Skip to search formSkip to main contentSkip to account menu

3p14.2

A chromosome band present on 3p
National Institutes of Health

Related topics

Related topics

3 relations
Chromosome 3 Short ArmChromosomesFHIT wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Allelic imbalance in oral lichen planus and assessment of its classification as a premalignant condition.
2005
2005
The Fragile Histidine Triad Gene: A Molecular Link Between Cigarette Smoking and Cervical Cancer
Purpose: Smoking is an epidemiologic risk factor for cervical cancer. The fragile histidine triad (FHIT) gene is a tumor… 
Highly Cited
2002
Highly Cited
2002
Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors.
The FRA3B, at 3p14.2, lies within the fragile histidine triad (FHIT) gene and is the most highly expressed of the common fragile… 
Highly Cited
2001
Highly Cited
2001
Loss of Fhit expression is a predictor of poor outcome in tongue cancer.
Abnormalities of FHIT, a candidate tumor suppressor gene located at 3pl4.2, have been found frequently in multiple tumor types… 
Highly Cited
2000
Highly Cited
2000
Loss of heterozygosity at chromosomes 3, 6, 8, 11, 16, and 17 in ovarian cancer: correlation to clinicopathological variables.
1999
1999
Genetic changes during the multistage pathogenesis of human papillomavirus positive and negative vulvar carcinomas.
Highly Cited
1996
Highly Cited
1996
Molecular analysis of the FHIT gene at 3p14.2 in lung cancer cell lines.
Chromosome 3p is frequently deleted in various cancers including examples in the lung. A novel gene, termed FHIT, was recently… 
Highly Cited
1996
Highly Cited
1996
Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2.
Despite several lines of evidence suggesting that common chromosomal fragile sites are biologically important as hot spots for… 
Highly Cited
1996
Highly Cited
1996
A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints.
The constitutive fragile site at human chromosomal band 3p14.2, FRA3B, has been described as the most active common fragile site… 
1988
1988
Do human renal cell carcinomas arise by a double-loss mechanism?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)