11q23.3

A chromosome band present on 11q
National Institutes of Health

Related topics

Related topics

14 relations
APOC3 wt AlleleARHGEF12 wt AlleleBLR1 wt AlleleCBL wt Allele
(More)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Association of sequence variants on chromosomes 20, 11, and 5 (20q13.33, 11q23.3, and 5p15.33) with glioma susceptibility in a Chinese population.
Two genome-wide association studies of glioma in European populations identified 14 genetic variants strongly associated with… (More)
  • table 1
  • table 2
  • table 3
  • table 4
  • table 5
Is this relevant?
Highly Cited
2010
Highly Cited
2010
High-risk neuroblastoma tumors with 11q-deletion display a poor prognostic, chromosome instability phenotype with later onset.
Analysis of chromosomal aberrations is used to determine the prognosis of neuroblastomas (NBs) and to aid treatment decisions… (More)
  • table 1
  • figure 1
  • figure 3
  • figure 2
  • figure 4
Is this relevant?
Highly Cited
2009
Highly Cited
2009
Genome-wide association study identifies five susceptibility loci for glioma
To identify risk variants for glioma, we conducted a meta-analysis of two genome-wide association studies by genotyping 550K… (More)
  • table 1
  • figure 1
  • figure 3
Is this relevant?
Highly Cited
2009
Highly Cited
2009
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus
We performed a genome-wide association study (GWAS) of systemic lupus erythematosus (SLE) in a Chinese Han population by… (More)
  • figure 2
  • figure 1
Is this relevant?
Highly Cited
2001
Highly Cited
2001
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on…
We have performed genetic linkage analysis in 13 large multiply affected families, to test the hypothesis that there is extensive… (More)
Is this relevant?
Highly Cited
2000
Highly Cited
2000
beta 3: an additional auxiliary subunit of the voltage-sensitive sodium channel that modulates channel gating with distinct kinetics.
The voltage-sensitive sodium channel confers electrical excitability on neurons, a fundamental property required for higher… (More)
  • figure 1
  • figure 2
  • table 1
  • table 1
  • figure 3
Is this relevant?
Highly Cited
1999
Highly Cited
1999
Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas
Deletions of the long arm of chromosome 11 (11q) have been noted in primary neuroblastomas, but a comprehensive analysis has not… (More)
  • table 1
  • table 2
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
Highly Cited
1995
Highly Cited
1995
Definition and refinement of chromosome 11 regions of loss of heterozygosity in breast cancer: identification of a new region at 11q23.3.
Chromosome 11 is frequently altered in several types of human neoplasms. In breast cancer, loss of heterozygosity has been… (More)
  • table 1
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
1994
1994
Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3.
Autosomal fragile sites, unlike their X-linked counterparts, are not known to be associated with disease. However, one case… (More)
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
1994
1994
Loss of heterozygosity in sporadic human breast carcinoma: a common region between 11q22 and 11q23.3.
The development of sporadic human breast cancer is associated with the accumulation of genetic alterations on several chromosomes… (More)
  • table 1
  • figure 2
Is this relevant?