অনুসন্ধান ফলাফলগুলি - Şükrü Öztürk
- প্রদর্শন 1 - 6 ফলাফল এর 6
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Genetic insights into non-obstructive azoospermia: Implications for diagnosis and TESE outcomes অনুযায়ী Shahrashoub Sharifi, Murat Dursun, Ayla Şahin, Serdar Turan, Ayşe Altun, Özden Özcan, Arif Kalkanlı, Kıvanç Çefle, Şükrü Öztürk, Şükrü Palanduz, Ateş Kadıoğlu
প্রকাশিত 2025Artigo -
2
REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis অনুযায়ী Yavuz Bayram, Janson J. White, Nursel Elçioğlu, Megan T. Cho, Neda Zadeh, Asuman Gedikbaşı, Şükrü Palanduz, Şükrü Öztürk, Kıvanç Çefle, Özgür Kasapçopur, Zeynep Coban‐Akdemir, Davut Pehli̇van, Amber Begtrup, Claudia M.B. Carvalho, Ingrid S. Paine, Ali Menteş, Kıvanç Bektaş Kayhan, Ender Karaca, Shalini N. Jhangiani, Donna M. Muzny, Richard A. Gibbs, James R. Lupski
প্রকাশিত 2017Artigo -
3
Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction অনুযায়ী Elena Bonora, Francesca Bianco, Lina Cordeddu, Michael J. Bamshad, Ludmila Francescatto, Dustin Dowless, Vincenzo Stanghellini, Rosanna Cogliandro, Greger Lindberg, Zeynel Mungan, Kıvanç Çefle, Tayfun Özçelık, Şükrü Palanduz, Şükrü Öztürk, Asuman Gedikbaşı, Alessandra Gori, Tommaso Pippucci, Claudio Graziano, Umberto Volta, Giacomo Caio, Giovanni Barbara, Mauro D’Amato, Marco Seri, Nicholas Katsanis, G. Cara Romeo, Roberto De Giorgio
প্রকাশিত 2015Artigo -
4
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey অনুযায়ী Ayşegül Ozantürk, Jan D. Marshall, Gayle B. Collin, Selma Düzenli, Robert Percy Marshall, Şükrü Candan, Tülay Tos, İhsan Esen, Mustafa Taşkesen, Atilla Çayır, Şükrü Öztürk, İhsan Üstün, Esra Ataman, Emin Karaca, Taha Reşid Özdemir, İlknur Erol, Fehime Kara Eroğlu, Deniz Torun, Erhan Parıltay, Elif Yılmaz Güleç, Ender Karaca, Mehmet Emre Atabek, Nursel Elçioğlu, İlhan Satman, Claes Möller, Jean Muller, Jürgen Κ. Naggert, Rıza Köksal Özgül
প্রকাশিত 2014Revisão -
5
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations অনুযায়ী Katrin Friedrich, Lin Lee, Dru F. Leistritz, Gudrun Nürnberg, Bidisha Saha, Fuki M. Hisama, Daniel Eyman, Davor Lessel, Peter Nürnberg, Chumei Li, María José García-F-Villalta, Carolien M. Kets, Joerg Schmidtke, Vítor Tedim Cruz, Peter C. van den Akker, Joseph Boak, Dincy Peter, Goli Compoginis, Kıvanç Çefle, Şükrü Öztürk, Norberto López, Theda Wessel, Martin Poot, P.F. Ippel, Birgit Groff-Kellermann, Holger Hoehn, George M. Martin, Christian Kubisch, Junko Oshima
প্রকাশিত 2010Artigo -
6
<i>WRN</i>Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects অনুযায়ী Koutaro Yokote, Sirisak Chanprasert, Lin Lee, Katharina Eirich, Minoru Takemoto, Aki Watanabe, Naoko Koizumi, Davor Lessel, Takayasu Mori, Fuki M. Hisama, Paula D. Ladd, Brad Angle, Hagit Baris, Kıvanç Çefle, Şükrü Palanduz, Şükrü Öztürk, Antoinette Chateau, Kentaro Deguchi, T.K.M Easwar, Antonio Federico, Amy Fox, Theresa A. Grebe, Beverly N. Hay, Sheela Nampoothiri, Karen Seiter, Elizabeth A. Streeten, Raúl E. Piña-Aguilar, Gemma Poke, Martin Poot, Renata Posmyk, George M. Martin, Christian Kubisch, Detlev Schindler, Junko Oshima
প্রকাশিত 2016Revisão
অনুসন্ধান সাধনীগুলি:
সম্পর্কিত বিষয়
Biology
Gene
Genetics
Mutation
Bioinformatics
Exome sequencing
Exon
Helicase
Medicine
Phenotype
RNA
Werner syndrome
Allele
Azoospermia
Context (archaeology)
DNA polymerase
DNA repair
Disease gene identification
Environmental health
Exonuclease
Founder effect
Genetic testing
Germline
Germline mutation
Haplotype
Human genetics
Infertility
Locus (genetics)
Male infertility
Messenger RNA