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14q13.3

Part of the chromosome bands present on the long (q) arm of chromosome 14.
National Institutes of Health

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4 relations
CTAGE5 wt AlleleChromosomesNKX2-8 wt Allelechromosome 14q

Papers overview

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2018
2018
Child Neurology: Siblings with infantile epilepsy and developmental delay
Objective Chromosome 14q11-q22 deletion syndrome (OMIM 613457) is a rare genomic disorder with a variable phenotype. Methods We… 
2018
2018
SNP Association with Risk for Sporadic Papillary Thyroid Carcinoma in Kazakh Population
Background: The recent genome-wide association studies (GWAS) including FOXE1 and NKX2-1 genes have represent associations for… 
2017
2017
Age at diagnosis and gender modify the risk of 9q22 and 14q13 polymorphisms for papillary thyroid carcinoma.
INTRODUCTION Papillary thyroid cancer (PTC) shows familial occurrence, and some susceptibility single nucleotide polymorphisms… 
2014
2014
Are the SNPs of NKX2-1 associated with papillary thyroid carcinoma in the Han population of Northern China?
Papillary thyroid carcinoma (PTC) is one of the most common tumors of the thyroid gland. The common risk factors of PTC include… 
2013
2013
Concurrent overexpression of RET/PTC1 and TTF1 confers tumorigenicity to thyrocytes
A variant located on 14q13.3 nearest to thyroid transcription factor-1 (TTF1) predisposes individuals to thyroid cancer, but… 
2012
2012
Identification of a Novel 14q13.3 Deletion Involving the SLC25A21 Gene Associated with Familial Synpolydactyly
Synpolydactyly is a relatively rare malformation. Recently, we came across a male infant with a familial synpolydactyly of the… 
2012
2012
Revision of “A 223-kb De Novo Deletion of PAX9 in a Patient With Oligodontia”
AbstractThe PAX (paired box) genes are a family of transcription factors critical for fetal growth and organogenesis… 
2010
2010
One Allele's Loss Is Another's Gain: Alterations of NKX2–8 in Non–Small Cell Lung Cancer
Large-scale genetic changes such as loss or gain of chromosomes are important drivers of solid tumor carcinogenesis. Recent… 
2008
2008
Use of co-activation of lung cancer specific developmental pathway genes, TTF-1, NKX2–8, and PAX9, to predict prognosis and guide therapeutic strategies
7511 Background: We recently described a novel, recurring amplicon (14q13.3) specific to NSCLC that harbors three genes, TTF- 1… 
2004
2004
Diagnostic and prognostic significance of genetic regional heterogeneity in meningiomas 1
We analyzed the frequency and regional distribution of cells with genetic abnormalities of chromosomes 1, 14, and 22 in… 
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