Publications by authors named "N Buyru"

Article Synopsis
  • The study used qRT-PCR to assess the expression of a specific gene and various miRNAs in thyroid tumors and nearby noncancerous tissues, as well as to check the methylation status of the gene's promoter.
  • There was a significant decrease in the gene's expression in tumors compared to noncancerous tissues, while the levels of miR-182, miR-183, and miR-375 were higher in the tumors.
  • The findings suggest that the gene plays a role in the development of papillary thyroid carcinoma and that its regulation is influenced more by miRNAs than by promoter methylation.
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To elucidate the pathogenesis of prostate diseases, following analysis, the gene was selected for further investigation. The gene has been associated with poor prognosis and is frequently mutated in different types of cancers. In this study, 50 benign prostatic hyperplasia (BPH) and 57 prostate cancer (PCa) tissues, including matched normal tissue for the patients, were analyzed by qRT-PCR and DNA sequencing for expression and the mutation profile, respectively.

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: Familial Mediterranean fever (FMF) is an autosomal recessive disorder characterized by recurrent short episodes (1-3 days) of inflammation and fever. FMF is associated with gene mutations but some patients with FMF symptoms do not have a mutation in the coding region of the gene. Vitamin D binding protein (VDBP) has important functions, including transporting vitamin D and its metabolites to target cells.

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: Wnt signaling pathway is associated with a variety of human cancers, including HNSCC. Wnt proteins control cellular events such as proliferation, fate specification, polarity, and migration by transducing signals to the nucleus through several cytoplasmic relay proteins. Although activation of the Wnt/β-catenin pathway is a frequent event in various cancers, there is limited knowledge on the contribution of this signaling mechanism in HNSCC.

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Breast cancer, which is the most common type of cancer among women, is a heterogenous disease. It results from progressive accumulation of genetic and epigenetic alterations in different genes. The Dok1 protein has been identified as the major substrate of protein tyrosine kinases in hematopoietic cells.

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