Search Results - "Mitev, Vanio"
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Insight into the Metabolite Pattern of Psoriasis: Correlation among Homocysteine, Methionine, and Polyamines
Published in Symmetry (Basel) (01-04-2021)“…Psoriasis is an incurable dermatological disorder, characterized by increased epidermal cell proliferation. Numerous studies have focused on the modulation of…”
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2
Rare host variants in ciliary expressed genes contribute to COVID-19 severity in Bulgarian patients
Published in Scientific reports (22-08-2024)“…Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19), a pneumonia with extremely heterogeneous clinical…”
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3
Promoter hypermethylation of CDKN2A, MGMT, MLH1, and DAPK genes in laryngeal squamous cell carcinoma and their associations with clinical profiles of the patients
Published in Head & neck (01-08-2014)“…Background Laryngeal squamous cell carcinoma (laryngeal SCC) is a frequently occurring cancer of the head and neck area. Epigenetic changes of tumor‐related…”
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4
The effect of sample size on polygenic hazard models for prostate cancer
Published in European journal of human genetics : EJHG (01-10-2020)“…We determined the effect of sample size on performance of polygenic hazard score (PHS) models in prostate cancer. Age and genotypes were obtained for 40,861…”
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5
Clinical and genetic variability among Bulgarian patients with autosomal recessive spastic ataxia of Charlevoix–Saguenay
Published in Molecular genetics & genomic medicine (01-07-2024)“…Background Autosomal recessive spastic ataxia ofCharlevoix–Saguenay (ARSACS) is a rare neurodegenerative disorder characterizedby early‐onset cerebellar…”
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A familial case of severe infantile nephronophthisis explained by oligogenic inheritance
Published in European journal of medical genetics (01-06-2017)“…Abstract Renal cysts are common malformation during the prenatal and postnatal period and frequent cause of chronic kidney or ESRD. More than 70 genes have…”
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Identification of a novel de novo mutation of CREBBP in a patient with Rubinstein-Taybi syndrome by targeted next-generation sequencing: a case report
Published in Human pathology (01-01-2016)“…Summary Rubinstein-Taybi syndrome (RSTS) is a rare autosomal dominant congenital disorder (prevalence, 1:125 000-720 000) characterized by broad thumbs and…”
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No evidence of association between 118A>G OPRM1 polymorphism and heroin dependence in a large Bulgarian case–control sample
Published in Drug and alcohol dependence (01-08-2011)“…Abstract The μ-opioid receptor is the primary site of action of most opioids. The 118A>G (rs1799971) polymorphism in exon 1 of the μ-opioid receptor gene (…”
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9
Determination of plasma aminothiols by high performance liquid chromatography after precolumn derivatization with N-(2-acridonyl)maleimide
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (01-07-2008)“…Design, synthesis and properties of new derivatization reagent N-(2-acridonyl)-maleimide (MIAC) for thiol groups is presented. The reaction of MIAC with…”
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10
Transmission disequilibrium of DISC1 haplotypes in Bulgarian families with affective disorder
Published in Psychiatry research (30-12-2013)Get full text
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11
CK2 Is Acting Upstream of MEK3/6 as a Part of the Signal Control of ERK1/2 and p38 MAPK during Keratinocytes Autocrine Differentiation
Published in Zeitschrift für Naturforschung C. A journal of biosciences (01-01-2011)“…Protein kinase CK2 (formerly termed “casein kinase II”) is a ubiquitously in mammalian cells distributed Ser/Thr kinase, with global role in cell regulation…”
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12
Investigation of candidate genes reveals significant statistical epistasis between DISC1 and TPH2 in Bulgarian affective disorder patients
Published in Biotechnology, biotechnological equipment (02-11-2017)“…The aim of the present study was to search for joint influence of variants in affective disorder (AD) candidate genes by investigating statistical epistasis…”
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13
Liquid chromatography method for simultaneous analysis of amino acids and biogenic amines in biological fluids with simultaneous gradient of pH and acetonitrile
Published in Journal of chromatography. B, Analytical technologies in the biomedical and life sciences (01-12-2007)“…A liquid chromatography method for simultaneous analysis of amino acids, polyamines, catecholeamines and metanephrines in human body fluids after…”
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14
Mutational Status of CDKN2A and TP53 Genes in Laryngeal Squamous Cell Carcinoma
Published in Pathology oncology research (01-04-2015)“…Laryngeal squamous cell carcinoma (LSCC) is the second most common tumour of the head and neck. It is characterized by frequent aberrations in two cell-cycle…”
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15
IL-1RN VNTR Polymorphism in Adult Dermatomyositis and Systemic Lupus Erythematosus
Published in Dermatology Research and Practice (01-01-2014)“…Polymorphisms in the cytokine genes and their natural antagonists are thought to influence the predisposition to dermatomyositis (DM) and systemic lupus…”
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16
Nafion®-Separated Electrode Solutions in Isoelectric Focusing
Published in Chromatographia (2012)“…In the present paper, we present our results from studies where the electrode solutions were separated from the carrier with the polytetrafluoroethylene-based…”
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Novel Methods for Controlling the Current During Isoelectric Focusing
Published in Chromatographia (01-09-2010)“…While studying the effect of electrochemical reactions occurring at the electrodes on achievement of steady state in isoelectric focusing (IEF) we observed an…”
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Electrochemical Reactions During Isoelectric Focusing and Their Role in Establishment of the pH Gradient
Published in Chromatographia (01-05-2009)“…The process occurring as the background to IEF is electrolysis of water. During IEF the yield of water ions decreases, following a non-linear relationship…”
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Novel MLH1 frameshift mutation in an extended hereditary nonpolyposis colorectal cancer family
Published in World journal of gastroenterology : WJG (28-12-2006)“…AIM: To present novel frameshift mutation c.31delC [p.L11X] in the MLH1 gene identified in an extended Bulgarian hereditary non-polyposis colorectal cancer…”
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Frequency and application of the hot spot BRAF gene mutation (p.V600E) in the diagnostic strategy for Hereditary Nonpolyposis Colorectal Cancer
Published in Cancer detection and prevention (01-01-2007)“…Abstract Background: BRAF somatic mutations were reported with high frequency in sporadic colorectal cancers (CRCs) with microsatellite instability (MSI). The…”
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