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PUBMED FOR HANDHELDS

Journal Abstract Search


97 related items for PubMed ID: 21987299

  • 41. Association between ABCB1 C3435T polymorphism and increased risk of cannabis dependence.
    Benyamina A, Bonhomme-Faivre L, Picard V, Sabbagh A, Richard D, Blecha L, Rahioui H, Karila L, Lukasiewicz M, Farinotti R, Picard V, Marill C, Reynaud M.
    Prog Neuropsychopharmacol Biol Psychiatry; 2009 Oct 01; 33(7):1270-4. PubMed ID: 19625010
    [Abstract] [Full Text] [Related]

  • 42. Contribution of OCTN variants within the IBD5 locus to pediatric onset Crohn's disease.
    Babusukumar U, Wang T, McGuire E, Broeckel U, Kugathasan S.
    Am J Gastroenterol; 2006 Jun 01; 101(6):1354-61. PubMed ID: 16771961
    [Abstract] [Full Text] [Related]

  • 43. Evidence for common genetic control in pathways of inflammation for Crohn's disease and psoriatic arthritis.
    Ho P, Bruce IN, Silman A, Symmons D, Newman B, Young H, Griffiths CE, John S, Worthington J, Barton A.
    Arthritis Rheum; 2005 Nov 01; 52(11):3596-602. PubMed ID: 16255050
    [Abstract] [Full Text] [Related]

  • 44. Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease.
    Baldassano RN, Bradfield JP, Monos DS, Kim CE, Glessner JT, Casalunovo T, Frackelton EC, Otieno FG, Kanterakis S, Shaner JL, Smith RM, Eckert AW, Robinson LJ, Onyiah CC, Abrams DJ, Chiavacci RM, Skraban R, Devoto M, Grant SF, Hakonarson H.
    Clin Gastroenterol Hepatol; 2007 Aug 01; 5(8):972-6. PubMed ID: 17618837
    [Abstract] [Full Text] [Related]

  • 45. Association of ATP-binding cassette transporter variants with the risk of Alzheimer's disease.
    Cascorbi I, Flüh C, Remmler C, Haenisch S, Faltraco F, Grumbt M, Peters M, Brenn A, Thal DR, Warzok RW, Vogelgesang S.
    Pharmacogenomics; 2013 Apr 01; 14(5):485-94. PubMed ID: 23556446
    [Abstract] [Full Text] [Related]

  • 46. Common ATP-binding cassette B1 variants are associated with increased digoxin serum concentration.
    Aarnoudse AJ, Dieleman JP, Visser LE, Arp PP, van der Heiden IP, van Schaik RH, Molokhia M, Hofman A, Uitterlinden AG, Stricker BH.
    Pharmacogenet Genomics; 2008 Apr 01; 18(4):299-305. PubMed ID: 18334914
    [Abstract] [Full Text] [Related]

  • 47. Association of ATG16L1 gene haplotype with inflammatory bowel disease in Indians.
    Pugazhendhi S, Baskaran K, Santhanam S, Ramakrishna BS.
    PLoS One; 2017 Apr 01; 12(5):e0178291. PubMed ID: 28542425
    [Abstract] [Full Text] [Related]

  • 48. Genetic susceptibility has a more important role in pediatric-onset Crohn's disease than in adult-onset Crohn's disease.
    de Ridder L, Weersma RK, Dijkstra G, van der Steege G, Benninga MA, Nolte IM, Taminiau JA, Hommes DW, Stokkers PC.
    Inflamm Bowel Dis; 2007 Sep 01; 13(9):1083-92. PubMed ID: 17476680
    [Abstract] [Full Text] [Related]

  • 49. Genes involved in the metabolism of poly-unsaturated fatty-acids (PUFA) and risk for Crohn's disease in children & young adults.
    Costea I, Mack DR, Israel D, Morgan K, Krupoves A, Seidman E, Deslandres C, Lambrette P, Grimard G, Levy E, Amre DK.
    PLoS One; 2010 Dec 20; 5(12):e15672. PubMed ID: 21187935
    [Abstract] [Full Text] [Related]

  • 50. Is there evidence to claim or deny association between variants of the multidrug resistance gene (MDR1 or ABCB1) and inflammatory bowel disease?
    Zintzaras E.
    Inflamm Bowel Dis; 2012 Mar 20; 18(3):562-72. PubMed ID: 21887726
    [Abstract] [Full Text] [Related]

  • 51. Runt-related transcription factor 3 is associated with ulcerative colitis and shows epistasis with solute carrier family 22, members 4 and 5.
    Weersma RK, Zhou L, Nolte IM, van der Steege G, van Dullemen HM, Oosterom E, Bok L, Peppelenbosch MP, Faber KN, Kleibeuker JH, Dijkstra G.
    Inflamm Bowel Dis; 2008 Dec 20; 14(12):1615-22. PubMed ID: 18668679
    [Abstract] [Full Text] [Related]

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  • 54. Clinical relevance of a pharmacogenetic approach using multiple candidate genes to predict response and resistance to imatinib therapy in chronic myeloid leukemia.
    Kim DH, Sriharsha L, Xu W, Kamel-Reid S, Liu X, Siminovitch K, Messner HA, Lipton JH.
    Clin Cancer Res; 2009 Jul 15; 15(14):4750-8. PubMed ID: 19584153
    [Abstract] [Full Text] [Related]

  • 55. Variants of OCTN1-2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis.
    Palmieri O, Latiano A, Valvano R, D'Incà R, Vecchi M, Sturniolo GC, Saibeni S, Peyvandi F, Bossa F, Zagaria C, Andriulli A, Devoto M, Annese V.
    Aliment Pharmacol Ther; 2006 Feb 15; 23(4):497-506. PubMed ID: 16441470
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  • 58. The influence of polymorphisms in the drug transporter, ABCB1 on the toxicity of glucocorticoids in Saudi children with acute lymphoblastic leukaemia.
    ElFayoumi RI, Hagras MM, Abozenadaha A, Gari M, Abosoudah I, Shinawi T, Mirza T, Bawazir W.
    Pharmacol Rep; 2019 Feb 15; 71(1):90-95. PubMed ID: 30508724
    [Abstract] [Full Text] [Related]

  • 59. ABCB1 gene variants and antidepressant treatment outcome: A meta-analysis.
    Breitenstein B, Brückl TM, Ising M, Müller-Myhsok B, Holsboer F, Czamara D.
    Am J Med Genet B Neuropsychiatr Genet; 2015 Jun 15; 168B(4):274-83. PubMed ID: 25847751
    [Abstract] [Full Text] [Related]

  • 60. Genetic variation in the farnesoid X-receptor predicts Crohn's disease severity in female patients.
    Wilson A, Wang Q, Almousa AA, Jansen LE, Choi YH, Schwarz UI, Kim RB.
    Sci Rep; 2020 Jul 16; 10(1):11725. PubMed ID: 32678214
    [Abstract] [Full Text] [Related]


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