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7q32.2

A chromosome band present on 7q.
National Institutes of Health

Related topics

Related topics

3 relations
ChromosomesMIR182 wt AlleleMIR183 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Computational systems biology analysis of biomarkers in lung cancer; unravelling genomic regions which frequently encode biomarkers, enriched pathways, and new candidates.
2016
2016
Assessment of the frequency of genetic alterations (LOH/MSI) in patients with intraepithelial cervical lesions with HPV infection: a pilot study
In the present study, we analyzed (1) the type of HPV infection and (2) the frequency of loss of heterozygosity and… 
2016
2016
Coronary artery disease variant and cell cycle
Genome wide association studies have to date identified multiple coronary artery disease (CAD) associated loci; however, for most… 
2016
2016
Abstract 1931: MiR182 mediated control over myeloid differentiation provides novel mechanism of Imatinib resistance in chronic myeloid leukemia
MiR182 is an evolutionarily conserved miR, present in a cluster with miR183, and miR96 on human chromosome 7q32.2. This cluster… 
2016
2016
Functional Analysis of a Coding Variant In ZC3HC1 at 7q32.2 Associated with Protection Against Coronary Artery Disease (CAD)
2015
2015
Deregulated microRNAs in triple-negative breast cancer revealed by deep sequencing
MicroRNAs (miRNAs) are short, non-coding RNA molecules that play critical roles in human malignancy. However, the regulatory… 
2015
2015
210 Investigation of the Functional Role of the Lead Variant at the ZC3HC1 Coronary Artery Disease Locus in Cell Cycle Regulation using a Genome Editing Approach
Genome wide association studies have identified 46 chromosomal loci that are associated with coronary artery disease (CAD… 
Review
2014
Review
2014
Isolated hypermethylation of GRB10 (7p12.2) in a Silver–Russell syndrome patient carrying a 20p13 microdeletion
To the Editor : Silver–Russell syndrome (SRS; OMIM 180860) is an imprinting disorder characterized by primordial growth… 
Review
2014
Review
2014
Isolated hypermethylation of GRB 10 ( 7 p 12 . 2 ) in a Silver – Russell syndrome patient carrying a 20 p 13 microdeletion
  • 2014
  • Corpus ID: 40833032
To the Editor : Silver–Russell syndrome (SRS; OMIM 180860) is an imprinting disorder characterized by primordial growth… 
Highly Cited
2012
Highly Cited
2012
Tumor microRNA-335 expression is associated with poor prognosis in human glioma
MicroRNA-335 (miR-335), as a transcript of genomic region chromosome 7q32.2, acts as a tumor suppressor or tumor promoter in… 
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