A novel 1p36.2 located gene, APITD1, with tumour-suppressive properties and a putative p53-binding domain, shows low expression in neuroblastoma tumours. (Q37355474)

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scientific article published on September 2004

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English	A novel 1p36.2 located gene, APITD1, with tumour-suppressive properties and a putative p53-binding domain, shows low expression in neuroblastoma tumours.	scientific article published on September 2004

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15328517%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

A novel 1p36.2 located gene, APITD1, with tumour-suppressive properties and a putative p53-binding domain, shows low expression in neuroblastoma tumours (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15328517%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

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Katarina Ejeskär

2

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1 January 2020

3

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1 January 2020

Tommy Martinsson

6

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1 January 2020

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C Krona

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1 January 2020

F Abel

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1 January 2020

R-M Sjöberg

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1 January 2020

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1 September 2004

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1 January 2020

British Journal of Cancer

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1 January 2020

91

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1 January 2020

6

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1 January 2020

1119-1130

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1 January 2020

https://scigraph.springernature.com/pub.10.1038/sj.bjc.6602083

0 references

Screening for gene mutations in a 500 kb neuroblastoma tumor suppressor candidate region in chromosome 1p; mutation and stage-specific expression in UBE4B/UFD2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

MethPrimer: designing primers for methylation PCRs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Analyses of apoptotic regulators CASP9 and DFFA at 1P36.2, reveal rare allele variants in human neuroblastoma tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Genetic analysis of childhood germ cell tumors with comparative genomic hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Comparative genomic and in situ hybridization of germ cell tumors of the infantile testis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Fine mapping of the human preprocortistatin gene (CORT) to neuroblastoma consensus deletion region 1p36.3-->p36.2, but absence of mutations in primary tumors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Interpreting cDNA sequences: some insights from studies on translation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Human TAFII31 protein is a transcriptional coactivator of the p53 protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Mutations in the p53 gene occur in diverse human tumour types

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

The p53 tumour suppressor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

6 September 2017

Three chromosomal rearrangements in neuroblastoma cluster within a 300-kb region on 1p36.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

28 September 2017

Chromosomal aberrations in human neuroblastomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

28 September 2017

Chromosome abnormalities of eighty-one pediatric germ cell tumors: sex-, age-, site-, and histopathology-related differences--a Children's Cancer Group study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

26 June 2018

Mutations of the p53 gene are involved in Ewing's sarcomas but not in neuroblastomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

26 June 2018

Cytogenetic aspects of pediatric germ cell tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

26 June 2018

Cytogenetic features of human neuroblastomas and cell lines.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

26 June 2018

Cytogenetic analysis of 124 prospectively ascertained male germ cell tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

26 June 2018

Smallest region of overlapping deletion in 1p36 in human neuroblastoma: a 1 Mbp cosmid and PAC contig

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

2 September 2018

Mutation of the p53 gene in neuroblastoma and its relationship with N-myc amplification.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747717

2 September 2018

International criteria for diagnosis, staging, and response to treatment in patients with neuroblastoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6602083

21 January 2018

High frequency of loss of heterozygosity for 1p35-p36 (D1S247) in Wilms tumor

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome bands 1p35-36 contain two distinct neuroblastoma tumor suppressor loci, one of which is imprinted

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comprehensive analysis of chromosome 1p deletions in neuroblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detailed molecular analysis of 1p36 in neuroblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fine mapping of a tumour suppressor candidate gene region in 1p36.2-3, commonly deleted in neuroblastomas and germ cell tumours

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of p53 gene mutations in primary neuroblastomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low frequency of the p53 gene mutations in neuroblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for two tumour suppressor loci on chromosomal bands 1p35-36 involved in neuroblastoma: one probably imprinted, another associated with N-myc amplification

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significance of chromosome 1p loss of heterozygosity in neuroblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

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

https://pubmed.ncbi.nlm.nih.gov/15328517

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

p73 at chromosome 1p36.3 is lost in advanced stage neuroblastoma but its mutation is infrequent

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel genomic imbalances in embryonal rhabdomyosarcoma revealed by comparative genomic hybridization and fluorescence in situ hybridization: an intergroup rhabdomyosarcoma study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15328517

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/SJ.BJC.6602083

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1 January 2020

PMC publication ID

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Europe PubMed Central

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1 January 2020

PubMed publication ID

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Europe PubMed Central

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1 January 2020

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