798299%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

L Chieco-Bianchi

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798299%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

E D'Andrea

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798299%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

publication date

1 January 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798299%20AND%20SRC:MED&resulttype=core&format=json

Journal of Cancer Research and Clinical Oncology

26 October 2019

published in

1 reference

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26 October 2019

volume

120

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798299%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

issue

12

1 reference

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26 October 2019

page(s)

732-736

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798299%20AND%20SRC:MED&resulttype=core&format=json

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

26 October 2019

cites work

1 reference

12 December 2020

Relaxation of imprinted genes in human cancer.

1 reference

12 December 2020

Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome.

1 reference

12 December 2020

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma

1 reference

12 December 2020

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

1 reference

12 December 2020

Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature

1 reference

12 December 2020

Parental imprinting of the mouse H19 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Preferential loss of maternal alleles in sporadic Wilms' tumour.

1 reference

12 December 2020

Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann—Beckwith syndrome

1 reference

12 December 2020

Molecular differential pathology of rhabdomyosarcoma

1 reference

12 December 2020

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

1 reference

12 December 2020

The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans

1 reference

12 December 2020

Three non-overlapping regions of chromosome arm 11p allele loss identified in infantile tumors of adrenal and liver

1 reference

12 December 2020

Report of the committee on the genetic constitution of chromosome 11.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching

1 reference

12 December 2020

Tumour-suppressor activity of H19 RNA

1 reference

12 December 2020

Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11

1 reference

12 December 2020

Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma

1 reference

12 December 2020

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

1 reference

12 December 2020

Dinucleotide repeat polymorphism at the IGF2R locus

1 reference

12 December 2020

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

12 December 2020

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

1 reference

12 December 2020

A routine method for the establishment of permanent growing lymphoblastoid cell lines

1 reference

12 December 2020

Genomic imprinting and carcinogenesis

1 reference

12 December 2020

The product of the H19 gene may function as an RNA

1 reference

12 December 2020

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

1 reference

12 December 2020

Loss of genes on the short arm of chromosome 11 in bladder cancer

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01194272

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7798299%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference