(Q41894867)

English

Intermediate grade osteosarcoma and chondrosarcoma arising in an osteochondroma. A case report of a patient with hereditary multiple exostoses

scientific article published on March 2002

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

0 references

Intermediate grade osteosarcoma and chondrosarcoma arising in an osteochondroma. A case report of a patient with hereditary multiple exostoses (English)

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

1 reference

based on heuristic

inferred from title

author name string

Bovée JV

1

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Sakkers RJ

2

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Geirnaerdt MJ

3

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Taminiau AH

4

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Hogendoorn PC

5

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

language of work or name

0 references

publication date

1 March 2002

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Journal of Clinical Pathology

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

55

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

3

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

226-229

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

Near-haploidy and subsequent polyploidization characterize the progression of peripheral chondrosarcoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

Tout-velu is a Drosophila homologue of the putative tumour suppressor EXT-1 and is needed for Hh diffusion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

The putative tumour suppressor EXT1 alters the expression of cell-surface heparan sulfate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

Positional cloning of a gene involved in hereditary multiple exostoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

A gene for hereditary multiple exostoses maps to chromosome 19p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

A cancer family syndrome in twenty-four kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1769605

5 June 2018

Up-regulation of PTHrP and Bcl-2 expression characterizes the progression of osteochondroma towards peripheral chondrosarcoma and is a late event in central chondrosarcoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/11896078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/11896078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteosarcoma arising in a solitary osteochondroma of the fibula

1 reference

https://pubmed.ncbi.nlm.nih.gov/11896078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity and DNA ploidy point to a diverging genetic mechanism in the origin of peripheral and central chondrosarcoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/11896078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11896078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic characterization of both components of a dedifferentiated chondrosarcoma, with implications for its histogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/11896078

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JCP.55.3.226

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 October 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q41894867&oldid=1929532657"