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Journal Abstract Search

97 related items for PubMed ID: 21987299

  • 21. [Associations of Crohn's disease with DR4 and DR5 gene polymorphisms].
    Lin X, Jin L, Pan C, Zheng S, Zhang D, Lin X, Ding R, Jiang L, Jiang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):715-22. PubMed ID: 26418999
    [Abstract] [Full Text] [Related]

  • 22. MDR1 gene C3435T polymorphism in chronic hepatitis C patients.
    Parsa Nahad M, Makvandi M, Teimoori A, Jalilian S, Kayedani GA, Mahmoodi S.
    Microb Pathog; 2018 Jan; 114():63-67. PubMed ID: 29155127
    [Abstract] [Full Text] [Related]

  • 23. Association between the PTPN2 gene and Crohn's disease: dissection of potential causal variants.
    Marcil V, Mack DR, Kumar V, Faure C, Carlson CS, Beaulieu P, Israel D, Krupoves A, Costea I, Lambrette P, Grimard G, Dong J, Seidman EG, Amre DK, Levy E.
    Inflamm Bowel Dis; 2013 May; 19(6):1149-55. PubMed ID: 23518806
    [Abstract] [Full Text] [Related]

  • 24. Genome-wide association study signal at the 12q12 locus for Crohn's disease may represent associations with the MUC19 gene.
    Kumar V, Mack DR, Marcil V, Israel D, Krupoves A, Costea I, Lambrette P, Grimard G, Dong J, Seidman EG, Amre DK, Levy E.
    Inflamm Bowel Dis; 2013 May; 19(6):1254-9. PubMed ID: 23619718
    [Abstract] [Full Text] [Related]

  • 25. Immediate and long-term outcomes of corticosteroid therapy in pediatric Crohn's disease patients.
    Krupoves A, Mack DR, Seidman EG, Deslandres C, Bucionis V, Amre DK.
    Inflamm Bowel Dis; 2011 Apr; 17(4):954-62. PubMed ID: 20684012
    [Abstract] [Full Text] [Related]

  • 26. Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children.
    Amre DK, Mack D, Israel D, Morgan K, Lambrette P, Law L, Grimard G, Deslandres C, Krupoves A, Bucionis V, Costea I, Bissonauth V, Feguery H, D'Souza S, Levy E, Seidman EG.
    Am J Gastroenterol; 2008 Mar; 103(3):615-20. PubMed ID: 18047539
    [Abstract] [Full Text] [Related]

  • 27. Smoking behaviour modifies IL23r-associated disease risk in patients with Crohn's disease.
    Doecke JD, Simms LA, Zhao ZZ, Roberts RL, Fowler EV, Croft A, Lin A, Huang N, Whiteman DC, Florin TH, Barclay ML, Merriman TR, Gearry RB, Montgomery GW, Radford-Smith GL.
    J Gastroenterol Hepatol; 2015 Feb; 30(2):299-307. PubMed ID: 24989722
    [Abstract] [Full Text] [Related]

  • 28. A non-synonymous coding variant (L616F) in the TLR5 gene is potentially associated with Crohn's disease and influences responses to bacterial flagellin.
    Sheridan J, Mack DR, Amre DK, Israel DM, Cherkasov A, Li H, Grimard G, Steiner TS.
    PLoS One; 2013 Feb; 8(4):e61326. PubMed ID: 23593463
    [Abstract] [Full Text] [Related]

  • 29. Genotype and haplotype analysis of ABCB1 at 1236, 2677 and 3435 among systemic sclerosis patients.
    Barańska M, Rychlik-Sych M, Skrętkowicz J, Dudarewicz M, Dziankowska-Bartkowiak B, Owczarek J, Waszczykowska E.
    Autoimmunity; 2017 Aug; 50(5):277-282. PubMed ID: 28534442
    [Abstract] [Full Text] [Related]

  • 30. Increased expression of IL12B mRNA transcribed from the risk haplotype for Crohn's disease is a risk factor for disease relapse in Japanese patients.
    Kakuta Y, Kimura T, Negoro K, Kuroha M, Shiga H, Endo K, Kinouchi Y, Shimosegawa T.
    J Gastroenterol; 2017 Dec; 52(12):1230-1239. PubMed ID: 28229296
    [Abstract] [Full Text] [Related]

  • 31. Association of TNFSF15 polymorphisms in Korean children with Crohn's disease.
    Lee YJ, Kim KM, Jang JY, Song K.
    Pediatr Int; 2015 Dec; 57(6):1149-53. PubMed ID: 25998826
    [Abstract] [Full Text] [Related]

  • 32. Association of genotypes and haplotypes of multi-drug transporter genes ABCB1 and ABCG2 with clinical response to imatinib mesylate in chronic myeloid leukemia patients.
    Au A, Aziz Baba A, Goh AS, Wahid Fadilah SA, Teh A, Rosline H, Ankathil R.
    Biomed Pharmacother; 2014 Apr; 68(3):343-9. PubMed ID: 24581936
    [Abstract] [Full Text] [Related]

  • 33. [Association of ABCB1 gene polymorphisms with aspirin resistance in patients with ischemic stroke].
    Wang ZY, Wang Y, Sui AH, Dong Y.
    Zhonghua Yi Xue Za Zhi; 2016 Dec 20; 96(47):3819-3824. PubMed ID: 28057098
    [Abstract] [Full Text] [Related]

  • 34. Two-Year Outcomes After Exclusive Enteral Nutrition Induction Are Superior to Corticosteroids in Pediatric Crohn's Disease Treated Early with Thiopurines.
    Grover Z, Lewindon P.
    Dig Dis Sci; 2015 Oct 20; 60(10):3069-74. PubMed ID: 26038093
    [Abstract] [Full Text] [Related]

  • 35. Association of ABCB1 gene polymorphisms and their haplotypes with response to antiepileptic drugs: a systematic review and meta-analysis.
    Haerian BS, Lim KS, Tan CT, Raymond AA, Mohamed Z.
    Pharmacogenomics; 2011 May 20; 12(5):713-25. PubMed ID: 21391884
    [Abstract] [Full Text] [Related]

  • 36. NELL1, NCF4, and FAM92B genes are not major susceptibility genes for Crohn's disease in Canadian children and young adults.
    Amre DK, Mack DR, Israel D, Krupoves A, Costea I, Lambrette P, Grimard G, Dong J, Levy E.
    Inflamm Bowel Dis; 2012 Mar 20; 18(3):529-35. PubMed ID: 21472827
    [Abstract] [Full Text] [Related]

  • 37. The role of ABC-transporter gene polymorphisms in chemotherapy induced immunosuppression, a retrospective study in childhood acute lymphoblastic leukaemia.
    Erdélyi DJ, Kámory E, Zalka A, Semsei AF, Csókay B, Andrikovics H, Tordai A, Borgulya G, Magyarosy E, Galántai I, Fekete G, Falus A, Szalai C, Kovács GT.
    Cell Immunol; 2006 Dec 20; 244(2):121-4. PubMed ID: 17434155
    [Abstract] [Full Text] [Related]

  • 38. Association between the C3435T polymorphism of the MDR1 gene and Crohn's disease.
    Lal S, Stempak JM, Law C, Elkadri AA, Steinhart AH, Silverberg MS.
    Inflamm Bowel Dis; 2006 Oct 20; 12(10):1006-7. PubMed ID: 17012973
    [No Abstract] [Full Text] [Related]

  • 39. Polymorphisms of tumor necrosis factor-alpha but not MDR1 influence response to medical therapy in pediatric-onset inflammatory bowel disease.
    Cucchiara S, Latiano A, Palmieri O, Canani RB, D'Incà R, Guariso G, Vieni G, De Venuto D, Riegler G, De'Angelis GL, Guagnozzi D, Bascietto C, Miele E, Valvano MR, Bossa F, Annese V, Italian Society of Pediatric Gastroenterology and Nutrition.
    J Pediatr Gastroenterol Nutr; 2007 Feb 20; 44(2):171-9. PubMed ID: 17255827
    [Abstract] [Full Text] [Related]

  • 40. The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.
    Schnitzler F, Friedrich M, Wolf C, Angelberger M, Diegelmann J, Olszak T, Beigel F, Tillack C, Stallhofer J, Göke B, Glas J, Lohse P, Brand S.
    PLoS One; 2014 Feb 20; 9(11):e108503. PubMed ID: 25365249
    [Abstract] [Full Text] [Related]

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