Hakutulokset - Aslıhan Tolun

  • Näytetään 1 - 12 yhteensä 12 tuloksesta
Tarkenna hakua
  1. 1
    Termination sites for adenovirus type 2 DNA replication

    Termination sites for adenovirus type 2 DNA replication Tekijä Aslıhan Tolun, U. Pettersson

    Julkaistu 1975
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  2. 2
    Truncating mutations in<i>TAF4B</i>and<i>ZMYND15</i>causing recessive azoospermia

    Truncating mutations in<i>TAF4B</i>and<i>ZMYND15</i>causing recessive azoospermia Tekijä Özgecan Ayhan, Mahmut Balkan, Ayşe Güven, Ronen Hazan, Murat Atar, Atalay Tok, Aslıhan Tolun

    Julkaistu 2014
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  3. 3
    A frameshift mutation of ERLIN2 in recessive intellectual disability, motor dysfunction and multiple joint contractures

    A frameshift mutation of ERLIN2 in recessive intellectual disability, motor dysfunction and multiple joint contractures Tekijä Yeşerin Yıldırım, Elif Kocasoy Orhan, Sı̇bel Aylı̇n Uğur İşerı̇, Piraye Oflazer, Bülent Kara, Seyhun Solakoğlu, Aslıhan Tolun

    Julkaistu 2011
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  4. 4
    Mutations in SLC34A2 Cause Pulmonary Alveolar Microlithiasis and Are Possibly Associated with Testicular Microlithiasis

    Mutations in SLC34A2 Cause Pulmonary Alveolar Microlithiasis and Are Possibly Associated with Testicular Microlithiasis Tekijä Ayse Corut, Abdurrahman Şenyiğit, Sı̇bel Aylı̇n Uğur İşerı̇, Sedat Altın, Uğur Özçelik, Haluk Çalışır, Zeki Yıldırım, Ayhan Göçmen, Aslıhan Tolun

    Julkaistu 2006
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  5. 5
    Splicing Defects in the Ataxia-Telangiectasia Gene, ATM: Underlying Mutations and Consequences

    Splicing Defects in the Ataxia-Telangiectasia Gene, ATM: Underlying Mutations and Consequences Tekijä Sharon N. Teraoka, Milhan Telatar, Sara Becker-Catania, Teresa Liang, Suna Önengüt, Aslıhan Tolun, Luciana Chessa, Özden Sanal, Ewa Bernatowska, Richard A. Gatti, Patrick Concannon

    Julkaistu 1999
    Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  6. 6
    Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay

    Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay Tekijä Myungjin Kim, Erin Sandford, Damián Gatica, Yu Qiu, Xu Liu, Yumei Zheng, Brenda A. Schulman, Jishu Xu, Ian Semple, Seung‐Hyun Ro, Bo Young Kim, Rezan Nehir Mavioğlu, Aslıhan Tolun, András Jipa, Szabolcs Takáts, Manuéla Kárpáti, Jun Z. Li, Zühal Yapıcı, Gábor Juhász, Jun Hee Lee, Daniel J. Klionsky, Margit Burmeister

    Julkaistu 2016
    Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  7. 7
    Large-scale recent expansion of European patrilineages shown by population resequencing

    Large-scale recent expansion of European patrilineages shown by population resequencing Tekijä Chiara Batini, Pille Hallast, Daniel Zadik, Pierpaolo Maisano Delser, Andrea Benazzo, Silvia Ghirotto, Eduardo Arroyo, Gianpiero L. Cavalleri, Peter de Knijff, Berit Myhre Dupuy, Heidi Eriksen, Turi King, Adolfo López de Munaín, Ana María López‐Parra, Aphrodite Loutradis, Jelena Milas̆in, Andrea Novelletto, Horolma Pamjav, Antti Sajantila, Aslıhan Tolun, Bruce Winney, Mark A. Jobling

    Julkaistu 2015
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  8. 8
    Mutation in protein disulfide isomerase A3 causes neurodevelopmental defects by disturbing endoplasmic reticulum proteostasis

    Mutation in protein disulfide isomerase A3 causes neurodevelopmental defects by disturbing endoplasmic reticulum proteostasis Tekijä Danilo B. Medinas, Sajid Malik, Esra Yıldız Bölükbaşı, Janina Borgonovo, Mirva J. Saaranen, Hery Urra, Eduardo Pulgar, Muhammad Afzal, Darwin Contreras, Madison T. Wright, Felipe Bodaleo, Gabriel Quiroz, Pablo Rozas, Sara Mumtaz, Rodrigo Dı́az, Carlos Rozas, Felipe Cabral‐Miranda, Ricardo Piña, Vicente Valenzuela, Özgün Uyan, Christopher Reardon, Ute Woehlbier, Robert H. Brown, Miguel Sena‐Esteves, Christian González‐Billault, Bernardo Morales, Lars Plate, Lloyd W. Ruddock, Miguel L. Concha, Claudio Hetz, Aslıhan Tolun

    Julkaistu 2021
    Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  9. 9
    The Y-Chromosome Tree Bursts into Leaf: 13,000 High-Confidence SNPs Covering the Majority of Known Clades

    The Y-Chromosome Tree Bursts into Leaf: 13,000 High-Confidence SNPs Covering the Majority of Known Clades Tekijä Pille Hallast, Chiara Batini, Daniel Zadik, Pierpaolo Maisano Delser, Jon H. Wetton, Eduardo Arroyo, Gianpiero L. Cavalleri, Peter de Knijff, Giovanni Destro‐Bisol, B.M. Dupuy, Heidi Eriksen, Lynn B. Jorde, Turi King, Maarten Larmuseau, Adolfo López de Munaín, Ana Marı́a López-Parra, Aphrodite Loutradis, Jelena Milašin, Andrea Novelletto, Horolma Pamjav, Antti Sajantila, W. Schempp, Mary Sears, Aslıhan Tolun, Chirs Tyler-Smith, Anneleen Van Geystelen, Scott Watkins, Bruce Winney, Mark A. Jobling

    Julkaistu 2014
    Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  10. 10
    Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

    Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders Tekijä Gaia Novarino, Ali G. Fenstermaker, Maha S. Zaki, Matan Hofree, Jennifer L. Silhavy, Andrew Heiberg, Mostafa Abdellateef, Başak Rosti, Eric Scott, Lobna Mansour, Amira Masri, Hülya Kayserili, Jumana Y. Al‐Aama, Ghada M. H. Abdel‐Salam, Ariana Karminejad, Majdi Kara, Bülent Kara, Babak Bozorgmehri, Tawfeg Ben‐Omran, Faezeh Mojahedi, Iman G. Mahmoud, Naïma Bouslam, Ahmed Bouhouche, Ali Benomar, Sylvain Hanein, Laure Raymond, Sylvie Forlani, Massimo Mascaro, Laila Selim, Nabil Shehata, Nasir Al‐Allawi, Parayil Sankaran Bindu, Matloob Azam, Murat Günel, Ahmet Okay Çağlayan, Kaya Bilgüvar, Aslıhan Tolun, Mahmoud Y. Issa, Jana Schroth, Emily Spencer, Rasim Özgür Rosti, Naiara Akizu, Keith K. Vaux, Anide Johansen, Alice A. Koh, Hisham Megahed, Alexandra Dürr, Alexis Brice, Giovanni Stévanin, Stacy Gabriel, Trey Ideker, Joseph G. Gleeson

    Julkaistu 2014
    Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  11. 11
    <i>TBC1D24</i> genotype–phenotype correlation

    <i>TBC1D24</i> genotype–phenotype correlation Tekijä Simona Balestrini, Mathieu Milh, Claudia Castiglioni, Kevin Lüthy, Mattéa J. Finelli, Patrik Verstreken, Aaron L. Cardon, Barbara Gnidovec Stražišar, J. Lloyd Holder, Gaëtan Lesca, Maria Margherita Mancardi, Anne Lise Poulat, Gabriela M. Repetto, Siddharth Banka, Leonilda Bilo, Laura E. Birkeland, Friedrich Bosch, Knut Brockmann, J. Helen Cross, Diane Doummar, Têmis Maria Félix, Fabienne Giuliano, Mutsuki Hori, Irina Hüning, Hulia Kayserili, Usha Kini, Melissa Lees, Girish Meenakshi, Leena Mewasingh, Alistair T. Pagnamenta, Silvio Peluso, Antje Mey, Gregory M. Rice, Jill A. Rosenfeld, Jenny C. Taylor, Matthew M. Troester, Christine M. Stanley, Dorothée Ville, Magdalena Walkiewicz, Antonio Falace, Anna Fassio, Johannes R. Lemke, Saskia Biskup, Jessica Tardif, Norbert Fonya Ajeawung, Aslıhan Tolun, Mark Corbett, Jozef Gécz, Zaid Afawi, Katherine B. Howell, Karen Oliver, Samuel F. Berkovic, Ingrid E. Scheffer, De Falco Fa, Peter L. Oliver, Pasquale Striano, Federico Zara, Philippe M. Campeau, Sanjay M. Sisodiya

    Julkaistu 2016
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:
  12. 12
    Y-Chromosomal Diversity in Europe Is Clinal and Influenced Primarily by Geography, Rather than by Language

    Y-Chromosomal Diversity in Europe Is Clinal and Influenced Primarily by Geography, Rather than by Language Tekijä Zoë H. Rosser, Tatiana Zerjal, Matthew E. Hurles, Maarja Adojaan, Dragan Alavantić, António Amorim, William Amos, Manuel Armenteros, Eduardo Arroyo, Guido Barbujani, G. Beckman, L. Beckman, Jaume Bertranpetit, Elena Bosch, Daniel G. Bradley, Gaute Brede, Gillian Cooper, Helena B.S.M. Côrte-Real, Peter de Knijff, Ronny Decorte, Yuri E. Dubrova, Oleg V. Evgrafov, Anja Gilissen, Sanja Glišić, Mukaddes Gölge, Emmeline W. Hill, Anna Jeziorowska, Luba Kalaydjieva, Manfred Kayser, Toomas Kivisild, С. А. Кравченко, Astrīda Krūmiņa, Vaidutis Kučinskas, João Lavinha, Л. А. Лившиц, Patrizia Malaspina, Syrrou Maria, Ken McElreavey, Thomas Meitinger, Aavo‐Valdur Mikelsaar, R.J. Mitchell, Khédoudja Nafa, Jayne Nicholson, Søren Nørby, Arpita Pandya, Jüri Parik, Philippos C. Patsalis, Luı́sa Pereira, Borut Peterlin, Gerli Pielberg, Maria João Prata, Carlo Previderé, Lutz Roewer, Siiri Rootsi, David C. Rubinsztein, Juliette Saillard, Fabrício R. Santos, Gheorghe Ştefănescu, Bryan Sykes, Aslıhan Tolun, Richard Villems, Chris Tyler‐Smith, Mark A. Jobling

    Julkaistu 2000
    Hae kokoteksti Hae kokoteksti
    Artigo
    Lisää suosikkeihin
    Tallennettuna:

Työkalut: