Search Results - "Hatırnaz, Özden"

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    PTEN and AKT1 Variations in Childhood T-Cell Acute Lymphoblastic Leukemia by Küçükcankurt, Fulya, Erbilgin, Yücel, Fırtına, Sinem, Hatırnaz Ng, Özden, Karakaş, Zeynep, Celkan, Tiraje, Ünüvar, Ayşegül, Özbek, Uğur, Sayitoğlu, Müge

    Published in Turkish journal of haematology (01-01-2020)
    “…PTEN/AKT pathway deregulations have been reported to be associated with treatment response in acute leukemia. This study examined pediatric T-cell acute…”
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    Journal Article
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    A Possible Role for WNT5A Hypermethylation in Pediatric Acute Lymphoblastic Leukemia by Hatırnaz Ng, Özden, Fırtına, Sinem, Can, İsmail, Karakaş, Zeynep, Ağaoğlu, Leyla, Doğru, Ömer, Celkan, Tiraje, Akçay, Arzu, Yıldırmak, Yıldız, Timur, Çetin, Özbek, Uğur, Sayitoğlu, Müge

    Published in Turkish journal of haematology (01-06-2015)
    “…WNT5A is one of the most studied noncanonical WNT ligands and is shown to be deregulated in different tumor types. Our aim was to clarify whether…”
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    Memantine and SKF82958 but not an enriched environment modulate naloxone-precipitated morphine abstinence syndrome without affecting hippocampal tPA mRNA levels in rats by Aslan, Abdurrahman, Hatırnaz-Ng, Özden, Taşar, Orçun, Özbek, Uğur, Yamantürk-Çelik, Pınar

    Published in Pharmacology, biochemistry and behavior (01-01-2024)
    “…There is accumulating evidence supporting the involvement of tissue-plasminogen activator (tPA) in the mechanisms underlying the effects of morphine and an…”
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    The potential protective roles of zinc, selenium and glutathione on hypoxia-induced TRPM2 channel activation in transfected HEK293 cells by Duzgun Ergun, Dilek, Dursun, Sefik, Pastaci Ozsobaci, Nural, Hatırnaz Ng, Ozden, Naziroglu, Mustafa, Ozcelik, Dervis

    “…Hypoxia induces cell death through excessive production of reactive oxygen species (ROS) and calcium (Ca 2+ ) influx in cells and TRPM2 cation channel is…”
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    Upregulation of T-Cell-Specific Transcription Factor Expression in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL) by Sayitoğlu, Müge, Erbilgin, Yücel, Hatırnaz Ng, Ozden, Yıldız, Inci, Celkan, Tiraje, Anak, Sema, Devecioğlu, Omer, Aydoğan, Gönül, Karaman, Serap, Sarper, Nazan, Timur, Cetin, Ure, Umit, Ozbek, Uğur

    Published in Turkish journal of haematology (01-12-2012)
    “…T-cell acute lymphoblastic leukemia (T-ALL) is associated with recurrent chromosomal aberrations andabnormal ectopic gene expression during T-cell development…”
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    Mutational landscape of SARS-CoV-2 genome in Turkey and impact of mutations on spike protein structure by Hatirnaz Ng, Ozden, Akyoney, Sezer, Sahin, Ilayda, Soykam, Huseyin Okan, Bayram Akcapinar, Gunseli, Ozdemir, Ozkan, Kancagi, Derya Dilek, Sir Karakus, Gozde, Yurtsever, Bulut, Kocagoz, Ayse Sesin, Ovali, Ercument, Ozbek, Ugur

    Published in PloS one (06-12-2021)
    “…The Coronavirus Disease 2019 (COVID-19) was declared a pandemic in March 2020 by the World Health Organization (WHO). As of May 25th, 2021 there were 2.059.941…”
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    Obstacles and expectations of rare disease patients and their families in Türkiye: ISTisNA project survey results by Hatirnaz Ng, Ozden, Sahin, Ilayda, Erbilgin, Yucel, Ozdemir, Ozkan, Yucesan, Emrah, Erturk, Nazli, Yemenici, Merve, Akgun Dogan, Ozlem, Ugur Iseri, Sibel Aylin, Satman, Ilhan, Alanay, Yasemin, Ozbek, Ugur

    Published in Frontiers in public health (04-01-2023)
    “…Rare disease patients constitute a significant part of the healthcare system of all countries. However, the information on the experiences during disease…”
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    Genomic disparity impacts variant classification of cancer susceptibility genes in Turkish breast cancer patients by Agaoglu, Nihat B., Unal, Busra, Hayes, Connor P., Walker, McKenzie, Ng, Ozden Hatirnaz, Doganay, Levent, Can, Nisan D., Rana, Huma Q., Ghazani, Arezou A.

    Published in Cancer medicine (Malden, MA) (01-02-2024)
    “…Objective Turkish genome is underrepresented in large genomic databases. This study aims to evaluate the effect of allele frequency in the Turkish population…”
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    A new line method; A direct test in spinal muscular atrophy screening for DBS by Kubar, Ayhan, Temel, Sehime Gülsüm, Beken, Serdar, Onder, Gizem, Hatirnaz, Ozden, Korkmaz, Ayse, Alanay, Yasemin, Ozbek, Ugur, Sag, Sebnem Ozemri, Ergoren, Mahmut Cerkez, Kubar, Elif, Sonmezalp, Candan Zeynep, Doğan, Ozlem

    Published in Molecular genetics & genomic medicine (01-12-2023)
    “…Background Nucleic acid‐based assays provide an opportunity to screen for genetically encoded diseases like spinal muscular atrophy (SMA), before the onset of…”
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    Impact of TP53 gene variants on prognosis and survival of childhood acute lymphoblastic leukemia by Firtina, Sinem, Erbilgin, Yucel, Hatirnaz Ng, Ozden, Karaman, Serap, Karakas, Zeynep, Celkan, Tulin Tiraje, Gelen, Sema Aylan, Yildirmak, Yildiz, Ozbek, Ugur, Sayitoglu, Muge

    “…The tumor suppressor protein 53 (TP53) gene is one of the most studied genes in cancer. Although TP53 variants are rare events in acute leukemia, recent…”
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    ABL gene kinase domain mutation scanning by denaturing high performance liquid chromatography sequencing method by Yücel Erbilgin, Suzin Çatal, Ahmet Emre Eşkazan, Özden Hatırnaz, Teoman Soysal, Uğur Özbek

    Published in Turkish journal of haematology (01-06-2011)
    “…Objective: Despite the efficacy of the BCR-ABL tyrosine kinase inhibitor imatinib, the development of resistance against imatinib has been observed. The most…”
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