Works matching AU Ryder, Edward


Results: 29
    1

    FBXO7 sensitivity of phenotypic traits elucidated by a hypomorphic allele.

    Published in:
    PLoS ONE, 2019, v. 14, n. 3, p. 1, doi. 10.1371/journal.pone.0212481
    By:
    • Ballesteros Reviriego, Carmen;
    • Clare, Simon;
    • Arends, Mark J.;
    • Cambridge, Emma L.;
    • Swiatkowska, Agnieszka;
    • Caetano, Susana;
    • Abu-Helil, Bushra;
    • Kane, Leanne;
    • Harcourt, Katherine;
    • Goulding, David A.;
    • Gleeson, Diane;
    • Ryder, Edward;
    • Doe, Brendan;
    • White, Jacqueline K.;
    • van der Weyden, Louise;
    • Dougan, Gordon;
    • Adams, David J.;
    • Speak, Anneliese O.
    Publication type:
    Article
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    Targeting of <i>Slc25a21</i> Is Associated with Orofacial Defects and Otitis Media Due to Disrupted Expression of a Neighbouring Gene.

    Published in:
    PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0091807
    By:
    • Maguire, Simon;
    • Estabel, Jeanne;
    • Ingham, Neil;
    • Pearson, Selina;
    • Ryder, Edward;
    • Carragher, Damian M.;
    • Walker, Nicolas;
    • Bussell, James;
    • Chan, Wai-In;
    • Keane, Thomas M.;
    • Adams, David J.;
    • Scudamore, Cheryl L.;
    • Lelliott, Christopher J.;
    • Ramírez-Solis, Ramiro;
    • Karp, Natasha A.;
    • Steel, Karen P.;
    • White, Jacqueline K.;
    • Gerdin, Anna-Karin
    Publication type:
    Article
    4

    Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 2, p. 291, doi. 10.1093/hmg/ddv471
    By:
    • Joyce, Peter I.;
    • Fratta, Pietro;
    • Landman, Allison S.;
    • Mcgoldrick, Philip;
    • Wackerhage, Henning;
    • Groves, Michael;
    • Busam, Bharani Shiva;
    • Galino, Jorge;
    • Corrochano, Silvia;
    • Beskina, Olga A.;
    • Esapa, Christopher;
    • Ryder, Edward;
    • Carter, Sarah;
    • Stewart, Michelle;
    • Codner, Gemma;
    • Hilton, Helen;
    • Teboul, Lydia;
    • Tucker, Jennifer;
    • Lionikas, Arimantas;
    • Estabel, Jeanne
    Publication type:
    Article
    5
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    The DrosDel Deletion Collection: A Drosophila Genomewide Chromosomal Deficiency Resource.

    Published in:
    Genetics, 2007, v. 177, n. 1, p. 615, doi. 10.1534/genetics.107.076216
    By:
    • Ryder, Edward;
    • Ashburner, Michael;
    • Bautista-Llacer, Rosa;
    • Drummond, Jenny;
    • Webster, Jane;
    • Johnson, Glynnis;
    • Morley, Tern;
    • Yuk Sang Chan;
    • Blows, Fiona;
    • Coulson, Darin;
    • Reuter, Gunter;
    • Baisch, Heiko;
    • Apelt, Christian;
    • Kauk, Andreas;
    • Rudolph, Thomas;
    • Kube, Maria;
    • Klimm, Melanie;
    • Nickel, Claudia;
    • Szidonya, Janos;
    • Maróy, Peter
    Publication type:
    Article
    7

    The DrosDel Collection: A Set of P-Element Insertions for Generating Custom Chromosomal Aberrations in Drosophila melanogaster.

    Published in:
    Genetics, 2004, v. 167, n. 2, p. 797, doi. 10.1534/genetics.104.026658
    By:
    • Ryder, Edward;
    • Blows, Fiona;
    • Ashburner, Michael;
    • Bautista-Llacer, Rosa;
    • Coulson, Darin;
    • Drummond, Jenny;
    • Webster, Jane;
    • Gubb, David;
    • Gunton, Nicola;
    • Johnson, Glynnis;
    • O'Kane, Cahir J.;
    • Huen, David;
    • Sharma, Punita;
    • Asztalos, Zoltan;
    • Baisch, Heiko;
    • Schulze, Janet;
    • Kube, Maria;
    • Kittlasu, Kathrin;
    • Reuter, Gunter;
    • Maroy, Peter
    Publication type:
    Article
    8
    9

    The Evolution of the DLK1-DIO3 Imprinted Domain in Mammals.

    Published in:
    PLoS Biology, 2008, v. 6, n. 6, p. e135, doi. 10.1371/journal.pbio.0060135
    By:
    • Edwards, Carol A.;
    • Mungall, Andrew J.;
    • Matthews, Lucy;
    • Ryder, Edward;
    • Gray, Dionne J.;
    • Pask, Andrew J.;
    • Shaw, Geoffrey;
    • Graves, Jennifer A. M.;
    • Rogers, Jane;
    • Dunham, Ian;
    • Renfree, Marilyn B.;
    • Ferguson-Smith, Anne C.
    Publication type:
    Article
    10
    11

    Tumors induce de novo steroid biosynthesis in T cells to evade immunity.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-17339-6
    By:
    • Mahata, Bidesh;
    • Pramanik, Jhuma;
    • van der Weyden, Louise;
    • Polanski, Krzysztof;
    • Kar, Gozde;
    • Riedel, Angela;
    • Chen, Xi;
    • Fonseca, Nuno A.;
    • Kundu, Kousik;
    • Campos, Lia S.;
    • Ryder, Edward;
    • Duddy, Graham;
    • Walczak, Izabela;
    • Okkenhaug, Klaus;
    • Adams, David J.;
    • Shields, Jacqueline D.;
    • Teichmann, Sarah A.
    Publication type:
    Article
    12

    Tiber thwarts tipburn.

    Published in:
    Agricultural Research, 1995, v. 43, n. 4, p. 23
    By:
    • Ryder, Edward J.
    Publication type:
    Article
    13

    Genomic analysis of a novel spontaneous albino C57BL/6N mouse strain.

    Published in:
    Genesis: The Journal of Genetics & Development, 2013, v. 51, n. 7, p. 523, doi. 10.1002/dvg.22398
    By:
    • Ryder, Edward;
    • Wong, Kim;
    • Gleeson, Diane;
    • Keane, Thomas M.;
    • Sethi, Debarati;
    • Vyas, Sapna;
    • Wardle‐Jones, Hannah;
    • Bussell, James N.;
    • Houghton, Richard;
    • Salisbury, Jennifer;
    • Harvey, Nina;
    • Adams, David J.;
    • Ramirez‐Solis, Ramiro
    Publication type:
    Article
    14

    Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines.

    Published in:
    Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-72418-8
    By:
    • Elrick, Hillary;
    • Peterson, Kevin A.;
    • Willis, Brandon J.;
    • Lanza, Denise G.;
    • Acar, Elif F.;
    • Ryder, Edward J.;
    • Teboul, Lydia;
    • Kasparek, Petr;
    • Birling, Marie-Christine;
    • Adams, David J.;
    • Bradley, Allan;
    • Braun, Robert E.;
    • Brown, Steve D.;
    • Caulder, Adam;
    • Codner, Gemma F.;
    • DeMayo, Francesco J.;
    • Dickinson, Mary E.;
    • Doe, Brendan;
    • Duddy, Graham;
    • Gertsenstein, Marina
    Publication type:
    Article
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    Blastocyst genotyping for quality control of mouse mutant archives: an ethical and economical approach.

    Published in:
    Transgenic Research, 2015, v. 24, n. 5, p. 921, doi. 10.1007/s11248-015-9897-1
    By:
    • Scavizzi, Ferdinando;
    • Ryder, Edward;
    • Newman, Stuart;
    • Raspa, Marcello;
    • Gleeson, Diane;
    • Wardle-Jones, Hannah;
    • Montoliu, Lluis;
    • Fernandez, Almudena;
    • Dessain, Marie-Laure;
    • Larrigaldie, Vanessa;
    • Khorshidi, Zuzana;
    • Vuolteenaho, Reetta;
    • Soininen, Raija;
    • André, Philippe;
    • Jacquot, Sylvie;
    • Hong, Yi;
    • Angelis, Martin;
    • Ramirez-Solis, Ramiro;
    • Doe, Brendan
    Publication type:
    Article
    19

    Rapid conversion of EUCOMM/KOMP-CSD alleles in mouse embryos using a cell-permeable Cre recombinase.

    Published in:
    Transgenic Research, 2014, v. 23, n. 1, p. 177, doi. 10.1007/s11248-013-9764-x
    By:
    • Ryder, Edward;
    • Doe, Brendan;
    • Gleeson, Diane;
    • Houghton, Richard;
    • Dalvi, Priya;
    • Grau, Evelyn;
    • Habib, Bishoy;
    • Miklejewska, Evelina;
    • Newman, Stuart;
    • Sethi, Debarati;
    • Sinclair, Caroline;
    • Vyas, Sapna;
    • Wardle-Jones, Hannah;
    • Bottomley, Joanna;
    • Bussell, James;
    • Galli, Antonella;
    • Salisbury, Jennifer;
    • Ramirez-Solis, Ramiro
    Publication type:
    Article
    20

    Common and distinct transcriptional signatures of mammalian embryonic lethality.

    Published in:
    Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-10642-x
    By:
    • Collins, John E.;
    • White, Richard J.;
    • Staudt, Nicole;
    • Sealy, Ian M.;
    • Packham, Ian;
    • Wali, Neha;
    • Tudor, Catherine;
    • Mazzeo, Cecilia;
    • Green, Angela;
    • Siragher, Emma;
    • Ryder, Edward;
    • White, Jacqueline K.;
    • Papatheodoru, Irene;
    • Tang, Amy;
    • Füllgrabe, Anja;
    • Billis, Konstantinos;
    • Geyer, Stefan H.;
    • Weninger, Wolfgang J.;
    • Galli, Antonella;
    • Hemberger, Myriam
    Publication type:
    Article
    21

    NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

    Published in:
    Science Immunology, 2024, v. 9, n. 95, p. 1, doi. 10.1126/sciimmunol.ade5705
    By:
    • Chen, Rui;
    • Lukianova, Elena;
    • van der Loeff, Ina Schim;
    • Spegarova, Jarmila Stremenova;
    • Willet, Joseph D.P.;
    • James, Kieran D.;
    • Ryder, Edward J.;
    • Griffin, Helen;
    • IJspeert, Hanna;
    • Gajbhiye, Akshada;
    • Lamoliatte, Frederic;
    • Marin-Rubio, Jose L.;
    • Woodbine, Lisa;
    • Lemos, Henrique;
    • Swan, David J.;
    • Pintar, Valeria;
    • Sayes, Kamal;
    • Ruiz-Morales, Elias R.;
    • Eastham, Simon;
    • Dixon, David
    Publication type:
    Article
    22

    Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation.

    Published in:
    PLoS Genetics, 2019, v. 15, n. 2, p. 1, doi. 10.1371/journal.pgen.1007917
    By:
    • O’Connell, Amy E.;
    • Gerashchenko, Maxim V.;
    • O’Donohue, Marie-Francoise;
    • Rosen, Samantha M.;
    • Huntzinger, Eric;
    • Gleeson, Diane;
    • Galli, Antonella;
    • Ryder, Edward;
    • Cao, Siqi;
    • Murphy, Quinn;
    • Kazerounian, Shideh;
    • Morton, Sarah U.;
    • Schmitz-Abe, Klaus;
    • Gladyshev, Vadim N.;
    • Gleizes, Pierre-Emmanuel;
    • Séraphin, Bertrand;
    • Agrawal, Pankaj B.
    Publication type:
    Article
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