(Q38312291)

English

Array-comparative genomic hybridization of central chondrosarcoma: identification of ribosomal protein S6 and cyclin-dependent kinase 4 as candidate target genes for genomic aberrations.

scientific article published on July 2006

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scholarly article

1 reference

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25 December 2019

Array-comparative genomic hybridization of central chondrosarcoma: identification of ribosomal protein S6 and cyclin-dependent kinase 4 as candidate target genes for genomic aberrations (English)

1 reference

Europe PubMed Central

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25 December 2019

1 reference

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2

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25 December 2019

Carla Rosenberg

4

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25 December 2019

8

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25 December 2019

Pancras C.W. Hogendoorn

9

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25 December 2019

author name string

Leida B Rozeman

1

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25 December 2019

Yvonne M Schrage

3

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25 December 2019

Hans J Tanke

5

1 reference

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25 December 2019

Antonie H M Taminiau

6

1 reference

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25 December 2019

Anne Marie Cleton-Jansen

7

1 reference

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25 December 2019

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publication date

1 July 2006

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25 December 2019

1 reference

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25 December 2019

107

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25 December 2019

380-388

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25 December 2019

2

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25 December 2019

Homozygous deletion frequency and expression levels of the CDKN2 gene in human sarcomas--relationship to amplification and mRNA levels of CDK4 and CCND1.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

21 January 2018

Prognostic factors in chondrosarcoma of bone: a clinicopathologic analysis with emphasis on histologic grading

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI 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://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome 9 alterations and trisomy 22 in central chondrosarcoma: a cytogenetic and DNA flow cytometric analysis of chondrosarcoma subtypes

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: chondrosarcoma and other cartilaginous neoplasms

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytogenetic aberrations and their prognostic impact in chondrosarcoma

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytogenetic findings in benign cartilaginous neoplasms

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Diagnosis and prognosis of chondrosarcoma of bone.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Changes of the p16 gene but not the p53 gene in human chondrosarcoma tissues

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular analysis of the INK4A/INK4A-ARF gene locus in conventional (central) chondrosarcomas and enchondromas: indication of an important gene for tumour progression.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Malignant progression in multiple enchondromatosis (Ollier's disease): an autopsy-based molecular genetic study

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion 1p in a low-grade chondrosarcoma in a patient with Ollier disease.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

A mutant PTH/PTHrP type I receptor in enchondromatosis

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150C.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

An association between cartilaginous tumours and breast cancer in the national pathology registration in The Netherlands points towards a possible genetic trait.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Insights from genomic microarrays into structural chromosome rearrangements

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

1-Mb resolution array-based comparative genomic hybridization using a BAC clone set optimized for cancer gene analysis

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Breakpoint identification and smoothing of array comparative genomic hybridization data

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

cDNA expression profiling of chondrosarcomas: Ollier disease resembles solitary tumours and alteration in genes coding for components of energy metabolism occurs with increasing grade.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

MYC amplification and polysomy 8 in chondrosarcoma: array comparative genomic hybridization, fluorescent in situ hybridization, and association with outcome

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Proliferation, but not growth, blocked by conditional deletion of 40S ribosomal protein S6

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Human tumor suppressor EXT gene family members EXTL1 and EXTL3 encode alpha 1,4- N-acetylglucosaminyltransferases that likely are involved in heparan sulfate/ heparin biosynthesis

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

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://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Absence of IHH and retention of PTHrP signalling in enchondromas and central chondrosarcomas.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Liprin beta 1, a member of the family of LAR transmembrane tyrosine phosphatase-interacting proteins, is a new target for the metastasis-associated protein S100A4 (Mts1).

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

SENP1 enhances androgen receptor-dependent transcription through desumoylation of histone deacetylase 1

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.22001

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/CNCR.22001

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16779802%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference

Europe PubMed Central

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25 December 2019

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