Read more about the article Contribution to the study of Acanthodactylus (Sauria: Lacertidae) mtDNA diversity focusing on the A. boskianus species group.
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Contribution to the study of Acanthodactylus (Sauria: Lacertidae) mtDNA diversity focusing on the A. boskianus species group.

Abstract The Acanthodactylus boskianus species group includes three species (A. boskianus, A. nilsoni, and A. schreiberi) of unclear phylogeny and phylogeographic history. By sequencing fragments of two mtDNA genes and…

Continue ReadingContribution to the study of Acanthodactylus (Sauria: Lacertidae) mtDNA diversity focusing on the A. boskianus species group.
Read more about the article Protease Inhibitors Drug Resistance Mutations in Turkish Patients with Chronic Hepatitis C.
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Protease Inhibitors Drug Resistance Mutations in Turkish Patients with Chronic Hepatitis C.

Abstract Drug resistance development is an expected problem during treatment with protease inhibitors (PIs), this is largely due to the fact that Pls are low-genetic barrier drugs. Resistance-associated variants (RAVs)…

Continue ReadingProtease Inhibitors Drug Resistance Mutations in Turkish Patients with Chronic Hepatitis C.
Read more about the article Canine Infections and Partial S Segment Sequence Analysis of Toscana Virus in Turkey.
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Canine Infections and Partial S Segment Sequence Analysis of Toscana Virus in Turkey.

Abstract Toscana virus (TOSV) is a sandfly-borne bunyavirus with a significant public health impact. Preliminary studies have revealed TOSV exposure in dogs and they were suggested as potential reservoirs. This…

Continue ReadingCanine Infections and Partial S Segment Sequence Analysis of Toscana Virus in Turkey.
Read more about the article A novel MC4R deletion coexisting with FTO and MC1R gene variants, causes severe early onset obesity.
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A novel MC4R deletion coexisting with FTO and MC1R gene variants, causes severe early onset obesity.

Abstract Heterozygous mutations on the melanocortin-4-receptor gene (MC4R) are the most frequent cause of monogenic obesity. We describe a novel MC4R deletion in a girl with severe early onset obesity,…

Continue ReadingA novel MC4R deletion coexisting with FTO and MC1R gene variants, causes severe early onset obesity.
Read more about the article Follicle-Stimulating Hormone Receptor (FSHR): A Promising Tool in Oncology?
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Follicle-Stimulating Hormone Receptor (FSHR): A Promising Tool in Oncology?

Abstract The cellular pathway of follicle-stimulating hormone (FSH) and its receptor (FSHR) is typically involved in reproduction in mammals. In humans, the FSHR is normally found in cells of the…

Continue ReadingFollicle-Stimulating Hormone Receptor (FSHR): A Promising Tool in Oncology?
Read more about the article The Relationship between Common Genetic Markers of Breast Cancer Risk and Chemotherapy-Induced Toxicity: A Case-Control Study.
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The Relationship between Common Genetic Markers of Breast Cancer Risk and Chemotherapy-Induced Toxicity: A Case-Control Study.

Abstract Ninety-four common genetic variants are confirmed to be associated with breast cancer. This study tested the hypothesis that breast cancer susceptibility variants may also be associated with chemotherapy-induced toxicity…

Continue ReadingThe Relationship between Common Genetic Markers of Breast Cancer Risk and Chemotherapy-Induced Toxicity: A Case-Control Study.
Read more about the article ESMO consensus guidelines for the management of patients with metastatic colorectal cancer.
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ESMO consensus guidelines for the management of patients with metastatic colorectal cancer.

Abstract Colorectal cancer (CRC) is one of the most common malignancies in Western countries. Over the last 20 years, and the last decade in particular, the clinical outcome for patients…

Continue ReadingESMO consensus guidelines for the management of patients with metastatic colorectal cancer.
Read more about the article Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation.
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Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation.

Abstract Congenital adrenal hyperplasia (CAH) is an endocrine autosomal recessive disorder with various symptoms of diverse severity. Mild hyperandrogenemia is the most commonclinical feature in non-classic CAH patients and 95%…

Continue ReadingGenetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation.
Read more about the article RARβ gene methylation is a candidate for primary glioblastoma treatment planning.
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RARβ gene methylation is a candidate for primary glioblastoma treatment planning.

Abstract We screened RARβ methylation in primary glioblastoma multiforme (GBM) and the results were evaluated based on the clinical data and treatment type. The objective of this study was to…

Continue ReadingRARβ gene methylation is a candidate for primary glioblastoma treatment planning.
Read more about the article Deregulated microRNA expression and its pathogenetic implications for myelodysplastic syndromes.
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Deregulated microRNA expression and its pathogenetic implications for myelodysplastic syndromes.

Abstract Myelodysplastic syndromes (MDS) include a heterogeneous group of clonal hematological stem cell disorders characterized by ineffective hematopoiesis, cytopenias. MicroRNAs (miRNAs) are short non-coding RNA molecules that repress gene expression…

Continue ReadingDeregulated microRNA expression and its pathogenetic implications for myelodysplastic syndromes.