Výsledky vyhledávání - Matthew Guille

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  1. 1
    Development of xenopus resource centers: The national xenopus resource and the european xenopus resource center

    Development of xenopus resource centers: The national xenopus resource and the european xenopus resource center Autor Esther J. Pearl, Robert M. Grainger, Matthew Guille, Marko E. Horb

    Vydáno 2012
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    Revisão
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  2. 2
    Overlapping sites for constitutive and induced DNA binding factors involved in interferon-stimulated transcription.

    Overlapping sites for constitutive and induced DNA binding factors involved in interferon-stimulated transcription. Autor Trevor Dale, Jeffrey M. Rosen, Matthew Guille, Andrew R. Lewin, Alan Porter, Ian M. Kerr, George R. Stark

    Vydáno 1989
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    Artigo
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  3. 3
    Adipose tissue macrophages develop from bone marrow–independent progenitors in <i>Xenopus laevis</i> and mouse

    Adipose tissue macrophages develop from bone marrow–independent progenitors in <i>Xenopus laevis</i> and mouse Autor Syed F. Hassnain Waqas, Anna Noble, Anh Cuong Hoang, Grace Ampem, M. Popp, Sarah Strauß, Matthew Guille, Tamás Rőszer

    Vydáno 2017
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    Artigo
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  4. 4
    Molecular insight into lignocellulose digestion by a marine isopod in the absence of gut microbes

    Molecular insight into lignocellulose digestion by a marine isopod in the absence of gut microbes Autor Andrew King, Simon M. Cragg, Yi Li, Jo Dymond, Matthew Guille, Dianna J. Bowles, Neil C. Bruce, Ian A. Graham, Simon J. McQueen‐Mason

    Vydáno 2010
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    Artigo
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  5. 5
    pTransgenesis: a cross-species, modular transgenesis resource

    pTransgenesis: a cross-species, modular transgenesis resource Autor Nick R. Love, Raphaël Thuret, Yaoyao Chen, Shoko Ishibashi, Nitin Sabherwal, Roberto Paredes, Juliana Alves‐Silva, Karel Dorey, Anna Noble, Matthew Guille, Yoshiki Sasai, Nancy Papalopulu, Enrique Amaya

    Vydáno 2011
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    Artigo
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  6. 6
    Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome

    Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome Autor Vardha Ismail, Linda G. Zachariassen, Annie Godwin, Mane Sahakian, Sian Ellard, Karen Stals, Emma L. Baple, Kate Tatton Brown, Nicola Foulds, Gabrielle Wheway, Matthew O. Parker, Signe Meisner Lyngby, Miriam G. Pedersen, Julie Désir, Allan Bayat, Maria Musgaard, Matthew Guille, Anders S. Kristensen, Diana Baralle

    Vydáno 2022
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  7. 7
    Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders

    Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders Autor Sónia Barbosa, Stephanie Greville‐Heygate, Maxime Bonnet, Annie Godwin, Christine Fagotto‐Kaufmann, Andrey V. Kajava, Damien Laouteouet, Rebecca Mawby, Htoo A. Wai, Alexander J.M. Dingemans, Jayne Y. Hehir‐Kwa, Marjorlaine Willems, Yline Capri, Sarju Mehta, Helen Cox, David Goudie, Fleur Vansenne, Peter D. Turnpenny, Marie Vincent, Benjamin Cogné, Gaëtan Lesca, Jozef Hertecant, Diana Rodriguez, Boris Keren, Lydie Bürglen, Marion Gérard, Audrey Putoux, Vincent Cantagrel, Karine Siquier-Pernet, Marlène Rio, Siddharth Banka, Ajoy Sarkar, Marcie Steeves, Michael Parker, Emma Clement, Sébastien Moutton, Frédéric Tran Mau‐Them, Amélie Piton, Bert B.A. de Vries, Matthew Guille, Anne Debant, Susanne Schmidt, Diana Baralle

    Vydáno 2020
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  8. 8
    Bi-allelic <i>ACBD6</i> variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders

    Bi-allelic <i>ACBD6</i> variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders Autor Rauan Kaiyrzhanov, Abolfazl Rad, Sheng‐Jia Lin, Aida M. Bertoli‐Avella, Wouter W. Kallemeijn, Annie Godwin, Maha S. Zaki, Kevin Huang, Tracy Lau, Cassidy Petree, Stéphanie Efthymiou, Ehsan Ghayoor Karimiani, Maja Hempel, Elizabeth A. Normand, Sabine Rudnik‐Schöneborn, Ulrich A. Schatz, Marc P. Baggelaar, Muhammad Ilyas, Tipu Sultan, Javeria Raza Alvi, Manizha Ganieva, Ben Fowler, Ruxandra Aanicai, Gulsen Akay Tayfun, Abdulaziz Al Saman, Abdulrahman Alswaid, Nafise Amiri, Nilufar Asilova, Vorasuk Shotelersuk, Patra Yeetong, Matloob Azam, Meisam Babaei, Gholamreza Bahrami Monajemi, Pouria Mohammadi, Saeed Samie, Selina Banu, Jorge Pinto Basto, Fanny Kortüm, Mislen Bauer, Peter Bauer, Christian Beetz, Masoud Garshasbi, Awatif Hameed Issa, Wafaa Eyaid, Hind Ahmed, Narges Hashemi, Kazem Hassanpour, Isabella Herman, Sherozjon Ibrohimov, Ban A. Abdul–Majeed, Maria Imdad, M.O. Isrofilov, Qassem Kaiyal, Suliman Khan, Brian Kirmse, Janet Koster, Charles Marques Lourenço, Tadahiro Mitani, Oana Moldovan, David Murphy, Maryam Najafi, Davut Pehli̇van, María Eugenia Rocha, Vincenzo Salpietro, Miriam Schmidts, Adel Shalata, Mohammad Mahroum, Jawabreh Kassem Talbeya, Robert W. Taylor, Dayana Vazquez, Annalisa Vetro, Hans R. Waterham, Mashaya Zaman, Tina A. Schrader, Wendy K. Chung, Renzo Guerrini, James R. Lupski, Joseph G. Gleeson, Mohnish Suri, Yalda Jamshidi, Kailash P. Bhatia, Barbara Vona, Michael Schrader, Mariasavina Severino, Matthew Guille, Edward W. Tate, Gaurav K. Varshney, Henry Houlden, Reza Maroofian

    Vydáno 2023
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