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Journal Abstract Search

223 related items for PubMed ID: 20079790

  • 21. Mannose binding lectin (+54) exon 1 gene polymorphism in Tunisian kidney transplant patients.
    Gorgi Y, Sfar I, Aouadi H, Makhlouf M, Abderrahim E, Jendoubiayed S, Bardi R, Ben Abdallah T, Ayed K.
    Transplant Proc; 2009 Mar; 41(2):660-2. PubMed ID: 19328949
    [Abstract] [Full Text] [Related]

  • 22. Association of interleukin-1 receptor-associated kinase M (IRAK-M) and inflammatory bowel diseases.
    Weersma RK, Oostenbrug LE, Nolte IM, Van Der Steege G, Oosterom E, Van Dullemen HM, Kleibeuker JH, Dijkstra G.
    Scand J Gastroenterol; 2007 Jul; 42(7):827-33. PubMed ID: 17558906
    [Abstract] [Full Text] [Related]

  • 23. [Inflammatory bowel diseases: an immunological approach].
    Sepúlveda SE, Beltrán CJ, Peralta A, Rivas P, Rojas N, Figueroa C, Quera R, Hermoso MA.
    Rev Med Chil; 2008 Mar; 136(3):367-75. PubMed ID: 18575665
    [Abstract] [Full Text] [Related]

  • 24. Lack of association between IBD5 and Crohn's disease in Japanese patients demonstrates population-specific differences in inflammatory bowel disease.
    Tosa M, Negoro K, Kinouchi Y, Abe H, Nomura E, Takagi S, Aihara H, Oomori S, Sugimura M, Takahashi K, Hiwatashi N, Takahashi S, Shimosegawa T.
    Scand J Gastroenterol; 2006 Jan; 41(1):48-53. PubMed ID: 16373276
    [Abstract] [Full Text] [Related]

  • 25. NOD2/CARD15 genotype and phenotype differences between Ashkenazi and Sephardic Jews with Crohn's disease.
    Karban A, Waterman M, Panhuysen CI, Pollak RD, Nesher S, Datta L, Weiss B, Suissa A, Shamir R, Brant SR, Eliakim R.
    Am J Gastroenterol; 2004 Jun; 99(6):1134-40. PubMed ID: 15180737
    [Abstract] [Full Text] [Related]

  • 26. Variants of CARD15 are associated with an aggressive clinical course of Crohn's disease--an IG-IBD study.
    Annese V, Lombardi G, Perri F, D'Incà R, Ardizzone S, Riegler G, Giaccari S, Vecchi M, Castiglione F, Gionchetti P, Cocchiara E, Vigneri S, Latiano A, Palmieri O, Andriulli A.
    Am J Gastroenterol; 2005 Jan; 100(1):84-92. PubMed ID: 15654786
    [Abstract] [Full Text] [Related]

  • 27. Genotype-phenotype analysis of the CXCL16 p.Ala181Val polymorphism in inflammatory bowel disease.
    Seiderer J, Dambacher J, Leistner D, Tillack C, Glas J, Niess JH, Pfennig S, Jürgens M, Müller-Myhsok B, Göke B, Ochsenkühn T, Lohse P, Reinecker HC, Brand S.
    Clin Immunol; 2008 Apr; 127(1):49-55. PubMed ID: 18248772
    [Abstract] [Full Text] [Related]

  • 28. Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease.
    Török HP, Glas J, Endres I, Tonenchi L, Teshome MY, Wetzke M, Klein W, Lohse P, Ochsenkühn T, Folwaczny M, Göke B, Folwaczny C, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2009 Jul; 104(7):1723-33. PubMed ID: 19455129
    [Abstract] [Full Text] [Related]

  • 29. Disease concordance, zygosity, and NOD2/CARD15 status: follow-up of a population-based cohort of Danish twins with inflammatory bowel disease.
    Jess T, Riis L, Jespersgaard C, Hougs L, Andersen PS, Orholm MK, Binder V, Munkholm P.
    Am J Gastroenterol; 2005 Nov; 100(11):2486-92. PubMed ID: 16279904
    [Abstract] [Full Text] [Related]

  • 30. Mannose-binding lectin and mannose-binding lectin-associated serine protease 2 in susceptibility, severity, and outcome of pneumonia in adults.
    Garcia-Laorden MI, Sole-Violan J, Rodriguez de Castro F, Aspa J, Briones ML, Garcia-Saavedra A, Rajas O, Blanquer J, Caballero-Hidalgo A, Marcos-Ramos JA, Hernandez-Lopez J, Rodriguez-Gallego C.
    J Allergy Clin Immunol; 2008 Aug; 122(2):368-74, 374.e1-2. PubMed ID: 18582923
    [Abstract] [Full Text] [Related]

  • 31. Interactions among genes influencing bacterial recognition increase IBD risk in a population-based New Zealand cohort.
    Petermann I, Huebner C, Browning BL, Gearry RB, Barclay ML, Kennedy M, Roberts R, Shelling AN, Philpott M, Han DY, Ferguson LR.
    Hum Immunol; 2009 Jun; 70(6):440-6. PubMed ID: 19275920
    [Abstract] [Full Text] [Related]

  • 32. Association of organic cation transporter risk haplotype with perianal penetrating Crohn's disease but not with susceptibility to IBD.
    Vermeire S, Pierik M, Hlavaty T, Claessens G, van Schuerbeeck N, Joossens S, Ferrante M, Henckaerts L, Bueno de Mesquita M, Vlietinck R, Rutgeerts P.
    Gastroenterology; 2005 Dec; 129(6):1845-53. PubMed ID: 16344053
    [Abstract] [Full Text] [Related]

  • 33. Mannose-binding lectin variant alleles and HLA-DR4 alleles are associated with giant cell arteritis.
    Jacobsen S, Baslund B, Madsen HO, Tvede N, Svejgaard A, Garred P.
    J Rheumatol; 2002 Oct; 29(10):2148-53. PubMed ID: 12375325
    [Abstract] [Full Text] [Related]

  • 34. Two factors of the lectin pathway of complement, l-ficolin and mannan-binding lectin, and their associations with prematurity, low birthweight and infections in a large cohort of Polish neonates.
    Swierzko AS, Atkinson AP, Cedzynski M, Macdonald SL, Szala A, Domzalska-Popadiuk I, Borkowska-Klos M, Jopek A, Szczapa J, Matsushita M, Szemraj J, Turner ML, Kilpatrick DC.
    Mol Immunol; 2009 Feb; 46(4):551-8. PubMed ID: 18950864
    [Abstract] [Full Text] [Related]

  • 35. Mannose-binding lectin (MBL) in adult patients with inflammatory bowel disease.
    Bąk-Romaniszyn L, Świerzko AS, Sokołowska A, Durko Ł, Mierzwa G, Szala-Poździej A, Małecka-Panas E, Cedzyński M.
    Immunobiology; 2020 Jan; 225(1):151859. PubMed ID: 31703823
    [Abstract] [Full Text] [Related]

  • 36. The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.
    Glas J, Konrad A, Schmechel S, Dambacher J, Seiderer J, Schroff F, Wetzke M, Roeske D, Török HP, Tonenchi L, Pfennig S, Haller D, Griga T, Klein W, Epplen JT, Folwaczny C, Lohse P, Göke B, Ochsenkühn T, Mussack T, Folwaczny M, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2008 Mar; 103(3):682-91. PubMed ID: 18162085
    [Abstract] [Full Text] [Related]

  • 37. Characterization of genotype-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markers.
    Crawford NP, Colliver DW, Funke AA, Young MN, Kelley S, Cobbs GA, Petras RE, Galandiuk S.
    Hum Mutat; 2005 Feb; 25(2):156-66. PubMed ID: 15643611
    [Abstract] [Full Text] [Related]

  • 38. Mannan-binding lectin deficiency results in unusual antibody production and excessive experimental colitis in response to mannose-expressing mild gut pathogens.
    Müller S, Schaffer T, Flogerzi B, Seibold-Schmid B, Schnider J, Takahashi K, Darfeuille-Michaud A, Vazeille E, Schoepfer AM, Seibold F.
    Gut; 2010 Nov; 59(11):1493-500. PubMed ID: 20682699
    [Abstract] [Full Text] [Related]

  • 39. Mannose-binding lectin deficiency confers risk for bacterial infections in a large Hungarian cohort of patients with liver cirrhosis.
    Altorjay I, Vitalis Z, Tornai I, Palatka K, Kacska S, Farkas G, Udvardy M, Harsfalvi J, Dinya T, Orosz P, Lombay B, Par G, Par A, Csak T, Osztovits J, Szalay F, Csepregi A, Lakatos PL, Papp M.
    J Hepatol; 2010 Sep; 53(3):484-91. PubMed ID: 20605050
    [Abstract] [Full Text] [Related]

  • 40. Evidence for association of OCTN genes and IBD5 with ulcerative colitis.
    Waller S, Tremelling M, Bredin F, Godfrey L, Howson J, Parkes M.
    Gut; 2006 Jun; 55(6):809-14. PubMed ID: 16361305
    [Abstract] [Full Text] [Related]

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