Search Results - "Vedat, Koksal"

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    Rapid diagnosis of spinal muscular atrophy using tetra-primer ARMS PCR assay: Simultaneous detection of SMN1 and SMN2 deletion by Baris, Ibrahim, Etlik, Ozdal, Koksal, Vedat, Arican-Baris, S. Tugba

    Published in Molecular and cellular probes (01-06-2010)
    “…Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive…”
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    Detection of Chlamydia pneumoniae and Helicobacter pylori in atherosclerotic plaques of carotid artery by polymerase chain reaction by Kaplan, Mehmet, Yavuz, Serap Simsek, Cinar, Bayer, Koksal, Vedat, Kut, Mustafa Sinan, Yapici, Fikri, Gercekoglu, Hakan, Demirtas, Mahmut Murat

    “…A possible role of some microorganisms has been proposed in the pathogenesis of atherosclerosis, but it is still an unresolved issue. We investigated the…”
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    Tumor Necrosis Factor Gene Polymorphisms in Turkish Patients with Sarcoidosis by Seyhan, Ekrem Cengiz, Cetinkaya, Erdogan, Altin, Sedat, Gunluoglu, Zeki, Demir, Adalet, Koksal, Vedat, Issever, Halim

    Published in Internal Medicine (01-01-2008)
    “…Background As reported recently, some gene polymorphisms are suspected to determine susceptibility to sarcoidosis and are held responsible for the extent and…”
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    SYBR green dye-based probe-free SNP genotyping: Introduction of T-Plex real-time PCR assay by Baris, Ibrahim, Etlik, Ozdal, Koksal, Vedat, Ocak, Zeynep, Baris, Saniye Tugba

    Published in Analytical biochemistry (15-10-2013)
    “…Single-nucleotide polymorphism (SNP) genotyping is widely used in genetic association studies to characterize genetic factors underlying inherited traits…”
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    Linezolid-resistant Enterococcus faecium: the first G2576T mutation in Turkey by Afşar, Ilhan, Barış, Ibrahim, Sener, Aslı Gamze, Köksal, Vedat, Demirci, Mustafa

    Published in Mikrobiyoloji bülteni (01-07-2012)
    “…Linezolid which is the first member of oxazolidinone class of synthetic antimicrobial agents, was licensed for the treatment of gram-positive coccal infections…”
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    Development and validation of a cost-effective in-house method, tetra-primer ARMS PCR assay, in genotyping of seven clinically important point mutations by Etlik, Ozdal, Koksal, Vedat, Arican-Baris, S. Tugba, Baris, Ibrahim

    Published in Molecular and cellular probes (01-08-2011)
    “…The single nucleotide polymorphism (SNP) genotyping is currently considered as a particularly valuable tool for the diagnosis of different pathologies. For…”
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    Role of MMP-1 1G/2G promoter gene polymorphism on the development of prostate cancer in the Turkish population by Albayrak, Selami, Cangüven, Onder, Göktaş, Cemal, Aydemir, Hüseyin, Köksal, Vedat

    Published in Urologia internationalis (01-01-2007)
    “…To investigate the association of 1G/2G polymorphism in matrix metalloproteinase-1 (MMP-1) promoter with susceptibility to prostate carcinoma in the Turkish…”
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    A single‐nucleotide polymorphism in the matrix metalloproteinase‐1 promoter enhances bladder cancer susceptibility by Tasci, Ali I., Tugcu, Volkan, Ozbek, Emin, Ozbay, Bedi, Simsek, Abdulmuttalip, Koksal, Vedat

    Published in BJU international (01-02-2008)
    “…OBJECTIVE To explore the association between the promoter polymorphism (that influences the transcriptional level) of matrix metalloproteinase‐1 (MMP‐1,…”
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    Facial Dysmorphism in Leigh Syndrome With SURF-1 Mutation and COX Deficiency by Yüksel, Adnan, Seven, Mehmet, Cetincelik, Ümran, Yeşil, Gözde, Köksal, Vedat

    Published in Pediatric neurology (01-06-2006)
    “…Leigh syndrome is an inherited, progressive neurodegenerative disorder of infancy and childhood. Mutations in the nuclear SURF-1 gene are specifically…”
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    Association between gene polymorphisms in TIM1, TSLP, IL18R1 and childhood asthma in Turkish population by Mete, Fatih, Ozkaya, Emin, Aras, Sukru, Koksal, Vedat, Etlik, Ozdal, Baris, Ibrahim

    “…Many immunologic and inflammatory mechanisms play a role in asthma etiology. The aim of this study was to investigate the susceptibility of asthma patients in…”
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    Possible association of the 5-HTTLPR serotonin transporter promoter gene polymorphism with premature ejaculation in a Turkish population by Ozbek, Emin, Tasci, Ali I, Tugcu, Volkan, Ilbey, Yusuf O, Simsek, Abdulmuttalip, Ozcan, Levent, Polat, Emre C, Koksal, Vedat

    Published in Asian journal of andrology (01-05-2009)
    “…We evaluated the genotypes of the serotonin transporter gene (5-HTT) in patients with premature ejaculation (PE) to determine the role of genetic factors in…”
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    Primer-engineered multiplex PCR–RFLP for detection of MTHFR C677T, prothrombin G20210A and factor V Leiden mutations by Koksal, Vedat, Baris, Ibrahim, Etlik, Ozdal

    Published in Experimental and molecular pathology (01-08-2007)
    “…Single-nucleotide polymorphisms in the genes that code for coagulation factors V (factor V Leiden) and II (prothrombin, G20210A), as well as the…”
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    An improved tetra-primer PCR approach for the detection of the FGFR3 G380R mutation responsible for achondroplasia by Etlik, Ozdal, Koksal, Vedat, Tugba Arican-Baris, Saniye, Baris, Ibrahim

    Published in Molecular and cellular probes (01-04-2008)
    “…Achondroplasia is the most common form of dwarfism and has an incidence of approximately 1/7500. In more than 98% of cases, the disease is associated with a G…”
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    The role of CYP1A1 Msp1 gene polymorphisms on lung cancer development in Turkey by Demir, Adalet, Altin, Sedat, Demir, Israfil, Köksal, Vedat, Cetinçelik, Umran, Dinçer, Ibrahim

    Published in Tüberküloz ve toraks (2005)
    “…Polymorphisms for genes encoding the metabolic enzymes cytochrome P450 1A1 (CYP1A1) might contribute to the variability in individual susceptibility to lung…”
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