Výsledky vyhledávání - Nejat Akar

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  1. 1
    Prothrombin gene 20210 G-A mutation in the Turkish population

    Prothrombin gene 20210 G-A mutation in the Turkish population Autor Nejat Akar, Müge Mısırlıoğlu, Ece Akar, Ferit Avcu, Atilla Yalçın, Ayşe Sözüöz

    Vydáno 1998
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    Carta
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  2. 2
    MEFV mutations in Turkish patients suffering from familial Mediterranean fever

    MEFV mutations in Turkish patients suffering from familial Mediterranean fever Autor Nejat Akar, M�ge Misiroglu, Fatoş Yalçınkaya, Ece Akar, Nilgün Çakar, Necmiye T�mer, Mustafa Akçakuş, Hakkı Taştan, Yaacov Matzner

    Vydáno 2000
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    Artigo
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  3. 3
    Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia

    Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia Autor Mustafa Tekin, Burcu Öztürk Hişmi, Suat Fítöz, Hi̇lal Özdağ, Filiz Başak Cengiz, Aslı Sırmacı, İdil Aslan, Bora İnceoğlu, E. Berrin Yüksel-Konuk, Seda Taşır Yılmaz, Öztan Yasun, Nejat Akar

    Vydáno 2007
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    Artigo
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  4. 4
    Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa

    Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa Autor Fulvio Cruciani, Roberta La Fratta, P. Santolamazza, Daniele Sellitto, R Pascone, Pedro Moral, Elizabeth Watson, Valentina Guida, Eliane Beraud Colomb, Boriana Zaharova, João Lavinha, Giuseppe Vona, Rashid Aman, Francesco Calı̀, Nejat Akar, Martin Richards, Antonio Torroni, Andrea Novelletto, Rosaria Scozzari

    Vydáno 2004
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    Artigo
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  5. 5
    Genome-Wide Transcriptional Reorganization Associated with Senescence-to-Immortality Switch during Human Hepatocellular Carcinogenesis

    Genome-Wide Transcriptional Reorganization Associated with Senescence-to-Immortality Switch during Human Hepatocellular Carcinogenesis Autor Gökhan Yıldız, Ayça Arslan-Ergül, Sevgi Baǧışlar, Özlen Konu, Haluk Yuzugullu, Özge Gürsoy-Yüzügüllü, Nuri Öztürk, Çigdem Özen, Hi̇lal Özdağ, Esra Erdal, Sedat Karademır, Özgül Sağol, Dılşa Mızrak, Hakan Bozkaya, Hakkı Gökhan İlk, Özlem İlk, Biter Bilen, Rengül Çetin-Atalay, Nejat Akar, Mehmet Öztürk

    Vydáno 2013
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    Artigo
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  6. 6
    Differential Structuring of Human Populations for Homologous X and Y Microsatellite Loci

    Differential Structuring of Human Populations for Homologous X and Y Microsatellite Loci Autor Rosaria Scozzari, Fulvio Cruciani, Patrizia Malaspina, P. Santolamazza, Bianca Maria Ciminelli, Antonio Torroni, David Modiano, Douglas C. Wallace, Kenneth K. Kídd, Antonel Olckers, Pedro Moral, L. Terrenato, Nejat Akar, Raheel Qamar, Atika Mansoor, S. Qasim Mehdi, Tullio Meloni, Giuseppe Vona, David E.C. Cole, Wangwei Cai, Andrea Novelletto

    Vydáno 1997
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    Artigo
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  7. 7
    A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

    A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss Autor Aslı Sırmacı, Seyra Erbek, Justin Price, Mingqian Huang, Duygu Duman, Filiz Başak Cengiz, Güney Bademci, Suna Tokgöz-Yılmaz, Burcu Öztürk Hişmi, Hi̇lal Özdağ, Banu Öztürk, Sevsen Kulaksızoğlu, Erkan Yıldırım, Haris Kokotas, Maria Grigoriadou, Michael B. Petersen, Hashem Shahin, Moien Kanaan, Mary‐Claire King, Zheng‐Yi Chen, Susan H. Blanton, Xue Z. Liu, Stephan Züchner, Nejat Akar, Mustafa Tekin

    Vydáno 2010
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    Artigo
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  8. 8
    Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls

    Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis inv... Autor Benedetto Simone, Valerio De Stefano, Emanuele Leoncini, Jeppe Zacho, Ida Martinelli, Joseph Emmerich, Elena Rossi, Aaron R. Folsom, Wassim Y. Almawi, Pierre Yves Scarabin, Martin den Heijer, Mary Cushman, Silvana Penco, Amparo Vayá, Pantep Angchaisuksiri, Gülfer Okumuş, Donato Gemmati, S. Cima, Nejat Akar, Kıvılcım Oğuzülgen, Véronique Ducros, Christoph Lichy, Consuelo Fernández‐Miranda, Andrzej Szczeklik, J. Aizpurua Nieto, José Domingo Torres, Véronique Le Cam‐Duchez, P Ivanov, Carlos Cantú‐Brito, В М Шмелева, Mojka Stegnar, Dotun Ogunyemi, Suhair S Eid, Nicola Nicolotti, Emma De Feo, Walter Ricciardi, Stefania Boccia

    Vydáno 2013
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    Revisão
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  9. 9
    A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis

    A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis Autor Heiko Witt, Miklós Sahin‐Tóth, Olfert Landt, Jian‐Min Chen, Thilo Kähne, Joost P.H. Drenth, Zoltán Kukor, Edit Szepessy, Walter Halangk, Stefan Dahm, Klaus Rohde, Hans-Ulrich Schulz, Cédric Le Maréchal, Nejat Akar, R Ammann, Kaspar Truninger, Mario Bargetzi, Eesh Bhatia, Carlo Castellani, Giulia Martina Cavestro, Miloš Černý, Giovanni Destro‐Bisol, Gabriella Spedini, Hans Eiberg, Jan B.�M.�J. Jansen, Monika Koudová, Eva Rausova, Milan Maçek, Núria Malats, Francisco X. Real, Hans‐Jürgen Menzel, Pedro Moral, Roberta Galavotti, Pier Franco Pignatti, Olga Rickards, Julius Špičák, Narcis Zarnescu, W. J. Bock, Thomas M. Gress, Helmut Frieß, Johann Ockenga, Hartmut Schmidt, Roland H. Pfützer, Matthias Löhr, Péter Simon, Frank Ulrich Weiß, Markus M. Lerch, Niels Teich, Volker Keim, Thomas Berg, Bertram Wiedenmann, W. A. P. Luck, David A. Groneberg, Michael Becker, Thomas Keil, Andreas Kage, Jana Bernardova, Markus Braun, Claudia Güldner, Juliane Halangk, Jonas Rosendahl, Ulrike Witt, Matthias Treiber, Renate Nickel, Claude Férec

    Vydáno 2006
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    Artigo
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