Search Results - "Toylu, Aslı"

Alterations in plasma miR-21, miR-590, miR-192 and miR-215 in idiopathic pulmonary fibrosis and their clinical importance by Dirol, Hulya, Toylu, Aslı, Ogus, Aliye C., Cilli, Aykut, Ozbudak, Omer, Clark, Ozden Altıok, Ozdemir, Tulay

“…Background Many studies have revealed that microRNA (miRNA) molecules may take part in idiopathic pulmonary fibrosis (IPF). But, the role of miRNAs in the…”
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Investigation of the relationship between reproductive disorders and chromosomal abnormalities in a large-scale, single-center 10-year retrospective study by Ertosun, Mustafa Gokhan, Araci, Duygu Gamze, Peker, Alp, Uzuner, Sezin Yakut, Toylu, Aslı, Ozekinci, Murat, Usta, Mustafa Faruk, Altiok Clark, Ozden

“…OBJECTIVEChromosomal changes are an important cause of reproductive disorders. This study investigated the chromosomal changes and prevalence of pathologies in…”
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Filamin a mediates HGF/c‐MET signaling in tumor cell migration by Zhou, Alex‐Xianghua, Toylu, Aslı, Nallapalli, Rajesh K., Nilsson, Gisela, Atabey, Neşe, Heldin, Carl‐Henrik, Borén, Jan, Bergo, Martin O., Akyürek, Levent M.

“…Deregulated hepatocyte growth factor (HGF)/c‐MET axis has been correlated with poor clinical outcome and drug resistance in many human cancers. Identification…”
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Canonical Wnt signaling is antagonized by noncanonical Wnt5a in hepatocellular carcinoma cells by Yuzugullu, Haluk, Benhaj, Khemais, Ozturk, Nuri, Senturk, Serif, Celik, Emine, Toylu, Asli, Tasdemir, Nilgun, Yilmaz, Mustafa, Erdal, Esra, Akcali, Kamil Can, Atabey, Nese, Ozturk, Mehmet

“…beta-catenin mutations that constitutively activate the canonical Wnt signaling have been observed in a subset of hepatocellular carcinomas (HCCs). These…”
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A Novel Coincidence: Essential Thrombocythemia with Facioscapulohumeral Muscular Dystrophy by Hangül, Ceren, Yücel, Orhan Kemal, Toylu, Aslı, Uysal, Hilmi, Berker Karaüzüm, Sibel

“…Essential thrombocythemia (ET) is a myeloproliferative disorder with elevated numbers of thrombocytes and facioscapulohumeral muscular dystrophy (FSHD) is the…”
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P1802EVALUATION OF THE GENETICAL FEATURES AFFECTING THE RENAL OUTCOMES IN CHILDREN WITH STEROID RESISTANT NEPHROTIC SYNDROME by Comak, Elif, Toylu, Aslı, Bilge, Ugur, Kaya Aksoy, Gülsah, Koyun, Mustafa, Akman, Sema

“…Abstract Background and Aims Nephrotic syndrome in childhood is characterized by proteinuria, hypoalbuminemia, edema, and hyperlipidemia. Although most…”
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The levels of hepatocyte growth factor in serum and follicular fluid and the expression of c-Met in granulosa cells in patients with polycystic ovary syndrome by Şahin, Nur, M.D, Toylu, Asl, M.D., Ph.D, Gülekli, Bülent, M.D, Doğan, Erbil, M.D, Kovali, Müge, M.Sc, Atabey, Neşe, Ph.D

“…Objective To evaluate the levels of hepatocyte growth factor (HGF) in follicular fluid (FF) and the expression of c-Met in granulosa cells (GCs) with respect…”
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Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMA by Arikan, Yunus, Berker Karauzum, Sibel, Uysal, Hilmi, Mihci, Ercan, Nur, Banu, Duman, Ozgur, Haspolat, Senay, Altiok Clark, Ozden, Toylu, Asli

“…•The clinical and genetic manifestations of SMA are diverse and heterogeneous.•In this paper, we report on the final mutation profiles of the SMN1 and SMN2…”
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Downregulation of VANGL1 inhibits cellular invasion rather than cell motility in hepatocellular carcinoma cells without stimulation by Cetin, Gokhan Ozan, Toylu, Asli, Atabey, Nese, Sercan, Zeynep, Sakizli, Meral

“…The Wnt planar cell polarity (PCP) pathway is one of the Wnt pathways which plays a critical role in cell proliferation and fate. The VANGL1 protein is one of…”
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The Expression of GDF-15 in the Human Vitreous in the Presence of Retinal Pathologies with an Inflammatory Component by Ilhan, Hatice Deniz, Bilgin, Ahmet Burak, Toylu, Asli, Dogan, Mehmet Erkan, Apaydin, Kadri Cemil

“…Purpose: The presence of growth differentiation factor-15 (GDF-15), a protein implicated in the regulation of the inflammatory response, was investigated in…”
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Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas by Güneş, Nilay, Uludağ Alkaya, Dilek, Toylu, Aslı, Özüdoğru, Püren, Çifçi Sunamak, Evrim, Şeker, Ali, Demir, Bilal, Kuruğoğlu, Sebuh, Mıhçı, Ercan, Tüysüz, Beyhan

“…Hereditary multiple osteochondromas is an autosomal dominant disorder caused by heterozygous pathogenic variants in EXT1 or EXT2. We aimed to evaluate the…”
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Increased Expression of NKX3.1 in Benign Prostatic Hyperplasia by Irer, Bora, Toylu, Asli, Aslan, Guven, Celebi, Ilhan, Yorukoglu, Kutsal, Atabey, Nese

“…Objectives To establish the role of the NKX3.1 gene in the development of benign prostatic hyperplasia by comparing the expression of NKX3.1 in messenger…”
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The association of Klinefelter syndrome and multiple pterygium syndrome: an unusual presentation by Nur, Banu Güzel, Altıok-Clark, Ozden, Toylu, Aslı, Lüleci, Güven, Mıhçı, Ercan

“…Multiple pterygium syndrome is characterized by a number of phenotypic features, small stature, webbing of the neck, elbows, and/or knees, and joint…”
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Hepatosellüler Karsinoma Hücre Dizilerinde, Hipoksi ve Radyasyon Stresine Karşı Hücrenin Direnç Geliştirmesinde HGF Sinyal Iletimi Sisteminin Rolünün Belirlenmesi by Toylu, Asli

“…Hepatosellüler karsinoma (HCC) vasküler bir tümördür ve hipoksi HCC gelişiminde ve ilerleyişinde önemli bir anjiyogenik faktördür. Hipoksi tarafından uyarılan…”
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