Clinical Characteristics and Mutation Spectrum of Neurofibromatosis Type 1 in 27 Turkish Families by Shahrashoub Sharifi, Tuğba Kalaycı, Şükrü Palanduz, Şükrü Öztürk, Kıvanç Cefle

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Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability [version 1; peer review: 2 approved] by Murat Kaya, İlknur Suer, Şükrü Öztürk, Kıvanç ÇEFLE, Birsen Karaman, Şükrü Palanduz

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Turmeric Inhibits MDA-MB-231 Cancer Cell Proliferation, Altering miR-638-5p and Its Potential Targets by Murat Kaya, Asmaa Abuaisha, Ilknur Suer, Selman Emiroglu, Fahrunnisa Abanoz, Sukru Palanduz, Kivanc Cefle, Sukru Ozturk

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Molecular Diagnosis Experience in Familial Mediterranean Fever: The Most Frequent Mutations in the MEFV Gene by Ender Coşkunpınar, Ayla Özvarnalı, Kıvanç Çefle, Ayşe Palanduz, Ahmet Gül, Derya Öztürk, Şükrü Öztürk, Şükrü Palanduz

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Could the ENPP1 p.D85H Mutation be Associated with Hypophosphatemic Rickets? by Ender COŞKUNPINAR, Sakin TEKİN, Şükrü PALANDUZ, Hakan AVCI, Kıvanç CEFLE, N. Ozan TİRYAKİOĞLU, Ayşe KUBAT ÜZÜM, Refik TANAKOL, İlhan SATMAN

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Investigation of ErbB and Insulin Signaling Pathways in the Pathogenesis of Multiple Myeloma by Derya Öztürk, Ender Mehmet Coşkunpınar, Emre Osmanbaşoğlu, Güven Çetin, Mustafa Nuri Yenerel, Mesut Ayer, Cumhur Gökhan Ekmekçi, Duran Üstek, Kıvanç Cefle, Şükrü Palanduz, Şükrü Öztürk

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Investigation of Gene Expressions of Myeloma Cells in the Bone Marrow of Multiple Myeloma Patients by Transcriptome Analysis by Melda Sarıman, Neslihan Abacı, Sema Sırma Ekmekçi, Aris Çakiris, Ferda Perçin Paçal, Duran Üstek, Mesut Ayer, Mustafa Nuri Yenerel, Sevgi Beşışık, Kıvanç Çefle, Şükrü Palandüz, Şükrü Öztürk

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