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Journal Abstract Search
151 related items for PubMed ID: 21633323
1. Variation in the glucocorticoid receptor gene (NR3C1) may be associated with corticosteroid dependency and resistance in children with Crohn's disease. Krupoves A, Mack D, Deslandres C, Seidman E, Amre DK. Pharmacogenet Genomics; 2011 Aug; 21(8):454-60. PubMed ID: 21633323 [Abstract] [Full Text] [Related]
2. Associations between variants in the ABCB1 (MDR1) gene and corticosteroid dependence in children with Crohn's disease. Krupoves A, Mack D, Seidman E, Deslandres C, Amre D. Inflamm Bowel Dis; 2011 Nov; 17(11):2308-17. PubMed ID: 21987299 [Abstract] [Full Text] [Related]
3. Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children. Amre DK, Mack DR, Morgan K, Fujiwara M, Israel D, Deslandres C, Seidman EG, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Grimard G, Levy E. Am J Gastroenterol; 2009 Nov; 104(11):2824-8. PubMed ID: 19623168 [Abstract] [Full Text] [Related]
4. Interleukin 10 (IL-10) gene variants and susceptibility for paediatric onset Crohn's disease. Amre DK, Mack DR, Morgan K, Israel D, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Grimard G, Deslandres C, Levy E, Seidman EG. Aliment Pharmacol Ther; 2009 May 01; 29(9):1025-31. PubMed ID: 19210299 [Abstract] [Full Text] [Related]
5. Glucocorticoid receptor polymorphisms and haplotypes associated with chronic fatigue syndrome. Rajeevan MS, Smith AK, Dimulescu I, Unger ER, Vernon SD, Heim C, Reeves WC. Genes Brain Behav; 2007 Mar 01; 6(2):167-76. PubMed ID: 16740143 [Abstract] [Full Text] [Related]
6. 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 01; 103(3):615-20. PubMed ID: 18047539 [Abstract] [Full Text] [Related]
7. The N363S and I559N single nucleotide polymorphisms of the h-GR/NR3C1 gene in patients with bronchial asthma. Panek M, Pietras T, Antczak A, Fabijan A, Przemęcka M, Górski P, Kuna P, Szemraj J. Int J Mol Med; 2012 Jul 01; 30(1):142-50. PubMed ID: 22469783 [Abstract] [Full Text] [Related]
8. Genetic variations of the NR3C1 gene in children with sporadic nephrotic syndrome. Ye J, Yu Z, Ding J, Chen Y, Huang J, Yao Y, Xiao H, Yang J, Shen Y, Meng Q. Biochem Biophys Res Commun; 2006 Sep 22; 348(2):507-13. PubMed ID: 16890204 [Abstract] [Full Text] [Related]
9. 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 22; 101(6):1354-61. PubMed ID: 16771961 [Abstract] [Full Text] [Related]
10. 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 22; 104(7):1723-33. PubMed ID: 19455129 [Abstract] [Full Text] [Related]
11. Sequence variants in Toll-like receptor gene cluster (TLR6-TLR1-TLR10) and prostate cancer risk. Sun J, Wiklund F, Zheng SL, Chang B, Bälter K, Li L, Johansson JE, Li G, Adami HO, Liu W, Tolin A, Turner AR, Meyers DA, Isaacs WB, Xu J, Grönberg H. J Natl Cancer Inst; 2005 Apr 06; 97(7):525-32. PubMed ID: 15812078 [Abstract] [Full Text] [Related]
12. KCNN4 gene variant is associated with ileal Crohn's Disease in the Australian and New Zealand population. Simms LA, Doecke JD, Roberts RL, Fowler EV, Zhao ZZ, McGuckin MA, Huang N, Hayward NK, Webb PM, Whiteman DC, Cavanaugh JA, McCallum R, Florin TH, Barclay ML, Gearry RB, Merriman TR, Montgomery GW, Radford-Smith GL. Am J Gastroenterol; 2010 Oct 06; 105(10):2209-17. PubMed ID: 20407432 [Abstract] [Full Text] [Related]
13. Glucocorticoid receptor gene haplotype predicts increased risk of hospital admission for depressive disorders in the Helsinki birth cohort study. Lahti J, Räikkönen K, Bruce S, Heinonen K, Pesonen AK, Rautanen A, Wahlbeck K, Kere J, Kajantie E, Eriksson JG. J Psychiatr Res; 2011 Sep 06; 45(9):1160-4. PubMed ID: 21477816 [Abstract] [Full Text] [Related]
14. Prior bowel resections, perianal disease, and a high initial Crohn's disease activity index are associated with corticosteroid resistance in active Crohn's disease. Gelbmann CM, Rogler G, Gross V, Gierend M, Bregenzer N, Andus T, Schölmerich J. Am J Gastroenterol; 2002 Jun 06; 97(6):1438-45. PubMed ID: 12094862 [Abstract] [Full Text] [Related]
15. Evidence for the involvement of the glucocorticoid receptor gene in bipolar disorder in an isolated northern Swedish population. Ceulemans S, De Zutter S, Heyrman L, Norrback KF, Nordin A, Nilsson LG, Adolfsson R, Del-Favero J, Claes S. Bipolar Disord; 2011 Jun 06; 13(7-8):614-23. PubMed ID: 22085474 [Abstract] [Full Text] [Related]
16. Glucocorticoid resistance in Crohn's disease and ulcerative colitis: an association study investigating GR and FKBP5 gene polymorphisms. Maltese P, Palma L, Sfara C, de Rocco P, Latiano A, Palmieri O, Corritore G, Annese V, Magnani M. Pharmacogenomics J; 2012 Oct 06; 12(5):432-8. PubMed ID: 21788965 [Abstract] [Full Text] [Related]
17. Polymorphisms of the TNF gene and the TNF receptor superfamily member 1B gene are associated with susceptibility to ulcerative colitis and Crohn's disease, respectively. Sashio H, Tamura K, Ito R, Yamamoto Y, Bamba H, Kosaka T, Fukui S, Sawada K, Fukuda Y, Tamura K, Satomi M, Shimoyama T, Furuyama J. Immunogenetics; 2002 Mar 06; 53(12):1020-7. PubMed ID: 11904678 [Abstract] [Full Text] [Related]
18. Tumor necrosis factor receptor gene polymorphisms in Crohn's disease: association with clinical phenotypes. Waschke KA, Villani AC, Vermeire S, Dufresne L, Chen TC, Bitton A, Cohen A, Thomson AB, Wild GE. Am J Gastroenterol; 2005 May 06; 100(5):1126-33. PubMed ID: 15842589 [Abstract] [Full Text] [Related]
19. The impact of catechol-O-methyltransferase SNPs and haplotypes on treatment response phenotypes in major depressive disorder: a case-control association study. Kocabas NA, Faghel C, Barreto M, Kasper S, Linotte S, Mendlewicz J, Noro M, Oswald P, Souery D, Zohar J, Massat I. Int Clin Psychopharmacol; 2010 Jul 06; 25(4):218-27. PubMed ID: 20531207 [Abstract] [Full Text] [Related]
20. Sex specific associations between common glucocorticoid receptor gene variants and hypothalamus-pituitary-adrenal axis responses to psychosocial stress. Kumsta R, Entringer S, Koper JW, van Rossum EF, Hellhammer DH, Wüst S. Biol Psychiatry; 2007 Oct 15; 62(8):863-9. PubMed ID: 17716631 [Abstract] [Full Text] [Related] Page: [Next] [New Search]