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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

171 related items for PubMed ID: 34320993

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  • 2. NR3C1 gene polymorphisms are associated with high-altitude pulmonary edema in Han Chinese.
    Yang Y, Du H, Li Y, Guan W, Tang F, Ga Q, Ge RL.
    J Physiol Anthropol; 2019 Apr 18; 38(1):4. PubMed ID: 30999951
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  • 3. The association of heat shock protein genetic polymorphisms with age-related hearing impairment in Taiwan.
    Chang NC, Yang HL, Dai CY, Lin WY, Hsieh MH, Chien CY, Ho KY.
    J Otolaryngol Head Neck Surg; 2021 Apr 29; 50(1):31. PubMed ID: 33926545
    [Abstract] [Full Text] [Related]

  • 4. Association of GRM7 variants with different phenotype patterns of age-related hearing impairment in an elderly male Han Chinese population.
    Luo H, Yang T, Jin X, Pang X, Li J, Chai Y, Li L, Zhang Y, Zhang L, Zhang Z, Wu W, Zhang Q, Hu X, Sun J, Jiang X, Fan Z, Huang Z, Wu H.
    PLoS One; 2013 Apr 29; 8(10):e77153. PubMed ID: 24146964
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  • 7. Polymorphisms in NR3C1 gene associated with risk of metabolic syndrome in a Chinese population.
    Yan YX, Dong J, Zhang J, Liu F, Wang W, Zhang L, He Y.
    Endocrine; 2014 Dec 29; 47(3):740-8. PubMed ID: 25104270
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  • 8. Association of cadherin23 single nucleotide polymorphism with age-related hearing impairment in Han Chinese.
    Hwang JH, Liu KS, Wu CC, Liu TC.
    Otolaryngol Head Neck Surg; 2012 Sep 29; 147(3):531-4. PubMed ID: 22581638
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  • 10. The grainyhead-like 2 gene (GRHL2) single nucleotide polymorphism is not associated with age-related hearing impairment in Han Chinese.
    Lin YH, Wu CC, Hsu CJ, Hwang JH, Liu TC.
    Laryngoscope; 2011 Jun 29; 121(6):1303-7. PubMed ID: 21557239
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  • 11. NR3C1 gene polymorphism for genetic susceptibility to infantile spasms in a Chinese population.
    Yang G, Zou LP, He B, Ding YX, Wang J, Shi XY, Sun YH, Jia FY.
    Life Sci; 2012 Jul 26; 91(1-2):37-43. PubMed ID: 22728713
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  • 12. Hearing impairment risk and interaction of folate metabolism related gene polymorphisms in an aging study.
    Uchida Y, Sugiura S, Ando F, Nakashima T, Shimokata H.
    BMC Med Genet; 2011 Mar 07; 12():35. PubMed ID: 21385350
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  • 13. Polymorphisms in the Glucocorticoid Receptor Gene and Associations with Glucocorticoid-Induced Avascular Osteonecrosis of the Femoral Head.
    Zhao Z, Xue Y, Hong D, Zhang H, Hu Z, Fan S, Chen H.
    Genet Test Mol Biomarkers; 2017 May 07; 21(5):322-327. PubMed ID: 28346829
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  • 14. Sequencing the exons of human glucocorticoid receptor (NR3C1) gene in Han Chinese with high-altitude pulmonary edema.
    Du H, Zhao J, Su Z, Liu Y, Yang Y.
    J Physiol Anthropol; 2018 Mar 27; 37(1):7. PubMed ID: 29587872
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  • 16. Association of polymorphisms in grainyhead-like-2 gene with the susceptibility to age-related hearing loss: A systematic review and meta-analysis.
    Han B, Yang X, Li Y, Hosseini DK, Tu Y, Dong Y, He Z, Yuan J, Cai H, Zhang K, Zhang X, Zhou T, Sun H.
    Medicine (Baltimore); 2019 Jun 27; 98(25):e16128. PubMed ID: 31232964
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  • 18. Association between allelic variants of the human glucocorticoid receptor gene and autoimmune diseases: A systematic review and meta-analysis.
    Herrera C, Marcos M, Carbonell C, Mirón-Canelo JA, Espinosa G, Cervera R, Chamorro AJ.
    Autoimmun Rev; 2018 May 27; 17(5):449-456. PubMed ID: 29526633
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  • 19. Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment.
    Van Eyken E, Van Camp G, Fransen E, Topsakal V, Hendrickx JJ, Demeester K, Van de Heyning P, Mäki-Torkko E, Hannula S, Sorri M, Jensen M, Parving A, Bille M, Baur M, Pfister M, Bonaconsa A, Mazzoli M, Orzan E, Espeso A, Stephens D, Verbruggen K, Huyghe J, Dhooge I, Huygen P, Kremer H, Cremers CW, Kunst S, Manninen M, Pyykkö I, Lacava A, Steffens M, Wienker TF, Van Laer L.
    J Med Genet; 2007 Sep 27; 44(9):570-8. PubMed ID: 17513527
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  • 20. Association of NR3C1/Glucocorticoid Receptor gene SNP with azoospermia in Japanese men.
    Chihara M, Yoshihara K, Ishiguro T, Adachi S, Okada H, Kashima K, Sato T, Tanaka A, Tanaka K, Enomoto T.
    J Obstet Gynaecol Res; 2016 Jan 27; 42(1):59-66. PubMed ID: 26556219
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