Investigation of cytokine changes and deiminated proteins in LPS-induced inflammation in BV2 microglial cells von Demirel, Gamze, Gürbilek, Mehmet, Koçak, Nadir, Özdemir, Ebru Marzioğlu, Deniz, Çiğdem Damla

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Variant Analysis of miRNA Regulatory Genes in 35 Sporadic Lung Carcinoma Tumors von Bağcı, Özkan, Özdemir, Ebru Marzioğlu, Şanlıtürk, Batuhan

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Influence of the IDOL Gene Variants on Low-Density Lipoprotein Cholesterol Levels in Turkish Patients with Familial Hypercholesterolemia von Duymus, Fahrettin, Kocak, Nadir, Özdemir, Ebru Marzioğlu, Esin, Deniz, Körez, Muslu Kazim, Cora, Tülün

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Investigation of the Frequency and Characteristic Features of De Novo Mutations in Clinical Exome Sequence Trio Samples von Koçak, Nadir, Torabi, Ali, Şanlıtürk, Batuhan, Bagci, Ozkan, Marzioğlu-özdemir, Ebru, Çora, Tülin

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Variant analysis of MiRNA regulatory genes in colorectal cancer von Bağcı, Özkan, Marzioğlu-özdemir, Ebru, Şanlıtürk, Batuhan

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A novel double hemizygous BTK mutation in a boy presenting with Pseudomonas skin abscesses von Guler, Tugba, Emiroglu, Melike, Duymus, Fahrettin, Marzioglu Ozdemir, Ebru, Artac, Hasibe

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A Case of Maturity onset diabetes of the young: just keep of mınd von AKYÜREK, Nesibe, ABİDİN, İlhan, MARZİOĞLU ÖZDEMİR, Ebru

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Unilateral Cataract and Vitreoretinopathy in a Case with Klippel-Trenaunay Syndrome von Olcaysu, Osman Okan, Altun, Ahmet, Olcaysu, Elif, Marzıoğlu Ozdemır, Ebru, Demır, Berrin

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The Relationship Between Endothelial Nitric Oxide Synthase Gene (NOS3) Polymorphisms, NOS3 Expression, and Varicocele von Kahraman, Cigdem Yuce, Tasdemir, Sener, Sahin, Ibrahim, Marzioglu Ozdemir, Ebru, Yaralı, Oguzhan, Ziypak, Tevfik, Adanur, Senol, Kahraman, Mustafa, Tatar, Abdulgani

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eP208 - A Turkish consanguineous family with a novel stop-gain mutation in SPTBN2 gene leads to spinocerebellar ataxia 14 von Duymus, Fahrettin, Ozdemir, Ebru Marzioglu, Kartal, Ayse

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A Turkish consanguineous family with a novel stop-gain mutation in SPTBN2 gene leads to spinocerebellar ataxia 14 von Duymus, Fahrettin, Ozdemir, Ebru Marzioglu, Kartal, Ayse

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Are Vascular Endothelium and Angiogenesis Effective MicroRNA Biomarkers Associated with the Prediction of Early-Onset Preeclampsia (EOPE) and Adverse Perinatal Outcomes? von Ozler, Sibel, Kebapcilar, Aysegul, Ozdemir, Ebru Marzioglu, Mert, Muhammed, Arıkan, Mehmet Nurullah, Celik, Cetin

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Phosphomannomutase 2-congenital disorder of glycosylation presenting with very early onset inflammatory bowel disease von Comert, Meltem, Guler, Tugba, Ergani, Anna Carina, Gumus, Meltem, Ozdemir, Ebru Marzioglu, Artac, Hasibe

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eP269 - In silico analysis of similar protein sequences between Sars-Cov-2 and BCG vaccine von Tulgar, Busra Goksel, Duymus, Fahrettin, Esin, Deniz, Maden, Fatma Betul, Ozdemir, Ebru Marzioglu, Kocak, Nadir

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eP220 - Case report: 10q26 deletion syndrome von Esin, Deniz, Duymus, Fahrettin, Tulgar, Busra Goksel, Ozdemir, Ebru Marzioglu, Cora, Tulun, Kartal, Ayse

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Case report: 10q26 deletion syndrome von Esin, Deniz, Duymus, Fahrettin, Tulgar, Busra Goksel, Ozdemir, Ebru Marzioglu, Cora, Tulun, Kartal, Ayse

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eP266 - Case report: A novel deletion in the NLRP7 gene in the genetic etiology of recurrent hydatidiform mole pregnancy von Tulgar, Busra Goksel, Esin, Deniz, Celik, Cetin, Ozdemir, Ebru Marzioglu, Duymus, Fahrettin

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In silico analysis of similar protein sequences between Sars-Cov-2 and BCG vaccine von Tulgar, Busra Goksel, Duymus, Fahrettin, Esin, Deniz, Maden, Fatma Betul, Ozdemir, Ebru Marzioglu, Kocak, Nadir

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A novel homozygous PGAP2 mutation causing hyperphosphatasia with mental retardation syndrome-3 von Esin, Deniz, Duymus, Fahrettin, Tulgar, Busra Goksel, Ozdemir, Ebru Marzioglu, Cora, Tulun, Kartal, Ayse

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eP264 - A novel homozygous PGAP2 mutation causing hyperphosphatasia with mental retardation syndrome-3 von Esin, Deniz, Duymus, Fahrettin, Tulgar, Busra Goksel, Ozdemir, Ebru Marzioglu, Cora, Tulun, Kartal, Ayse

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