(Q39708109)

14 September 2017

Aberrant transcripts of the FHIT gene are expressed in normal and leukaemic haemopoietic cells (English)

1 reference

14 September 2017

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Carapeti M

1

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14 September 2017

Aguiar RC

2

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14 September 2017

Sill H

3

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14 September 2017

Goldman JM

4

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14 September 2017

Cross NC

5

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14 September 2017

language of work or name

English

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publication date

1 September 1998

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British Journal of Cancer

14 September 2017

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14 September 2017

78

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14 September 2017

5

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14 September 2017

601-605

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https://scigraph.springernature.com/pub.10.1038/bjc.1998.547

14 September 2017

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cites work

The FHIT gene is alternatively spliced in normal kidney and renal cell carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Fhit, a putative tumor suppressor in humans, is a dinucleoside 5',5"'-P1,P3-triphosphate hydrolase

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

FHIT gene alterations in head and neck squamous cell carcinomas

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Variable FHIT transcripts in non-neoplastic tissues

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

FHIT gene alterations in esophageal cancer and ulcerative colitis (UC).

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Potential gastrointestinal tumor suppressor locus at the 3p14.2 FRA3B site identified by homozygous deletions in tumor cell lines

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Deletions of the short arm of chromosome 3 in solid tumors and the search for suppressor genes.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Loss of heterozygosity of chromosome 3p markers in small-cell lung cancer

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Dominant-negative mutations of the Wilms' tumour predisposing gene (WT1) are infrequent in CML blast crisis and de novo acute leukaemia.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

FHIT mutations in human primary gastric cancer

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Abnormal FHIT transcripts in human breast carcinomas: a clinicopathological and epidemiological analysis of 61 Japanese cases.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

The diversity of BCR-ABL fusion proteins and their relationship to leukemia phenotype

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

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

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Homozygous deletions of the p16 tumor-suppressor gene are associated with lymphoid transformation of chronic myeloid leukemia.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2063063

Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma

20 August 2018

1 reference

12 December 2020

FHIT gene expression in human ovarian, endometrial, and cervical cancer cell lines

1 reference

12 December 2020

Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma

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12 December 2020

Molecular analysis of the short arm of chromosome 3 in small-cell and non-small-cell carcinoma of the lung

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12 December 2020

Simple non-invasive method to obtain DNA for gene analysis

1 reference

12 December 2020

Loss of heterozygosity on the short arm of chromosome 3 in mesothelioma cell lines and solid tumors

1 reference

12 December 2020

Precise localization of aphidicolin-induced breakpoints on the short arm of human chromosome 3

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12 December 2020

Detection of Genetic Loss in Tumors by Representational Difference Analysis

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12 December 2020

Aberrant FHIT transcripts in Merkel cell carcinoma

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12 December 2020

Evaluation of the FHIT gene in colorectal cancers

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12 December 2020

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

1 reference

12 December 2020

Frequent breakpoints in the 3p14.2 fragile site, FRA3B, in pancreatic tumors

1 reference

12 December 2020

The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14

1 reference

12 December 2020

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

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12 December 2020

High levels of allele loss at the FHIT and ATM genes in non-comedo ductal carcinoma in situ and grade I tubular invasive breast cancers

1 reference

12 December 2020

Molecular analysis of the FHIT gene at 3p14.2 in lung cancer cell lines

1 reference

12 December 2020

Identifiers

DOI

10.1038/BJC.1998.547

1 reference

14 September 2017

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14 September 2017

PubMed publication ID

9744498

1 reference