Search Results - "Tuncel, Gulten"

Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome by Temel, Sehime Gulsun, Ergoren, Mahmut Cerkez, Manara, Elena, Paolacci, Stefano, Tuncel, Gulten, Gul, Seref, Bertelli, Matteo

“…Neonatal progeroid syndrome or Wiedemann-Rautenstrauch syndrome (WRS; MIM 264090) is a rare genetic disorder that has clinical symptoms including premature…”
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Impact of SARS-CoV-2 Delta and Omicron variants on viral burden and cycle threshold in BNT162b2-vaccinated 12–18 years group by Ergoren, Mahmut Cerkez, Komurcu, Kubra, Tuncel, Gulten, Akan, Gokce, Ozverel, Cenk Serhan, Dalkan, Ceyhun, Kalayci, Melis, Sanlıdag, Tamer

“…The SARS-CoV-2 pandemic continues to impact the medical, economic, social, and political areas worldwide. Although it has been claimed that children are the…”
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Designing In-House SARS-CoV-2 RT-qPCR Assay for Variant of Concerns by Ergoren, Mahmut Cerkez, Tuncel, Gulten, Ozverel, Cenk Serhan, Sanlidag, Tamer

“…Abstract Variants (Alfa, Gamma, Beta, and Delta) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are circulating worldwide. These variants of…”
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Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS‐CoV‐2 from 946 whole‐exome sequencing data in the Turkish population by Duman, Nilgun, Tuncel, Gulten, Bisgin, Atil, Bozdogan, Sevcan Tug, Sag, Sebnem Ozemri, Gul, Seref, Kiraz, Aslihan, Balta, Burhan, Erdogan, Murat, Uyanik, Bulent, Canbek, Sezin, Ata, Pinar, Geckinli, Bilgen Bilge, Arslan Ates, Esra, Alavanda, Ceren, Yesim Ozdemir, Sevda, Sezer, Ozlem, Ozgon, Gulay Oner, Gurkan, Hakan, Guler, Kubra, Boga, Ibrahim, Kaya, Niyazi, Alemdar, Adem, Sayan, Murat, Dundar, Munis, Ergoren, Mahmut Cerkez, Temel, Sehime Gulsun

“…Heterogeneity in symptoms associated with COVID‐19 in infected patients remains unclear. ACE2 and TMPRSS2 gene variants are considered possible risk factors…”
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Lessons from Real Life Experience: Importance of In-House Sequencing and Smart Ratio-Based Real-Time PCR Outperform Multiplex Ligation-Dependent Probe Amplification in Prenatal Diagnosis for Spinal Muscular Atrophy: Bench to Bedside Diagnosis by Tuncel, Gulten, Sanlıdag, Burcin, Dirik, Eray, Baris, Tugba, Ergoren, Mahmut Cerkez, Temel, Sehime Gulsun

“…Abstract Spinal muscular atrophy (SMA) is a rare, recessively inherited neurodegenerative disorder caused by the presence of pathogenic variants in the SMN…”
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Adult-onset glutaric aciduria type I: rare presentation of a treatable disorder by Gelener, Pınar, Severino, Mariasavina, Diker, Sevda, Teralı, Kerem, Tuncel, Gulten, Tuzlalı, Hatice, Manara, Elena, Paolacci, Stefano, Bertelli, Matteo, Ergoren, Mahmut Cerkez

“…Glutaric aciduria type I (GA1; OMIM #231670) is an autosomal recessively inherited and treatable disorder characterized by the accumulation and irregular…”
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WNT signaling pathway genes expression profile in isolated hypodontia by Kashoura, Yaman, Serakinci, Nedime, Beleva, Nadejda, Kaçamak, Nazlı Idil, Tuncel, Gulten, Oz, Ulas

“…The aim of this study is to investigate the potential role and the association of PAX9 , WNT10a , and AXIN2 genes during the development of hypodontia. A total…”
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Strong Association between Vitamin D Receptor Gene and Severe Acute Respiratory Syndrome coronavirus 2 Infectious Variants by Mamurova, Begimai, Akan, Gokce, Mogol, Evren, Turgay, Ayla, Tuncel, Gulten, Evren, Emine Unal, Evren, Hakan, Suer, Kaya, Sanlidag, Tamer, Ergoren, Mahmut Cerkez

“…A coronavirus disease 2019 (COVID-19) disease, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has created significant concern…”
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Sex and ABO Blood Differences in SARS-CoV-2 Infection Susceptibility by Ergoren, Mahmut Cerkez, Akan, Gokce, Guler, Emrah, Tuncel, Gulten, Akovalı, Damla, Evren, Emine Unal, Evren, Hakan, Suer, Huseyin Kaya, Sanlidag, Tamer

“…Data consisting of millions of cases cannot still explain the immunopathogenesis mechanism between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)…”
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The Biennial report: The collaboration between MAGI Research, Diagnosis and Treatment Center of Genetic and Rare Diseases and Near East University DESAM Institute by Ergoren, Mahmut Cerkez, Manara, Elena, Paolacci, Stefano, Cobanogullari, Havva, Tuncel, Gulten, Betmezoglu, Meryem, Bertelli, Matteo, Sanlidag, Tamer

“…Abstract Background Scientific collaboration is more common now than it was before. In many areas of biomedical science, collaborations between researchers…”
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Comparison of RT-qPCR results of different gene targets for SARS-CoV-2 in asymptomatic individuals during COVID-19 pandemic by Tuncel, Gulten, Ergoren, Mahmut Cerkez, Baddal, Buket, Tulay, Pinar, Arikan, Ayse, Guler, Emrah, Ozverel, Cenk Serhan, Kaya Suer, H., Sayan, Murat, Sanlidag, Tamer

“…A reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR) is regarded as the most sensitive method available and is being used for screening…”
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Importance of m N 6 -methyladenosine (m 6 A) RNA modification in cancer by Tuncel, Gulten, Kalkan, Rasime

“…RNA methylation, which was identified back in 1970s, has gained remarkable interest in recent years as it was shown to be a reversible modification involved in…”
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Importance of m N{sup 6}-methyladenosine (m{sup 6}A) RNA modification in cancer by Tuncel, Gulten, Kalkan, Rasime

“…RNA methylation, which was identified back in 1970s, has gained remarkable interest in recent years as it was shown to be a reversible modification involved in…”
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Receptor tyrosine kinase-Ras-PI 3 kinase-Akt signaling network in glioblastoma multiforme by Tuncel, Gulten, Kalkan, Rasime

“…Glioblastoma multiforme (GBM) is the most malignant form of the brain tumors and shows different genetic and epigenetic abnormalities. Gene amplification,…”
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Comparing expression levels of PERIOD genes PER1, PER2 and PER3 in chronic insomnia patients and medical staff working in the night shift by Emeklİ, Rabia, İsmaİloğullari, Sevda, Bayram, Arslan, Akalin, Hilal, Tuncel, Gülten, Dündar, Munis

“…This study was done to determine the changes in expression levels of PERIOD family genes in chronic insomnia patients and night shift healthcare staff with…”
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Oxford nanopore sequencing-based assay for BTD gene screening: Design, clinical validation, and variant frequency assessment in the Turkish population by Kazan, Hasan Hüseyin, Karaca, Meryem, Akan, Gökçe, Özgen, Özge, Tuncel, Gülten, Özketen, Ahmet Çağlar, Balcı, Mehmet Cihan, Körbeyli, Hüseyin Kutay, Atalar, Fatmahan, Gökçay, Gülden Fatma

“…Amplification-based ONT sequencing using two primer pools and long PCR results in fast, cheap and accurate screening of BTD gene. [Display omitted] •Molecular…”
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Importance of m N6-methyladenosine (m6A) RNA modification in cancer by Tuncel, Gulten, Kalkan, Rasime

“…RNA methylation, which was identified back in 1970s, has gained remarkable interest in recent years as it was shown to be a reversible modification involved in…”
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Natural selection at work? Vitamin D deficiency rates and rising health problems in young Turkish Cypriot professionals by Kandemiş, Emine, Tuncel, Gülten, Fahrioğlu, Umut, Temel, Şehime Gülsün, Mocan, Gamze, Ergören, Mahmut Çerkez

“…Objectives: Vitamin D is a fat-soluble, prohormone vitamin that is important especially for bone mineralization and skeletal health. In recent years, vitamin D…”
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A review of the Mediterranean diet and nutritional genomics in relation to cancer in women by Tuncel, Gulten, Hoti, Qendresa, Mocan, Gamze, Ergoren, Mahmut Cerkez

“…Cancer is the leading cause of death among women all over the world. Female tissue-specific cancers are the most commonly diagnosed among women and account for…”
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Altered expression levels of TAS1R2 and TAS1R3 genes among SARS-CoV-2 variants of concerns by Hoti, Qendresa, Akan, Gokce, Tuncel, Gulten, Evren, Emine Unal, Evren, Hakan, Suer, Kaya, Sanlidag, Tamer, Ergoren, Mahmut Cerkez

“…Background The most common symptoms of coronavirus infections are fever, cough, shortness of breath, headache, ache of joints, a loss of smell and loss of…”
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