(Q40994571)

1 July 2018

title

Abnormalities of the FHIT transcripts in osteosarcoma and Ewing sarcoma (English)

1 reference

1 July 2018

author name string

S Hinohara

1

1 reference

1 July 2018

N Satake

2

1 reference

1 July 2018

K Sekine

3

1 reference

1 July 2018

Y Kaneko

4

1 reference

1 July 2018

publication date

1 September 1998

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1 July 2018

number of pages

8

1 reference

Japanese Journal of Cancer Research

inferred from page(s)

published in

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1 July 2018

volume

89

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1 July 2018

issue

9

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1 July 2018

page(s)

887-894

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1 July 2018

Absence of Fhit protein in primary lung tumors and cell lines with FHIT gene abnormalities.

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

Variable FHIT transcripts in non-neoplastic tissues

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

FHIT gene alterations in head and neck squamous cell carcinomas

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

Combinatorial generation of variable fusion proteins in the Ewing family of tumours.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

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

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

A second Ewing's sarcoma translocation, t(21;22), fuses the EWS gene to another ETS-family transcription factor, ERG

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

Molecular cloning of the chromosomal breakpoint of B-cell lymphomas and leukemias with the t(11;14) chromosome translocation

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

Molecular structure of the human cytoplasmic beta-actin gene: interspecies homology of sequences in the introns

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

The FHIT gene 3p14.2 is abnormal in lung cancer.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

Narrow spectrum of infrequent p53 mutations and absence of MDM2 amplification in Ewing tumours.

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921954

The FHIT gene at 3p14.2 is abnormal in breast carcinomas

19 August 2018

1 reference

12 December 2020

Mutation spectrum of the retinoblastoma gene in osteosarcomas

1 reference

12 December 2020

Frequent abnormalities of FHIT, a candidate tumor suppressor gene, in head and neck cancer cell lines

1 reference

12 December 2020

Evaluation of the FHIT gene in colorectal cancers

1 reference

12 December 2020

Mutation spectrum of the p53 gene in bone and soft tissue sarcomas

1 reference

12 December 2020

Aberrant FHIT transcripts in Merkel cell carcinoma

1 reference

12 December 2020

Disappearance of AML1-MTG8(ETO) fusion transcript in acute myeloid leukaemia patients with t(8;21) in long-term remission

1 reference

12 December 2020

Loss of heterozygosity of the RB gene is a poor prognostic factor in patients with osteosarcoma

1 reference

12 December 2020

10.1111/J.1349-7006.1998.TB00645.X

Identifiers

DOI

1 reference

1 July 2018

PMCID

5921954

1 reference

1 July 2018

PubMed ID

9818023

1 reference

1 July 2018