Comparison of miRNA expressions among benign, premalignant and malignant lesions of the larynx: could they be transformation biomarkers? von Tuncturk, Fatma Ruya, Akalin, Ibrahim, Uzun, Lokman, Zenginkinet, Tulay

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Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome von Ozlu, Emin, Karadag, Ayse Serap, Akalın, Ibrahim, Yesil, Gozde, Yılmaz, Sarenur, Zindancı, Ilkin, Uzuncakmak, Tugba Kevser, Ozkanlı, Seyma, Akdeniz, Necmettin

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DNA methylation in hearing-related genes in non-syndromic sensorineural hearing loss patients von Eğilmez, Oğuz Kadir, Can, Sermet, Kalcıoğlu, M. Tayyar, Tan, Berna Demircan, Yılmaz, Sarenur, Yiğit, Özgür, Durna, Muhammed Yusuf, Akdeniz, Esra, Akalin, Ibrahim

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Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: An array CGH analysis and review von Akalin, Ibrahim, Bozdag, Senol, Spielmann, Malte, Basaran, Sarenur Yilmaz, Nanda, Indrajit, Klopocki, Eva

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Ear atresia: Is there a role of apoptosis-regulating miRNAs? von Aslan, Ezgi, Akbas, Emre, Yilmaz, Sena, Karaoglu, Ahmet Salih, Telli, Ubeyde, Yildirim, Salih, Gudek, Hilal, Kalcioglu, Mahmut Tayyar, Yilmaz, Sarenur, Akalin, Ibrahim

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Novel PTCH1 Gene Mutation in a Patient with Gorlin-Goltz Syndrome von Emin Ozlu, Ayse Serap Karadag, Ibrahim Akalın, Gozde Yesil, Sarenur Yılmaz, Ilkin Zindancı, Tugba Kevser Uzuncakmak, Seyma Ozkanlı, Necmettin Akdeniz

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Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders von Mitani, Tadahiro, Punetha, Jaya, Akalin, Ibrahim, Pehlivan, Davut, Dawidziuk, Mateusz, Coban Akdemir, Zeynep, Yilmaz, Sarenur, Aslan, Ezgi, Hunter, Jill V., Hijazi, Hadia, Grochowski, Christopher M., Jhangiani, Shalini N., Karaca, Ender, Fatih, Jawid M., Iwanowski, Piotr, Gambin, Tomasz, Wlasienko, Pawel, Goszczanska-Ciuchta, Alicja, Bekiesinska-Figatowska, Monika, Hosseini, Masoumeh, Arzhangi, Sanaz, Najmabadi, Hossein, Rosenfeld, Jill A., Du, Haowei, Marafi, Dana, Blaser, Susan, Teitelbaum, Ronni, Silver, Rachel, Posey, Jennifer E., Ropers, Hans-Hilger, Gibbs, Richard A., Wiszniewski, Wojciech, Lupski, James R., Chitayat, David, Kahrizi, Kimia, Gawlinski, Pawel

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Folate receptor α expression and significance in endometrioid endometrium carcinoma and endometrial hyperplasia von Senol, Serkan, Ceyran, Ayse Bahar, Aydin, Abdullah, Zemheri, Ebru, Ozkanli, Seyma, Kösemetin, Duygu, Sehitoglu, Ibrahim, Akalin, Ibrahim

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Fever-induced Brugada syndrome in a 9-year-old boy presenting with acute chest pain von Besli, Gülser Esen, Yıldırım, Sema, Akalın, İbrahim, Ayhan, Yusuf İzzet, Kısıoğlu, Merve, Berdeli, Afig

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A New Promising Pathway in Aggressive Prostate Cancer: Treg/mir-let8c/lin28b von Akalin, Ibrahim, Erol, Bulent, Aslan, Ezgi, Ozkanli, S. Seyma, Efiloglu, Ozgur, Yildirim, Salih, Caskurlu, Turhan, Yildirim, Asif, Karaman, M. Ihsan

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The Thrombotic Events in Polycythemia Vera Patients May Be Related to Increased Oxidative Stress von Durmus, Ahmet, Mentese, Ahmet, Yilmaz, Mustafa, Sumer, Aysegul, Akalin, Ibrahim, Topal, Cevat, Alver, Ahmet

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Prognostic significance of survivin, β-catenin and p53 expression in urothelial carcinoma von Senol, Serkan, Yildirim, Asif, Ceyran, Bahar, Uruc, Fatih, Zemheri, Ebru, Ozkanli, Seyma, Akalin, Ibrahim, Ulus, Ismail, Caskurlu, Turhan, Aydin, Abdullah

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Acute in Vitro effects of ABS (Ankaferd Hemostat) on the Lymphoid Neoplastic Cells (B-CLL and RAJI Tumor Cell Lines) von HAZNEDAROGLU, IBRAHIM

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Neonatal Polycythemia May be Free of JAK2V617F Mutation/Yenidogan Polisitemisi JAK2V617F Mutasyonundan Bagimsiz Olabilir von Akalin, Ibrahim, Armangil, Didem, Durmus, Ahmet

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MİLLÎ MÜCADELE’DE KULLANILAN İLETİŞİM KAYNAKLARI: URFA SAVUNMASI ÖRNEĞİ von AKALIN, İbrahim Engin

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Neonatal Polycythemia May be Free of JAK2V617F Mutation von AKALIN, İbrahim, ARMANGİL, Didem, DURMUŞ, Ahmet

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Relation of stem cell markers ALDH1 and CD44 with clinicopathological factors in urothelial carcinomas of urinary bladder von Senol, Serkan, Yildırım, Asif, Akalin, Ibrahim, Uruç, Fatih, Çobanoğlu, Bengü, Yilmaz, Sarenur, Ceyran, Bahar, Kösemetin, Duygu, Ece, Dilek, Aydın, Abdullah

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Lentiginoses in polycythemia vera patient: Is there a role for JAK2 (V617F) mutation? von Uzuncakmak, Tugba Kevser, Yilmaz, Sarenur, Karadag, Ayse Serap, Akdeniz, Necmettin, Akalin, Ibrahim

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Akut miyeloid lösemide kromozomal anomaliler: Tek merkezden 417 olgunun sitogenetik sonuçları von Akalın,İbrahim, Karabulut,Halil Gürhan, Yürür Kutlay,Nüket, Ilgın Ruhi,Hatice, Tükün,Fatma Ajlan, Sağlam,Burcu, Tuncalı,Timur, Vicdan,Nedime Arzu, Sadeghi,Faika

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Angiotensin Converting Enzyme Insertion/Deletion Gene Polymorphisms in Leukemic Hematopoiesis von AKALIN, Ibrahim

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