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PUBMED FOR HANDHELDS

Journal Abstract Search

257 related items for PubMed ID: 24937328

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  • 3. Exome Sequencing and Genotyping Identify a Rare Variant in NLRP7 Gene Associated With Ulcerative Colitis.
    Onoufriadis A, Stone K, Katsiamides A, Amar A, Omar Y, de Lange KM, Taylor K, Barrett JC, Pollok R, Hayee B, Mansfield JC, Sanderson JD, Simpson MA, Mathew CG, Prescott NJ.
    J Crohns Colitis; 2018 Feb 28; 12(3):321-326. PubMed ID: 29211899
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  • 4. Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
    Christodoulou K, Wiskin AE, Gibson J, Tapper W, Willis C, Afzal NA, Upstill-Goddard R, Holloway JW, Simpson MA, Beattie RM, Collins A, Ennis S.
    Gut; 2013 Jul 28; 62(7):977-84. PubMed ID: 22543157
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  • 5. Whole genome and exome sequencing of monozygotic twins discordant for Crohn's disease.
    Petersen BS, Spehlmann ME, Raedler A, Stade B, Thomsen I, Rabionet R, Rosenstiel P, Schreiber S, Franke A.
    BMC Genomics; 2014 Jul 05; 15(1):564. PubMed ID: 24996980
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  • 7. Role of the novel Th17 cytokine IL-17F in inflammatory bowel disease (IBD): upregulated colonic IL-17F expression in active Crohn's disease and analysis of the IL17F p.His161Arg polymorphism in IBD.
    Seiderer J, Elben I, Diegelmann J, Glas J, Stallhofer J, Tillack C, Pfennig S, Jürgens M, Schmechel S, Konrad A, Göke B, Ochsenkühn T, Müller-Myhsok B, Lohse P, Brand S.
    Inflamm Bowel Dis; 2008 Apr 05; 14(4):437-45. PubMed ID: 18088064
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  • 8. Association of T Helper 1 Cytokine Gene Single Nucleotide Polymorphisms with Ulcerative Colitis and Crohn's Disease.
    Ebrahimi Daryani N, Sadr M, Soltani S, Saghazadeh A, Moossavi S, Shahkarami S, Farhadi E, Rezaei N.
    Dig Dis; 2019 Apr 05; 37(1):21-32. PubMed ID: 30134230
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  • 9. Single nucleotide polymorphisms in C-type lectin genes, clustered in the IBD2 and IBD6 susceptibility loci, may play a role in the pathogenesis of inflammatory bowel diseases.
    Wolfkamp SC, Verstege MI, Vogels EW, Meisner S, Verseijden C, Stokkers PC, te Velde AA.
    Eur J Gastroenterol Hepatol; 2012 Aug 05; 24(8):965-70. PubMed ID: 22664939
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  • 10. Exome sequencing identifies novel compound heterozygous IFNA4 and IFNA10 mutations as a cause of impaired function in Crohn's disease patients.
    Xiao CX, Xiao JJ, Xu HZ, Wang HH, Chen X, Liu YS, Li P, Shi Y, Nie YZ, Li S, Wu KC, Liu ZJ, Ren JL, Guleng B.
    Sci Rep; 2015 May 22; 5():10514. PubMed ID: 26000985
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  • 12. Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.
    Yang SK, Hong M, Zhao W, Jung Y, Baek J, Tayebi N, Kim KM, Ye BD, Kim KJ, Park SH, Lee I, Lee EJ, Kim WH, Cheon JH, Kim YH, Jang BI, Kim HS, Choi JH, Koo JS, Lee JH, Jung SA, Lee YJ, Jang JY, Shin HD, Kang D, Youn HS, Liu J, Song K.
    Gut; 2014 Jan 22; 63(1):80-7. PubMed ID: 23850713
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  • 14. Low-Frequency IL23R Coding Variant Associated with Crohn's Disease Susceptibility in Japanese Subjects Identified by Personal Genomics Analysis.
    Onodera K, Arimura Y, Isshiki H, Kawakami K, Nagaishi K, Yamashita K, Yamamoto E, Niinuma T, Naishiro Y, Suzuki H, Imai K, Shinomura Y.
    PLoS One; 2015 Jan 22; 10(9):e0137801. PubMed ID: 26375822
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  • 19. Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families.
    Levine AP, Pontikos N, Schiff ER, Jostins L, Speed D, NIDDK Inflammatory Bowel Disease Genetics Consortium, Lovat LB, Barrett JC, Grasberger H, Plagnol V, Segal AW.
    Gastroenterology; 2016 Oct 22; 151(4):698-709. PubMed ID: 27373512
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