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Pubmed for Handhelds

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Journal Abstract Search

129 related items for PubMed ID: 27511505

  • 21. Association of MMP-9 gene polymorphisms with Behçet's disease risk.
    Naouali A, Kaabachi W, Tizaoui K, Amor AB, Hamzaoui A, Hamzaoui K.
    Immunol Lett; 2015 Mar; 164(1):18-24. PubMed ID: 25639450
    [Abstract] [Full Text] [Related]

  • 22. Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haplotype and in silico analysis.
    Azani A, Hosseinzadeh A, Azadkhah R, Zonouzi AAP, Zonouzi AP, Aftabi Y, Khani H, Heidary L, Danaii S, Bargahi N, Pouladi N, Hosseini SM.
    Eur J Obstet Gynecol Reprod Biol; 2017 Aug; 215():93-100. PubMed ID: 28605668
    [Abstract] [Full Text] [Related]

  • 23. Posterior tibial tendinopathy associated with matrix metalloproteinase 13 promoter genotype and haplotype.
    de Araujo Munhoz FB, Baroneza JE, Godoy-Santos A, Fernandes TD, Branco FP, Alle LF, de Souza RL, Dos Santos MC.
    J Gene Med; 2016 Nov; 18(11-12):325-330. PubMed ID: 27886420
    [Abstract] [Full Text] [Related]

  • 24. Association of PTEN gene polymorphisms with liver cancer risk.
    Li HG, Liu FF, Zhu HQ, Zhou X, Lu J, Chang H, Hu JH.
    Int J Clin Exp Pathol; 2015 Nov; 8(11):15198-203. PubMed ID: 26823866
    [Abstract] [Full Text] [Related]

  • 25. Analysis of cytotoxic T lymphocyte antigen-4 (CTLA-4) promoter -318C/T and +49A/G gene polymorphisms in Turkish patients with familial Mediterranean fever.
    Gunesacar R, Erken E, Dinkci S.
    Cell Biochem Biophys; 2013 Mar; 65(2):181-6. PubMed ID: 22923220
    [Abstract] [Full Text] [Related]

  • 26. Single nucleotide polymorphisms in the FOXP3 gene are associated with increased risk of relapsing-remitting multiple sclerosis.
    Eftekharian MM, Sayad A, Omrani MD, Ghannad MS, Noroozi R, Mazdeh M, Mirfakhraie R, Movafagh A, Roshanaei G, Azimi T, Inoko H, Taheri M.
    Hum Antibodies; 2016 Mar; 24(3-4):85-90. PubMed ID: 27792007
    [Abstract] [Full Text] [Related]

  • 27. Association of adiponectin (AdipoQ) and sulphonylurea receptor (ABCC8) gene polymorphisms with Type 2 Diabetes in North Indian population of Punjab.
    Matharoo K, Arora P, Bhanwer AJ.
    Gene; 2013 Sep 15; 527(1):228-34. PubMed ID: 23764562
    [Abstract] [Full Text] [Related]

  • 28. No Association of Polymorphisms in the Genes Encoding Interleukin-6 and Interleukin-6 Receptor Subunit Alpha with the Risk of Keloids in Polish Patients.
    Dmytrzak A, Lewandowska K, Boroń A, Łoniewska B, Grzesch N, Brodkiewicz A, Clark JSC, Ciechanowicz A, Kostrzewa-Nowak D.
    Int J Mol Sci; 2024 May 13; 25(10):. PubMed ID: 38791322
    [Abstract] [Full Text] [Related]

  • 29. Osteoporotic fractures are associated with an 86-base pair repeat polymorphism in the interleukin-1--receptor antagonist gene but not with polymorphisms in the interleukin-1beta gene.
    Langdahl BL, Løkke E, Carstens M, Stenkjaer LL, Eriksen EF.
    J Bone Miner Res; 2000 Mar 13; 15(3):402-14. PubMed ID: 10750554
    [Abstract] [Full Text] [Related]

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  • 31. Interleukin-10 gene promoter polymorphisms and the risk of nasopharyngeal carcinoma.
    Wei YS, Kuang XH, Zhu YH, Liang WB, Yang ZH, Tai SH, Zhao Y, Zhang L.
    Tissue Antigens; 2007 Jul 13; 70(1):12-7. PubMed ID: 17559576
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  • 33. [Association of single nucleotide polymorphisms in VEGF gene with the risk of endometriosis and adenomyosis].
    Liu Q, Li Y, Zhao J, Zhou RM, Wang N, Sun DL, Duan YN, Kang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr 13; 26(2):165-9. PubMed ID: 19350508
    [Abstract] [Full Text] [Related]

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  • 35. Haplotypes defined by promoter and intron 1 polymorphisms of the COLIA1 gene regulate bone mineral density in women.
    Stewart TL, Jin H, McGuigan FE, Albagha OM, Garcia-Giralt N, Bassiti A, Grinberg D, Balcells S, Reid DM, Ralston SH.
    J Clin Endocrinol Metab; 2006 Sep 13; 91(9):3575-83. PubMed ID: 16804049
    [Abstract] [Full Text] [Related]

  • 36. [Preliminary study on the association of chemokine RANTES gene polymorphisms with HIV-1 infection in Chinese Han population].
    Liu XL, Wang FS, Jin L, Liu MX, Xu DZ.
    Zhonghua Liu Xing Bing Xue Za Zhi; 2003 Nov 13; 24(11):971-5. PubMed ID: 14687494
    [Abstract] [Full Text] [Related]

  • 37. COL1A1, ESR1, VDR and TGFB1 polymorphisms and haplotypes in relation to BMD in Spanish postmenopausal women.
    Bustamante M, Nogués X, Enjuanes A, Elosua R, García-Giralt N, Pérez-Edo L, Cáceres E, Carreras R, Mellibovsky L, Balcells S, Díez-Pérez A, Grinberg D.
    Osteoporos Int; 2007 Feb 13; 18(2):235-43. PubMed ID: 17021946
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  • 39. Associations of collagen type 1 α1 gene polymorphisms and musculoskeletal soft tissue injuries: a meta-analysis with trial sequential analysis.
    Guo R, Gao S, Shaxika N, Aizezi A, Wang H, Feng X, Wang Z.
    Aging (Albany NY); 2024 May 22; 16(10):8866-8879. PubMed ID: 38787354
    [Abstract] [Full Text] [Related]

  • 40. Susceptibility to osteoporotic fracture is determined by allelic variation at the Sp1 site, rather than other polymorphic sites at the COL1A1 locus.
    McGuigan FE, Reid DM, Ralston SH.
    Osteoporos Int; 2000 May 22; 11(4):338-43. PubMed ID: 10928224
    [Abstract] [Full Text] [Related]

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