Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Guthery, Sl"'
Autor:
Momozawa, Y, Dmitrieva, J, Theatre, E, Deffontaine, V, Rahmouni, S, Charloteaux, B, Crins, F, Docampo, E, Elansary, M, Gori, AS, Lecut, C, Mariman, R, Mni, M, Oury, C, Altukhov, I, Alexeev, D, Aulchenko, Y, Amininejad, L, Bouma, G, Hoentjen, F, Lowenberg, M, Oldenburg, B, Pierik, MJ, de Jong, AE, van der Woude, C.J., Visschedijk, MC, Lathrop, M, Hugot, JP, Weersma, RK, Vos, M, Franchimont, D, Vermeire, S, Kubo, M, Louis, E, Georges, M, Abraham, C, Achkar, JP, Ahmad, T, Ananthakrishnan, AN, Andersen, V, Anderson, CA, Andrews, JM, Annese, V, Aumais, G, Baidoo, L, Baldassano, RN, Bampton, PA, Barclay, M, Barrett, JC, Bayless, TM, Bethge, J, Bitton, A, Boucher, G, Brand, S, Brandt, B, Brant, SR, Buning, C, Chew, A, Cho, JH, Cleynen, I, Cohain, A, Croft, A, Daly, MJ, D'Amato, M, Danese, S, Jong, D, Denapiene, G, Denson, LA, Devaney, KL, Dewit, O, D'Inca, R, Dubinsky, M, Duerr, RH, Edwards, C, Ellinghaus, D, Essers, J, Ferguson, LR, Festen, EA, Fleshner, P, Florin, T, Franke, A, Fransen, K, Gearry, R, Gieger, C, Glas, J, Goyette, P, Green, T, Griffiths, AM, Guthery, SL, Hakonarson, H, Halfvarson, J, Hanigan, K, Haritunians, T, de Hart, A, Hawkey, C, Hayward, NK, Hedl, M, Henderson, P, Hu, XH, Huang, HL, Hui, KY, Imielinski, M, Ippoliti, A, Jonaitis, L, Jostins, L, Karlsen, TH, Kennedy, NA, Khan, MA, Kiudelis, G, Krishnaprasad, K, Kugathasan, S, Kupcinskas, L, Latiano, A, Laukens, D, Lawrance, IC, Lee, JC, Lees, CW, Leja, M, van Limbergen, J, Lionetti, P, Liu, JZ, Mahy, G, Mansfield, J, Massey, D, Mathew, CG, McGovern, DPB, Milgrom, R, Mitrovic, M, Montgomery, GW, Mowat, C, Newman, W, Ng, A, Ng, SC, Ng, SME, Nikolaus, S, Ning, K, Nothen, M, Oikonomou, I, Palmieri, O, Parkes, M, Phillips, A, Ponsioen, CY, Potocnik, U, Prescott, NJ, Proctor, DD, Radford-Smith, G, Rahier, JF, Raychaudhuri, S, Regueiro, M, Rieder, F, Rioux, JD, Ripke, S, Roberts, R, Russell, RK, Sanderson, JD, Sans, M, Satsangi, J, Schadt, EE, Schreiber, S, Schulte, D, Schumm, LP, Scott, R, Seielstad, M, Sharma, Y, Silverberg, MS, Simms, LA, Skieceviciene, J, Spain, SL, Steinhart, AH, Stempak, JM, Stronati, L, Sventoraityte, J, Targan, SR, Taylor, KM, Velde, A, Torkvist, L, Tremelling, M, van Sommeren, S, Vasiliauskas, E, Verspaget, HW, Walters, T, Wang, K, Wang, MH, Wei, Z, Whiteman, D, Wijmenga, C, Wilson, DC, Winkelmann, J, Xavier, RJ, Zhang, B, Zhang, CK, Zhang, H, Zhang, W, Zhao, HY, Zhao, ZZ
Publikováno v:
NATURE COMMUNICATIONS
Momozawa, Y, Dmitrieva, J, Théâtre, E, Deffontaine, V, Rahmouni, S, Charloteaux, B, Crins, F, Docampo, E, Elansary, M, Gori, A-S, Lecut, C, Mariman, R, Mni, M, Oury, C, Altukhov, I, Alexeev, D, Aulchenko, Y, Amininejad, L, Bouma, G, Hoentjen, F, Löwenberg, M, Oldenburg, B, Pierik, M J, Vander Meulen-de Jong, A E, Janneke van der Woude, C, Visschedijk, M C, Lathrop, M, Hugot, J-P, Weersma, R K, De Vos, M, Franchimont, D, Vermeire, S, Kubo, M & Louis, E & Georges, M 2018, ' IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes ', Nature Communications, vol. 9, no. 1, pp. 2427 . https://doi.org/10.1038/s41467-018-04365-8
Nature Communications
Nature Communications, 9:2427. Nature Publishing Group
Nature communications, Vol. 9, no. 1, p. 2427 (2018)
Momozawa, Y, Dmitrieva, J, Théâtre, E, Deffontaine, V, Rahmouni, S, Charloteaux, B, Crins, F, Docampo, E, Elansary, M, Gori, A-S, Lecut, C, Mariman, R, Mni, M, Oury, C, Altukhov, I, Alexeev, D, Aulchenko, Y, Amininejad, L, Bouma, G, Hoentjen, F, Löwenberg, M, Oldenburg, B, Pierik, M J, Vander Meulen-de Jong, A E, Janneke van der Woude, C, Visschedijk, M C, Lathrop, M, Hugot, J-P, Weersma, R K, De Vos, M, Franchimont, D, Vermeire, S, Kubo, M & Louis, E & Georges, M 2018, ' IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes ', Nature Communications, vol. 9, no. 1, pp. 2427 . https://doi.org/10.1038/s41467-018-04365-8
Nature Communications
Nature Communications, 9:2427. Nature Publishing Group
Nature communications, Vol. 9, no. 1, p. 2427 (2018)
GWAS have identified >200 risk loci for Inflammatory Bowel Disease (IBD). The majority of disease associations are known to be driven by regulatory variants. To identify the putative causative genes that are perturbed by these variants, we generate a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0dfdfd477db43cfdeff0fe3f26a98b51
https://biblio.ugent.be/publication/8582997/file/8582999
https://biblio.ugent.be/publication/8582997/file/8582999
Autor:
Denson, LA, Jurickova, I, Karns, R, Shaw, KA, Cutler, DJ, Okou, D, Alexander Valencia, C, Dodd, A, Mondal, K, Aronow, BJ, Haberman, Y, Linn, A, Price, A, Bezold, R, Lake, K, Jackson, K, Walters, TD, Griffiths, A, Baldassano, RN, Noe, JD, Hyams, JS, Crandall, WV, Kirschner, BS, Heyman, MB, Snapper, S, Guthery, SL, Dubinsky, MC, Leleiko, NS, Otley, AR, Xavier, RJ, Stevens, C, Daly, MJ, Zwick, ME, Kugathasan, S
Publikováno v:
Inflammatory bowel diseases, vol 25, iss 3
Denson, LA; Jurickova, I; Karns, R; Shaw, KA; Cutler, DJ; Okou, D; et al.(2018). Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease.. Inflammatory bowel diseases. doi: 10.1093/ibd/izy265. UCSF: Retrieved from: http://www.escholarship.org/uc/item/9pw1s15v
Denson, LA; Jurickova, I; Karns, R; Shaw, KA; Cutler, DJ; Okou, D; et al.(2018). Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte-Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease.. Inflammatory bowel diseases. doi: 10.1093/ibd/izy265. UCSF: Retrieved from: http://www.escholarship.org/uc/item/9pw1s15v
BACKGROUND:Granulocyte-macrophage colony-stimulating factor auto-antibodies (GMAbs) suppress neutrophil-extrinsic GM-CSF signaling and increase risk for stricturing behavior in Crohn's disease (CD). We aimed to define clinical, genomic, and functiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3ff2148ee5ce136c1e832ebafd64c520
https://escholarship.org/uc/item/9pw1s15v
https://escholarship.org/uc/item/9pw1s15v
Autor:
Leiding, JW, Okada, S, Hagin, D, Abinun, M, Shcherbina, A, Balashov, DN, Kim, VHD, Ovadia, A, Guthery, SL, Pulsipher, M, Lilic, D, Devlin, LA, Christie, S, Depner, M, Fuchs, S, van Royen-Kerkhof, A, Lindemans, C, Petrovic, A, Sullivan, KE, Bunin, N, Kilic, SS, Arpaci, F, de la Calle-Martin, O, Martinez-Martinez, L, Aldave, JC, Kobayashi, M, Ohkawa, T, Imai, K, Iguchi, A, Roifman, CM, Gennery, AR, Slatter, M, Ochs, HD, Morio, T, Torgerson, TR, Inborn Errors Working Party, European Soc Blood Marrow, Primary Immune Deficiency
Publikováno v:
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Background: Gain-of-function (GOF) mutations in signal transducer and activator of transcription 1 (STAT1) cause susceptibility to a range of infections, autoimmunity, immune dysregulation, and combined immunodeficiency. Disease manifestations can be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::1af22e603ade6f55ed89266cc666c46e
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=3954
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=3954
Autor:
Cleynen, Isabelle, Boucher, Gabrielle, Jostins, Luke, Schumm, L. Philip, Zeissig, Sebastian, Ahmad, Tariq, Andersen, Vibeke, Andrews, Jane M., Annese, Vito, Brand, Stephan, Brant, Steven R., Cho, Judy H., Daly, Mark J., Dubinsky, Marla, Duerr, Richard H., Ferguson, Lynnette R., Franke, Andre, Gearry, Richard B., Goyette, Philippe, Hakonarson, Hakon, Halfvarson, Jonas, Hov, Johannes R., Huang, Hailang, Kennedy, Nicholas A., Kupcinskas, Limas, Lawrance, Ian C., Lee, James C., Satsangi, Jack, Schreiber, Stephan, Théâtre, Emilie, Van Der Meulen De Jong, Andrea E, Weersma, Rinse K., Wilson, David C., Parkes, Miles, Vermeire, Severine, Rioux, John D., Mansfield, John, Silverberg, Mark S., Radford Smith, Graham, Mcgovern, Dermot P. B., Barrett, Jeffrey C., Lees, Charlie W, Abraham, C, Achkar, Jp, Ahmad, T, Amininejad, L, Ananthakrishnan, An, Andersen, V, Anderson, Ca, Andrews, Jm, Annese, V, Aumais, G, Baidoo, L, Baldassano, Rn, Bampton, Pa, Barclay, M, Barrett, Jc, Bayless, Tm, Bethge, J, Bis, Jc, Bitton, A, Boucher, G, Brand, S, Brandt, B, Brant, Sr, Büning, C, Chew, A, Cho, Jh, Cleynen, I, Cohain, A, Croft, A, Daly, Mj, D'Amato, M, Danese, S, De Jong, D, De Vos, M, Denapiene, G, Denson, La, Devaney, K, Dewit, O, D'Inca, R, Dubinsky, M, Duerr, Rh, Edwards, C, Ellinghaus, D, Essers, J, Ferguson, Lr, Festen, Ea, Fleshner, P, Florin, T, Franchimont, D, Franke, A, Fransen, K, Gearry, R, Georges, M, Gieger, C, Glas, J, Goyette, P, Green, T, Griffiths, Am, Guthery, Sl, Hakonarson, H, Halfvarson, J, Hanigan, K, Haritunians, T, Hart, A, Hawkey, C, Hayward, Nk, Hedl, M, Henderson, P, Hu, X, Huang, H, Hui, Ky, Imielinski, M, Ippoliti, A, Jonaitis, L, Jostins, L, Karlsen, Th, Kennedy, Na, Khan, Ma, Kiudelis, G, Krishnaprasad, K, Kugathasan, S, Kupcinskas, L, Latiano, A, Laukens, D, Lawrance, Ic, Lee, Jc, Lees, Cw, Leja, M, Van Limbergen, J, Lionetti, P, Liu, Jz, Louis, E, Mahy, G, Mansfield, J, Massey, D, Mathew, Cg, Mcgovern, Dp, Milgrom, R, Mitrovic, M, Montgomery, Gw, Mowat, C, Newman, W, Ng, A, Ng, Sc, Ng, Sm, Nikolaus, S, Ning, K, Nöthen, M, Oikonomou, I, Palmieri, O, Parkes, M, Phillips, A, Ponsioen, Cy, Potocnik, U, Prescott, Nj, Proctor, Dd, Radford Smith, G, Rahier, Jf, Raychaudhuri, S, Regueiro, M, Rieder, F, Rioux, Jd, Ripke, S, Roberts, R, Russell, Rk, Sanderson, Jd, Sans, M, Satsangi, J, Schadt, Ee, Schreiber, S, Schumm, Lp, Scott, R, Seielstad, M, Sharma, Y, Silverberg, Ms, Simms, La, Skieceviciene, J, Spain, Sl, Steinhart, A, Stempak, Jm, Stronati, Laura, Sventoraityte, J, Targan, Sr, Taylor, Km, ter Velde, A, Theatre, E, Torkvist, L, Tremelling, M, van der Meulen, A, van Sommeren, S, Vasiliauskas, E, Vermeire, S, Verspaget, Hw, Walters, T, Wang, K, Wang, Mh, Weersma, Rk, Wei, Z, Whiteman, D, Wijmenga, C, Wilson, Dc, Winkelmann, J, Xavier, Rj, Zeissig, S, Zhang, B, Zhang, Ck, Zhang, H, Zhang, W, Zhao, H, Zhao, Zz
Publikováno v:
Cleynen, I, Boucher, G, Jostins, L, Schumm, L P, Zeissig, S, Ahmad, T, Andersen, V, Andrews, J M, Annese, V, Brand, S, Brant, S R, Cho, J H, Daly, M J, Dubinsky, M, Duerr, R H, Ferguson, L R, Franke, A, Gearry, R B, Goyette, P, Hakonarson, H, Halfvarson, J, Hov, J R, Huang, H, Kennedy, N A, Kupcinskas, L, Lawrance, I C, Lee, J C, Satsangi, J, Schreiber, S, Théâtre, E, van der Meulen-de Jong, A E, Weersma, R K, Wilson, D C, Parkes, M, Vermeire, S, Rioux, J D, Mansfield, J, Silverberg, M S, Radford-Smith, G, McGovern, D P B, Barrett, J C, Lees, C W & International Inflammatory Bowel Disease Genetics Consortium 2016, ' Inherited determinants of Crohn's disease and ulcerative colitis phenotypes : a genetic association study ', The Lancet, vol. 387, no. 10014, pp. 156-167 . https://doi.org/10.1016/S0140-6736(15)00465-1
LANCET
Lancet, 387(10014), 156-167
Lancet (London, England)
Cleynen, I, Boucher, G, Jostins, L, Schumm, L P, Zeissig, S, Ahmad, T, Andersen, V, Andrews, J M, Annese, V, Brand, S, Brant, S R, Cho, J H, Daly, M J, Dubinsky, M, Duerr, R H, Ferguson, L R, Franke, A, Gearry, R B, Goyette, P, Hakonarson, H, Halfvarson, J, Hov, J R, Huang, H, Kennedy, N A, Kupcinskas, L, Lawrance, I C, Lee, J C, Satsangi, J, Schreiber, S, Théâtre, E, van der Meulen-de Jong, A E, Weersma, R K, Wilson, D C, Parkes, M, Vermeire, S, Rioux, J D, Mansfield, J, Silverberg, M S, Radford-Smith, G, McGovern, D P B & Barrett, J C & Lees, C W 2016, ' Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study ', The Lancet, vol. 387, no. 10014, pp. 156-167 . https://doi.org/10.1016/S0140-6736(15)00465-1
Lancet (London, England), Vol. 387, no. 10014, p. 156-67 (2016)
The Lancet, 387(10014), 156-167. ELSEVIER SCIENCE INC
LANCET
Lancet, 387(10014), 156-167
Lancet (London, England)
Cleynen, I, Boucher, G, Jostins, L, Schumm, L P, Zeissig, S, Ahmad, T, Andersen, V, Andrews, J M, Annese, V, Brand, S, Brant, S R, Cho, J H, Daly, M J, Dubinsky, M, Duerr, R H, Ferguson, L R, Franke, A, Gearry, R B, Goyette, P, Hakonarson, H, Halfvarson, J, Hov, J R, Huang, H, Kennedy, N A, Kupcinskas, L, Lawrance, I C, Lee, J C, Satsangi, J, Schreiber, S, Théâtre, E, van der Meulen-de Jong, A E, Weersma, R K, Wilson, D C, Parkes, M, Vermeire, S, Rioux, J D, Mansfield, J, Silverberg, M S, Radford-Smith, G, McGovern, D P B & Barrett, J C & Lees, C W 2016, ' Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study ', The Lancet, vol. 387, no. 10014, pp. 156-167 . https://doi.org/10.1016/S0140-6736(15)00465-1
Lancet (London, England), Vol. 387, no. 10014, p. 156-67 (2016)
The Lancet, 387(10014), 156-167. ELSEVIER SCIENCE INC
Background: Crohn's disease and ulcerative colitis are the two major forms of inflammatory bowel disease; treatment strategies have historically been determined by this binary categorisation. Genetic studies have identified 163 susceptibility loci fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50f04919d18474155a26114385411d1b
https://findresearcher.sdu.dk:8443/ws/files/128924437/Inherited_determinants_of_Crohn_s_disease_and_ulcerative_colitis_phenotypes.pdf
https://findresearcher.sdu.dk:8443/ws/files/128924437/Inherited_determinants_of_Crohn_s_disease_and_ulcerative_colitis_phenotypes.pdf
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Autor:
Willson TA, Kuhn BR, Jurickova I, Gerad S, Moon D, Bonkowski E, Carey R, Collins MH, Xu H, Jegga AG, Guthery SL, Denson LA, Willson, Tara A, Kuhn, Benjamin R, Jurickova, Ingrid, Gerad, Shaina, Moon, David, Bonkowski, Erin, Carey, Rebecca, Collins, Margaret H
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition; 2012 Jul, Vol. 55 Issue 1, p32-43, 12p
Akademický článek
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Autor:
Prahalad S, Hansen S, Whiting A, Guthery SL, Clifford B, McNally B, Zeft AS, Bohnsack JF, Jorde LB
Publikováno v:
Arthritis & Rheumatism; Jul2009, Vol. 60 Issue 7, p2124-2130, 7p