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ZNF516 gene

Known as: ZINC FINGER PROTEIN 516, HsT287, KIAA0222 
 

Topic mentions per year

Topic mentions per year

2003-2017
012320032017

Papers overview

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2017
2017
ZNF516 suppresses EGFR by targeting the CtBP/LSD1/CoREST complex to chromatin
EGFR is required for animal development, and dysregulation of EGFR is critically implicated in malignant transformation. However… (More)
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2016
2016
Molecular Triage of Premalignant Lesions in Liquid-Based Cervical Cytology and Circulating Cell-Free DNA from Urine, Using a Panel of Methylated Human Papilloma Virus and Host Genes.
Clinically useful molecular tools to triage women for a biopsy upon referral to colposcopy are not available. We aimed to develop… (More)
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2015
2015
Screening of candidate genes in fibroblasts derived from patients with Dupuytren’s contracture using bioinformatics analysis
Our study aimed to identify candidate genes associated with Dupuytren’s contracture (DC) and elucidate their roles in DC… (More)
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2014
2014
Genome-wide methylation profiling reveals Zinc finger protein 516 (ZNF516) and FK-506-binding protein 6 (FKBP6) promoters frequently methylated in cervical neoplasia, associated with HPV status and…
Cervical cancer is a major health concern among women in Latin America due to its high incidence and mortality. Therefore, the… (More)
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2014
2014
Response to Bakhoum et al.
reflect differences in experimental conditions or divergence between cell line isolates. These are mitigated in our analysis by… (More)
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2013
2013
Gene-gene interaction between RBMS3 and ZNF516 influences bone mineral density.
Osteoporosis is characterized by low bone mineral density (BMD), a highly heritable trait that is determined, in part, by the… (More)
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2013
2013
RBMS3 versus ZNF516: interaction between SNPs in two genes impacts on BMD.
  • BoneKEy reports
  • 2013
 
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2013
2013
Narrowing the critical region for congenital vertical talus in patients with interstitial 18q deletions.
Interstitial deletions of 18q lead to a number of phenotypic features, including multiple types of foot deformities. Many of… (More)
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Review
2006
Review
2006
Identification of 2.3-Mb gene locus for congenital aural atresia in 18q22.3 deletion: a case report analyzed by comparative genomic hybridization.
OBJECTIVE 18q deletion syndrome is a multiple-anomaly mental retardation syndrome associated with congenital aural atresia. The… (More)
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2003
2003
Identification of the DNA binding specificity of the human ZNF219 protein and its function as a transcriptional repressor.
The ZNF219 gene is a member of the Kruppel-like zinc finger gene family that is involved in a diverse range of biological… (More)
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