Gain of chromosome arm 17q is associated with unfavourable prognosis in neuroblastoma, but does not involve mutations in the somatostatin receptor 2(SSTR2) gene at 17q24. (Q36620037)

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scientific article published on December 1999

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English	Gain of chromosome arm 17q is associated with unfavourable prognosis in neuroblastoma, but does not involve mutations in the somatostatin receptor 2(SSTR2) gene at 17q24.	scientific article published on December 1999

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scholarly article

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Europe PubMed Central

PMC publication ID

2362984

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

title

Gain of chromosome arm 17q is associated with unfavourable prognosis in neuroblastoma, but does not involve mutations in the somatostatin receptor 2(SSTR2) gene at 17q24 (English)

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Europe PubMed Central

PMC publication ID

2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

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2 November 2019

main subject

neuroblastoma

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inferred from title

author

Katarina Ejeskär

series ordinal

2

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Europe PubMed Central

PMC publication ID

2362984

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

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2 November 2019

Per Kogner

series ordinal

3

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Europe PubMed Central

PMC publication ID

2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

Tommy Martinsson

series ordinal

4

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Europe PubMed Central

PMC publication ID

2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

author name string

F Abel

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

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2 November 2019

language of work or name

English

0 references

publication date

1 December 1999

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stated in

Europe PubMed Central

PMC publication ID

2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

published in

British Journal of Cancer

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stated in

Europe PubMed Central

PMC publication ID

2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

volume

81

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Europe PubMed Central

PMC publication ID

2362984

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

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2 November 2019

issue

8

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Europe PubMed Central

PMC publication ID

2362984

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

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2 November 2019

page(s)

1402-1409

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Europe PubMed Central

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2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

cites work

Gain of chromosome 17 is the most frequent abnormality detected in neuroblastoma by comparative genomic hybridization

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PubMed Central

reference URL

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

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Multiple gene transcripts of the somatostatin receptor SSTR2: tissue selective distribution and cAMP regulation.

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30 September 2017

Point mutation of the somatostatin receptor 2 gene in the human small cell lung cancer cell line COR-L103.

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30 September 2017

Cloning and functional characterization of a family of human and mouse somatostatin receptors expressed in brain, gastrointestinal tract, and kidney

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30 September 2017

Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines.

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28 June 2018

Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity

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28 June 2018

Regression and progression in neuroblastoma. Does genetics predict tumour behaviour?

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PubMed Central

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28 June 2018

1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines

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PubMed Central

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28 June 2018

Genetic heterogeneity of neuroblastoma studied by comparative genomic hybridization.

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20 September 2018

Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma

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12 December 2020

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Additional copies of a 25 Mb chromosomal region originating from 17q23.1-17qter are present in 90% of high-grade neuroblastomas

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

based on heuristic

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Promiscuous translocations of chromosome arm 17q in human neuroblastomas

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gain of chromosome arm 17q predicts unfavourable outcome in neuroblastoma patients. U.K. Children's Cancer Study Group and the U.K. Cancer Cytogenetics Group

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delimitation of a critical tumour suppressor region at distal 1p in neuroblastoma tumours

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

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Somatostatin in neuroblastoma and ganglioneuroma

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitation of somatostatin receptor type 2 gene expression in neuroblastoma cell lines and primary tumors using competitive reverse transcription-polymerase chain reaction

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

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Cancer in neonates: the experience at the Children's Hospital of Philadelphia

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical relevance of tumor cell ploidy and N-myc gene amplification in childhood neuroblastoma: a Pediatric Oncology Group study

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of chromosome 1p loci and microsatellite instability in neuroblastomas analyzed with short-tandem repeat polymorphisms

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/10604740

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/SJ.BJC.6692231

1 reference

stated in

Europe PubMed Central

PMC publication ID

2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

PMC publication ID

2362984

1 reference

stated in

Europe PubMed Central

PMC publication ID

2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

PubMed publication ID

10604740

1 reference

stated in

Europe PubMed Central

PMC publication ID

2362984

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10604740%20AND%20SRC:MED&resulttype=core&format=json

retrieved

2 November 2019

ResearchGate publication ID

12696216

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