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3p14.1

A chromosome band present on 3p
National Institutes of Health

Related topics

Related topics

3 relations
Chromosome 3 Short ArmChromosomesMAGI1 wt Allele

Papers overview

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2013
2013
Investigation of tumor suppressor genes apart from VHL on 3p by deletion mapping in sporadic clear cell renal cell carcinoma (cRCC).
2013
2013
Integrative analysis of prostate cancer aggressiveness
Clinical management of prostate cancer (PC) is still highly demanding on the identification of robust biomarkers which will allow… 
2010
2010
FOXP1 protein overexpression is associated with inferior outcome in nodal diffuse large B‐cell lymphomas with non‐germinal centre phenotype, independent of gains and structural aberrations at 3p14.1
Hoeller S, Schneider A, Haralambieva E, Dirnhofer S & Tzankov A
(2010) Histopathology 57, 73–80
FOXP1 protein overexpression is… 
2008
2008
Minimal deletion regions in lung squamous cell carcinoma: association with abnormality of the DNA double-strand break repair genes and their applications on gene identification and prognostic…
2008
2008
Investigation of allelic imbalances on chromosome 3p in nasopharyngeal carcinoma in Tunisia: high frequency of microsatellite instability in patients with early-onset of the disease.
2008
2008
Amplicons on chromosome 3 contain oncogenes induced by recurrent exposure to 12-O-tetradecanoylphorbol-13-acetate and sodium n-butyrate and Epstein-Barr virus reactivation in a nasopharyngeal…
2006
2006
Meta-analysis of genome-wide linkage studies for bone mineral density
AbstractGenome-wide linkage studies have shown several chromosome loci that may harbor genes that regulate bone mineral density… 
1998
1998
Minimal deletion of 3p13→14.2 associated with immortalization of human uroepithelial cells
Immortalization and tumorigenic transformation of many human cell types, including human uroepithelial cells (HUCs), are… 
Highly Cited
1995
Highly Cited
1995
Frequent microsatellite alterations on chromosome 3p in esophageal squamous cell carcinoma.
By the microsatellite assay, two types of genetic alterations, loss of heterozygosity (LOH) and replication error (RER), were… 
1993
1993
Determination of the specificity of aphidicolin-induced breakage of the human 3p14.2 fragile site.
The constitutive 3p14.2 fragile site is the most highly inducible fragile site in the human genome. This locus may predispose… 
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