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13q31.3

A chromosome band present on 13q.
National Institutes of Health

Related topics

Related topics

3 relations
ChromosomesMIR17 wt AlleleMIR18A wt Allele

Papers overview

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2018
2018
Genomic profiling identifies GPC5 amplification in association with sarcomatous transformation in a subset of uterine carcinosarcomas
Uterine carcinosarcoma, also known as Malignant Mixed Müllerian Tumour, is a high‐grade biphasic neoplasm composed of sarcomatous… 
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… 
2014
2014
Overexpression of miR‐17 in gastric cancer is correlated with proliferation‐associated oncogene amplification
The molecular mechanism underlying microRNA (miR)‐17 overexpression has not been clearly evaluated in gastric cancer. We aimed to… 
Review
2013
Review
2013
Post-axial polydactyly type A2, overgrowth and autistic traits associated with a chromosome 13q31.3 microduplication encompassing miR-17-92 and GPC5.
2013
2013
Abstract 1352: Epithelial-mesenchymal transition (EMT) gene variants influence epithelial ovarian cancer risk in women of European, African and Asian ancestry.
Introduction The epithelial-mesenchymal transition (EMT) pathway contributes to epithelial ovarian cancer (EOC) progression… 
2012
2012
Immunohistochemical Detection of Glypican-5 in Paraffin-embedded Material: An Optimized Method for a Novel Research Antibody
Glypican-5 (GPC5) is a cell surface heparan sulfate proteoglycan and 1 of 6 closely related members of the glypican family in… 
2009
2009
Novel PNLIPRP3 and DOCK8 gene expression and prognostic implications of DNA loss on chromosome 10q25.3 in hepatocellular carcinoma.
Our previous study of gene alterations in 29 hepatocellular carcinoma (HCC) using AP-PCR amplified with 59 different 10-mer… 
2007
2007
Scotosensitive and Photosensitive Myoclonic Seizures in an Infant with Trisomy 13
We describe a male carrier of trisomy 13 with scotosensitive and photosensitive myoclonic seizures appearing at the age of 8… 
2006
2006
Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13
We report a young girl with microphthalmia, conductive deafness, aortic isthmus stenosis, laryngomalacia, and laryngeal stenosis… 
1989
1989
[Lethal polymalformative syndrome with 13q deletion secondary to a maternal X; 13 translocation].
The authors report the case of a newborn full term delivered by cesarean section for evolutive hydrocephalus, in the last month… 
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