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Journal Abstract Search

173 related items for PubMed ID: 17295929

  • 1. Frequency and significance of the novel single nucleotide missense polymorphism Val109Asp in the human gene encoding omentin in Caucasian patients with type 2 diabetes mellitus or chronic inflammatory bowel diseases.
    Schäffler A, Zeitoun M, Wobser H, Buechler C, Aslanidis C, Herfarth H.
    Cardiovasc Diabetol; 2007 Feb 13; 6():3. PubMed ID: 17295929
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  • 2. Association of Omentin rs2274907 and FTO rs9939609 gene polymorphisms with insulin resistance in Iranian individuals with newly diagnosed type 2 diabetes.
    Khoshi A, Bajestani MK, Shakeri H, Goodarzi G, Azizi F.
    Lipids Health Dis; 2019 Jun 14; 18(1):142. PubMed ID: 31200723
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  • 3. Circulatory Omentin-1 levels but not genetic variants influence the pathophysiology of Type 2 diabetes.
    Rathwa N, Patel R, Pramanik Palit S, Jadeja SD, Narwaria M, Ramachandran AV, Begum R.
    Cytokine; 2019 Jul 14; 119():144-151. PubMed ID: 30909150
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  • 4. Val109Asp Polymorphism of the Omentin-1 Gene and Incidence of Knee Osteoarthritis in a Chinese Han Population: A Correlation Analysis.
    Chen R, Zhang Y, Xu H, Hu H, Chen M, Shuai Z.
    Drug Des Devel Ther; 2021 Jul 14; 15():5075-5086. PubMed ID: 34992344
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  • 5. The common polymorphism Val109Asp in the omentin gene is associated with daily energy intake in the Central-European population.
    Splichal Z, Bienertova-Vasku J, Novak J, Zlamal F, Tomandl J, Tomandlova M, Forejt M, Havlenova S, Jackowska A, Vasku A.
    Nutr Neurosci; 2015 Jan 14; 18(1):41-8. PubMed ID: 24552613
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  • 6. Omentin Val109Asp polymorphism and risk of coronary artery disease.
    Jamshidi J, Ghanbari M, Asnaashari A, Jafari N, Valizadeh GA.
    Asian Cardiovasc Thorac Ann; 2017 Mar 14; 25(3):199-203. PubMed ID: 28325076
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  • 9. Omentin serum levels and omentin gene Val109Asp polymorphism in patients with psoriasis.
    Turan H, Yaykasli KO, Soguktas H, Yaykasli E, Aliagaoglu C, Erdem T, Karkucak M, Kaya E, Ucgun T, Bahadir A.
    Int J Dermatol; 2014 May 14; 53(5):601-5. PubMed ID: 24321036
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  • 15. [The significance of IL-13 gene +2044G/A mutation in patients with inflammatory bowel disease].
    Waterman M, Karban A, Nesher S, Weiss B, Shamir R, Eliakim R.
    Harefuah; 2006 Nov 14; 145(11):789-92, 864. PubMed ID: 17183946
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  • 16. OCTN1 variant L503F is associated with familial and sporadic inflammatory bowel disease.
    Lin Z, Nelson L, Franke A, Poritz L, Li TY, Wu R, Wang Y, MacNeill C, Thomas NJ, Schreiber S, Koltun WA.
    J Crohns Colitis; 2010 Jun 14; 4(2):132-8. PubMed ID: 21122496
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  • 17. Decreased levels of serum omentin-1 in patients with inflammatory bowel disease.
    Yin J, Hou P, Wu Z, Nie Y.
    Med Sci Monit; 2015 Jan 10; 21():118-22. PubMed ID: 25576244
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  • 18. High-resolution melting curve analysis for high-throughput genotyping of NOD2/CARD15 mutations and distribution of these mutations in Slovenian inflammatory bowel diseases patients.
    Mitrovič M, Potočnik U.
    Dis Markers; 2011 Jan 10; 30(5):265-74. PubMed ID: 21734346
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