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8p21.3

A chromosome band present on 8p.
National Institutes of Health

Related topics

Related topics

4 relations
ChromosomesLOXL2 wt AlleleMIR320A wt AllelePDLIM2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
8p21.3 deletion suggesting a probable role of TRAIL-R1 and TRAIL-R2 as candidate tumor suppressor genes in the pathogenesis of multiple myeloma
Abstract8p21.3 deletion was recently characterized in B cell lymphoma suggesting that TRAIL-R1 and TRAIL-R2 may be the target of… 
2008
2008
Protein phosphatase and TRAIL receptor genes as new candidate tumor genes on chromosome 8p in prostate cancer.
BACKGROUND Allelic losses on chromosome 8p are common in prostate carcinoma, but it is not known exactly how they contribute to… 
2007
2007
Integration of somatic deletion analysis of prostate cancers and germline linkage analysis of prostate cancer families reveals two small consensus regions for prostate cancer genes at 8p.
The evidence for tumor suppressor genes at 8p is well supported by many somatic deletion studies and genetic linkage studies… 
Highly Cited
2007
Highly Cited
2007
More evidence supports the association of PPP3CC with schizophrenia
Calcineurin is a calcium/calmodulin-dependent protein phosphatase composed of two subunits, a regulatory subunit of calcineurin B… 
2007
2007
Haploinsufficiency of 8p22 may influence cancer-specific survival in prostate cancer.
Highly Cited
2005
Highly Cited
2005
Perturbation of the Tumor Necrosis Factor–Related Apoptosis-Inducing Ligand Cascade in Ovarian Cancer: Overexpression of FLIPL and Deregulation of the Functional Receptors DR4 and DR5
Purpose: Epithelial ovarian cancer is the most common cause of mortality from gynecologic malignancies. Due to advanced stage at… 
2004
2004
Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1·1‐cM interval at 8p21.3
Background  Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal congenital alopecia with progressive hair loss… 
2001
2001
Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features.
We report six cases in two families and a sporadic case with a direct duplication of region 8p21.3-->23.1. In one family, the… 
2000
2000
Molecular cloning and characterization of two novel genes on chromosome 8p21.3
AbstractThrough large-scale sequencing of genomic DNA from human chromosome 8p22–p21.3 we have isolated two novel genes… 
1992
1992
Interstitial deletion 8p21.3----p23.1 in a 6-year-old girl.
We present a 6-year-old mentally retarded girl. Chromosome analysis showed an interstitial deletion of chromosome 8; 46,XX,del(8… 
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