Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

11q13.3

A chromosome band present on 11q
National Institutes of Health

Related topics

Related topics

7 relations
AIP wt AlleleANO1 wt AlleleCLCF1 wt AlleleChromosomes
Expand

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Identification of genomic alterations in oesophageal squamous cell cancer
Oesophageal cancer is one of the most aggressive cancers and is the sixth leading cause of cancer death worldwide. Approximately… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2012
Highly Cited
2012
Common genetic variants at the 11q13.3 renal cancer susceptibility locus influence binding of HIF to an enhancer of cyclin D1 expression
Although genome-wide association studies (GWAS) have identified the existence of numerous population-based cancer susceptibility… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2012
Highly Cited
2012
Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned
Major depressive disorder (MDD) is a common complex disorder with a partly genetic etiology. We conducted a genome-wide… Expand
  • figure 1
Is this relevant?
Highly Cited
2011
Highly Cited
2011
Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3
We conducted a two-stage genome-wide association study of renal cell carcinoma (RCC) in 3,772 affected individuals (cases) and 8… Expand
  • figure 1
  • figure 2
Is this relevant?
Highly Cited
2011
Highly Cited
2011
Identification of a therapeutic strategy targeting amplified FGF19 in liver cancer by Oncogenomic screening.
We screened 124 genes that are amplified in human hepatocellular carcinoma (HCC) using a mouse hepatoblast model and identified… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2007
Highly Cited
2007
Amplicon Mapping and Expression Profiling Identify the Fas-Associated Death Domain Gene as a New Driver in the 11q13.3 Amplicon in Laryngeal/Pharyngeal Cancer
Purpose: Amplification of the 11q13 region is a frequent event in human cancer. The highest incidence (36%) is found in head and… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2006
2006
High-resolution mapping identifies a commonly amplified 11q13.3 region containing multiple genes flanked by segmental duplications
DNA amplification of the 11q13 region is observed frequently in many carcinomas. Within the amplified region several candidate… Expand
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
1998
Highly Cited
1998
Chromosomal gains and losses in primary cutaneous melanomas detected by comparative genomic hybridization.
The analysis of genetic changes in primary cutaneous melanoma has been limited by the need for fixation for diagnostic purposes… Expand
  • figure 1
  • figure 2
  • table I
  • figure 3
  • table 2
Is this relevant?
Highly Cited
1996
Highly Cited
1996
Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma.
In multiple myeloma, karyotopic 14q32 translocations have been identified at a variable frequency (10-60% in different studies… Expand
Is this relevant?
Highly Cited
1991
Highly Cited
1991
Folate-binding protein is a marker for ovarian cancer.
We describe the isolation of a complementary DNA (cDNA) sequence encoding the ovarian cancer-associated antigen recognized by… Expand
  • table 1
  • table 2
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE