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Recent Publications

Found 447 results
Author Title Type [ Year(Asc)]
Mackley EC, Houston S, Marriott CL, Halford EE, Lucas B, Cerovic V, Filbey KJ, Maizels RM, Hepworth MR, Sonnenberg GF et al..  2015.  CCR7-dependent trafficking of RORγ⁺ ILCs creates a unique microenvironment within mucosal draining lymph nodes.. Nat Commun. 6:5862.
Frykman PK, Nordenskjöld A, Kawaguchi A, Hui TT, Granström AL, Cheng Z, Tang J, Underhill DM, Iliev ID, Funari VA et al..  2015.  Characterization of Bacterial and Fungal Microbiome in Children with Hirschsprung Disease with and without a History of Enterocolitis: A Multicenter Study.. PLoS One. 10(4):e0124172.
Steinberg-Neifach O, Wellington K, Vazquez L, Lue NF.  2015.  Combinatorial recognition of a complex telomere repeat sequence by the Candida parapsilosis Cdc13AB heterodimer.. Nucleic Acids Res.
Iliev ID.  2015.  Dectin-1 Exerts Dual Control in the Gut.. Cell Host Microbe. 18(2):139-41.
Seehus CR, Aliahmad P, de la Torre B, Iliev ID, Spurka L, Funari VA, Kaye J.  2015.  The development of innate lymphoid cells requires TOX-dependent generation of a common innate lymphoid cell progenitor.. Nat Immunol. 16(6):599-608.
de Sena-Tomás C, Yu EYoung, Calzada A, Holloman WK, Lue NF, Pérez-Martín J.  2015.  Fungal Ku prevents permanent cell cycle arrest by suppressing DNA damage signaling at telomeres.. Nucleic Acids Res.
Brestoff JR, Kim BS, Saenz SA, Stine RR, Monticelli LA, Sonnenberg GF, Thome JJ, Farber DL, Lutfy K, Seale P et al..  2015.  Group 2 innate lymphoid cells promote beiging of white adipose tissue and limit obesity.. Nature. 519(7542):242-6.
Yu EYoung, Pérez-Martín J, Holloman WK, Lue NF.  2015.  Mre11 and Blm-Dependent Formation of ALT-Like Telomeres in Ku-Deficient Ustilago maydis.. PLoS Genet. 11(10):e1005570.
Tang J, Iliev ID, Brown J, Underhill DM, Funari VA.  2015.  Mycobiome: Approaches to analysis of intestinal fungi.. J Immunol Methods. 421:112-21.
Müller S, Wolf AJ, Iliev ID, Berg BL, Underhill DM, Liu GY.  2015.  Poorly Cross-Linked Peptidoglycan in MRSA Due to mecA Induction Activates the Inflammasome and Exacerbates Immunopathology.. Cell Host Microbe. 18(5):604-12.
Steinberg-Neifach O, Lue NF.  2015.  Telomere DNA recognition in Saccharomycotina yeast: potential lessons for the co-evolution of ssDNA and dsDNA-binding proteins and their target sites.. Front Genet. 6:162.
Janovitz T, Sadelain M, Falck-Pedersen E.  2014.  Adeno-associated virus type 2 preferentially integrates single genome copies with defined breakpoints.. Virol J. 11:15.
Lam E, Stein S, Falck-Pedersen E.  2014.  Adenovirus detection by the cGAS/STING/TBK1 DNA sensing cascade.. J Virol. 88(2):974-81.
Fung TC, Artis D, Sonnenberg GF.  2014.  Anatomical localization of commensal bacteria in immune cell homeostasis and disease.. Immunol Rev. 260(1):35-49.
Sinha A, Hughes KR, Modrzynska KK, Otto TD, Pfander C, Dickens NJ, Religa AA, Bushell E, Graham AL, Cameron R et al..  2014.  A cascade of DNA-binding proteins for sexual commitment and development in Plasmodium.. Nature. 507(7491):253-7.
Lue NF, Chan J, Wright WE, Hurwitz J.  2014.  The CDC13-STN1-TEN1 complex stimulates Pol α activity by promoting RNA priming and primase-to-polymerase switch.. Nat Commun. 5:5762.
Osborne LC, Monticelli LA, Nice TJ, Sutherland TE, Siracusa MC, Hepworth MR, Tomov VT, Kobuley D, Tran SV, Bittinger K et al..  2014.  Coinfection. Virus-helminth coinfection reveals a microbiota-independent mechanism of immunomodulation.. Science. 345(6196):578-82.
Sander AF, Lavstsen T, Rask TS, Lisby M, Salanti A, Fordyce SL, Jespersen JS, Carter R, Deitsch K, Theander TG et al..  2014.  DNA secondary structures are associated with recombination in major Plasmodium falciparum variable surface antigen gene families.. Nucleic Acids Res. 42(4):2270-81.
Zhou Q, Holloman WK.  2014.  Dual DNA-binding domains shape the interaction of Brh2 with DNA.. DNA Repair (Amst). 22:104-11.
Janovitz T, Oliveira T, Sadelain M, Falck-Pedersen E.  2014.  Highly divergent integration profile of adeno-associated virus serotype 5 revealed by high-throughput sequencing.. J Virol. 88(5):2481-8.
Puckett S, Trujillo C, Eoh H, Marrero J, Spencer J, Jackson M, Schnappinger D, Rhee K, Ehrt S.  2014.  Inactivation of fructose-1,6-bisphosphate aldolase prevents optimal co-catabolism of glycolytic and gluconeogenic carbon substrates in Mycobacterium tuberculosis.. PLoS Pathog. 10(5):e1004144.
Gaur RL, Ren K, Blumenthal A, Bhamidi S, Gibbs S, Jackson M, Zare RN, Ehrt S, Ernst JD, Banaei N.  2014.  LprG-mediated surface expression of lipoarabinomannan is essential for virulence of Mycobacterium tuberculosis.. PLoS Pathog. 10(9):e1004376.
Kirkman L, Lawrence EA, Deitsch K.  2014.  Malaria parasites utilize both homologous recombination and alternative end joining pathways to maintain genome integrity.. Nucleic Acids Res. 42(1):370-9.
Gouzy A, Larrouy-Maumus G, Bottai D, Levillain F, Dumas A, Wallach JB, Caire-Brandli I, de Chastellier C, Di Wu T-, Poincloux R et al..  2014.  Mycobacterium tuberculosis exploits asparagine to assimilate nitrogen and resist acid stress during infection.. PLoS Pathog. 10(2):e1003928.
Underhill DM, Iliev ID.  2014.  The mycobiota: interactions between commensal fungi and the host immune system.. Nat Rev Immunol. 14(6):405-16.