Works matching AU Jackson, Andrew P.

Results: 87
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    A comprehensive evaluation of rodent malaria parasite genomes and gene expression.

    Published in:
    BMC Biology, 2014, v. 12, n. 1, p. 2, doi. 10.1186/s12915-014-0086-0
    By:
    • Otto, Thomas D.;
    • Böhme, Ulrike;
    • Jackson, Andrew P.;
    • Hunt, Martin;
    • Franke-Fayard, Blandine;
    • Hoeijmakers, Wieteke A. M.;
    • Religa, Agnieszka A.;
    • Robertson, Lauren;
    • Sanders, Mandy;
    • Ogun, Solabomi A.;
    • Cunningham, Deirdre;
    • Erhart, Annette;
    • Billker, Oliver;
    • Khan, Shahid M.;
    • Stunnenberg, Hendrik G.;
    • Langhorne, Jean;
    • Holder, Anthony A.;
    • Waters, Andrew P.;
    • Newbold, Chris I.;
    • Pain, Arnab
    Publication type:
    Article
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    ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy.

    Published in:
    PLoS Genetics, 2019, v. 15, n. 3, p. 1, doi. 10.1371/journal.pgen.1007605
    By:
    • Handley, Mark T.;
    • Reddy, Kaalak;
    • Wills, Jimi;
    • Rosser, Elisabeth;
    • Kamath, Archith;
    • Halachev, Mihail;
    • Falkous, Gavin;
    • Williams, Denise;
    • Cox, Phillip;
    • Meynert, Alison;
    • Raymond, Eleanor S.;
    • Morrison, Harris;
    • Brown, Stephen;
    • Allan, Emma;
    • Aligianis, Irene;
    • Jackson, Andrew P.;
    • Ramsahoye, Bernard H.;
    • von Kriegsheim, Alex;
    • Taylor, Robert W.;
    • Finch, Andrew J.
    Publication type:
    Article
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    A Cell-surface Phylome for African Trypanosomes.

    Published in:
    PLoS Neglected Tropical Diseases, 2013, v. 7, n. 3, p. 1, doi. 10.1371/journal.pntd.0002121
    By:
    • Jackson, Andrew P.;
    • Allison, Harriet C.;
    • Barry, J. David;
    • Field, Mark C.;
    • Hertz-Fowler, Christiane;
    • Berriman, Matthew
    Publication type:
    Article
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    A Cell-surface Phylome for African Trypanosomes.

    Published in:
    PLoS Neglected Tropical Diseases, 2013, v. 7, n. 3, p. 1, doi. 10.1371/journal.pntd.0002121
    By:
    • Jackson, Andrew P.;
    • Allison, Harriet C.;
    • Barry, J. David;
    • Field, Mark C.;
    • Hertz-Fowler, Christiane;
    • Berriman, Matthew
    Publication type:
    Article
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    Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 4, p. 350, doi. 10.1038/ng.776
    By:
    • Bicknell, Louise S.;
    • Walker, Sarah;
    • Klingseisen, Anna;
    • Stiff, Tom;
    • Leitch, Andrea;
    • Kerzendorfer, Claudia;
    • Martin, Carol-Anne;
    • Yeyati, Patricia;
    • Al Sanna, Nouriya;
    • Bober, Michael;
    • Johnson, Diana;
    • Wise, Carol;
    • Jackson, Andrew P.;
    • O'Driscoll, Mark;
    • Jeggo, Penny A.
    Publication type:
    Article
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    Hypomorphic PCNA mutation underlies a human DNA repair disorder.

    Published in:
    Journal of Clinical Investigation, 2014, v. 124, n. 7, p. 3137, doi. 10.1172/JCI74593
    By:
    • Baple, Emma L.;
    • Chambers, Helen;
    • Cross, Harold E.;
    • Fawcett, Heather;
    • Nakazawa, Yuka;
    • Chioza, Barry A.;
    • Harlalka, Gaurav V.;
    • Mansour, Sahar;
    • Sreekantan-Nair, Ajith;
    • Patton, Michael A.;
    • Muggenthaler, Martina;
    • Rich, Phillip;
    • Wagner, Karin;
    • Coblentz, Roselyn;
    • Stein, Constance K.;
    • Last, James I.;
    • Taylor, A. Malcolm R.;
    • Jackson, Andrew P.;
    • Ogi, Tomoo;
    • Lehmann, Alan R.
    Publication type:
    Article
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    Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy.

    Published in:
    Nature Genetics, 2014, v. 46, n. 12, p. 1283, doi. 10.1038/ng.3122
    By:
    • Martin, Carol-Anne;
    • Klingseisen, Anna;
    • Bicknell, Louise S;
    • Leitch, Andrea;
    • Murray, Jennie E;
    • Hunt, David;
    • Ding, James;
    • Harley, Margaret E;
    • Heyn, Patricia;
    • Jackson, Andrew P;
    • Daire, Valérie Cormier;
    • Dollfus, Hélène;
    • Dupuis, Lucie;
    • Mendoza-Londono, Roberto;
    • Bashamboo, Anu;
    • McElreavey, Kenneth;
    • Kariminejad, Ariana;
    • Moore, Anthony T;
    • Saggar, Anand;
    • Schlechter, Catie
    Publication type:
    Article
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    RNase H2, mutated in Aicardi‐Goutières syndrome, promotes LINE‐1 retrotransposition.

    Published in:
    EMBO Journal, 2018, v. 37, n. 15, p. 1, doi. 10.15252/embj.201798506
    By:
    • Benitez‐Guijarro, Maria;
    • Lopez‐Ruiz, Cesar;
    • Tarnauskaitė, Žygimantė;
    • Murina, Olga;
    • Mian Mohammad, Mahwish;
    • Williams, Thomas C.;
    • Fluteau, Adeline;
    • Sanchez, Laura;
    • Vilar‐Astasio, Raquel;
    • Garcia‐Canadas, Marta;
    • Cano, David;
    • Kempen, Marie‐Jeanne H. C.;
    • Sanchez‐Pozo, Antonio;
    • Heras, Sara R.;
    • Jackson, Andrew P.;
    • Reijns, Martin A. M.;
    • Garcia‐Perez, Jose L.
    Publication type:
    Article
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    Ribonuclease H2 mutations induce a cGAS/ STING-dependent innate immune response.

    Published in:
    EMBO Journal, 2016, v. 35, n. 8, p. 831, doi. 10.15252/embj.201593339
    By:
    • Mackenzie, Karen J;
    • Carroll, Paula;
    • Lettice, Laura;
    • Tarnauskaitė, Žygimantė;
    • Reddy, Kaalak;
    • Dix, Flora;
    • Revuelta, Ailsa;
    • Abbondati, Erika;
    • Rigby, Rachel E;
    • Rabe, Björn;
    • Kilanowski, Fiona;
    • Grimes, Graeme;
    • Fluteau, Adeline;
    • Devenney, Paul S;
    • Hill, Robert E;
    • Reijns, Martin AM;
    • Jackson, Andrew P
    Publication type:
    Article
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    RNA: DNA hybrids are a novel molecular pattern sensed by TLR9.

    Published in:
    EMBO Journal, 2014, v. 33, n. 6, p. 542, doi. 10.1002/embj.201386117
    By:
    • Rigby, Rachel E;
    • Webb, Lauren M;
    • Mackenzie, Karen J;
    • Li, Yue;
    • Leitch, Andrea;
    • Reijns, Martin A M;
    • Lundie, Rachel J;
    • Revuelta, Ailsa;
    • Davidson, Donald J;
    • Diebold, Sandra;
    • Modis, Yorgo;
    • MacDonald, Andrew S;
    • Jackson, Andrew P
    Publication type:
    Article
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    Vivaxin genes encode highly immunogenic, non-variant antigens on the Trypanosoma vivax cell-surface.

    Published in:
    PLoS Neglected Tropical Diseases, 2022, v. 16, n. 9, p. 1, doi. 10.1371/journal.pntd.0010791
    By:
    • Romero-Ramirez, Alessandra;
    • Casas-Sánchez, Aitor;
    • Autheman, Delphine;
    • Duffy, Craig W.;
    • Brandt, Cordelia;
    • Clare, Simon;
    • Harcourt, Katherine;
    • André, Marcos Rogério;
    • de Almeida Castilho Neto, Kayo José Garcia;
    • Teixeira, Marta M. G.;
    • Machado, Rosangela Zacharias;
    • Coombes, Janine;
    • Flynn, Robin J.;
    • Wright, Gavin J.;
    • Jackson, Andrew P.
    Publication type:
    Article
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    Microcephalin.

    Published in:
    Cell Cycle, 2006, v. 5, n. 20, p. 2339
    By:
    • O'Driscoll, Mark;
    • Jackson, Andrew P.;
    • Jeggo, Penny A.
    Publication type:
    Article
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    Meier-Gorlin syndrome.

    Published in:
    2015
    By:
    • de Munnik, Sonja A.;
    • Hoefsloot, Elisabeth H.;
    • Roukema, Jolt;
    • Schoots, Jeroen;
    • Knoers, Nine V. A. M.;
    • Brunner, Han G.;
    • Jackson, Andrew P.;
    • Bongers, Ernie M. H. F.;
    • Knoers, Nine Vam;
    • Bongers, Ernie Mhf
    Publication type:
    journal article
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    Transcriptome, proteome and draft genome of Euglena gracilis.

    Published in:
    BMC Biology, 2019, v. 17, n. 1, p. 1, doi. 10.1186/s12915-019-0626-8
    By:
    • Ebenezer, ThankGod E.;
    • Zoltner, Martin;
    • Burrell, Alana;
    • Nenarokova, Anna;
    • Novák Vanclová, Anna M. G.;
    • Prasad, Binod;
    • Soukal, Petr;
    • Santana-Molina, Carlos;
    • O'Neill, Ellis;
    • Nankissoor, Nerissa N.;
    • Vadakedath, Nithya;
    • Daiker, Viktor;
    • Obado, Samson;
    • Silva-Pereira, Sara;
    • Jackson, Andrew P.;
    • Devos, Damien P.;
    • Lukeš, Julius;
    • Lebert, Michael;
    • Vaughan, Sue;
    • Hampl, Vladimίr
    Publication type:
    Article
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    The evolutionary dynamics of variant antigen genes in Babesia reveal a history of genomic innovation underlying host–parasite interaction.

    Published in:
    Nucleic Acids Research, 2014, v. 42, n. 11, p. 7113, doi. 10.1093/nar/gku322
    By:
    • Jackson, Andrew P.;
    • Otto, Thomas D.;
    • Darby, Alistair;
    • Ramaprasad, Abhinay;
    • Xia, Dong;
    • Echaide, Ignacio Eduardo;
    • Farber, Marisa;
    • Gahlot, Sunayna;
    • Gamble, John;
    • Gupta, Dinesh;
    • Gupta, Yask;
    • Jackson, Louise;
    • Malandrin, Laurence;
    • Malas, Tareq B.;
    • Moussa, Ehab;
    • Nair, Mridul;
    • Reid, Adam J.;
    • Sanders, Mandy;
    • Sharma, Jyotsna;
    • Tracey, Alan
    Publication type:
    Article
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    The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.

    Published in:
    Nucleic Acids Research, 2014, v. 42, n. D1, p. D966
    By:
    • Köhler, Sebastian;
    • Doelken, Sandra C.;
    • Mungall, Christopher J.;
    • Bauer, Sebastian;
    • Firth, Helen V.;
    • Bailleul-Forestier, Isabelle;
    • Black, Graeme C. M.;
    • Brown, Danielle L.;
    • Brudno, Michael;
    • Campbell, Jennifer;
    • FitzPatrick, David R.;
    • Eppig, Janan T.;
    • Jackson, Andrew P.;
    • Freson, Kathleen;
    • Girdea, Marta;
    • Helbig, Ingo;
    • Hurst, Jane A.;
    • Jähn, Johanna;
    • Jackson, Laird G.;
    • Kelly, Anne M.
    Publication type:
    Article
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    Growth in individuals with Saul–Wilson syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2020, v. 182, n. 9, p. 2110, doi. 10.1002/ajmg.a.61754
    By:
    • Ferreira, Carlos R.;
    • Niiler, Timothy;
    • Duker, Angela L.;
    • Jackson, Andrew P.;
    • Bober, Michael B.
    Publication type:
    Article
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