Design and characterisation of a thin-film electrode array with shared reference/counter electrodes for electrochemical detection von Uludag, Yildiz, Olcer, Zehra, Samil Sagiroglu, Mahmut

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Coffin-Siris syndrome with café-au-lait spots, obesity and hyperinsulinism caused by a mutation in the ARID1B gene von Sonmez, Fatma Mujgan, Uctepe, Eyyup, Gunduz, Mehmet, Gormez, Zeliha, Erpolat, Seval, Oznur, Murat, Sagiroglu, Mahmut Samil, Demirci, Huseyin, Gunduz, Esra

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Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene von Bayrakli, Fatih, Poyrazoglu, Hatice Gamze, Yuksel, Sirin, Yakicier, Cengiz, Erguner, Bekir, Sagiroglu, Mahmut Samil, Yuceturk, Betul, Ozer, Bugra, Doganay, Selim, Tanrikulu, Bahattin, Seker, Askin, Akbulut, Fatih, Ozen, Ali, Per, Huseyin, Kumandas, Sefer, Altuner Torun, Yasemin, Bayri, Yasar, Sakar, Mustafa, Dagcinar, Adnan, Ziyal, Ibrahim

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HomSI: a homozygous stretch identifier from next-generation sequencing data von Görmez, Zeliha, Bakir-Gungor, Burcu, Sagiroglu, Mahmut Samil

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Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction von Akizu, Naiara, Cantagrel, Vincent, Zaki, Maha S, Al-Gazali, Lihadh, Wang, Xin, Rosti, Rasim Ozgur, Dikoglu, Esra, Gelot, Antoinette Bernabe, Rosti, Basak, Vaux, Keith K, Scott, Eric M, Silhavy, Jennifer L, Schroth, Jana, Copeland, Brett, Schaffer, Ashleigh E, Gordts, Philip L S M, Esko, Jeffrey D, Buschman, Matthew D, Field, Seth J, Napolitano, Gennaro, Abdel-Salam, Ghada M, Ozgul, R Koksal, Sagıroglu, Mahmut Samil, Azam, Matloob, Ismail, Samira, Aglan, Mona, Selim, Laila, Mahmoud, Iman G, Abdel-Hadi, Sawsan, Badawy, Amera El, Sadek, Abdelrahim A, Mojahedi, Faezeh, Kayserili, Hulya, Masri, Amira, Bastaki, Laila, Temtamy, Samia, Müller, Ulrich, Desguerre, Isabelle, Casanova, Jean-Laurent, Dursun, Ali, Gunel, Murat, Gabriel, Stacey B, de Lonlay, Pascale, Gleeson, Joseph G

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Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling von Cetinkaya, Arda, Xiong, Jingwei Rachel, Vargel, İbrahim, Kösemehmetoğlu, Kemal, Canter, Halil İbrahim, Gerdan, Ömer Faruk, Longo, Nicola, Alzahrani, Ahmad, Camps, Mireia Perez, Taskiran, Ekim Zihni, Laupheimer, Simone, Botto, Lorenzo D., Paramalingam, Eeswari, Gormez, Zeliha, Uz, Elif, Yuksel, Bayram, Ruacan, Şevket, Sağıroğlu, Mahmut Şamil, Takahashi, Tokiharu, Reversade, Bruno, Akarsu, Nurten Ayse

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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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Generating a detailed protein profile of Fasciola hepatica during the chronic stage of infection in cattle von Haçarız, Orçun, Baykal, Ahmet Tarık, Akgün, Mete, Kavak, Pınar, Sağıroğlu, Mahmut Şamil, Sayers, Gearóid Patrick

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A System Architecture for Efficient Transmission of Massive DNA Sequencing Data von Sağiroğlu, Mahmut Şamİl, Külekcİ, M Oğuzhan

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TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia von Alanay, Yasemin, Ergüner, Bekir, Utine, Eda, Haçarız, Orçun, Kiper, Pelin Ozlem Simsek, Taşkıran, Ekim Zihni, Perçin, Ferda, Uz, Elif, Sağıroğlu, Mahmut Şamil, Yuksel, Bayram, Boduroglu, Koray, Akarsu, Nurten Ayse

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Robustness of Massively Parallel Sequencing Platforms von Kavak, Pınar, Yüksel, Bayram, Aksu, Soner, Kulekci, M Oguzhan, Güngör, Tunga, Hach, Faraz, Şahinalp, S Cenk, Alkan, Can, Sağıroğlu, Mahmut Şamil

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Highly accurate and sensitive short read aligner von GÖK, MEHMET YAĞMUR, UĞURDAĞ, SEZER GÖREN, ÜNSALAN, CEM, SAĞIROĞLU, MAHMUT ŞAMİL

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Improving Genome Assemblies Using Multi-platform Sequence Data von Kavak, Pınar, Ergüner, Bekir, Üstek, Duran, Yüksel, Bayram, Sağıroğlu, Mahmut Şamil, Güngör, Tunga, Alkan, Can

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Whole-exome sequencing revealed two novel mutations in Usher syndrome von Koparir, Asuman, Karatas, Omer Faruk, Atayoglu, Ali Timucin, Yuksel, Bayram, Sagiroglu, Mahmut Samil, Seven, Mehmet, Ulucan, Hakan, Yuksel, Adnan, Ozen, Mustafa

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Comparative transcriptome profiling approach to glean virulence and immunomodulation-related genes of Fasciola hepatica von Haçarız, Orçun, Akgün, Mete, Kavak, Pınar, Yüksel, Bayram, Sağıroğlu, Mahmut Şamil

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Optimization for automated assembly of puzzles von Sağıroğlu, Mahmut Şamil, Erçil, Aytül

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A patient with mitochondrial disorder due to a novel mutation in MRPS22 von Kılıç, Mustafa, Oğuz, Kader-Karli, Kılıç, Esra, Yüksel, Deniz, Demirci, Hüseyin, Sağıroğlu, Mahmut Şamil, Yücel-Yılmaz, Didem, Özgül, Rıza Köksal

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Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype von Bayrakli, Fatih, Guclu, Bulent, Yakicier, Cengiz, Balaban, Hatice, Kartal, Ugur, Erguner, Bekir, Sagiroglu, Mahmut Samil, Yuksel, Sirin, Ozturk, Ahmet Rasit, Kazanci, Burak, Ozum, Unal, Kars, Hamit Zafer

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A Texture Based Matching Approach for Automated Assembly of Puzzles von Sagiroglu, M.S., Ercil, A.

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METHOD FOR ANALYSIS OF NUCLEOTIDE SEQUENCE DATA BY JOINT USE OF MULTIPLE CALCULATION UNITS AT DIFFERENT LOCATIONS von KÜLEKCI, Muhammed Oguzhan, SAGIROGLU, Mahmut Samil

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