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

4q35.1

A chromosome band present on 4q
National Institutes of Health

Related topics

Related topics

3 relations
ChromosomesING2 wt AlleleSORBS2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
Several chronic lymphocytic leukaemia (CLL) susceptibility loci have been reported; however, much of the heritable risk remains… Expand
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2012
2012
Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region.
Chromosome 4q deletion syndrome (4q- syndrome) is a rare condition, with an estimated incidence of 1 in 100,000. Although… Expand
Is this relevant?
2008
2008
Frequent deletion of ING2 locus at 4q35.1 associates with advanced tumor stage in head and neck squamous cell carcinoma
BackgroundLoss of heterozygosity (LOH) in the ING family members has been shown in head and neck squamous cell carcinoma (HNSCC… Expand
  • table 1
  • figure 1
  • figure 2
  • table 2
  • table 3
Is this relevant?
2007
2007
Deletions in chromosome 4 differentially associated with the development of cervical cancer: evidence of slit2 as a candidate tumor suppressor gene
The aim of this study was to locate the candidate tumor suppressor genes (TSGs) loci in the chromosomal 4p15-16, 4q22-23 and 4q34… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 6
  • figure 4
Is this relevant?
Highly Cited
2005
Highly Cited
2005
Genome-wide aberrations in pancreatic adenocarcinoma.
Chromosomal instability, manifesting as copy number alterations (CNAs), is characteristic of pancreatic adenocarcinoma. We used… Expand
Is this relevant?
Highly Cited
2004
Highly Cited
2004
Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.
Bietti crystalline corneoretinal dystrophy (BCD) is an autosomal recessive retinal dystrophy characterized by multiple glistening… Expand
Is this relevant?
Highly Cited
2003
Highly Cited
2003
CLDN23 gene, frequently down-regulated in intestinal-type gastric cancer, is a novel member of CLAUDIN gene family.
Microarray analyses combined with laser-capture microdissection have been applied for risk assessments of gastric cancer as well… Expand
Is this relevant?
2003
2003
A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
Low copy repeats (LCRs) located in 22q11.2, especially LCR-B, are susceptible to rearrangements associated with several… Expand
  • figure 1
  • figure 2
  • table 1
  • figure 4
  • figure 3
Is this relevant?
1995
1995
Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a).
The pineal hormone melatonin elicits potent circadian and reproductive effects in mammals. We report the chromosomal location of… Expand
Is this relevant?
Highly Cited
1994
Highly Cited
1994
Structure and regulation of the human interferon regulatory factor 1 (IRF-1) and IRF-2 genes: implications for a gene network in the interferon system.
Interferon regulatory factor 1 (IRF-1) and IRF-2 are structurally similar DNA-binding factors which were originally identified as… Expand
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