Works matching AU Gleeson, Diane

Results: 8
    1

    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
    2

    Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease.

    Published in:
    PLoS Genetics, 2010, v. 6, n. 2, p. 1, doi. 10.1371/journal.pgen.1000833
    By:
    • Morgan, Neil V.;
    • Morris, Mark R.;
    • Cangul, Hakan;
    • Gleeson, Diane;
    • Straatman-Iwanowska, Anna;
    • Davies, Nicholas;
    • Keenan, Stephen;
    • Pasha, Shanaz;
    • Rahman, Fatimah;
    • Gentle, Dean;
    • Vreeswijk, Maaike P. G.;
    • Devilee, Peter;
    • Knowles, Margaret A.;
    • Ceylaner, Serdar;
    • Trembath, Richard C.;
    • Dalence, Carlos;
    • Kismet, Erol;
    • Köseoğ lu, Vedat;
    • Rossbach, Hans-Christoph;
    • Gissen, Paul
    Publication type:
    Article
    3

    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
    4

    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
    5

    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
    6

    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
    7
    8

    Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole-body energy expenditure.

    Published in:
    Journal of Pathology, 2016, v. 239, n. 3, p. 374, doi. 10.1002/path.4737
    By:
    • Liakath‐Ali, Kifayathullah;
    • Vancollie, Valerie E;
    • Lelliott, Christopher J;
    • Speak, Anneliese O;
    • Lafont, David;
    • Protheroe, Hayley J;
    • Ingvorsen, Camilla;
    • Galli, Antonella;
    • Green, Angela;
    • Gleeson, Diane;
    • Ryder, Ed;
    • Glover, Leanne;
    • Vizcay‐Barrena, Gema;
    • Karp, Natasha A;
    • Arends, Mark J;
    • Brenn, Thomas;
    • Spiegel, Sarah;
    • Adams, David J;
    • Watt, Fiona M;
    • van der Weyden, Louise
    Publication type:
    Article