Aberrant transcripts of the FHIT gene are expressed in normal and leukaemic haemopoietic cells (Q39708109)

14 September 2017

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

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

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, 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

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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

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12 December 2020

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

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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

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12 December 2020

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

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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

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12 December 2020

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

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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

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