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181 related items for PubMed ID: 29987165

  • 1. Fine mapping MHC associations in Graves' disease and its clinical subtypes in Han Chinese.
    Chu X, Yang M, Song ZJ, Dong Y, Li C, Shen M, Zhu YQ, Song HD, Chen SJ, Chen Z, Huang W.
    J Med Genet; 2018 Oct; 55(10):685-692. PubMed ID: 29987165
    [Abstract] [Full Text] [Related]

  • 2. Fine mapping the MHC region identified four independent variants modifying susceptibility to chronic hepatitis B in Han Chinese.
    Zhu M, Dai J, Wang C, Wang Y, Qin N, Ma H, Song C, Zhai X, Yang Y, Liu J, Liu L, Li S, Liu J, Yang H, Zhu F, Shi Y, Shen H, Jin G, Zhou W, Hu Z.
    Hum Mol Genet; 2016 Mar 15; 25(6):1225-32. PubMed ID: 26769676
    [Abstract] [Full Text] [Related]

  • 3. Fine-mapping the MHC region in Asian populations identified novel variants modifying susceptibility to lung cancer.
    Qin N, Wang C, Zhu M, Lu Q, Ma Z, Huang M, Dai J, Ma H, Jin G, Hu Z, Shen H.
    Lung Cancer; 2017 Oct 15; 112():169-175. PubMed ID: 29191591
    [Abstract] [Full Text] [Related]

  • 4. Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
    Nakabayashi K, Tajima A, Yamamoto K, Takahashi A, Hata K, Takashima Y, Koyanagi M, Nakaoka H, Akamizu T, Ishikawa N, Kubota S, Maeda S, Tsunoda T, Kubo M, Kamatani N, Nakamura Y, Sasazuki T, Shirasawa S.
    J Hum Genet; 2011 Nov 15; 56(11):772-8. PubMed ID: 21900946
    [Abstract] [Full Text] [Related]

  • 5. Fine mapping of the MHC region identifies major independent variants associated with Han Chinese primary biliary cholangitis.
    Wang C, Zheng X, Tang R, Han C, Jiang Y, Wu J, Shao Y, Gao Y, Yu J, Hu Z, Zang Z, Zhao Y, Dai N, Liu L, Wu X, Nie J, Jiang B, Lin M, Li L, Wei Y, Li Y, Gong Y, Dai Y, Wang L, Ding N, Xu P, Chen S, Jiang P, Wang L, Qiu F, Wu Q, Zhang M, Jawed R, Chen R, Zhang Y, Shi X, Zhu Z, Pei H, Huang L, Tian Y, Zhang K, Qiu H, Zhao W, Gershwin ME, Chen W, Seldin MF, Liu X, Ma X, Sun L.
    J Autoimmun; 2020 Feb 15; 107():102372. PubMed ID: 31810856
    [Abstract] [Full Text] [Related]

  • 6. The amino acid variants in HLA II molecules explain the major association with adult-onset Still's disease in the Han Chinese population.
    Teng JL, Chen X, Chen J, Zeng T, He L, Li M, Luo CN, Liu S, Ding TT, Yimaiti K, Li X, Ding Y, Cheng XB, Zhou J, Ye JN, Ji J, Su YT, Shi H, Sun Y, Gao C, Hu QY, Chi HH, Yuan X, Zhou ZC, Wang D, Wang K, Feng D, Li C, Sun Y, Niu Y, Xu X, Chen LJ, Xu J, Wu LJ, Zhou Z, Pan D, Niu H, Yang CD, Yongyong Shi, Li Z, Liu HL.
    J Autoimmun; 2021 Jan 15; 116():102562. PubMed ID: 33168359
    [Abstract] [Full Text] [Related]

  • 7. Risk for ACPA-positive rheumatoid arthritis is driven by shared HLA amino acid polymorphisms in Asian and European populations.
    Okada Y, Kim K, Han B, Pillai NE, Ong RT, Saw WY, Luo M, Jiang L, Yin J, Bang SY, Lee HS, Brown MA, Bae SC, Xu H, Teo YY, de Bakker PI, Raychaudhuri S.
    Hum Mol Genet; 2014 Dec 20; 23(25):6916-26. PubMed ID: 25070946
    [Abstract] [Full Text] [Related]

  • 8. Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis.
    Raychaudhuri S, Sandor C, Stahl EA, Freudenberg J, Lee HS, Jia X, Alfredsson L, Padyukov L, Klareskog L, Worthington J, Siminovitch KA, Bae SC, Plenge RM, Gregersen PK, de Bakker PI.
    Nat Genet; 2012 Jan 29; 44(3):291-6. PubMed ID: 22286218
    [Abstract] [Full Text] [Related]

  • 9. Fine-mapping analysis of the MHC region for vitiligo based on a new Han-MHC reference panel.
    Yang C, Wu J, Zhang X, Wen L, Sun J, Cheng Y, Tang X, Liang B, Chen G, Zhou F, Cui Y, Zhang A, Zhang X, Zheng X, Yang S, Sun L.
    Gene; 2018 Mar 30; 648():76-81. PubMed ID: 29355683
    [Abstract] [Full Text] [Related]

  • 10. The HLA-DRβ1 amino acid positions 11-13-26 explain the majority of SLE-MHC associations.
    Kim K, Bang SY, Lee HS, Okada Y, Han B, Saw WY, Teo YY, Bae SC.
    Nat Commun; 2014 Dec 23; 5():5902. PubMed ID: 25533202
    [Abstract] [Full Text] [Related]

  • 11. Refined association of TSH receptor susceptibility locus to Graves' disease in the Chinese Han population.
    Liu BL, Yang SY, Liu W, Xue LQ, Chen X, Pan CM, Gu ZH, Zhan M, Zhang XM, Liang J, Gao GQ, Du WH, Yuan GY, Ying R, Zhao SX, Song HD.
    Eur J Endocrinol; 2014 Jan 23; 170(1):109-19. PubMed ID: 24144966
    [Abstract] [Full Text] [Related]

  • 12. Genetic heterogeneity of susceptibility gene in different ethnic populations: refining association study of PTPN22 for Graves' disease in a Chinese Han population.
    Xue L, Pan C, Gu Z, Zhao S, Han B, Liu W, Yang S, Yu S, Sun Y, Liang J, Gao G, Zhang X, Yuan G, Li C, Du W, Chen G, Chen J, Song H.
    PLoS One; 2013 Jan 23; 8(12):e84514. PubMed ID: 24386393
    [Abstract] [Full Text] [Related]

  • 13. Histocompatibility leucocyte antigens and closely linked immunomodulatory genes in autoimmune thyroid disease.
    Hunt PJ, Marshall SE, Weetman AP, Bunce M, Bell JI, Wass JA, Welsh KI.
    Clin Endocrinol (Oxf); 2001 Oct 23; 55(4):491-9. PubMed ID: 11678832
    [Abstract] [Full Text] [Related]

  • 14. TNFSF15 Polymorphisms are Associated with Graves' Disease and Graves' Ophthalmopathy in a Han Chinese Population.
    Zhang M, Liu S, Xu J, Lv S, Fan Y, Zhang Y, Zhang Y, Wu Y, Su Y, Yu H, Song S, He J, Li H.
    Curr Eye Res; 2020 Jul 23; 45(7):888-895. PubMed ID: 31869260
    [Abstract] [Full Text] [Related]

  • 15. Trans-Ethnic Fine-Mapping of the Major Histocompatibility Complex Region Linked to Parkinson's Disease.
    Naito T, Satake W, Ogawa K, Suzuki K, Hirata J, Foo JN, Tan EK, Toda T, Okada Y.
    Mov Disord; 2021 Aug 23; 36(8):1805-1814. PubMed ID: 33973677
    [Abstract] [Full Text] [Related]

  • 16. Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles.
    Chen PL, Fann CS, Chu CC, Chang CC, Chang SW, Hsieh HY, Lin M, Yang WS, Chang TC.
    PLoS One; 2011 Jan 28; 6(1):e16635. PubMed ID: 21307958
    [Abstract] [Full Text] [Related]

  • 17. Polymorphisms in the ADRB2 gene and Graves disease: a case-control study and a meta-analysis of available evidence.
    Chu X, Dong Y, Shen M, Sun L, Dong C, Wang Y, Wang B, Zhang K, Hua Q, Xu S, Huang W.
    BMC Med Genet; 2009 Mar 13; 10():26. PubMed ID: 19284637
    [Abstract] [Full Text] [Related]

  • 18. Predisposition to Graves' disease and Graves' ophthalmopathy by genetic variants of IL2RA.
    Du J, Wang X, Tan G, Wei W, Zhou F, Liang Z, Li H, Yu H.
    J Mol Med (Berl); 2021 Oct 13; 99(10):1487-1495. PubMed ID: 34287665
    [Abstract] [Full Text] [Related]

  • 19. Dense mapping of IL2RA shows no association with Graves' disease in Chinese Han population.
    Song ZY, Liu W, Xue LQ, Pan CM, Wang HN, Gu ZH, Yang SY, Cao HM, Zuo CL, Zhang XN, Jiang H, Liu BL, Bi YX, Zhang XM, Zhao SX, Song HD.
    Clin Endocrinol (Oxf); 2013 Aug 13; 79(2):267-74. PubMed ID: 23170961
    [Abstract] [Full Text] [Related]

  • 20. Fine mapping major histocompatibility complex associations in psoriasis and its clinical subtypes.
    Okada Y, Han B, Tsoi LC, Stuart PE, Ellinghaus E, Tejasvi T, Chandran V, Pellett F, Pollock R, Bowcock AM, Krueger GG, Weichenthal M, Voorhees JJ, Rahman P, Gregersen PK, Franke A, Nair RP, Abecasis GR, Gladman DD, Elder JT, de Bakker PI, Raychaudhuri S.
    Am J Hum Genet; 2014 Aug 07; 95(2):162-72. PubMed ID: 25087609
    [Abstract] [Full Text] [Related]

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