Kết quả tìm kiếm - Guille, Matthew
- Đang hiển thị 1 - 20 kết quả của 20
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The Maternal CCAAT Box Transcription Factor Which Controls GATA-2 Expression Is Novel and Developmentally Regulated and Contains a Double-Stranded-RNA-Binding Subunit Bằng Orford, Robert L., Robinson, Carl, Haydon, Joanna M., Patient, Roger K., Guille, Matthew J.
Được phát hành 1998Text -
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Catalyst-free Click PEGylation reveals substantial mitochondrial ATP synthase sub-unit alpha oxidation before and after fertilisation Bằng Cobley, James N., Noble, Anna, Jimenez-Fernandez, Eduardo, Valdivia Moya, Manuel-Thomas, Guille, Matthew, Husi, Holger
Được phát hành 2019Text -
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Chytrid fungus infections in laboratory and introduced Xenopus laevis populations: assessing the risks for U.K. native amphibians Bằng Tinsley, Richard C., Coxhead, Peter G., Stott, Lucy C., Tinsley, Matthew C., Piccinni, Maya Z., Guille, Matthew J.
Được phát hành 2015Text -
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RNA-dependent cytoplasmic anchoring of a transcription factor subunit during Xenopus development Bằng Brzostowski, Joseph, Robinson, Carl, Orford, Robert, Elgar, Stuart, Scarlett, Garry, Peterkin, Tessa, Malartre, Marianne, Kneale, Geoffrey, Wormington, Michael, Guille, Matthew
Được phát hành 2000Text -
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Molecular insight into lignocellulose digestion by a marine isopod in the absence of gut microbes Bằng King, Andrew J., Cragg, Simon M., Li, Yi, Dymond, Jo, Guille, Matthew J., Bowles, Dianna J., Bruce, Neil C., Graham, Ian A., McQueen-Mason, Simon J.
Được phát hành 2010Text -
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Xenopus Resources: Transgenic, Inbred and Mutant Animals, Training Opportunities, and Web-Based Support Bằng Horb, Marko, Wlizla, Marcin, Abu-Daya, Anita, McNamara, Sean, Gajdasik, Dominika, Igawa, Takeshi, Suzuki, Atsushi, Ogino, Hajime, Noble, Anna, Robert, Jacques, James-Zorn, Christina, Guille, Matthew
Được phát hành 2019Text -
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pTransgenesis: a cross-species, modular transgenesis resource Bằng Love, Nick R., Thuret, Raphael, Chen, Yaoyao, Ishibashi, Shoko, Sabherwal, Nitin, Paredes, Roberto, Alves-Silva, Juliana, Dorey, Karel, Noble, Anna M., Guille, Matthew J., Sasai, Yoshiki, Papalopulu, Nancy, Amaya, Enrique
Được phát hành 2011Text -
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Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly Bằng Macken, William L., Godwin, Annie, Wheway, Gabrielle, Stals, Karen, Nazlamova, Liliya, Ellard, Sian, Alfares, Ahmed, Aloraini, Taghrid, AlSubaie, Lamia, Alfadhel, Majid, Alajaji, Sulaiman, Wai, Htoo A., Self, Jay, Douglas, Andrew G. L., Kao, Alexander P., Guille, Matthew, Baralle, Diana
Được phát hành 2021Text -
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Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome Bằng Ismail, Vardha, Zachariassen, Linda G., Godwin, Annie, Sahakian, Mane, Ellard, Sian, Stals, Karen L., Baple, Emma, Brown, Kate Tatton, Foulds, Nicola, Wheway, Gabrielle, Parker, Matthew O., Lyngby, Signe M., Pedersen, Miriam G., Desir, Julie, Bayat, Allan, Musgaard, Maria, Guille, Matthew, Kristensen, Anders S., Baralle, Diana
Được phát hành 2022Text -
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Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders Bằng Barbosa, Sónia, Greville-Heygate, Stephanie, Bonnet, Maxime, Godwin, Annie, Fagotto-Kaufmann, Christine, Kajava, Andrey V., Laouteouet, Damien, Mawby, Rebecca, Wai, Htoo Aung, Dingemans, Alexander J.M., Hehir-Kwa, Jayne, Willems, Marjorlaine, Capri, Yline, Mehta, Sarju G., Cox, Helen, Goudie, David, Vansenne, Fleur, Turnpenny, Peter, Vincent, Marie, Cogné, Benjamin, Lesca, Gaëtan, Hertecant, Jozef, Rodriguez, Diana, Keren, Boris, Burglen, Lydie, Gérard, Marion, Putoux, Audrey, Cantagrel, Vincent, Siquier-Pernet, Karine, Rio, Marlene, Banka, Siddharth, Sarkar, Ajoy, Steeves, Marcie, Parker, Michael, Clement, Emma, Moutton, Sébastien, Tran Mau-Them, Frédéric, Piton, Amélie, de Vries, Bert B.A., Guille, Matthew, Debant, Anne, Schmidt, Susanne, Baralle, Diana
Được phát hành 2020Text