Search Results - "Bağcı, Gülseren"

Extract of Calvatia gigantea inhibits proliferation of A549 human lung cancer cells by Eroğlu, Canan, Seçme, Mücahit, Atmaca, Pelin, Kaygusuz, Oğuzhan, Gezer, Kutret, Bağcı, Gülseren, Dodurga, Yavuz

“…In this study, in order to investigate the anticancer mechanism of Calvatia gigantea extract, edible mushroom species, which belong to Lycoperdaceae family,…”
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Anti-tumor effects of bemiparin in HepG2 and MIA PaCa-2 cells by Alur, İhsan, Dodurga, Yavuz, Seçme, Mücahit, Elmas, Levent, Bağcı, Gülseren, Gökşin, İbrahim, Avcı, Çığır Biray

“…Recent researches have demonstrated improved survival in oncologic patients treated with low molecular weight heparins (LMWHs) which are anticoagulant drugs…”
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Investigation of the effects of a sulfite molecule on human neuroblastoma cells via a novel oncogene URG4/URGCP by Dodurga, Yavuz, Seçme, Mücahit, Eroğlu, Canan, Gündoğdu, Gülşah, Avcı, Çığır Biray, Bağcı, Gülseren, Küçükatay, Vural, Lale Şatıroğlu-Tufan, N.

“…The aim of this study is to determine the anticancer effect of sulfite on SH-SY5Y neuroblastoma cells in vitro conditions and elucidate underlying molecular…”
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Possible Role of GADD45γ Methylation in Diffuse Large B-Cell Lymphoma: Does It Affect the Progression and Tissue Involvement? by Barış, İkbal Cansu, Caner, Vildan, Şen Türk, Nilay, Sarı, İsmail, Hacıoğlu, Sibel, Doğu, Mehmet Hilmi, Çetin, Ozan, Tepeli, Emre, Can, Özge, Bağcı, Gülseren, Keskin, Ali

“…Diffuse large B-cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma among adults and is characterized by heterogeneous clinical,…”
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Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer by Tepeli, Emre, Caner, Vildan, Büyükpınarbaşılı, Nur, Çetin, G. Ozan, Düzcan, Füsun, Elmas, Levent, Bağcı, Gülseren

“…Excision Repair Cross - Complementing Group 1 ( ERCC1 ) is an important DNA repair gene, playing critical role in nucleotide excision repair pathway and having…”
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The determination of relationship between “excision repair cross-complementing group 1” (ERCC1) gene T19007C and C8092A single nucleotide polymorphisms and clinicopathological parameters in non-small cell lung cancer by Koç, Esin, Caner, Vildan, Büyükpınarbaşılı, Nur, Tepeli, Emre, Türk, Nilay Şen, Ozan Çetin, G., Bağcı, Gülseren

“…DNA repair plays a key role in prevention of carcinogenesis and one of the most important DNA repair mechanisms is nucleotide excision repair (NER) pathway…”
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Dicentric Recombinant Chromosome 18 due to Maternal Paracentric Inversion Analyzed by Array CGH by Anlaş, Özlem, Ölmez, Akgün, Karaman, Birsen, Düzcan, Füsun, Yüksel, Selçuk, Tümkaya, Funda, Bağcı, Gülseren, Semerci Gündüz, Cavidan Nur

“…Introduction: Chromosomal abnormalities are mostly found in 0.5–0.8% of live-born infants with developmental and morphological defects. Paracentric inversions…”
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Investigation of anticancer mechanism of oleuropein via cell cycle and apoptotic pathways in SH-SY5Y neuroblastoma cells by Seçme, Mücahit, Eroğlu, Canan, Dodurga, Yavuz, Bağcı, Gülseren

“…Neuroblastoma is one of the most common types of pediatric tumors that can spread quickly in neuronal tissues. Oleuropein which is active compound of olive…”
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Assessment of the anticancer mechanism of ferulic acid via cell cycle and apoptotic pathways in human prostate cancer cell lines by Eroğlu, Canan, Seçme, Mücahit, Bağcı, Gülseren, Dodurga, Yavuz

“…Studies on genetic changes underlying prostate cancer and the possible signaling pathways are getting increased day by day, and new treatment methods are being…”
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A case of recombinant chromosome 4: further delineation of the clinical features by ANLAŞ, Özlem, ÇETİN, Gökhan Ozan, YARARBAŞ, Kanay, DÜZCAN, Füsun, Cavidan Nur SEMERCİ GÜNDÜZ, AYAZ, Akif, BAĞCI, Gülseren

“…Recombinant chromosome 4 is a very rare chromosomal aberration with eleven cases reported in the literature up to date. Here we report a five years old male…”
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Maternal origin and clinical findings in a case with trisomy 22 by Mihçi, Ercan, Taçoy, Sükran, Yakut, Sezin, Ongun, Hakan, Keser, Ibrahim, Kiliçarslan, Bahar, Bağci, Gülseren, Lüleci, Güven

“…We report a newborn girl with multiple congenital anomalies whose chromosomal analysis showed complete trisomy 22. Her phenotype included microcephaly,…”
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A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type by Albuz, Burcu, Çetin, Gökhan Ozan, Özhan, Bayram, Sarikepe, Bilge, Anlaş, Özlem, Öztürk, Menekşe, Zeybek, Selcan, Sabir, Nuran, Bağci, Gülseren, Semerci Gündüz, Cavidan Nur

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Co-existence of Goldenhar and Klinefelter Syndromes in a Patient Born Following ICSI by Zeybek, Selcan, Sarikepe, Bilge, Bagci, Gulseren, Alatas, Erkan, Duzcan, Fusun

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In vitro testing for genotoxicity of 4-CPA by sister chromatid exchange in human lymphocyte culture by AÇIKBAŞ, İbrahim, BAĞCI, Gülseren, DEMİR, Göksemin, BAĞCI, Hüseyin

“…Certain phenoxyacetate derivatives used as plant growth regulators act as plant hormones. 2,4-D dichlorophenoxyacetic acid and 4-chlorophenoxyacetic acid are…”
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Utility of serum DNA and pyrosequencing for the detection of EGFR mutations in non-small cell lung cancer by Akca, Hakan, Demiray, Aydn, Yaren, Arzu, Bir, Ferda, Koseler, Aylin, Iwakawa, Reika, Bagci, Gulseren, Yokota, Jun

“…Mutations in the EGFR gene are critical determinants of treatment with EGFR tyrosine kinase inhibitors (TKIs) for non-small cell lung cancer (NSCLC) patients…”
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Familial Translocation (2;18) Ascertained Through Recurrent Spontaneous Abortions by Gülseren Bağcı, Emre Tepeli, Füsun Düzcan, Ozan Çetin, Erkan Alataş

“…We report a young woman who presented with a reproductive history of two recurrent spontaneous abortions. Genetic etiology of recurrent fetal loss is…”
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Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype by Bagci, Gulseren, Ph.D, Bisgin, Atil, M.D., Ph.D, Karauzum, Sibel Berker, Ph.D, Trak, Bilal, M.D, Luleci, Guven, Ph.D

“…Objective To present a familial case of Swyer syndrome. Design Case report. Setting Academic medical center. Patient(s) Two sisters with a main complaint of…”
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Determination of O⁶-methylguanine DNA methyltransferase promoter methylation in non-small cell lung cancer by Ekim, Mehmet, Caner, Vildan, Büyükpınarbaşılı, Nur, Tepeli, Emre, Elmas, Levent, Bağcı, Gülseren

“…Aberrant methylation of promoter CpG islands is known to be a major inactivation mechanism of the tumor-related genes including DNA repair genes. The objective…”
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Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation by Bağcı, Gülseren, Çetin, Gökhan Ozan, Semerci, Nur, Toruner, Gokce A., Cinbiş, Mine

“…Terminal deletions of chromosome 14q are very rarely reported. Schneider et al. (2008) reviewed about 20 cases of 14q32 region deletion in a previous article…”
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Dicentric Recombinant Chromosome 18 due to Maternal Paracentric Inversion Analyzed by Array CGH by Anlaş, Özlem, Ölmez, Akgün, Karaman, Birsen, Düzcan, Füsun, Yüksel, Selçuk, Tümkaya, Funda, Bağcı, Gülseren, Semerci Gündüz, Cavidan Nur

“…IntroductionChromosomal abnormalities are mostly found in 0.5-0.8% of live-born infants with developmental and morphological defects. Paracentric inversions…”
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