Chromosomal breakage and sister chromatid exchange analysis in breast cancer patients with heterozygous BLM gene variants von Yararbas, Kanay, Sayar, Ceyhan, Tavukcu, Cemre, Korkmaz, Taner, Çankaya, Dilara Çakmak, Mutlu, Elif Karabacak, Özbek, Uğur

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Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span von Yücel-Yılmaz, Didem, Yücesan, Emrah, Yalnızoğlu, Dilek, Oğuz, Kader Karlı, Sağıroğlu, Mahmut Şamil, Özbek, Uğur, Serdaroğlu, Esra, Bilgiç, Başar, Erdem, Sevim, İşeri, Sibel Aylin Uğur, Hanağası, Haşmet, Gürvit, Hakan, Özgül, Rıza Köksal, Dursun, Ali

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

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The Role of the Local Bone Marrow Renin-Angiotensin System in Multiple Myeloma von Saka, Bülent, Sayitoğlu, Müge, İstemihan, Zülal, Karan, M. Akif, Erten, Nilgün, Doğan, Öner, Özbek, Uğur, Genç, Sema, Taşçıoğlu, Cemil, Kalayoğlu-Beşışık, Sevgi

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Aberrant Methylation Profile and Microsatellit Instability in Turkish Sporadic Colorectal Carcinoma von EKMEKÇİ, Cumhur Gökhan, GÜLLÜOĞLU, Mine, KAPRAN, Yersu, DİZDAROĞLU, Ferhunde, ÖZBEK, Uğur

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SCREENING SLC2A1 GENE FOR SEQUENCE AND COPY NUMBER VARIATIONS ASSOCİATED WITH GLUT-1 DEFICIENCY SYNDROME von ÖRNEK ERGÜZELOĞLU, Cemre, KARA, Bülent, KARACAN, İlker, ÖZDEMİR, Özkan, KESİM, Yeşim, BEBEK, Nerses, ÖZBEK, Uğur, UĞUR İŞERİ, Sibel Aylin

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Determining T and B Cell development by TREC/KREC analysis in primary immunodeficiency patients and healthy controls von Şentürk, Gizem, Ng, Yuk Yin, Eltan, Sevgi Bilgiç, Başer, Dilek, Ogulur, Ismail, Altındirek, Didem, Fırtına, Sinem, Yılmaz, Hülya, Kocamış, Burcu, Kıykım, Ayça, Camcıoğlu, Yıldız, Ar, Muhlis Cem, Sudutan, Tuğçe, Beken, Serdar, Temel, Şehime G., Alanay, Yasemin, Karakoc‐Aydiner, Elif, Barış, Safa, Özen, Ahmet, Özbek, Uğur, Sayitoğlu, Müge, Hatırnaz Ng, Özden

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A Novel and Mosaic WDR45 Nonsense Variant Causes Beta-Propeller Protein-Associated Neurodegeneration Identified Through Whole Exome Sequencing and X chromosome Heterozygosity Analy... von Akçakaya, Nihan Hande, Salman, Barış, Görmez, Zeliha, Tarkan Argüden, Yelda, Çırakoğlu, Ayşe, Çakmur, Raif, Dönmez Çolakoğlu, Berril, Hacıhanefioğlu, Seniha, Özbek, Uğur, Yapıcı, Zuhal, Uğur İşeri, Sibel Aylin

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Digital distraction levels of university students in emergency remote teaching von Göl, Burak, Özbek, Uğur, Horzum, Mehmet Barış

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Clinical and genetic spectrum of an orphan disease MPAN: a series with new variants and a novel phenotype von Akçakaya, Nihan Hande, Haryanyan, Garen, Mercan, Sevcan, Sozer, Nejla, Ali, Asuman, Tombul, Temel, Ozbek, Ugur, Uğur İşeri, Sibel Aylin, Yapıcı, Zuhal

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Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia von Altıokka‐Uzun, Güneş, Özdemir, Özkan, Uğur‐İşeri, Sibel, Bebek, Nerses, Gürses, Candan, Özbek, Uğur, Baykan, Betül

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Association of Pro-apoptotic Bad Gene Expression Changes with Benign Thyroid Nodules von Gül, Nurdan, Temel, Berna, Ustek, Duran, Sirma-Ekmekçi, Sema, Kapran, Yersu, Tunca, Fatih, Giles-Şenyürek, Yasemin, Özbek, Uğur, Alagöl, Faruk

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A Possible Role for WNT5A Hypermethylation in Pediatric Acute Lymphoblastic Leukemia von 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

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High MN1 expression increases the in vitro clonogenic activity of primary mouse B-cells von Numata, Masashi, Yener, Mehmet Deniz, Ekmekçi, Sema Sırma, Aydın, Müge, Grosveld, Gerard, Cardone, Monica, Terranova, Sabrina, Geltink, Ramon Klein, Özbek, Uğur, Özçelik, Emrah, Güleç, Çağrı, Anak, Sema, Karaman, Serap, Öztürk, Gülyüz, Akbıyık, Meral, Kandilci, Ayten

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Cosmic Whirl: Navigating the Comet Trail in DNA: H2AX Phosphorylation and the Enigma of Uncertain Significance Variants von Ustun Yilmaz, Sevdican, Agaoglu, Nihat Bugra, Manto, Karin, Muftuoglu, Meltem, Özbek, Ugur

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ABL gene kinase domain mutation scanning by denaturing high performance liquid chromatography sequencing method von Erbilgin, Yücel, Çatal, Suzin, Eşkazan, Ahmet Emre, Hatırnaz, Özden, Soysal, Teoman, Özbek, Uğur

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Anti-neuronal and stress-induced-phosphoprotein 1 antibodies in neuro-Behçet's disease von Vural, Burçak, Uğurel, Elif, Tüzün, Erdem, Kürtüncü, Murat, Zuliani, Luigi, Çavuş, Filiz, İçöz, Sema, Erdağ, Ece, Gül, Ahmet, Güre, Ali O, Vincent, Angela, Özbek, Uğur, Eraksoy, Mefkure, Akman-Demir, Gülşen

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Perception and management of cancer predisposition in pediatric cancer centers: A European‐wide questionnaire‐based survey von Lazic, Jelena, Haas, Oskar A, Özbek, Ugur, Ripperger, Tim, Byrjalsen, Anna, te Kronnie, Geertruij, Sayitoğlu, Muge, Ng, Ozden Hatirnaz, Agaoglu, Nihat Bugra, Erbilgin, Yucel, Senturk, Gizem, Khodzhoev, Khusan, Sudutan, Tugce, Altıner, Sule, Ozdemir, Gul Nihal, Demirsoy, Ugur, Yilmaz, Ceren Damla, Ruml, Jelena, Yalcin, Koray, Ili, Ezgi Gökpinar, Pantic, Ivana, Vukovic, Milica, Mlynarski, Wojciech, Pastorczak, Agata, Bosch, Jutte van der Werff Ten, Schlegelberger, Brigitte, Slamova, Lucie, Loeffen, Jan, Garcia‐Orad, Africa, Metzler, Markus, Reismüller, Bettina

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Does normoxemic cardiopulmonary bypass prevent myocardial reoxygenation injury in cyanotic children? von Bulutcu, Füsun S., Bayındır, Osman, Polat, Bülent, Yalcın, Yalım, Özbek, Uğur, Cakalı, Emine

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Which may be effective to reduce blood loss after cardiac operations in cyanotic children: tranexamic acid, aprotinin or a combination? von BULUTCU, FÜSUN S., ÖZBEK, UĞUR, POLAT, BÜLENT, YALÇIN, YALIM, KARACI, A.R., BAYINDIR, OSMAN

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