Somatic glypican 3 (GPC3) mutations in Wilms' tumour (Q38283630)

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Language	Label	Description	Also known as
English	Somatic glypican 3 (GPC3) mutations in Wilms' tumour	scientific article

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

title

Somatic glypican 3 (GPC3) mutations in Wilms' tumour (English)

1 reference

stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

author name string

G R M White

series ordinal

1

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stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

A M Kelsey

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2

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stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

J M Varley

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

J M Birch

series ordinal

4

1 reference

stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

language of work or name

English

0 references

publication date

1 June 2002

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stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

published in

British Journal of Cancer

1 reference

stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

volume

86

1 reference

stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

issue

12

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stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

page(s)

1920-1922

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stated in

Europe PubMed Central

PMC publication ID

2375433

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1 September 2017

cites work

Developmental roles of the glypicans

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

Proteoglycans and pattern formation: sugar biochemistry meets developmental genetics

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

Frequent silencing of the GPC3 gene in ovarian cancer cell lines

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

A small interstitial deletion in the GPC3 gene causes Simpson-Golabi-Behmel syndrome in a Dutch-Canadian family

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

Wilms tumor genetics

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

OCI-5/GPC3, a glypican encoded by a gene that is mutated in the Simpson-Golabi-Behmel overgrowth syndrome, induces apoptosis in a cell line-specific manner.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

Analysis of exon/intron structure and 400 kb of genomic sequence surrounding the 5'-promoter and 3'-terminal ends of the human glypican 3 (GPC3) gene

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

6 September 2017

The genetics of Wilms' tumor--a case of disrupted development

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

14 September 2017

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2375433

retrieved

23 June 2018

Expression of glypican 3 (GPC3) in embryonal tumors

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12085187

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PCR buffer optimization with uniform temperature regimen to facilitate automation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12085187

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns and temporal trends in the incidence of malignant disease in children: II. Solid tumours of childhood

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12085187

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12085187

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/SJ.BJC.6600417

1 reference

stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

Dimensions Publication ID

1000956987

0 references

PMC publication ID

2375433

1 reference

stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

PubMed publication ID

12085187

1 reference

stated in

Europe PubMed Central

PMC publication ID

2375433

retrieved

1 September 2017

ResearchGate publication ID

11290537

0 references

 

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