Multidisciplinary treatment of non-syndromic oligodontia

por Bural, Canan, Oztas, Evren, Ozturk, Sukru, Bayraktar, Gulsen
Publicado 2012

The Effects of Etodolac, Nimesulid and Naproxen Sodium on the Frequency of Sister Chromatid Exchange after Enclused Third Molars Surgery

por Köseoğlu, Banu Gürkan, Öztürk, Şükrü, Koçak, Hülya, Palanduz, Şükrü, Çefle, Kıvanç
Publicado 2008

Coculture model of blood–brain barrier on electrospun nanofibers

por ÖZYURT, Mustafa Görkem, BAYIR, Ece, DOĞAN, Şule, ÖZTÜRK, Şükrü, ŞENDEMİR, Aylin
Publicado en Turk J Biol (2020)

Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability

por Kaya, Murat, Suer, İlknur, Öztürk, Şükrü, ÇEFLE, Kıvanç, Karaman, Birsen, Palanduz, Şükrü
Publicado en F1000Res (2019)

Roles of Signal Transducer Pathways in Investigation of Biopsies from Patients with Bladder Tumors

por Bayrak, Aysegul, Palanduz, Sukru, Coskunpinar, Ender, Sanli, Oner, Armagan, Abdullah, Karakus, Serkan, Topaktas, Ramazan, Cefle, Kivanc, Ozturk, Sukru, Ucur, Ali
Publicado en Asian Pac J Cancer Prev (2017)

DNA damage effects of inhalation anesthetics in human bronchoalveolar cells

por Cukurova, Zafer, Cetingok, Halil, Ozturk, Sukru, Gedikbasi, Asuman, Hergunsel, Oya, Ozturk, Derya, Don, Burak, Cefle, Kivanc, Palanduz, Sukru, Ertem, Devrimsel Harika
Publicado en Medicine (Baltimore) (2019)

Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus

por Kürklü, Esma, Öztürk, Şükrü, Cassidy, Andrew J., Ak, Gülsüm, Koray, Meltem, Çefle, Kıvanç, Palandüz, Şükrü, Güllüoğlu, Mine G, Tanyeri, Hakkı, McLean, William-Henry-Irwin
Publicado en Med Oral Patol Oral Cir Bucal (2018)

Investigation of Gene Expressions of Myeloma Cells in the Bone Marrow of Multiple Myeloma Patients by Transcriptome Analysis

por Sarıman, Melda, Abacı, Neslihan, Sırma Ekmekçi, Sema, Çakiris, Aris, Perçin Paçal, Ferda, Üstek, Duran, Ayer, Mesut, Yenerel, Mustafa Nuri, Beşışık, Sevgi, Çefle, Kıvanç, Palandüz, Şükrü, Öztürk, Şükrü
Publicado en Balkan Med J (2019)

Mutations in RAD21 Disrupt Regulation of APOB in Patients with Chronic Intestinal Pseudo-obstruction

por Bonora, Elena, Bianco, Francesca, Cordeddu, Lina, Bamshad, Michael, Francescatto, Ludmila, Dowless, Dustin, Stanghellini, Vincenzo, Cogliandro, Rosanna F., Lindberg, Greger, Mungan, Zeynel, Cefle, Kivanc, Ozcelik, Tayfun, Palanduz, Sukru, Ozturk, Sukru, Gedikbasi, Asuman, Gori, Alessandra, Pippucci, Tommaso, Graziano, Claudio, Volta, Umberto, Caio, Giacomo, Barbara, Giovanni, D'Amato, Mauro, Seri, Marco, Katsanis, Nicholas, Romeo, Giovanni, De Giorgio, Roberto
Publicado en Gastroenterology (2015)

REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis

por Bayram, Yavuz, White, Janson J., Elcioglu, Nursel, Cho, Megan T., Zadeh, Neda, Gedikbasi, Asuman, Palanduz, Sukru, Ozturk, Sukru, Cefle, Kivanc, Kasapcopur, Ozgur, Coban Akdemir, Zeynep, Pehlivan, Davut, Begtrup, Amber, Carvalho, Claudia M.B., Paine, Ingrid Sophie, Mentes, Ali, Bektas-Kayhan, Kivanc, Karaca, Ender, Jhangiani, Shalini N., Muzny, Donna M., Gibbs, Richard A., Lupski, James R.
Publicado en Am J Hum Genet (2017)

The phenotypic and molecular genetic spectrum of Alström Syndrome in 44 Turkish kindreds and a literature review of Alström Syndrome in Turkey

por Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M. Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Müller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal
Publicado en J Hum Genet (2014)

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

por Friedrich, Katrin, Lee, Lin, Leistritz, Dru F., Nürnberg, Gudrun, Saha, Bidisha, Hisama, Fuki M., Eyman, Daniel K., Lessel, Davor, Nürnberg, Peter, Li, Chumei, Garcia-F-Villalta, María J., Kets, Carolien M., Schmidtke, Joerg, Cruz, Vítor Tedim, Van den Akker, Peter C., Boak, Joseph, Peter, Dincy, Compoginis, Goli, Cefle, Kivanc, Ozturk, Sukru, López, Norberto, Wessel, Theda, Poot, Martin, Ippel, P. F., Groff-Kellermann, Birgit, Hoehn, Holger, Martin, George M., Kubisch, Christian, Oshima, Junko
Publicado en Hum Genet (2010)

WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects

por Yokote, Koutaro, Chanprasert, Sirisak, Lee, Lin, Eirich, Katharina, Takemoto, Minoru, Watanabe, Aki, Koizumi, Naoko, Lessel, Davor, Mori, Takayasu, Hisama, Fuki M., Ladd, Paula D., Angle, Brad, Baris, Hagit, Cefle, Kivanc, Palanduz, Sukru, Ozturk, Sukru, Chateau, Antoinette, Deguchi, Kentaro, Easwar, T.K.M, Federico, Antonio, Fox, Amy, Grebe, Theresa A., Hay, Beverly, Nampoothiri, Sheela, Seiter, Karen, Streeten, Elizabeth, Piña-Aguilar, Raul E., Poke, Gemma, Poot, Martin, Posmyk, Renata, Martin, George M., Kubisch, Christian, Schindler, Detlev, Oshima, Junko
Publicado en Hum Mutat (2016)