(Q35747975)

10 August 2017

title

Fragile histidine triad gene abnormalities in the pathogenesis of gallbladder carcinoma (English)

1 reference

10 August 2017

1

Ignacio I Wistuba

1 reference

10 August 2017

3

Anirban Maitra

1 reference

10 August 2017

Raheela Ashfaq

2

1 reference

10 August 2017

Hector Alvarez

series ordinal

4

1 reference

10 August 2017

Erick Riquelme

series ordinal

5

1 reference

10 August 2017

Adi F Gazdar

series ordinal

6

1 reference

10 August 2017

language of work or name

English

0 references

publication date

1 June 2002

1 reference

The American Journal of Pathology

10 August 2017

published in

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10 August 2017

volume

160

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10 August 2017

issue

6

1 reference

10 August 2017

page(s)

2073-2079

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Epidemiology and molecular pathology of gallbladder cancer

10 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

High-resolution chromosome 3p allelotyping of breast carcinomas and precursor lesions demonstrates frequent loss of heterozygosity and a discontinuous pattern of allele loss

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Genome-wide allelotyping analysis reveals multiple sites of allelic loss in gallbladder carcinoma

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Genetic abnormalities involved in the pathogenesis of gallbladder carcinoma

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Sequential molecular abnormalities are involved in the multistage development of squamous cell lung carcinoma

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Methylation of the 5' CpG island of the FHIT gene is closely associated with transcriptional inactivation in esophageal squamous cell carcinomas

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Comparison of molecular changes in lung cancers in HIV-positive and HIV-indeterminate subjects

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Replacement of Fhit in cancer cells suppresses tumorigenicity

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Deletions of chromosome 3p are frequent and early events in the pathogenesis of uterine cervical carcinoma

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Hereditary cancer, oncogenes, and antioncogenes.

12 July 2018

1 reference

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A genetic model for colorectal tumorigenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

5' CpG island methylation of the FHIT gene is correlated with loss of gene expression in lung and breast cancer

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Abnormal Fhit expression in malignant and premalignant lesions of the cervix.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

FHIT and FRA3B 3p14.2 allele loss are common in lung cancer and preneoplastic bronchial lesions and are associated with cancer-related FHIT cDNA splicing aberrations.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B.

25 September 2018

1 reference

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Field cancerization in the aerodigestive tract--its etiology, manifestation, and significance

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850840

Role of FHIT in human cancer

25 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1016/S0002-9440(10)61157-1

Frequent deletions of FHIT and FRA3B in Barrett's metaplasia and esophageal adenocarcinomas

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016/S0002-9440(10)61157-1

Genomic FHIT analysis in RER and RER- adenocarcinomas of the pancreas

7 January 2021

1 reference

Crossref

https://api.crossref.org/works/10.1016/S0002-9440(10)61157-1

Analysis of the FHIT gene and FRA3B region in sporadic breast cancer, preneoplastic lesions, and familial breast cancer probands

7 January 2021

1 reference

12 December 2020

Loss of FHIT function in lung cancer and preinvasive bronchial lesions

1 reference

12 December 2020

The FHIT gene is expressed in pancreatic ductular cells and is altered in pancreatic cancers

1 reference

12 December 2020

Loss of fragile histidine triad expression in colorectal carcinomas and premalignant lesions

1 reference

12 December 2020

High resolution chromosome 3p allelotyping of human lung cancer and preneoplastic/preinvasive bronchial epithelium reveals multiple, discontinuous sites of 3p allele loss and three regions of frequent breakpoints

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

10.1016/S0002-9440(10)61157-1

Identifiers

DOI

1 reference

10 August 2017

1 reference

10 August 2017

1 reference